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线性分子式:
H2NC6H4OH · HCl
化学文摘社编号:
分子量:
145.59
UNSPSC Code:
12352107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
200-122-6
Beilstein/REAXYS Number:
3911747
MDL number:
Form:
powder
SMILES string
Cl[H].Nc1ccc(O)cc1
InChI
1S/C6H7NO.ClH/c7-5-1-3-6(8)4-2-5;/h1-4,8H,7H2;1H
InChI key
RVGOBWDGAVAVPJ-UHFFFAOYSA-N
form
powder
color
gray
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Application
4-Aminophenol (p-aminophenol, PAP), a nephrotoxin and hepatotoxin, may be used to study its mechanisms of biological toxicity and glutathione depletion.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Sens. 1 - STOT RE 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
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This theoretical and experimental study describes the design and evaluation of the free-radical scavenging effect for the molecular association of 4-aminophenol and salicylate derivatives. For this purpose, we employed theoretical methods for the selection of antioxidant drugs and the rapid
Hyeok-Jin Ko et al.
Biotechnology letters, 34(4), 677-682 (2011-12-02)
Aryl acylamidase (EC 3.5.1.13, AAA) acts on the amide bond between aryl and acyl groups. Whole cells of Escherichia coli overexpressing a novel bacterial AAA synthesized p-acetaminophenol (p-AAP) from p-aminophenol (p-AP, aryl compound) and acetate (acyl donor). Optimum conditions were
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