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09170

4-Aminophenol hydrochloride

≥99.0% (AT)

Sinonimo/i:

4-Hydroxyaniline hydrochloride

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Informazioni su questo articolo

Formula condensata:
H2NC6H4OH · HCl
Numero CAS:
Peso molecolare:
145.59
UNSPSC Code:
12352107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
200-122-6
Beilstein/REAXYS Number:
3911747
MDL number:


Quality Segment

assay

≥99.0% (AT)

mp

300-305 °C (dec.)

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

Application

4-Aminophenol hydrochloride can be used to study cell biology, bioactive small molecules, chemical synthesis, organic building blocks, oxygen compounds and phenols. 4-Aminophenol hydrochloride has been used to study ferrihemoglobin and kidney lesions in rats.


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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

Classe di stoccaggio

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



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M Kiese et al.
Archives of toxicology, 34(4), 337-340 (1975-12-18)
4-Dimethylaminophenol hydrochloride (DMAP), 20mg/kg i.v., was found to oxidize in rats as much as 50% of the hemoglobin to ferrihemoglobin but did not cause kidney lesions. 4-Aminophenol hydrochloride, 400 mg/kg i.v., oxidized only 25% of the hemoglobin and produced large
Tomoyuki Yasukawa et al.
Biosensors & bioelectronics, 37(1), 19-23 (2012-05-23)
In this work, a novel immunosensing method has been developed on the basis of the sensitive determination of a product generated by an enzyme reaction with dual amplification system combining an electrochemical-redox cycling and coulometric signal transduction using a galvanic
Rosivaldo S Borges et al.
Chemical biology & drug design, 81(3), 414-419 (2013-02-15)
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



Numero articolo commerciale globale

SKUGTIN
112038-100ML04061838699466
09170-500G04061833439814
09170-100G04061838653673

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