P15102
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:
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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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, 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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