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A3035

Sigma-Aldrich

Acetaminofene

analytical standard

Sinonimo/i:

4′-idrossiacetanilide, 4-acetamidofenolo, N-(4-idrossifenil)acetammide, N-acetil-4-amminofenolo, APAP, Paracetamolo

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About This Item

Formula condensata:
CH3CONHC6H4OH
Numero CAS:
103-90-2
Peso molecolare:
151.16
Beilstein:
2208089
Numero CE:
203-157-5
Numero MDL:
MFCD00002328
Codice UNSPSC:
41116107
ID PubChem:
24890717
NACRES:
NA.21

Grado

analytical standard

Livello qualitativo

300

Forma fisica

powder

Confezionamento

vial of 1 g

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

168-172 °C (lit.)

applicazioni

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Stringa SMILE

CC(=O)Nc1ccc(O)cc1

InChI

1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)
RZVAJINKPMORJF-UHFFFAOYSA-N

Informazioni sul gene

human ... FAAH(2166) , PTGS1(5742) , PTGS2(5743) , TRPV1(7442)

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Applicazioni

Analgesico.

Confezionamento

Supplied in amber screw-cap vials

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

364.3 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

184.6 °C - Pensky-Martens closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
SLCB0560
SLBX2188
SLBQ8819V
SLBK4475V
SLBD2576V

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Sigma-Aldrich

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4-Aminophenol ≥98%

Sigma-Aldrich

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4-Aminophenol

Aspirin United States Pharmacopeia (USP) Reference Standard

USP

1044006

Aspirin

Phenacetin ≥98.0% (HPLC)

Sigma-Aldrich

77440

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Sigma-Aldrich

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USP

1374306

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Acetaminophen solution 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

Supelco

A-064

Acetaminophen solution

Ibuprofene

Supelco

I110

Ibuprofene

S M de Morais et al.
Gastroenterology, 102(2), 577-586 (1992-02-01)
Gilbert's syndrome occurs in 5%-7% of the human population and is caused by an inherited deficiency in the glucuronidation of endogenous bilirubin, resulting in its accumulation and jaundice. The authors of the present study have previously shown that rats with
Edward Munsterhjelm et al.
Anesthesiology, 103(4), 712-717 (2005-09-30)
Acetaminophen (paracetamol) is widely used for postoperative analgesia. Its mechanism of action is inhibition of prostaglandin synthesis in the central nervous system, and acetaminophen is traditionally not considered to influence platelet function. The authors studied the dose-dependent inhibition of platelet
Mitchell R McGill et al.
Pharmaceutical research, 30(9), 2174-2187 (2013-03-07)
Acetaminophen (APAP) is one of the most widely used drugs. Though safe at therapeutic doses, overdose causes mitochondrial dysfunction and centrilobular necrosis in the liver. The first studies of APAP metabolism and activation were published more than 40 years ago.
Garry G Graham et al.
Drug safety, 28(3), 227-240 (2005-03-01)
The excellent tolerability of therapeutic doses of paracetamol (acetaminophen) is a major factor in the very wide use of the drug. The major problem in the use of paracetamol is its hepatotoxicity after an overdose. Hepatotoxicity has also been reported
Garry G Graham et al.
Inflammopharmacology, 21(3), 201-232 (2013-05-31)
Paracetamol is used worldwide for its analgesic and antipyretic actions. It has a spectrum of action similar to that of NSAIDs and resembles particularly the COX-2 selective inhibitors. Paracetamol is, on average, a weaker analgesic than NSAIDs or COX-2 selective
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