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Merck
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Documentos

A7085

Sigma-Aldrich

Acetaminofeno

BioXtra, ≥99.0%

Sinônimo(s):

4′-Hidroxiacetanilida, 4-Acetamidofenol, N-(4-Hidroxifenil)acetamida, N-Acetil-4-aminofenol, APAP, Paracetamol

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About This Item

Fórmula linear:
CH3CONHC6H4OH
Número CAS:
Peso molecular:
151.16
Beilstein:
2208089
Número CE:
Número MDL:
Código UNSPSC:
12352111
ID de substância PubChem:
NACRES:
NA.25

linha de produto

BioXtra

Nível de qualidade

Ensaio

≥99.0%

forma

powder

Impurezas

≤0.0005% Phosphorus (P)
≤0.1% Insoluble matter

resíduo de ignição

≤0.1%

pf

168-172 °C (lit.)

solubilidade

ethanol: 0.5 M, clear, colorless

traços de ânion

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

traços de cátion

Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%

cadeia de caracteres SMILES

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)

chave InChI

RZVAJINKPMORJF-UHFFFAOYSA-N

Informações sobre genes

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Descrição geral

Acetaminophen or paracetamol is an analgesic and antipyretic. It is however a weak non opioid analgesic.

Aplicação

Acetaminophen has been used:
  • as an anti-inflammatory drug to test its effect in lipid peroxidation in marine mussels
  • to test its effect on neurite outgrowth in gamma-aminobutyric acid-ergic and glutamatergic neurons
  • as a hepatocellular injury inducing agent in mice

Analgésico.

Ações bioquímicas/fisiológicas

Acetaminophen or paracetamol is an inhibitor of prostaglandin synthesis. It is complexed with arachidonic acid in central nervous system resulting in the formation of N-arachidonoylphentolamine, which is essential for the activation of cannabinoid receptor. Acetaminophen is metabolized to toxic N-acetyl-p-benzoquinone imine. Paracetamol is prescribed for osteoarthritis pain and inhibits cyclooxygenase 1 and 2 activities. It is metabolized by the cytochrome P450 enzymes in liver and is implicated in liver toxicity.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Classificações de perigo

Acute Tox. 4 Oral

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

364.3 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

184.6 °C - Pensky-Martens closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Paracetamol: mechanisms and updates
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Continuing education in anaesthesia, critical care & pain, 14(4), 153-158 (2013)
Interactions between Acetaminophen and Phytotherapies: Overview for the Rational Use of Phytotherapics
Ribeiro J, et al.
Journal of Natural Product and Plant Resources, 8(3), 1-14 (2018)
Early detection of acute druginduced liver injury in mice by non-invasive NIR fluorescence imaging
Vasquez KO and Peterson JD
Journal of Pharmacology and Experimental Therapeutics, 1(4), 23-23 (2017)
Effects on feeding rate and biomarker responses of marine mussels experimentally exposed to propranolol and acetaminophen
Sole M, et al.
Analytical and Bioanalytical Chemistry, 396(2), 649-656 (2010)
Comparative Sensitivity of Human-Induced Pluripotent Stem Cell-Derived Neuronal Subtypes to Chemically Induced Neurodegeneration
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