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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

Stato

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
0000373100
0000366464
0000373099
0000321410
0000373100

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Sigma-Aldrich

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USP

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Sigma-Aldrich

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USP

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Ibuprofene

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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
Karel Allegaert et al.
Archives of disease in childhood, 98(6), 462-466 (2013-04-23)
There remains a need for alternative medical treatments for patent ductus arteriosus (PDA) closure in extreme preterm neonates because of therapeutic failure and adverse effects associated with non-selective cyclo-oxygenase inhibitors. Reports of an association between paracetamol exposure and PDA closure
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
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.
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