Basic information
- CAS
4075-79-0- Standard SMILES
CC(=O)Nc1ccc(-c2ccccc2)cc1- InChIKey
SVLDILRDQOVJED-UHFFFAOYSA-N- Molecular formula
- C14H13NO
- Average molar mass
- 211.26 g/mol
- Monoisotopic mass
- 211.09971404
Overview
4-Acetylaminobiphenyl is a member of biphenyls.
Names & identifiers
- Preferred name
- N-Acetyl-4-aminobiphenyl
- IUPAC
- N-(4-phenylphenyl)acetamide
- English name
- 4-acetylaminobiphenyl
- Molecular formula
- C14H13NO
- Molecular weight
- 211.26
Names & synonyms
Show more names
Database identifiers
- CAS
4075-79-0- PubChem CID
- 19998
- DTXSID
DTXSID8039243- ChEMBL
CHEMBL300429- ChEBI
CHEBI:177487- UNII
- U9BHQ2TJ87
- EC Number
- 817-898-2
- Nikkaji
- J2.205E
Properties
Computed structural properties
- XLogP
- 3
- Topological polar surface area
- 29.1 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 2
- Heavy atoms
- 16
- Formal charge
- 0
- Complexity
- 225
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 171 °C · 171°C
- Boiling point
- 350.95 °C · 350.95°C (rough estimate)
- Density
- 1.0694 · 1.0694 (rough estimate)
- refractive index
- 1.578 · 1.5780 (estimate)
- storage temp.
- Refrigerator
- solubility
- Chloroform, Methanol
- form
- Solid
- color
- Crystals from MeOH (aq)
- InChI
- InChI=1S/C14H13NO/c1-11(16)15-14-9-7-13(8-10-14)12-5-3-2-4-6-12/h2-10H,1H3,(H,15,16)
- InChIKey
- SVLDILRDQOVJED-UHFFFAOYSA-N
- SMILES
- C(NC1=CC=C(C2=CC=CC=C2)C=C1)(=O)C
- FDA UNII
- 9 BHQ2TJ87 · U9BHQ2TJ87
- EPA Substance Registry System
- 1 · Acetamide, N-[1,1'-biphenyl]-4-yl- (4075-79-0)
- Symbol(GHS)
- 7 · GHS07,GHS08
- Signal word
- Warning
- Hazard statements
- 312 · H312-H315-H319-H332-H302-H335-H351
- Precautionary statements
- 264 · P264-P280-P305+P351+P338-P337+P313P-P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P201-P202-P281-P308+P313-P405-P501
- TSCA
- TSCA listed
- Hazardous Substances Data
- 4075 · 4075-79-0(Hazardous Substances Data)
- Toxicity
- 2770 mg/kg/21W-C:CAR · TDLo orl-rat: 2770 mg/kg/21W-C:CAR CNREA8 15,188,55 orl-rat TD:4070 mg/kg/34W-C:CAR CNREA8 16,525,56
Safety & regulation
GHS classification
GHS Classification
Warning
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
P203, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P318, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Toxicology
Non-Human Toxicity Excerpts
NEONATAL ICR/HA MICE WERE INJECTED SC WITH SINGLE DOSE OF 25, 50, & 100 MUG OF 4-ACETYLAMINOBIPHENYL ALONE OR TOGETHER WITH 2.5% PIPERONYL BUTOXIDE IN TRICAPRYLIN. PB INDUCED SYNERGISTIC TOXICITY AND AAB INDUCED DOSE-RELATED HEPATOCARCINOGENICITY IN MALE.
N-HYDR OXY-N-ACETYL-4-AMINOBIPHENYL, CARCINOGENIC METABOLITE OF CANCER-INDUCING N-ACETYL-4-AMINOBIPHENYL, INDUCED ATP-ENERGIZED MITOCHONDRIAL VOL CHANGE IN AN IN VITRO MITOCHONDRIAL SYSTEM WHEN COMBINED WITH THIOL REAGENT SUCH AS SHOWDOMYCIN.
ACTIVATION OF GUANYLATE CYCLASE DURING THE OXIDATION OF ARYLAMINE CARCINOGENS.
Safety data
- tsca
- TSCA listed
- Toxicity
- TDLo orl-rat: 2770 mg/kg/21W-C:CAR CNREA8 15,188,55 orl-rat TD:4070 mg/kg/34W-C:CAR CNREA8 16,525,56
- Signal word
- Warning
- Symbol(GHS)
- GHS07,GHS08
- Hazard statements
- H312-H315-H319-H332-H302-H335-H351
- Precautionary statements
- P264-P280-P305+P351+P338-P337+P313P-P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P201-P202-P281-P308+P313-P405-P501
- Hazardous Substances Data
- 4075-79-0(Hazardous Substances Data)
Chemistry & industry
Pharmacology
Metabolism/Metabolites
REDUCTION OF N-HYDROXY-4-ACETYLAMINOBIPHENYL BY INTESTINAL MICROFLORA OF THE RAT TO 4-ACETYLAMINOBIPHENYL WAS EXAMINED.
...NONBASIC NITROGEN-CONTAINING COMPD...4-ACETYLAMINOBIPHENYL UTILIZE A CYTOCHROME P-450-DEPENDENT SYSTEM.
ABILITY OF ARYLACETAMINE DEACETYLASE ENZYME SYSTEMS OF DOG LIVER TO DEACETYLATE 4-ACETYLAMINOBIPHENYL WAS EXAMINED. ENZYME ACTIVITY WAS GREATEST IN LIVER TISSUE, WAS LOCALIZED IN MICROSOMAL SUBCELLULAR FRACTION & REQUIRED NO COFACTORS.
Uses & manufacturing
Uses
Not commercially used or produced in the US; [HSDB]
NO EVIDENCE OF CURRENT USE IN US
U.S. Exports
(1977) No Data
(1979) No Data
U.S. Imports
(1977) No Data
(1979) No Data
U.S. Production
(1977) NOT PRODUCED COMMERCIALLY IN US
(1979) NOT PRODUCED COMMERCIALLY IN US
Applications
UsesN-Acetyl-4-aminobiphenyl is a metabolite of 4-Aminobiphenyl, a procarcinogenic agent.
Upstream & downstream products
Downstream products
Suppliers21 total
Additional notes
DefinitionChEBI: 4-Acetylaminobiphenyl is a member of biphenyls.
Related reactions
Compound notes
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