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Merck

36684

3-Aminophenol

PESTANAL®, analytical standard

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About This Item

Linear Formula:
H2NC6H4OH
CAS Number:
591-27-5
Molecular Weight:
109.13
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755450
EC Number:
209-711-2
Beilstein/REAXYS Number:
636059
MDL number:
MFCD00007786

Key Documents

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InChI key

CWLKGDAVCFYWJK-UHFFFAOYSA-N

InChI

1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2

SMILES string

Nc1cccc(O)c1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

164 °C/11 mmHg (lit.)

Quality Level

100

mp

120-124 °C (lit.)

application(s)

agriculture
environmental

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH6730
BCBW5080

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A new twist to an old tale: novel insights into the differential toxicities of acetaminophen and its regioisomer N-acetyl-meta-aminophenol (AMAP).
J Gerry Kenna
Archives of toxicology, 87(1), 15-18 (2012-09-25)
Mutsuko Koizumi et al.
The Journal of toxicological sciences, 27(5), 411-421 (2003-01-22)
Repeated dose toxicity of 3-aminophenol was examined on oral administration to newborn and young rats, and susceptibility was analyzed in terms of the no observed adverse effect level (NOAEL) and the unequivocally toxic level. In the 18-day newborn rat study
P Nagaraja et al.
Farmaco (Societa chimica italiana : 1989), 58(12), 1295-1300 (2003-11-25)
A rapid, simple and sensitive spectrophotometric method for the determination of some sulfa drugs is described. The method is based on the formation of orange yellow colored azo product by the diazotization of sulfonamides, viz., dapsone (DAP), sulfathiazole (SFT), sulfadiazine
R Kutty et al.
Canadian journal of microbiology, 46(3), 211-217 (2000-04-05)
Pseudomonas sp. strain PH1 was isolated from soil contaminated with pharmaceutical and dye industry waste. The isolate PH1 could use m-aminophenol as a sole source of carbon, nitrogen, and energy to support the growth. PH1 could degrade up to 0.32
Hung-Kuang Chang et al.
Biochemical and biophysical research communications, 371(1), 149-153 (2008-04-18)
The gene encoding m-hydroxybenzoate hydroxylase (mobA) was cloned from Comamonas testosteroni GZ39. MobA converts m-hydroxybenzoate and to a lesser extent p-hydroxybenzoate to protocatechuate. To explore the structural and functional relationships in phenolic acid monooxygenases, MobA was subjected to in vitro
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