2013年11月26日星期二

Naproxen Properties

Naproxen (naprosyn) is one of the nonsteroidal anti-inflammatory drugs (NSAIDs) used to treat certain types of arthritis. Naproxen tablets were approved by the FDA in 1976. On January 11, 1994, the FDA approved naproxen in a nonprescription form.Naproxen  is commonly used for relief of a wide variety of pain, fever, inflammations, and stiffness.

Naproxen is one kind of white to light yellow crystal powder and belongs to the classes of Carboxylic Acids (Chiral); Chiral Building Blocks; for Resolution of Bases; Optical Resolution; Synthetic Organic Chemistry; Intermediates & Fine Chemicals; Pharmaceuticals. The IUPAC name is (2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid. In addition, the Classification Code is Analgesic; Analgesics; Analgesics, Non-Narcotic; Anti-Inflammatory Agents; Anti-inflammatory; Anti-inflammatory agents, non-steroidal; Antipyretic; Antirheumatic Agents; Cyclooxygenase inhibitors; Drug / Therapeutic Agent; Enzyme Inhibitors; Gout suppressants; Human Data; Mutation data; Peripheral Nervous System Agents; Reproductive Effect; Sensory System Agents. Naproxen can soluble in organic solvents.




Name:Naproxene

EINECS:244-838-7

Molecular Formula:C14H14O3

CAS Registry Number:22204-53-1

Synonyms:(S)-(+)-2-(6-Methoxy-2-naphthyl)propionic acid; (+)-6-Methoxy-alpha-methyl-2-naphthaleneacetic acid; Naproxen
InChI:InChI=1/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)/t9-/m0/s1

Appearance:white powder

Molecular Weight:230.26

Density:1.197g/cm3

Boiling Point:403.9°Cat760mmHg

Melting Point:153-154℃

Flash Point:154.5°C

Storage Temperature:Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage.

Refractive index:67.5 ° (C=1, CHCl3)

Solubility:practically insoluble at low and soluble at high

Stability:No data.

Usage:An anti-inflammatory, analgesic, antipyretic. A non-steroidal anti-inflammatory

4-Bromofluorobenzene Properties

4-Bromofluorobenzene,  its cas register number is 460-00-4. It also can be called 1-bromo-4-fluoro-benzen; 1-Fluoro-4-bromobenzene; 4-Bromfluorbenzol; 4-Fluorbrombenzol; 4-Fluoro-1-bromobenzene; 4-Fluorophenyl bromide; 4-fluorophenylbromide; Benzene, 1-bromo-4-fluoro. 4-Bromofluorobenzene(CAS NO.460-00-4) is a clear colorless liquid and belongs to the Organic chemicals and Derivatives.  4-Bromofluorobenzene is used in pharmaceutical, pesticide synthesis.


Name:4-Bromofluorobenzene

EINECS:207-300-2

Molecular Formula:C6H4BrF

CAS Registry Number:460-00-4

InChI:InChI=1/C6H4BrF/c7-5-1-3-6(8)4-2-5/h1-4H

HS Code:29036990

Appearance:White to pale yellow crystalline powder

Molecular Weight:175

Density:1.593

Boiling Point:151-153℃

Melting Point:-16℃

Flash Point:53℃

Storage Temperature:0-6°C

Refractive index:1.526-1.528

Solubility:Insoluble

Stability:Stable under normal temperatures and pressures.

Chemical Properties: clear colorless liquid

General Description: Colorless liquid.

Air & Water Reactions: Highly flammable. Insoluble in water.

Reactivity Profile: Simple aromatic halogenated organic compounds, such as 4-Bromofluorobenzene, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

Health Hazard: Acute/Chronic Hazards: Irritant.


When you are using this chemical, please be cautious about it as the following:

1. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;

2. Wear suitable protective clothing, gloves and eye/face protection;

3. Keep away from sources of ignition - No smoking;

4. In case of accident or if you feel unwell, seek medical advice immediately (show label where possible);

5. Wear suitable protective clothing and gloves;

6. Keep container tightly closed.

2013年11月25日星期一

Arginine hydrochloride Properties

Arginine hydrochloride contains not less than 98.5 per cent and not more than the equivalent of 101.0 per cent of the hydrochloride of (S)-2-amino-5-guanidinopentanoic acid,calculated with reference to the dried substance.It is a  white or almost white, crystalline powder or colourless crystals, freely soluble in water, very slightly soluble in alcohol.

Arginine hydrochloride C6H14N4O2.HCl (cas 1119-34-2) Molecular Structure
Name:Arginine hydrochloride

EINECS:214-275-1

Molecular Formula:C6H14N4O2.HCl

CAS Registry Number:1119-34-2

Synonyms:Arginine,monohydrochloride, L- (8CI); L-Arginine, monohydrochloride (9CI); Argamine; L-Arginine HCl

InChI:InChI=1S/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)

HS Code:29252000

Appearance:White crystalline powder

Molecular Weight:210.70

Density:1.46 g/cm3

Boiling Point:409.1°C at 760 mmHg

Melting Point:226-230 °C

Flash Point:201.2°C

Alpha:22 o (C=8,6N HCL)

Storage Temperature:2-8°C

Solubility:H2O: 100 mg/mL

Stability:Stable. Incompatible with strong oxidizing agents.

Usage:Biologically significant amino acid.

Methanaminium,1-carboxy-N,N,N-trimethyl-, chloride (1:1)

Methanaminium,1-carboxy-N,N,N-trimethyl-, chloride (1:1) C5H12ClNO2 (cas 590-46-5) Molecular Structure

Name:Methanaminium,1-carboxy-N,N,N-trimethyl-, chloride (1:1)

EINECS:209-683-1

Molecular Formula:C5H12ClNO2

CAS Registry Number:590-46-5

Synonyms:1-Carboxy-N,N,N-trimethylmethanaminium chloride; Betaine HCl; BETAINE CHLORIDE

InChI:InChI=1/C5H11NO2.ClH/c1-6(2,3)4-5(7)8;/h4H2,1-3H3;1H

HS Code:29239000

Appearance:colorless to white crystals

Molecular Weight:153.6

Density:1 g/cm3

Melting Point:241-242℃

Storage Temperature:Store in a cool, dry place. Store in a tightly closed container.

Solubility:64.7 g/100 mL (25 °C) in water

Stability:Stable under normal temperatures and pressures.

Usage:Used to treat a lack of or defect in certain enzymes that causes too much homocysteine in the blood and urine.

Cinnamyl alcohol Identification

Cinnamyl alcohol is an organic compound that is found in esterified form in storax, balsam Peru and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure. It can be produced by the hydrolysis of storax. Cinnamyl alcohol has a distinctive odour described as "sweet, balsam, hyacinth, spicy, green, powdery, cinnamic" and is used in perfumery and as a deodorant.

1. Properties

Name:Cinnamyl alcohol

EINECS:203-212-3

Molecular Formula:C9H10O

Percent Composition: C 80.56%, H 7.51%, O 11.92%

Literature References: The trans-form occurs (in the esterified form) in storax and in balsam Peru, cinnamon leaves, hyacinth oil. Obtained by the alkaline hydrolysis of storax. Prepd synthetically by reducing cinnamal diacetate with iron filings and acetic acid; from cinnamaldehyde by Meerwein-Ponndorf reduction with aluminum isopropoxide:

CAS Registry Number:104-54-1

Synonyms:3-Phenyl-2-propene-1-ol; 3-Phenyl-2-propen-1-ol; Cinnamic alcohol

InChI:InChI=1/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+

Index of refraction: nD20 1.58190; nD33 1.57580

Appearance:colourless solid

Molecular Weight:134.18

Density:1.044

Boiling Point:258℃

Melting Point:31-35℃

Flash Point:126℃

Storage Temperature:Store at 32F (0C) in a standard flammable liquids storage warehouse, room, or cabinet. Special vented containers may be required. Separate from oxidizing materials, acids, and alkalies. Protect against damage. Keep in containers made of fluorosilicone glass or stainless steel in a standard combustible material store at or near 0C.

Solubility:1.8 g/L (20 oC) in water

Stability:Stable. Incompatible with strong oxidizing agents.

Usage:Chemical intermediate for acetoacetic esters & acetoacetanilides, n,n-dialkylacetoacetamides, dyes, pharmaceuticals, for pigments & toners, food preservatives, insecticides, dicrotophos, & the fungicide, dehydroacetic acid.

Toxicity data: LD50 (g/kg): 2.0 orally in rats; >5.0 dermally in rabbits (Letizia)

2. Safety

The Cinnamyl alcohol is harmful if swallowed .It is irritating to eyes and skin .And it may cause sensitization by skin contact,so you need avoid contact with skin. When you use it ,wear suitable protective clothing ,gloves and eye/face protection.In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.


Cinnamyl alcohol has been found to have a sensitising effect on some people and as a result is the subject of a Restricted Standard issued by IFRA (International Fragrance Association).

Metformin hydrochloride Properties

Metformin hydrochloride is one kind of crystalline solid or white powder. The IUPAC Name of this chemical is 3-(Diaminomethylidene)-1,1-dimethylguanidine hydrochloride. Besides, Metformin hydrochloride belongs to Intermediates & Fine Chemicals; Pharmaceuticals; API's; Miscellaneous Compounds. In addition, Metformin hydrochloride Classification Code is Antidiabetic; Drug / Therapeutic Agent; Skin / Eye Irritant. Metformin hydrochloride is freely soluble in water and is practically insoluble in acetone, ether and chloroform.

1. Properties of Metformin hydrochloride

Name:Metformin hydrochloride

EINECS:214-230-6

Molecular Formula:C4H12ClN5

CAS Registry Number:1115-70-4

Appearance:crystalline solid

Molecular Weight:165.62

Boiling Point:224.1 °C at 760 mmHg

Melting Point:223-226℃

Flash Point:89.3 °C

Solubility:Soluble in water, 95% alcohol. Practically insoluble in ether, chloroform.

Biological Activity:Antidiabetic agent; lowers plasma glucose levels and improves insulin sensitivity. Inhibits hepatic gluconeogenesis via activation of the LKB1/AMPK pathway. Displays antiproliferative effects in cancer cell lines.

Usage:An oral hypoglycemic agent

2. Safety information of Metformin hydrochloride
Hazard Codes: Xn

Risk Statements: 22-36/38

R22:Harmful if swallowed.

R36/38:Irritating to eyes and skin.

Safety Statements: 26-36

S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

S36:Wear suitable protective clothing.

WGK Germany: 3

RTECS: DU1800000

3. Uses of Metformin hydrochloride

Metformin hydrochloride is an oral hypoglycemic agent. It can lower plasma glucose levels and improves insulin sensitivity. Metformin hydrochloride Inhibits hepatic gluconeogenesis via activation of the LKB1/AMPK pathway. Displays antiproliferative effects in cancer cell lines.


4. Production of Metformin hydrochloride

Metformin hydrochloride is derived by Dimethylamine salt reacting with Dicyandiamide.

2013年11月22日星期五

How Cisplatin Works on treating cancer

Cisplatin(CAS.NO:15663-27-1), cisplatinum, or cis-diamminedichloridoplatinum(II) is a chemotherapy drug. It was the first member of a class of platinum-containing anti-cancer drugs, which now also includes carboplatin and oxaliplatin. These platinum complexes react in vivo, binding to and causing crosslinking of DNA, which ultimately triggers apoptosis (programmed cell death).

Cancerous tumors are characterized by cell division, which is no longer controlled as it is in normal tissue.   "Normal" cells stop dividing when they come into contact with like cells, a mechanism known as contact inhibition.  Cancerous cells lose this ability.  Cancer cells no longer have the normal checks and balances in place that control and limit cell division.  The process of cell division, whether normal or cancerous cells, is through the cell cycle.  The cell cycle goes from the resting phase, through active growing phases, and then to mitosis (division).

The ability of chemotherapy to kill cancer cells depends on its ability to halt cell division.  Usually, the drugs work by damaging the RNA or DNA that tells the cell how to copy itself in division.  If the cells are unable to divide, they die.  The faster the cells are dividing, the more likely it is that chemotherapy will kill the cells, causing the tumor to shrink.  They also induce cell suicide (self-death or apoptosis).

Chemotherapy drugs that affect cells only when they are dividing are called cell-cycle specific.  Chemotherapy drugs that affect cells when they are at rest are called cell-cycle non-specific.  The scheduling of chemotherapy is set based on the type of cells, rate at which they divide, and the time at which a given drug is likely to be effective.  This is why chemotherapy is typically given in cycles.

Chemotherapy is most effective at killing cells that are rapidly dividing.  Unfortunately, chemotherapy does not know the difference between the cancerous cells and the normal cells. The "normal" cells will grow back and be healthy but in the meantime, side effects occur.  The "normal" cells most commonly affected by chemotherapy are the blood cells, the cells in the mouth, stomach and bowel, and the hair follicles; resulting in low blood counts, mouth sores, nausea, diarrhea, and/or hair loss.  Different drugs may affect different parts of the body.

Cisplatin is classified as an alkylating agent.  Alkylating agents are most active in the resting phase of the cell.  These drugs are cell cycle non-specific.


Following administration, one of the chloride ligands is slowly displaced by water (an aqua ligand), in a process termed aquation. The aqua ligand in the resulting [PtCl(H2O)(NH3)2]+ is itself easily displaced, allowing the platinum atom to bind to bases. Of the bases on DNA, guanine is preferred. Subsequent to formation of [PtCl(guanine-DNA)(NH3)2]+, crosslinking can occur via displacement of the other chloride ligand, typically by another guanine. Cisplatin crosslinks DNA in several different ways, interfering with cell division by mitosis. The damaged DNA elicits DNA repair mechanisms, which in turn activate apoptosis when repair proves impossible. Recently it was shown that the apoptosis induced by cisplatin on human colon cancer cells depends on the mitochondrial serine-protease Omi/Htra2. Since this was only demonstrated for colon carcinoma cells, it remains an open question if the Omi/Htra2 protein participates in the cisplatin-induced apoptosis in carcinomas from other tissues.

Most notable among the changes in DNA are the 1,2-intrastrand cross-links with purine bases. These include 1,2-intrastrand d(GpG) adducts which form nearly 90% of the adducts and the less common 1,2-intrastrand d(ApG) adducts. 1,3-intrastrand d(GpXpG) adducts occur but are readily excised by the nucleotide excision repair (NER). Other adducts include inter-strand crosslinks and nonfunctional adducts that have been postulated to contribute to cisplatin's activity. Interaction with cellular proteins, particularly HMG domain proteins, has also been advanced as a mechanism of interfering with mitosis, although this is probably not its primary method of action.


Note that although cisplatin is frequently designated as an alkylating agent, it has no alkyl group and so cannot carry out alkylating reactions. It is correctly classified as alkylating-like.

Luteolin:anti-inflammation and anticancer

Luteolin, 3',4',5,7-tetrahydroxyflavone, is a common flavonoid that exists in many types of plants including fruits, vegetables, and medicinal herbs. Plants rich in luteolin have been used in Chinese traditional medicine for treating various diseases such as hypertension, inflammatory disorders, and cancer.

Luteolin(CAS.NO:491-70-3) has multiple biological effects such as anti-inflammation, anti-allergy and anticancer, luteolin functions as either an antioxidant or a pro-oxidant biochemically. The biological effects of luteolin could be functionally related to each other. For instance, the anti-inflammatory activity may be linked to its anticancer property. Luteolin's anticancer property is associated with the induction of apoptosis, and inhibition of cell proliferation, metastasis and angiogenesis. Furthermore, luteolin sensitizes cancer cells to therapeutic-induced cytotoxicity through suppressing cell survival pathways such as phosphatidylinositol 3'-kinase (PI3K)/Akt, nuclear factor kappa B (NF-kappaB), and X-linked inhibitor of apoptosis protein (XIAP), and stimulating apoptosis pathways including those that induce the tumor suppressor p53. These observations suggest that luteolin could be an anticancer agent for various cancers.


When compared to other flavonoids, only luteolin and quercetin inhibited platelet-activating factor and suppressed a type of inflammatory response induced by allergens by inhibiting lipoxygenase.   Luteolin inhibited the excess production of TNF-alpha, which directly causes inflammation and apoptosis  (cell death). The scientists who conducted the study concluded that luteolin could be used to develop a novel type of anti-inflammatory and anti-allergic drugs. .

A study assessed the antioxidant potencies of several dietary flavonoids compared with vitamin C. Pretreatment with all flavonoids and vitamin C produced dose-dependent reductions in oxidative DNA damage. When ranked in order of potency, luteolin was two times more effective than vitamin C by the Trolox test and more effective than seven other flavonoids in reducing DNA oxidative damage.

A 2010 University of Illinois study funded by the National Institutes of Health found that luteolin, a super-nutrient that had already been documented as having anti-inflammatory effects in the body, can also reduce brain inflammation and reverse age-related memory deficits by directly blocking the release of inflammatory molecules in the brain.


It’s common knowledge that antioxidants reduce inflammation in the body and that inflammation is the cause behind much illness, including many auto-immune diseases. Inflammation in the brain seems to play a major role in age-related memory loss. The University of Illinois study suggests that luteolin acts directly on the immune cells in the brain and spinal cord (known as microglial cells), reducing their production of inflammatory cytokines in the brain, small proteins that affect communication between and behavior of cells. Luteolin’s effect in decreasing the release of these proteins helps protect,


Luteolin has been studied in several preliminary in vitro scientific investigations. Proposed activities include antioxidant activity (ie. scavenging of free radicals), promotion of carbohydrate metabolism, and immune system modulation. Other in vitro studies suggest luteolin has anti-inflammatory activity, and that it acts as a monoamine transporter activator, a phosphodiesterase inhibitor,and an interleukin 6 inhibitor. In vivo studies show luteolin affects xylazine/ketamine-induced anesthesia in mice. In vitro and in vivo experiments also suggest luteolin may inhibit the development of skin cancer. Importantly, the therapeutic value of the above findings is unclear, and will remain so until further detailed in vivo, toxicity, and clinical studies are performed.

Introduction to 1,2,4-1H-Triazole

1,2,4-1H-Triazole is one of a pair of isomeric chemical compounds with molecular formula C2H3N3, called triazoles, which have a five-membered ring of two carbon atoms and three nitrogen atoms. 1,2,4-1H-Triazole is a basic aromatic heterocycle. 1,2,4-1H-Triazole derivatives find use in a wide variety of applications, most notably as antifungals such as fluconazole and itraconazole.


1.Chemical properties


Name:1,2,4-1H-Triazole

EINECS:206-022-9

Molecular Formula:C2H3N3

CAS Registry Number:288-88-0

Synonyms:1H-1,2,4-1H-Triazole; 1,2,4-Triazole; 1H-1,2,4Triazole; 1,2,4-1H-1,2,4-1H-Triazole; Triazole

InChI:InChI=1/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5)

HS Code:29339990

Appearance:white crystalline powder and flakes

Molecular Weight:69.07

Density:1.274g/cm3

Boiling Point:260℃

Melting Point:119-122℃

Flash Point:140℃

Storage Temperature:Store at 0-5°C

Refractive index:1.534

Solubility:Water solubility: 1250 g/L at 20 °C

Stability:Stable under normal temperatures and pressures.

Usage:Used to produce antifungals.

2. First Aid Measures

Ingestion:Get medical aid. Wash mouth out with water.

Inhalation:Remove from exposure to fresh air immediately.

Skin:Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes.

Eyes:Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids.

3. Handling and Storage

Storage:Store in a cool, dry place. Store in a tightly closed container.

Handling:Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.

4.Hazards Identification
Ingestion:Harmful if swallowed. May cause irritation of the digestive tract.

Inhalation:May cause respiratory tract irritation. May be harmful if inhaled.

Skin:May be harmful if absorbed through the skin.

Eyes:Causes eye irritation.

EC Risk Phrase:R 22 36 63

EC Safety Phrase:S 36/37

5. Exposure Controls/Personal Protection

1)Personal Protection:

Skin: Wear appropriate protective gloves to prevent skin exposure.

Clothing: Wear appropriate protective clothing to prevent skin exposure.

2)Respirators:


Follow the OSHA respirator regulations found in 29CFR 1910.134 or European Standard EN 149. Always use a NIOSH or European Standard EN 149 approved respirator when necessary.

2013年11月20日星期三

Neomycin sulfate

Neomycin is produced by Streptomyces fradiae. Polymyxin B Sulfate acts by binding to the 30S subunit of the bacterial ribosome leading to inhibition of protein synthesis and death in susceptible bacteria. Neomycin Sulfate is used for the prevention of bacterial contamination of cell cultures. This antibiotic is highly active against gram-negative bacteria. The recommended working concentration is 50 µg/ml. Life Technologies offers a variety of antibiotics and antimycotics for cell culture applications.


Name:Neomycin sulfate

EINECS:215-773-1

Molecular Formula:C23H46N6O13.3(H2SO4)

CAS Registry Number:1405-10-3

HS Code:29419000

Appearance:Tan powder.

Molecular Weight:908.87

Boiling Point:1046.1°C at 760 mmHg

Flash Point:586.5°C

Storage Temperature:2-8°C

Refractive index:56 ° (C=10, H2O)

Solubility:500 g/L (20 C)

Stability:Stable. Incompatible with strong oxidizing agents.

Usage:Antibacterial.

Indications: It is prescribed orally to treat hepatic coma and infections of the intestine and to prepare the gastrointestinal tract for surgery. It is prescribed topically to treat skin infections.

Contraindications: Renal dysfunction, intestinal obstruction, or known hypersensitivity to this drug or to any aminoglycoside medication prohibits its use. Neomycin is not administered parenterally.


Adverse effects: Among the more serious adverse effects are nausea, vomiting, diarrhea, malabsorption, or superinfection. Prolonged treatment in patients with impaired renal function may result in the toxicities of systemic aminoglycosides (e.g., ototoxicity, nephrotoxicity, neuromuscular toxicity). Hypersensitivity reactions may occur with topical administration of this drug.

Side effect of Pregabalin

Pregabalin is used to relieve neuropathic pain (pain from damaged nerves) that can occur in your arms, hands, fingers, legs, feet, or toes if you have diabetes or in the area of your rash if you have had shingles (a painful rash that occurs after infection with herpes zoster). It is also used to treat fibromyalgia (a long-lasting condition that may cause pain, muscle stiffness and tenderness, tiredness, and difficulty falling asleep or staying asleep). Pregabalin is used with other medications to treat certain types of seizures in people with epilepsy. Pregabalin is in a class of medications called anticonvulsants. It works by decreasing the number of pain signals that are sent out by damaged nerves in the body.

Along with their useful effects, most medicines can cause unwanted side-effects although not everyone experiences them. These usually improve as your body adjusts to the new medicine, but speak with your doctor or pharmacist if any of the following side-effects continue or become troublesome.


Adverse drug reactions associated with the use of pregabalin include:

Very common (>10% of patients): dizziness, drowsiness.

Common (1–10% of patients): blurred vision, diplopia, increased appetite and subsequent weight gain, euphoria, confusion, vivid dreams, changes in libido (increase or decrease), irritability, ataxia, attention changes, abnormal coordination, memory impairment, tremors, dysarthria, parasthesia, vertigo, dry mouth and constipation, vomiting and flatulence, erectile dysfunction, fatigue, peripheral edema, drunkenness, abnormal walking, asthenia, nasopharyngitis, increased creatine kinase level.

Infrequent (0.1–1% of patients): depression, lethargy, agitation, anorgasmia, hallucinations, myoclonus, hypoaesthesia, hyperaesthesia, tachycardia, excessive salivation, sweating, flushing, rash, muscle cramp, myalgia, arthralgia, urinary incontinence, dysuria, thrombocytopenia, kidney calculus.

Rare (<0.1% of patients): neutropenia, first degree heart block, hypotension, hypertension, pancreatitis, dysphagia, oliguria, rhabdomyolysis, suicidal thoughts or behavior.


Pregabalin may also cause withdrawal effects after long-term use if discontinued abruptly. When prescribed for seizures, quitting “cold turkey” can increase the strength of the seizures and possibly cause the seizures to reoccur. Withdrawal symptoms include restlessness, insomnia, and anxiety. Pregabalin should be reduced gradually when finishing treatment. Because of complication risk associated with certain common side effects in patients affected by other health issues, Pregabalin should not be used without regular medical supervision and any side effect should immediately be reported.

Pregabalin: an anticonvulsant drug

Pregabalin is an anticonvulsant drug used for neuropathic pain and as an adjunct therapy for partial seizures with or without secondary generalization in adults. It has also been found effective for generalized anxiety disorder and is (as of 2007) approved for this use in the European Union and Russia.

Pregabalin is used alongside other medicines in the treatment of focal seizures, which is a type of epilepsy. A seizure is a short episode of symptoms which is caused by a burst of abnormal electrical activity in the brain. With a focal (sometimes called 'partial') seizure, the burst of electrical activity stays in one part of the brain. Therefore, you tend to have localised or 'focal' symptoms. Pregabalin is used to control the symptoms of seizures.

Pregabalin(CAS.NO:148553-50-8) is also used either alone or alongside other medicines to treat certain types of long-lasting pain caused by damage to nerves. This type of pain, called neuropathic pain, can be caused by a number of different conditions including diabetes and shingles.

1. Medical uses

Pregabalin appears to be as effective as gabapentin for neuropathic pain; however costs more. It is effective for some people with postherpetic neuralgia and fibromyalgia. There is not enough data to state that it should be used in all neuropathic pain. It has not been found to be effective for HIV-associated peripheral neuropathy. It has not been shown to be useful for cancer related neuropathic pain. There is no evidence for use in acute pain. Pregabalin is also used for the treatment perioperative pain. There is no evidence for its use in the prevention of migraines and gabapentin has been found not to be useful.
Pregabalin may be used as a second line medication in general anxiety disorder. It appears to have anxiolytic effects similar to benzodiazepines.

2. Usage
Pregabalin comes as a capsule to take by mouth. It is usually taken with or without food two or three times a day. Take pregabalin at around the same times every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand.

3. Storage

Store at room temperature away from light and moisture. Do not store in the bathroom. If you are using the liquid, after you open the bottle, discard any unused liquid after 45 days. Keep all medications away from children and pets.

4. Overdosage


Several renal failure patients developed myoclonus while receiving pregabalin, apparently as a result of gradual accumulation of the drug. Acute overdosage may be manifested by somnolence, tachycardia and hypertonicity. Plasma, serum or blood concentrations of pregabalin may be measured to monitor therapy or to confirm a diagnosis of poisoning in hospitalized patients.

2013年11月19日星期二

Introduction of Di-tert-butyl dicarbonate

Di-tert-butyl dicarbonate is a reagent widely used in organic synthesis.This carbonate ester reacts with amines to give N-tert-butoxycarbonyl or so-called t-BOC derivatives. These derivatives do not behave as amines, which allows certain subsequent transformations to occur that would have otherwise affected the amine functional group. The t-BOC can later be removed from the amine using acids. Thus, t-BOC serves as a protective group, for instance in solid phase peptide synthesis. It is unreactive to most bases and nucleophiles, allowing for an orthogonal Fmoc protection.

The IUPAC name of Boc anhydride is tert-butyl (2-methylpropan-2-yl)oxycarbonyl carbonate. With the CAS registry number 24424-99-5, it is also named as Di-tert-butyl dicarbonate. The product's categories are Amino Acid Derivatives; Starting Raw Materials & Intermediates; Organics; N-Protecting Reagents; Biochemistry; Peptide Synthesis; Protection & Derivatization Reagents (for Synthesis); Protective Reagents (Peptide Synthesis); Reagents for Oligosaccharide Synthesis; Synthetic Organic Chemistry; Boc-Amino Acid Series. Besides, it is white to off-white microcrystalline powder, which should be stored in closed containers in a cool, dry place at 2-8 °C.

1. Chemical Properties


Name:Di-tert butyl dicarbonate

EINECS:246-240-1

Molecular Formula:C10H18O5

CAS Registry Number:24424-99-5

Synonyms:Di-tert-butyl pyrocarbonate; di(tert-butyl) carbonate; di-t-Butyl-dicarbonate Dicarbonic acid, bis(1,1-dimethylethyl)ester; (t.-Boc)2O; DIBOC; Dibutyldicarbonate; BOC anhydride; BOC-20; Di-t-butyl pyrocarbonate; Di-tert butyl dicarbonate; Di-tert-butyl dicarbonate; Di-t-Butyl DICARBONATE; (BOC)2O; Di-tert-butyldicarbonate; Dicarbonic acid, C,C'-bis(1,1-dimethylethyl) ester; Dicarbonic acid, bis(1,1-dimethylethyl) ester

InChI:InChI=1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3

HS Code:29209010

Appearance:white solid and/or colorless liquid

Molecular Weight:218.24692

Density:0.949

Boiling Point:56-57°C(0.5 torr)

Melting Point:22-24°C

Flash Point:37°C

Storage Temperature:2-8°C

Refractive index:1.4075-1.4095

Solubility:insoluble

Stability:Stable under normal temperatures and pressures.

Vapour Pressure: 0.049 mmHg at 25 °C

Enthalpy of Vaporization: 47.26 kJ/mol

Surface Tension: 31.2 dyne/cm

2. Preparation of Di-tert-butyl dicarbonate

Di-tert-butyl dicarbonate can be prepared from tert-Butanol, Carbon dioxide, Phosgene, using DABCO as a base.

3. Uses of Di-tert-butyl dicarbonate

The Di-tert-butyl dicarbonate is an intermediate and amino-protecting agent widely used in organic synthesis. It is also used in the Synthesis of 6-acetyl-1,2,3,4-tetrahydropyridine. Simlilarly, it can react with 3-Amino-benzoic acid to get 3-tert-Butoxycarbonylamino-benzoic acid.(This reaction needs Et3N, H2O and Dioxane at temperature of 20 °C for 24 hours. The yield is 100 %.)

4. Safety information of Di-tert-butyl dicarbonate


The Di-tert-butyl dicarbonate is highly flammable that may form explosive peroxides. Please keep away from sources of ignition. It is also very toxic by inhalation, so you should keep container tightly closed in a well-ventilated place. Moreover, it is irritating to eyes, respiratory system and skin. And it may cause sensitization by skin contact. In case of contact with eyes, please rinse immediately with plenty of water and seek medical advice. Additionally, you should wear suitable protective clothing, gloves and eye/face protection to avoid contact with skin. After contact with skin, please wash immediately with plenty of soap-suds. And please take precautionary measures against static discharges. What's more, in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible).

Zinc: History,Application and Production

Zinc, also referred to in nonscientific contexts as spelter, is a bluish-white, lustrous, diamagnetic metal, though most common commercial grades of the metal have a dull finish. It is somewhat less dense than iron and has a hexagonal crystal structure.

Zinc , with CAS number of 7440-66-6, can be called Asarco L 15 ; Blue powder ; CCRIS 1582 ; Emanay zinc dust ; Granular zinc ; Lead refinery vacuum zinc ; Rheinzink ; Merrillite .

The metal is hard and brittle at most temperatures but becomes malleable between 100 and 150 °C. Above 210 °C, the metal becomes brittle again and can be pulverized by beating. Zinc is a fair conductor of electricity. For a metal, zinc has relatively low melting (419.5 °C, 787.1 F) and boiling points (907 °C). Its melting point is the lowest of all the transition metals aside from mercury and cadmium.


Many alloys contain zinc, including brass, an alloy of copper and zinc. Other metals long known to form binary alloys with zinc are aluminium, antimony, bismuth, gold, iron, lead, mercury, silver, tin, magnesium, cobalt, nickel, tellurium and sodium. While neither zinc nor zirconium are ferromagnetic, their alloy ZrZn2 exhibits ferromagnetism below 35 K.

1. History

1). Ancient use

Various isolated examples of the use of impure zinc in ancient times have been discovered.Ornaments made of alloys that contain 80–90% zinc with lead, iron, antimony, and other metals making up the remainder, have been found that are 2500 years old.

2). Early studies and naming

Zinc was distinctly recognized as a metal under the designation of Fasada in the medical Lexicon ascribed to the Hindu king Madanapala and written about the year 1374. Smelting and extraction of impure zinc by reducing calamine with wool and other organic substances was accomplished in the 13th century in India.The Chinese did not learn of the technique until the 17th century.

Some alchemists called zinc oxide lana philosophica, Latin for "philosopher's wool".a Swiss-born German alchemist referred to the metal as "zincum" or "zinken" in his book Liber Mineralium II, in the 16th century. The metal was also called Indian tin, tutanego, calamine, and spinter.

3). Isolation of the pure element

William Champion's brother, John, patented a process in 1758 for calcining zinc sulfide into an oxide usable in the retort process. Prior to this only calamine could be used to produce zinc. In 1798, Johann Christian Ruberg improved on the smelting process by building the first horizontal retort smelter. Jean-Jacques Daniel Dony built a different kind of horizontal zinc smelter in Belgium, which processed even more zinc.

Italian doctor Luigi Galvani discovered in 1780 that connecting the spinal cord of a freshly dissected frog to an iron rail attached by a brass hook caused the frog's leg to twitch.The galvanic cell and the process of galvanization were both named for Luigi Galvani and these discoveries paved the way for electrical batteries, galvanization and cathodic protection.

Galvani's friend, Alessandro Volta, continued researching this effect and invented the Voltaic pile in 1800.The basic unit of Volta's pile was a simplified galvanic cell.

The non-magnetic character of zinc and its lack of color in solution delayed discovery of its importance to biochemistry and nutrition. This changed in 1940 when carbonic anhydrase, an enzyme that scrubs carbon dioxide from blood, was shown to have zinc in its active site. The digestive enzyme carboxypeptidase became the second known zinc-containing enzyme in 1955.

2. Uses

Zinc (CAS NO.7440-66-6) metal is most commonly used as an anti-corrosion agent. The zinc metal was used for galvanization, which is used on chain-link fencing, guard rails, suspension bridges, lightposts, metal roofs, heat exchangers, and car bodies. Zinc is also used to cathodically protect metals that are exposed to sea water from corrosion. With an electrochemical potential of ?0.7618 volts, zinc makes a good material for the negative terminus or anode in batteries.Powdered zinc is used in this way in alkaline batteries and sheets of zinc metal form the cases for and act as anodes in zinc-carbon batteries.

A widely used alloy of zinc is brass, which is useful in communication equipment, hardware, musical instruments, and water valves. Other widely used alloys that contain zinc include nickel silver, typewriter metal, soft and aluminum solder, and commercial bronze.Zinc is also used in contemporary pipe organs as a substitute for the traditional lead/tin alloy in pipes. Alloys of primarily zinc with small amounts of copper, aluminium, and magnesium are useful in die casting as well as spin casting, especially in the automotive, electrical, and hardware industries.

Zinc oxide is widely used as a white pigment in paints, and as a catalyst in the manufacture of rubber. It is also used as a heat disperser for the rubber and acts to protect its polymers from ultraviolet radiation. Zinc chloride can be used as a wood preservative.It is also used to make other chemicals. Zinc methyl (Zn(CH3)2) is used in a number of organic syntheses.Zinc sulfide (ZnS) is used in luminescent pigments such as on the hands of clocks, X-ray and television screens, and luminous paints.Crystals of ZnS are used in lasers that operate in the mid-infrared part of the spectrum. Zinc sulphate is a chemical in dyes and pigments. Zinc pyrithione is used in antifouling paints. Zinc powder is sometimes used as a propellant in model rockets.Zinc sheet metal is used to make zinc bars.
Zinc is included in most single tablet over-the-counter daily vitamin and mineral supplements. Zinc gluconate glycine and zinc acetate are used in throat lozenges or tablets to reduce the duration and the severity of cold symptoms. Zinc lactate is used in toothpaste to prevent halitosis.

3. Production

Roasting converts the zinc sulfide concentrate produced during processing to zinc oxide:

2ZnS + 3 O2 → 2ZnO + 2SO2

Pyrometallurgy processing reduces zinc oxide with carbon or carbon monoxide at 950 °C (1,740 °F) into the metal, which is distilled as zinc vapor.

2 ZnO + C → 2 Zn + CO2


2 ZnO + 2CO → 2 Zn + 2 CO2

Compounds:Zinc

Zinc, in commerce also spelter, is a metallic chemical element; it has the symbol Zn and atomic number 30. It is the first element of group 12 of the periodic table. Zinc is, in some respects, chemically similar to magnesium, because its ion is of similar size and its only common oxidation state is +2. Zinc is the 24th most abundant element in the Earth's crust and has five stable isotopes. The most common zinc ore is sphalerite (zinc blende), a zinc sulfide mineral. The largest mineable amounts are found in Australia, Asia, and the United States. Zinc production includes froth flotation of the ore, roasting, and final extraction using electricity (electrowinning).


1. Chemical properties

Name:Zinc

EINECS:231-175-3

Molecular Formula:Zn

CAS Registry Number:7440-66-6

InChI:InChI=1/Zn

Appearance:silver or blueish-white foil or powder

Molecular Weight:65.39

Density:7.14

Boiling Point:907℃

Melting Point:420℃

Flash Point:-17℃

Storage Temperature:2-8°C

Solubility:Soluble in acids and alkalies; insoluble in water

Stability:Stable. Incompatible with amines, cadmium, sulfur, chlorinated solvents, strong acids, strong bases. Air and moisture sensitive. Zinc powder is very flammable.

2. Safety information

Hazard Codes: N,F,Xi,Xn

Risk Statements: 52/53-50/53-17-15-36/37/38-51/53-36/37-22-19

R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment.

R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.

R17:Spontaneously flammable in air.

R15:Contact with water liberates extremely flammable gases.

R36/37/38:Irritating to eyes, respiratory system and skin.

R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.

R36/37:Irritating to eyes and respiratory system.

R22:Harmful if swallowed.

R19:May form explosive peroxides.

Safety Statements: 26-61-60-46-43-36

S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

S61:Avoid release to the environment. Refer to special instructions / safety data sheets.

S60:This material and its container must be disposed of as hazardous waste.

S46:If swallowed, seek medical advice immediately and show this container or label.

S43:In case of fire use ... (there follows the type of fire-fighting equipment to be used.)

S36:Wear suitable protective clothing.

RIDADR: UN 3264 8/PG 3

WGK Germany: 3

RTECS: ZH1400000

F: 3

HazardClass: 8

PackingGroup: III

Human systemic effects by ingestion: cough, dyspnea, and sweating. A human skin irritant. Pure zinc powder, dust, and fume are relatively nontoxic to humans by inhalation. The difficulty arises from oxidation of zinc fumes immediately prior to inhalation or presence of impurities such as Cd, Sb, As, Pb. Inhalation may cause sweet taste, throat dryness, cough, weakness, generalized aches, chills, fever, nausea, vomiting.


Flammable in the form of dust when exposed to heat or flame. May ignite spontaneously in air when dry. Explosive in the form of dust when reacted with acids. Incompatible with NH4NO3, BaO2, Ba(NO3)2, Cd, CS2, chlorates, Cl2, ClF3, CrO3, (ethyl acetoacetate + tribromoneopentyl alcohol), F2, hydrazine mononitrate, hydroxylamine, Pb(N3)2, (Mg + Ba(NO3)2 + BaO2), MnCl2, HNO3, performic acid, KClO3, KNO3, K2O2, Se, NaClO3, Na2O2, S, Te, H2O, (NH4)2S, As2O3, CS2, CaCl2, NaOH, chlorinated rubber, catalytic metals, halocarbons, o-nitroanisole, nitrobenzene, nonmetals, oxidants, paint primer base, pentacarbonyliron, transition metal halides, seleninyl bromide. To fight fire, use special mixtures of dry chemical. When heated to decomposition it emits toxic fumes of ZnO.

2013年11月16日星期六

Glimepiride: type 2 diabetes

Insulin is a hormone that is made naturally in your body, in the pancreas. It helps to control the levels of sugar in your blood. If your body does not make enough insulin to meet its needs, or if it does not use the insulin it makes effectively, this results in the condition called diabetes mellitus (sugar diabetes).


People with diabetes need treatment to control the amount of sugar in their blood. This is because good control of blood sugar levels reduces the risk of complications later on. Some people can control the sugar in their blood by making changes to the food they eat but for other people, medicines like glimepiride are given alongside the changes in diet.

Glimepiride(CAS.NO:93479-97-1) works by increasing the amount of insulin that your pancreas releases. It can be given on its own or alongside other antidiabetic medicines or insulin.

Diabetes mellitus type 2 (formerly noninsulin-dependent diabetes mellitus (NIDDM) or adult-onset diabetes) is a metabolic disorder that is characterized by high blood glucose in the context of insulin resistance and relative insulin deficiency. This is in contrast to diabetes mellitus type 1, in which there is an absolute insulin deficiency due to destruction of islet cells in the pancreas. The classic symptoms are excess thirst, frequent urination, and constant hunger. Type 2 diabetes makes up about 90% of cases of diabetes with the other 10% due primarily to diabetes mellitus type 1 and gestational diabetes. Obesity is thought to be the primary cause of type 2 diabetes in people who are genetically predisposed to the disease.

Type 2 diabetes is initially managed by increasing exercise and dietary modification. If blood glucose levels are not adequately lowered by these measures, medications such as metformin or insulin may be needed. In those on insulin, there is typically the requirement to routinely check blood sugar levels.

Type 2 diabetes is due to insufficient insulin production from beta cells in the setting of insulin resistance.Insulin resistance, which is the inability of cells to respond adequately to normal levels of insulin, occurs primarily within the muscles, liver, and fat tissue.In the liver, insulin normally suppresses glucose release. However, in the setting of insulin resistance, the liver inappropriately releases glucose into the blood. The proportion of insulin resistance versus beta cell dysfunction differs among individuals, with some having primarily insulin resistance and only a minor defect in insulin secretion and others with slight insulin resistance and primarily a lack of insulin secretion.

Glimepiride is indicated to treat type 2 diabetes mellitus; its mode of action is to increase insulin production by the pancreas. It is not used for type 1 diabetes because in type 1 diabetes the pancreas is not able to produce insulin.
Glimepiride is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes (non-insulin-dependent diabetes). It may also be used with other diabetes medications. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Glimepiride belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin.


Glimepiride is used along with diet and exercise, and sometimes with other medications, to treat type 2 diabetes (condition in which the body does not use insulin normally and, therefore, cannot control the amount of sugar in the blood). Glimepiride lowers blood sugar by causing the pancreas to produce insulin (a natural substance that is needed to break down sugar in the body) and helping the body use insulin efficiently. This medication will only help lower blood sugar in people whose bodies produce insulin naturally. Glimepiride is not used to treat type 1 diabetes (condition in which the body does not produce insulin and, therefore, cannot control the amount of sugar in the blood) or diabetic ketoacidosis (a serious condition that may occur if high blood sugar is not treated).

Bicalutamide chemical properties

Bicalutamide is in a class of medications called nonsteroidal antiandrogens. Bicalutamide is used with another medication to treat metastatic prostate cancer .  It works by blocking the effect of androgen (a male hormone), to stop the growth and spread of cancer cells.

Name:Bicalutamide

Molecular Formula:C18H14F4N2O4S

CAS Registry Number:90357-06-5

Appearance:off-white crystalline solid

Molecular Weight:430.373373

Density:1.52 g/cm3

Boiling Point:650.3 °C at 760 mmHg

Melting Point:191-193°C

Flash Point:347.1 °C

Storage Temperature:Store in original container in a cool dark place.

Refractive index:1.577

Solubility:Insoluble in water

Chemical Properties: Off-White Crystalline Solid

Biological Activity:Orally active non-steroidal androgen receptor antagonist (IC 50 = 190 nM). Displays peripheral selectivity and does not effect serum levels of LH and testosterone. Exhibits potent anticancer activity in vivo .

Usage:Non-steroidal peripherally active antiandrogen. Used as an antiandrogen, antineoplastic (hormonal)


Side effect:Flushing and sweating (hot flashes), body aches and pains, breast swelling/tenderness/pain, headache, dizziness, drowsiness, trouble sleeping, weakness, hair loss, weight changes, constipation, diarrhea, stomach upset, gas, nausea, vomiting, and loss of appetite may occur.

Properties of Antimony(III) oxide

Antimony(III) oxide is the inorganic compound with the formula Sb2O3. It is the most important commercial compound of antimony. It is found in nature as the minerals valentinite and senarmontite. Like most polymeric oxides, Sb2O3 dissolves in aqueous solutions only with hydrolysis.

Antimony(III) oxide is an amphoteric oxide, it dissolves in aqueous sodium hydroxide solution to give the meta-antimonite NaSbO2, which can be isolated as the trihydrate. Antimony(III) oxide also dissolves in concentrated mineral acids to give the corresponding salts, which hydrolyzes upon dilution with water. With nitric acid, the trioxide is oxidized to antimony(V) oxide.

When heated with carbon, the oxide is reduced to antimony metal. With other reducing agents such as sodium borohydride or lithium aluminium hydride, the unstable and very toxic gas stibine is produced. When heated with potassium bitartrate, a complex salt potassium antimony tartrate, KSb(OH)2•C4H2O6 is formed.
  
Name:Antimony(III) oxide

EINECS:215-175-0

Molecular Formula:Sb2O3

CAS Registry Number:1309-64-4

Synonyms:Antimony trioxide; diantimony trioxide; Antimonyoxideelecgrwhitepowder; Antimonyoxidepowder

InChI:InChI=1/3O.2Sb/q3*-2;2*+3

Appearance:White Powder

Molecular Weight:291.52

Density:5.2

Boiling Point:1456°C

Melting Point:656°C (subl.)

Solubility:Slightly soluble

Stability:Stable.

Chemical Properties: White Powder

General Description: Diantimony trioxide is a white crystalline solid. Diantimony trioxide is insoluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Diantimony trioxide is used to fireproof fabrics, paper and plastics, as a paint pigment and for many other uses.

Air & Water Reactions: Insoluble in water.

Reactivity Profile: Idiantimony trioxide ignites and burns when heated in powdered form in air . Reacts violentlhy with bromine trifluoride.

Health Hazard :Dust: P oisonous if inhaled or if skin is exposed. If inhaled will cause coughing, difficult breathing or loss of consciousness. Sllid: Poisonous if swallowed or if skin is exposed. If swallowed will cause dizziness, nausea, vomiting or loss of consciousness.

Fire Hazard: Not flammable.

Uses:

The annual consumption of antimony(III) oxide in the United States and Europe is approximately 10,000 and 25,000 tonnes, respectively. The main application is for flame retardants in combination with halogenated materials. The combination of the halides and the antimony being key to the flame-retardant action for polymers, helping to form less flammable chars. Such flame retardants are found in electrical apparatus, textiles, leather, and coatings.

Other applications:


1.Antimony(III) oxide is an opacifying agent for glasses, ceramics and enamels.

2.Some specialty pigments contain antimony.

3.Antimony(III) oxide is a useful catalyst in the production of polyethylene terephthalate (PET plastic) and the vulcanization of rubber.

4.Flame retardant for textiles, leather, polymers, and coatings.

2013年11月15日星期五

What's the application of the Chitosan?

Chitosan  is a linear polysaccharide composed of randomly distributed β-(1-4)-linked D-glucosamine (deacetylated unit) and N-acetyl-D-glucosamine (acetylated unit). It is made by treating shrimp and other crustacean shells with the alkali sodium hydroxide.

Chitosan(CAS.NO:9012-76-4) has a number of commercial and possible biomedical uses. It can be used in agriculture as a seed treatment and biopesticide, helping plants to fight off fungal infections. In winemaking it can be used as a fining agent, also helping to prevent spoilage. In industry, it can be used in a self-healing polyurethane paint coating. In medicine, it may be useful in bandages to reduce bleeding and as an antibacterial agent; it can also be used to help deliver drugs through the skin.


1. Agricultural and horticultural use
The agricultural and horticultural uses for chitosan, primarily for plant defense and yield increase, are based on how this glucosamine polymer influences the biochemistry and molecular biology of the plant cell. The cellular targets are the plasma membrane and nuclear chromatin. Subsequent changes occur in cell membranes, chromatin, DNA, calcium, MAP Kinase, oxidative burst, reactive oxygen species, callose pathogenesis-related (PR) genes and phytoalexins.

Agricultural applications of chitosan can reduce environmental stress due to drought and soil deficiencies, strengthen seed vitality, improve stand quality, increase yields, and reduce fruit decay of vegetables, fruits and citrus crops (see photo right).Horticultural application of chitosan increases blooms and extends the life of cut flowers and Christmas trees.The US Forest Service has conducted research on chitosan to control pathogens in pine trees and increase resin pitch outflow which resists pine beetle infestation.

2. Potential industrial use
Scientists have recently developed a polyurethane coating that heals its own scratches when exposed to sunlight, offering the promise of scratch-free cars and other products. The self-healing coating uses chitosan incorporated into traditional polymer materials, such as those used in coatings on cars, to protect paint. When a scratch damages the chemical structure, the chitosan responds to ultraviolet light by forming chemical chains that begin bonding with other materials in the substance, eventually smoothing the scratch. The process can take less than an hour.


3. Biomedical uses
Chitosan's properties allow it to rapidly clot blood, and has recently gained approval in the United States and Europe for use in bandages and other hemostatic agents. Chitosan hemostatic products have been shown in testing by the U.S. Marine Corps to quickly stop bleeding and to reduce blood loss, and result in 100% survival of otherwise lethal arterial wounds in swine. Chitosan hemostatic products reduce blood loss in comparison to gauze dressings and increase patient survival. Chitosan hemostatic products have been sold to the U.S. Army and are currently used by the UK military. Both the US and UK have already used the bandages on the battlefields of Iraq and Afghanistan. Chitosan is hypoallergenic and has natural antibacterial properties, which further support its use in field bandages.

4. Chitosan is under research for several potential clinical applications:

As a soluble dietary fiber, it increases gastrointestinal lumen viscosity and slows down the emptying of the stomach.

It alters bile acid composition, increasing the excretion of sterols and reducing the digestibility of ileal fats.It is unclear how chitosan does this, but the currently favored hypotheses involve the increase of intestinal viscosity or bile acid-binding capacity.

Chitosan is relatively insoluble in water, but can be dissolved by dilute acids, which would make it a highly-viscous dietary fiber. Such fibers might inhibit the uptake of dietary lipids by increasing the thickness of the boundary layer of the intestinal lumen, which has been observed in animal experiments.


Having very few acetyl groups, chitosan contains cationic groups. This may cause chitosan to have bile acid-binding capacity, which causes mixed micelles to be entrapped or disintegrated in the duodenum and ileum. This would interrupt bile acid circulation, causing reduced lipid absorption and increased sterol excretion, which has also been observed in animal experiments.

Compounds: Chitosan

The Chitosan, with the cas registry number 9012-76-4, is a kind of white colorless solid. This is stable but incompatible with strong oxidizing agents. And its product categories are including Miscellaneous Natural Products; Biochemistry; Polysaccharides; Sugars; Nutritional Supplements; Dextrins Sugar & Carbohydrates.

Chitosan Unspecified (cas 9012-76-4) Molecular Structure
Name:Chitosan

EINECS:222-311-2

Molecular Formula:Unspecified

CAS Registry Number:9012-76-4

Appearance:faintly beige solid

Molecular Weight:179.17112

Density:1.75g/cm3

Melting Point:88 deg C

Storage Temperature:Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Refractive index:1.7

Solubility:insoluble in water

Stability:Stable. Incompatible with strong oxidizing agents.

Usage:Claimed to have the ability to retain fats and cholesterol in the stomach.
The production method of this chemical is below: Add 20g Chitosan into the 300mL 50% NaOH solvent and wait for its complete infiltration; Then heat to 95℃ for about 1.5 hours, filter out the alkali liquor and then wash to be neutral; Lastly cool and dry to have colorless transparent schistose products 15.6g.

As to its usage, it is widely applied in many ways. It could be used as antistaling agent which is usually used in food industry, and thickening agent, flocculating agent; It could also be used in pharmaceutic, agricultural seed, daily expenses, waste water treatment.


When you are dealing with this chemical, you should be very cautious. Being a kind of harmful chemicals, it may cause damage to health. If by inhalation, in contact with skin and if swallowed, it is dangerous. Then it is irritating to eyes, respiratory system and skin. Therefore, you shoud take the following instructions. Wear suitable protective clothing, and then avoid contacting with skin and eyes. If in case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

2013年11月14日星期四

Application and Production of 2-Chloronicotinic acid

2-Chloronicotinic acid , its cas register number is 2942-59-8. It also can be called 2-Chloro-3-pyridinecarboxylic acid ; Nicotinic acid, 2-chloro- ; 3-Pyridinecarboxylic acid, 2-chloro- .It is a white to cream powder.



1. General description and application

Niacin (also called Nicotinic Acid) and Niacinamide (also called Nicotinamide), two compounds of water-soluble vitamin B complex, are active in the metabolism of body. Chemically they are 3-Pyridinecarboxylic acid and 3-Pyridinecarboxamide respectively. Commercially, niacin is obtained from beta -picoline or from quinoline, which are both obtainable from coal tar. Niacinamide, more water soluble, is the amide form of niacin. When an amide molecule attaches itself to niacin, it becomes niacinamide. The B vitamins niacin and niacinamide are known as preventives of pellagra. Niacin is interchangeable in metabolism with its amide, niacinamide. Nicotinamide is hydrolyzed to the acid in the digestive tract of non-ruminants. After absorption in the mucosa, the amide is formed again. In the rumen of ruminants, nicotinamide is converted in a short time to nicotinic acid. Nicotinamide and nicotinic acid are therefore equivalent in action in the case of farm animals. These are key ingredients in animal feed and animal feed premixes as these contribute to numerous metabolic reactions  as hydrogen-transferring coenzymes. 2-Chloronicotinic acid is used as an intermediate for agrochemicals, feed additives, pharmaceuticals and animal food enrichments. Niacin acts to reduce plasma cholesterol, as a vasodilator and to treat pellagra.  Niacin is used for the prophylaxis. Their derivatives are used for these effects.

It Used as pharmaceutical intermediates for the manufacture of cigarettes mefenamic acid , smoke flufenamic acid ; pesticide intermediates for the manufacture of nicosulfuron , Diflufenican etc.

2. The preparation method  

(1) With 3 - methylpyridine as a raw material , the first reaction with hydrogen peroxide, N- oxo-3 - methyl pyridine , and the acid-binding agent the presence of diisopropylamine in a solvent oxychloride was added dropwise phosphorus chloride, ring chlorination agent , to give 2 - chloro-5 - methyl- pyridine and 2 - chloro -3 - methyl pyridine was , crystallization and distillation using separation techniques combination , respectively to give 2 - chloro- - 5 - methylpyridine and 2 - chloro -3 - methyl pyridine. 2 - chloro -3 - methyl pyridine side-chain chlorinated to give 2 - chloro-3 - trichloromethylpyridine further hydrolysis to give 2 - chloro-3 - pyridine chloride or 2 - chloro-3 - pyridine carboxylic acid (2 - chloro- nicotinic acid ) .


(2) In phosphorus oxychloride and phosphorus trichloride mixture leads to chlorine , temperature controlled at about 60 ℃ until there is residual chlorine escape until cooled and nicotinic acid N-oxide was added in portions , heating and mixing liquid at . 100 ~ 105 ℃ reaction 1 ~ 1.5h, until the reaction mixture was then stirred transparent 30min, and the phosphorus oxychloride removed under reduced pressure , the resulting residue was cooled to room temperature, water was finished .

2-Chloronicotinic acid properties

2-Chloronicotinic acid , its cas register number is 2942-59-8. It also can be called 2-Chloro-3-pyridinecarboxylic acid ; Nicotinic acid, 2-chloro- ; 3-Pyridinecarboxylic acid, 2-chloro- .It is a white to cream powder.


1. Chemistry

Product Name: 2-Chloronicotinic acid

CAS Registry Number: 2942-59-8

IUPAC Name: 2-chloropyridine-3-carboxylic Acid

Molecular Weight: 157.55446 [g/mol]

Molecular Formula: C6H4ClNO2

Appearance:off-white to brown powder

XLogP3-AA: 1.3

H-Bond Donor: 1

H-Bond Acceptor: 3

EINECS: 220-937-0

Melting Point: 176-178 °C (dec.)(lit.)

Index of Refraction: 1.59

Molar Refractivity: 36.16 cm3

Molar Volume: 107.1 cm3

Surface Tension: 61 dyne/cm

Density: 1.47 g/cm3

Flash Point: 145.4 °C

Enthalpy of Vaporization: 58.93 kJ/mol

Boiling Point: 316.8 °C at 760 mmHg

Vapour Pressure: 0.000168 mmHg at 25 °C

Product Categories: blocks;Carboxes;Pyridines;Pyridine;Acids and Derivatives;Heterocycles;Pyridines, Pyrimidines, Purines and Pteredines;Carboxylic Acids;Organic acids;Diflufenican;Chloropyridines;Halopyridines;Carboxylic Acids

Canonical SMILES: C1=CC(=C(N=C1)Cl)C(=O)O

InChI: InChI=1S/C6H4ClNO2/c7-5-4(6(9)10)2-1-3-8-5/h1-3H,(H,9,10)

InChIKey: IBRSSZOHCGUTHI-UHFFFAOYSA-N

2. Storage and uses

Storage Temperature:Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
Solubility:Slightly solubleStability:Stable under normal temperatures and pressures.

Uses:2-Chloronicotinic acid (CAS NO.2942-59-8) can be used as an intermediate for agrochemicals, feed additives, pharmaceuticals and animal food enrichments.

3. Safety Profile

Safty information about 2-Chloronicotinic acid (CAS NO.2942-59-8) is:

Hazard Codes: IrritantXi

Risk Statements: 36/37/38

R36/37/38:Irritating to eyes, respiratory system and skin.

Safety Statements: 22-24/25-37/39-26-36

S22:Do not breathe dust.

S24/25:Avoid contact with skin and eyes.

S37/39:Wear suitable gloves and eye/face protection.

S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

S36:Wear suitable protective clothing.

WGK Germany: 3

Hazard Note: Irritant

TSCA: T

HazardClass: IRRITANT

HS Code: 29333999

Vitamin A and Beta Carotene

Beta Carotene is a carotenoid compound responsible for giving fruits and vegetables their orange pigment. A powerful antioxidant, beta carotene has been found to help protect against cancer and aging. Beta-carotene is a fat soluble vitamin.

Vitamin A is a fat-soluble vitamin that is naturally present in many foods. Vitamin A is important for normal vision, the immune system, and reproduction. Vitamin A also helps the heart, lungs, kidneys, and other organs work properly. The most common type of provitamin A in foods and dietary supplements is beta-carotene.

Beta Carotene(CAS.NO:7235-40-7), along with other carotenoids, is a molecule that the body easily changes into Vitamin A.  While most nutrition labels will list a recommended amount of vitamin A to include in a healthy diet, most health professionals will recommend that beta carotene be the main source of that vitamin A consumption.  The reason for this is that beta carotene and other carotenoids are found mainly in fruits and vegetables which contain a host of other vitamins and minerals and are very low in fat.  Vitamin A, however, if consumed in its full form, is mainly found in butter and eggs.  Getting your recommenced daily allowance of vitamin A without using beta carotene would mean eating large amounts of saturated fats that would be incredibly unhealthy.  Once absorbed by the small intestines, beta carotene is changed directly into Vitamin A.

In 1831, beta-carotene was first isolated from the roots of carrots, but it was not until the Nobel prize-winning research of Paul Karrer in the early 1930s that the structure of the substance was determined. The earliest use of synthesized beta-carotene was as a food colorant, but during the 1980s the vitamin precursor抯 growing reputation as an antioxidant and a possible cancer-fighter resulted in its frequent inclusion in vitamin supplements. Since that time, however, conflicting findings about the benefits of taking synthesized beta-carotene have surfaced.

Beta-carotene belongs to a class of chemical compounds called carotenoids. Among many other positive health benefits, carotenoids act as a precursor to vitamin A, so if you know about the benefits of vitamin A, you will completely understand the importance of beta-carotene.

Basically, when you consume foods or ingest supplements containing beta-carotene, it breaks down into vitamin A in your liver.

Beta-carotene is thought to possess many positive health benefits and in particular helps prevent night blindness and other eye problems.

It also effective in skin disorders, enhances immunity, protects against toxins and cancer formations, colds, flu, and infections. It is an antioxidant and protector of the cells while slowing the aging process.

It is considered that natural Beta-Carotene aids in cancer prevention. It is important in the formation of bones and teeth. No vitamin overdose can occur with natural Beta-Carotene. It has been reported that beta carotene offers a notable measure of photoprotection to individuals with porphyria. (Beta-Carotene helps to protect the eye and vision).

Vitamin A is necessary for a large number of metabolic functions similar to other vitamins.  One of the major unique functions of vitamin A is it磗 role in vision, especially dim-light vision.  In third world countries where fruit and vegetables are not readily available, vitamin A deficiency is the leading cause of blindness in children.  Beta carotene is a rather cheap vitamin to produce, which means this type of blindness is easily preventable.

Vitamin A produced from beta carotene is also necessary for normal cell growth and cell division.  DNA replication requires the presence of vitamin A to function properly.  Because of this, rapidly dividing cells often give the first signs of vitamin A deficiency.  These symptoms include poor skin quality, brittle hair and nausea because of problems with the lining of the stomach.  Vitamin A is also an important part of bone and teeth development.  Inadequate Vitamin A during the growing years will lead to abnormal growth of the extremities.

Another important function of vitamin A includes its use by the body as an antioxidant.  An antioxidant is a molecule that the body can use to block a number of harmful chemical reactions.  One of these harmful reactions involves the interference of DNA replication by free radicals.  Vitamin A and other antioxidants bind with the free radicals and keep them from disrupting cell division.  Another very important action of antioxidants and vitamin A involve the formation of plaques by cholesterol.  Once inside the bloodstream, cholesterol binds together and forms plaques which then attach to the inside of the artery wall and restrict blood flow.  Antioxidants including vitamin A, keep the cholesterol from binding together, and also prevent it from attaching to the walls of the arteries.

Beta-Carotene Sources in the diet

β-Carotene(CAS.NO:7235-40-7) contributes to the orange color of many different fruits and vegetables. Vietnamese gac (Momordica cochinchinensis Spreng.) and crude palm oil are particularly rich sources, as are yellow and orange fruits, such as cantaloupe, mangoes and papayas, and orange root vegetables such as carrots and yams. The color of β-carotene is masked by chlorophyll in green leafy vegetables such as spinach, kale, sweet potato leaves, and sweet gourd leaves. Vietnamese gac and crude palm oil have the highest content of β-carotene of any known fruit or vegetable, 10 times higher than carrots, for example. However, gac is quite rare and unknown outside its native region of Southeast Asia, and crude palm oil is typically processed to remove the cartenoids before sale to improve the color and clarity.


Below is a list of high beta-carotene foods.

1. Sweet Potato
Perhaps the most orange of all fruits and vegetables, sweet potatoes will provide 9444μg of beta carotene per 100g serving. That is 14260μg in a medium sized potato(150g).

2. Kale
Kale is considered to be an early form of cabbage, and is delicious steamed with wine. 100 grams of raw kale will provide 9226μg of beta-carotene, 100 grams cooked will provide 8173μg.

3. Carrots
The beta-carotene in carrots gives them their orange color. 100 grams of raw carrots provides 8285μg of beta-carotene, one medium sized carrot(61g) will provide 5053μg, and one baby carrot(10g) will provide 639μg.

4. Turnip Greens
Turnip greens add a nice note of spice to any salad or soup. 100 grams of raw turnip greens provides 6952μg of beta-carotene, 100 grams cooked provides 4575μg.

5. Mustard Greens

Mustard green have even more spice than turnip greens and are great in a salad or wrap. Mustard greens provide 6300μg of beta-carotene per 100g serving, cooked mustard greens will provide 3794μg.

6. Spinach
An excellent vegetable to add to a wrap or calzone, raw spinach provides 5626μg of beta-carotene per 100g serving. Due to water loss during cooking, cooked spinach provides even more beta-carotene with 6288μg per 100g serving.

7. Dried Herbs
Dried herbs are so packed with vitamins they appear on practically every HealthAliciousNess top 10 list. Make it a habit to add a pinch of dried herb to everything you prepare. Dried Basil provides the most beta-carotene with 5584μg per 100g serving, it is followed by Dried Parsley (5380μg), Marjoram (4806μg), Dried Oregano (4112μg), Ground Sage (3485μg), Dried Coriander (3407μg), and Fresh Thyme (2851μg).

8. Butternut Squash
This dark orange squash has a delicious nutty and sweet flavor. 100 grams baked provides 4570μg of beta-carotene, 100 grams raw will provide 4226μg.

9. Lettuce
In regards to beta-carotene, the kind of lettuce does matter. Dark colorful lettuces provide the most beta-carotene with Red-Leaf Lettuce providing 4495μg per 100g, Green-Leaf providing 4443μg per 100g, and Iceberg only providing 299μg per 100g.

10. Collards
A cousin of cabbage and also a good source of calcium, collards provide 3842μg of beta-carotene per 100g serving. Cooked collards provide even more with 4814μg per 100g serving.

Cyclohexanone application

Cyclohexanone is a colourless liquid used as a solvent for cellulose lacquers. It is the organic compound with the formula (CH2)5CO. The molecule consists of six-carbon cyclic molecule with a ketone functional group. This colorless oil has an odor reminiscent of peardrop sweets as well as acetone. Over time, samples assume a yellow color due to oxidation. Cyclohexanone is slightly soluble in water, but miscible with common organic solvents.

Cyclohexanone(CAS.NO:108-94-1) is a synthetic organic liquid used primarily as an intermediate in the production of nylon. Other minor applications are as an intermediate, additive and solvent in a variety of products.

Cyclohexanone is used in organic synthesis, particularly in the production of adipic acid and caprolactam (ca. 95%), polyvinyl chloride and its copolymers, and methacrylate ester polymers. Additional uses include wood stains, paint and varnish removers, spot remover, degreasing of metals, polishes, levelling agents, dyeing and delustering silk, lubricating oil additives, solvent for herbicides, cellulosics, natural and synthetic resins, waxes, fats, etc.

The great majority of cyclohexanone is consumed in the production of precursors to Nylon 6,6 and Nylon 6. About half of the world's supply is converted to adipic acid, one of two precursors for nylon 6,6. For this application, the KA oil (see above) is oxidized with nitric acid. The other half of the cyclohexanone supply is converted to the oxime. In the presence of sulfuric acid catalyst, the oxime rearranges to caprolactam, a precursor to nylon 6:

When used in industrial coating processes, cyclohexanone is maintained within a closed vessel. Also used in such products as accelerators,developers, paints and lacquers, printing inks, laboratory chemicals, adhesives, regulators, cleaning agents and as diluents.

Intermediate for E. caprolactam Herbicides, insecticides, pharmaceuticals, polycondensates.Used as solvent for plant protection agents .Used as PVC dyes and varnish.

For Du Pont, cyclohexanone is produced and further processed in a closed system as an intermediate in the production of adipic acid.

For others (producers excluding Du Pont), sixty percent of imported quantities is used as a solvent in herbicides. Application rate is estimated to be 200 mL/hectare.However, cyclohexanone is being replaced by other solvents; therefore its use in this application is  expected to be reduced.The remainder is for undetermined uses.


Transport:The product is transported in road tank cars, containers and railway tank wagons. Cyclohexanone is a hazardous material.

2013年11月13日星期三

Intro to Metronidazole

Metronidazole's brand name is Flagyl. It is an antibiotic effective against anaerobic bacteria and certain parasites. Anaerobic bacteria are single-celled, living organisms that thrive in environments in which there is little oxygen (anaerobic environments) and can cause disease in the abdomen (bacterial peritonitis), liver (liver abscess), and pelvis (abscess of the ovaries and the Fallopian tubes). Giardia lamblia and ameba are intestinal parasites that can cause abdominal pain and diarrhea in infected individuals. Trichomonas is a vaginal parasite that causes inflammation of the vagina (vaginitis). Metronidazole selectively blocks some of the functions within the bacterial cells and the parasites resulting in their death.


Name:Metronidazole

EINECS:207-136-1

Molecular Formula:C6H9N3O3

CAS Registry Number:443-48-1

Appearance:white to slightly yellow crystalline powder

Molecular Weight:171.15

Density:1.45 g/cm3

Boiling Point:405.4 °C at 760 mmHg

Melting Point:159-163℃

Flash Point:199 °C

Storage Temperature:2-8°C

Refractive index:1.612

Solubility:<0.1 g/100 mL at 20 °C in water

Stability:Stable. Incompatible with strong oxidizing agents.

Usage:Microbiocide.

Chemical Properties: white to slightly yellow crystalline powder

Usage: Used as an antibacterial in the treatment of rosacea. Antiprotozoal (trichomonas). A potential human carcinogen.

General Description: White to pale-yellow crystalline powder with a slight odor. Bitter and saline taste. pH (saturated aqueous solution) about 6.5.

Air & Water Reactions: Insoluble in water.

Reactivity Profile: Metronidazole darkens on exposure to light. Metronidazole is incompatible with strong oxidizing agents. .


Fire Hazard :Flash point data for Metronidazole are not available; however, Metronidazole is probably combustible.

Where can you buy Sulfur(α)?

Sulfur or sulphur  is a chemical element with symbol S and atomic number 16. It is an abundant, multivalent non-metal. Under normal conditions, sulfur atoms form cyclic octatomic molecules with chemical formula S8. Elemental sulfur is a bright yellow crystalline solid when at room temperature. Chemically, sulfur can react as either an oxidant or reducing agent. It oxidizes most metals and several nonmetals, including carbon, which leads to its negative charge in most organosulfur compounds, but it reduces several strong oxidants, such as oxygen and fluorine.


Sulfur(α) is one of the Allotropes of sulfur. There are a large number of allotropes of sulfur. In this respect, sulfur is second only to carbon. The most common form found in nature is yellow orthorhombic Sulfur(α), which contains puckered rings of S.

Sulfur(α) is the form most commonly found in nature. When pure it has a greenish-yellow colour (traces of cyclo-S7 in commercially available samples make it appear yellower). It is practically insoluble in water and is a good electrical insulator with poor thermal conductivity. It is quite soluble in carbon disulfide: 35.5 g/100 g solvent at 25 °C. It has a rhombohedral crystal structure. This is the predominant form found in "flowers of sulfur", "roll sulfur" and "milk of sulfur". It contains S8 puckered rings, alternatively called a crown shape.The S-S bond lengths are all 206 pm and the S-S-S angles are 108° with a dihedral angle of 98°. At 95.3 °C, α-sulfur converts to β-sulfur.
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