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CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2

CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2

  • CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2
  • CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2
CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2
Product Details:
Place of Origin: China
Brand Name: Top Pharm
Certification: IOS 901
Model Number: 103-90-2
Payment & Shipping Terms:
Minimum Order Quantity: 10g
Price: Negotiable
Packaging Details: As your requirments
Delivery Time: 3-6 working days
Payment Terms: T/T, Western Union, MoneyGram,bitcoin
Supply Ability: bulk stock
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Detailed Product Description
Appearance: White Or White Crystalline Powder Other Names: Acetaminophen
Purity: 99% Molecular Weight: 151.165
Molecular Formula: C8H9NO2
High Light:

ghrp 6 acetate


active raw material

Pain killers 99% purity Pharmaceutical raw materials Paracetamol/Acetaminophen white powder CAS number: 103-90-2
Chemical Names: Acetaminophen; 4-Acetamidophenol; Paracetamol;
CAS: 103-90-2
Molecular Formula: C8H9NO2 or HOC6H4NHCOCH3
Molecular Weight: 151.165 g/mol
Paracetamol belongs to a group of medicines known as analgesics, or painkillers. It is used to relieve mild-to-moderate pain. It is also useful for lowering a raised temperature (fever), such as after childhood immunisation.
Paracetamol is a common painkiller and is available to buy from many retail outlets as tablets/capsules and as liquid medicine. Many brands of 'over-the-counter' combination painkillers contain paracetamol, as do many cold and flu remedies. It is important that you check the label on any preparation that you buy to make sure that you are not taking more than one preparation containing paracetamol.
Since their synthesis in the late 1800s paracetamol (acetaminophen) and phenacetin have followed divergent pathways with regard to their popularity as mild analgesic/antipyretic drugs. Initially, paracetamol was discarded in favour of phenacetin because the latter drug was supposedly less toxic. Today the opposite is true, and paracetamol, along with aspirin, has become one of the two most popular 'over-the-counter' non-narcotic analgesic agents. This marked increase in the wide approval attained by paracetamol has been accompanied by the virtual commercial demise of phenacetin because of its role, albeit somewhat circumstantial, in causing analgesic nephropathy. Both paracetamol and phenacetin are effective mild analgesics, suitable for treating mild to moderate pain, and their actions are broadly comparable with those of aspirin and related salicylates, although they do not appear to possess significant anti-inflammatory activity. Since a major portion of a dose of phenacetin is rapidly metabolised to paracetamol, it seems possible that phenacetin owes some of its therapeutic activity to its main metabolite, paracetamol, whereas its most troublesome side effect (methaemoglobinaemia) is due to another metabolite, p-phenetidine. The mechanism of action of paracetamol is poorly defined, although it has been speculated that it may selectively inhibit prostaglandin production in the central nervous system, which would account for its analgesic/antipyretic properties. The lack of any significant influence on peripheral cyclooxygenase would explain the absence of anti-inflammatory activity. At therapeutic doses paracetamol is well tolerated and produces fewer side effects than aspirin. The most frequently reported adverse effect associated with paracetamol is hepatotoxicity, which occurs after acute overdosage (usually doses greater than 10 to 15g are needed) and, very rarely, during long term treatment with doses at the higher levels of the therapeutic range. Paracetamol damages the liver through the formation of a highly reactive metabolite which is normally inactivated by conjugation with glutathione. Overdoses of paracetamol exhaust glutathione stores, thus allowing the accumulation of this toxic metabolite which covalently binds with vital cell elements and can result in liver necrosis. Glutathione precursors (notably intravenous N-acetylcysteine) have proved remarkably successful in treating paracetamol overdose, as long as treatment is initiated within 10 hours.

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CAS 103-90-2 Paracetamol Pain Relief 4 Acetamidophenol Molecular Formula C8H9NO2 0



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