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Merck
CN

P15102

4-苯氧基苯胺

97%

别名:

4-氨基二苯醚

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线性分子式:
C6H5OC6H4NH2
化学文摘社编号:
分子量:
185.22
EC Number:
205-367-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
777708
MDL number:
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产品名称

4-苯氧基苯胺, 97%

InChI key

WOYZXEVUWXQVNV-UHFFFAOYSA-N

InChI

1S/C12H11NO/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9H,13H2

SMILES string

Nc1ccc(Oc2ccccc2)cc1

assay

97%

form

solid

mp

82-84 °C (lit.)

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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R L Gupta et al.
Mutation research, 334(3), 273-281 (1995-06-01)
Nitroscanate (NSC) was found to be a direct acting mutagen in the Ames Salmonella tester strains TA100 and TA98 and this activity increased further in the presence of rat liver S9 mix. It was inactive in TA98NR and TA100NR, and
Clarina I Manley-King et al.
Bioorganic & medicinal chemistry, 19(1), 261-274 (2010-12-08)
Previous studies have shown that (E)-5-styrylisatin and (E)-6-styrylisatin are reversible inhibitors of human monoamine oxidase (MAO) A and B. Both homologues are reported to exhibit selective binding to the MAO-B isoform with (E)-5-styrylisatin being the most potent inhibitor. To further
S Torres-Cartas et al.
European journal of medicinal chemistry, 42(11-12), 1396-1402 (2007-05-08)
Mutagenicity is a toxicity endpoint associated with the chronic exposure to chemicals. Aromatic amines have considerable industrial and environmental importance due to their widespread use in industry and their mutagenic capacity. Biopartitioning micellar chromatography (BMC), a mode of micellar liquid

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