36684
3-氨基苯酚
PESTANAL®, analytical standard
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线性分子式:
H2NC6H4OH
化学文摘社编号:
分子量:
109.13
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
209-711-2
Beilstein/REAXYS Number:
636059
MDL number:
产品名称
3-氨基苯酚, 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
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相关类别
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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2
存储类别
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
法规信息
危险化学品
此项目有
[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)
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)
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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