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Merck
CN

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:
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grade

analytical standard

Quality Level

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

SMILES string

Nc1cccc(O)c1

InChI

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

InChI key

CWLKGDAVCFYWJK-UHFFFAOYSA-N

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


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Warning

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
Toxic effects of aminophenols on aquatic life using the zebrafish embryo test and the comet assay.
L W Sun et al.
Bulletin of environmental contamination and toxicology, 73(4), 628-634 (2004-09-25)
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