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Merck
CN

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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Product Name

3-Aminophenol, PESTANAL®, analytical standard

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.)

mp

120-124 °C (lit.)

application(s)

agriculture
environmental

format

neat

Quality Level

100

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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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH6730
BCBW5080

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[Experimental data for the substantiation of the maximum allowable concentration of meta-aminophenol in the air of work areas].
K L Markarian et al.
Gigiena truda i professional'nye zabolevaniia, (1)(1), 49-50 (1988-01-01)
Frank Filsinger et al.
Physical review letters, 100(13), 133003-133003 (2008-06-04)
We have selected and spatially separated the two conformers of 3-aminophenol (C(6)H(7)NO) present in a molecular beam. Analogous to the separation of ions based on their mass-to-charge ratios in a quadrupole mass filter, the neutral conformers are separated based on
Woon Yong Sohn et al.
Physical chemistry chemical physics : PCCP, 13(15), 7037-7042 (2011-03-15)
3-Aminophenol (3AP) has two conformers, cis and trans, depending on the orientation of the OH group relative to the NH(2) group. While both conformers are found in the jet-cooled spectra of 3AP, only the trans isomer was found in the
Simultaneous spectrophotometric determination of PAS and its degradation product m-aminophenol.
C Vetuschi et al.
Pharmaceutica acta Helvetiae, 63(11), 290-293 (1988-01-01)
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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