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Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin

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Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin

China Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin supplier
Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin supplier Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin supplier

Large Image :  Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin

Product Details:

Place of Origin: CN
Brand Name: LSW
Certification: ISO9001,BRC, KOSHER
Model Number: 62-44-2

Payment & Shipping Terms:

Minimum Order Quantity: 10g
Price: Negotiation
Packaging Details: Discreet package
Delivery Time: 5-8 working days
Payment Terms: T/T, Western Union, MoneyGram,Bitcoin
Supply Ability: 5000kg/month
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Detailed Product Description
CAS: 62-44-2 MF: C10H13NO2
MW: 179.2157 Purity: 99.00%
Appearance: White Crystalline Powder Grade: Pharmaceutical Grade

 

Bulk Stocks on USA and Canada Powder Phenacetin Pharmaceutical Grade CAS 62-44-2 

 

Phenacetin Quick Details

 

 

Phenacetin
CAS: 62-44-2
EINECS Number: 200-533-0
Formula: C10H13NO2
MW: 179.2157
Density: 1.099g / cm3
Melting point: 133-138 ℃
Boiling point: 355.1 ° C at 760 mmHg
Flash Point: 168.5 ° C
Water-soluble: 0.076 g / 100 mL
Vapor Pressure: 3.21E-05mmHg at 25 ° C
Uses: Anti-inflammatory drugs
Assay: 99%
Appearance: White or almost white crystalline powder

Phenacetin is a pain-relieving and fever-reducing drug, widely used from its introduction in 1887 until banned in the US by the FDA in 1983. Its use has declined because of its adverse effects, which include increased risk of certain cancers and kidney damage. It is metabolized into paracetamol, which replaced it in some over-the-counter medications following the ban on phenacetin.

 

 

Phenacetin Description


The painkiller phenacetin was the world's first synthetic pharmaceutical drug. Phenacetin was often accompanied by aspirin and caffeine in what were called APC pills, which were widely distributed during and after World War II. The use of phenacetin in the U.S. was discontinued in the 1980s because of links to cancer and other adverse side effects, but it remains available in some countries.

 

Phenacetin is a white crystalline powder with the chemical composition C10H13NO2. It was first developed by Harmon Northrop Morse in 1878. In addition to its pain-reducing properties, it also has been used as a fever-reducer, a treatment for rheumatoid arthritis and a treatment for intercostal neuralgia, a rare disorder that causes pain in the nerves around the ribs. It was one of the first painkillers that was not derived from opium while at the same time being absent of anti-inflammatory qualities.

 

In 1983, the U.S. Food and Drug Administration (FDA) banned phenacetin in the U.S. because of its discovered carcinogenic properties and its link to kidney failure. The FDA stated that phenacetin alone is reasonably believed to be a human carcinogen, or cancer-causing agent, and that painkiller mixtures containing the drug are known human carcinogens. There has been little evidence found that phenacetin alone is a human carcinogen because it usually has been administered in combination with other drugs.

 

 

Pharma Grade Local Anaesthesia Drugs White Crystalline Powder Phenacetin

 

 

Applications

 

Phenacetin was widely used until the third quarter of the twentieth century, often in the form of an "A.P.C." or aspirin-phenacetin-caffeine compound analgesic, as a remedy for fever and pain. An early formulation (1919) was Vincent's APC in Australia. However the U.S. Food and Drug Administration ordered the withdrawal of drugs containing phenacetin in November 1983, owing to its carcinogenic and kidney-damaging properties (Federal Register of October 5, 1983 (48 FR 45466)).

 

It was also banned in India.As a result some branded, previously phenacetin-based preparations continued to be sold, but with the phenacetin replaced by safer alternatives. A popular brand of phenacetin was Roche's Saridon, which was reformulated in 1983 to contain propyphenazone, paracetamol and caffeine. Coricidin was also reformulated without phenacetin. Paracetamol is a metabolite of phenacetin with similar analgesic and antipyretic effects, but the new formulation has not been found to have phenacetin's carcinogenicity.

 

Phenacetin is now being used as a cutting agent to adulterate cocaine in the UK and Canada, owing to the similar physical features of the two drugs.Due to low cost phenacetin is used for research into the physical and refractive properties of crystals. It is an ideal compound for this type of research.

 

 

 

COA

 

 

 

Product name Phenacetin
CAS No. 62-44-2 Outer Packing 25KG
Production date 2016.05.07 Shelf life 2019.05.05
Standard adopted BP68
Items of analysis Specification Results
Description Should comply with the standard Comforms
Identification Positive Positive
Melting point 134℃ to 136.5℃ 134.5℃ to 136.5℃
4-chloroacetanilide BP1968 <3.5ml/0.6g
P-Phenetidine BP1968 Comforms
Sulphated ash ≤0.1% 0.07%
Assay ≥99% 99.1%
through a uss#80   98%
Conclusion Qualified

 

 

 

 

History:

 

Phenacetin was introduced in 1887 in Elberfeld, Germany by German company Bayer, and was used principally as an analgesic; it was one of the first synthetic fever reducers to go on the market. It is also known historically to be one of the first non-opioid analgesics without anti-inflammatory properties.

Prior to World War One, Britain imported phenacetin from Germany.During the war, a team including Jocelyn Field Thorpe and Martha Annie Whiteley developed a synthesis in Britain.

 

 

Known mechanism of action:

 

Phenacetin's analgesic effects are due to its actions on the sensory tracts of the spinal cord. In addition, phenacetin has a depressant action on the heart, where it acts as a negative inotrope. It is an antipyretic, acting on the brain to decrease the temperature set point. It is also used to treat rheumatoid arthritis (subacute type) and intercostal neuralgia.

It is metabolized in the body to paracetamol (acetaminophen), which is also a clinically relevant analgesic.

 

 

Uses:

 

Phenacetin was widely used until the third quarter of the twentieth century, often in the form of an A.P.C., or "aspirin-phenacetin-caffeine" compound analgesic, as a remedy for fever and pain. An early formulation (1919) was Vincent's APC in Australia.

 

In the United States, the Food and Drug Administration ordered the withdrawal of drugs containing phenacetin in November 1983, due to its carcinogenic and kidney-damaging properties.It was also banned in India.As a result, some branded, and previously phenacetin-based, preparations continued to be sold, but with the phenacetin replaced by safer alternatives. A popular brand of phenacetin was Roche's Saridon, which was reformulated in 1983 to contain propyphenazone, paracetamol and caffeine. Coricidin was also reformulated without phenacetin. Paracetamol is a metabolite of phenacetin with similar analgesic and antipyretic effects, but the new formulation has not been found to have phenacetin's carcinogenicity.

 

Phenacetin has been used as a cutting agent to adulterate cocaine in the UK and Canada, due to the similar physical properties.

Due to its low cost, phenacetin is used for research into the physical and refractive properties of crystals. It is an ideal compound for this type of research.

 

 

Effects:

 

Phenacetin Usage Analgesic, antipyretic. Component of APC tablets, analgesic mixture also containing aspirin and caffeine. Phenacetin is reasonably anticipated to be a human carcinogen; analgesic mixtures containing Phenacetin are listed as known human carcinogens.

 

Paracetamol is a metabolite of phe-nacetin with similar analgesic and antipyretic effects, but the new formulation has not been found to have phe-nacetin's carcinogenicity.
Phenacetin is now being used as a cutting agent to adulterate in the UK and Canada, owing to the similar physical features of the two drugs.

 

 

Phenacetin Function


Antipyretic effect is stronger than the analgesic effect. Effect of strength is slow and long-lasting as aspirin,low toxicity. Research shows that: This product and its metabolites acetaminophen have the antipyreticeffect. Because the enzyme inhibitor make Phenacet-Acetate not be converted into paracetamol, still showed
obvious antipyretic effect,thus the antipyretic effect after the product line not converrt to paracetamol.Themild Phenacet-Acetate analgesic effect usually lasts 3 to 4 hours; and synergistic effect, of alicylic acid coadministrationmake the analgesic effect enhancement. The main clinical is for small animal antipyretic analgesic. This product is also a component of the APC tablet.

 

 

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