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Key Documents

P15102

Sigma-Aldrich

4-Phenoxyaniline

97%

Synonym(s):

4-Aminophenyl phenyl ether

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About This Item

Linear Formula:
C6H5OC6H4NH2
CAS Number:
Molecular Weight:
185.22
Beilstein/REAXYS Number:
777708
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

97%

form

solid

mp

82-84 °C (lit.)

SMILES string

Nc1ccc(Oc2ccccc2)cc1

InChI

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

InChI key

WOYZXEVUWXQVNV-UHFFFAOYSA-N

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signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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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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