N-Acetyl-4-aminobiphenyl

HCID 19998

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

4075-79-0N-Acetyl-4-aminobiphenyl4-ACETYLAMINOBIPHENYL4'-Phenylacetanilide4-AcetamidobiphenylN-(4-Biphenylyl)acetamideAcetanilide, 4'-phenyl-4-BiphenylacetamideBiphenyl, 4-acetamidoN-(1,1'-Biphenyl)-4-ylacetamideU9BHQ2TJ87NSC-3134
Show more names
NSC2271924-PHENYLACETANILIDEN-(p-Phenylphenyl)acetamideN-(1,1'-Biphenyl-4-yl)acetamideAcetamide, N-[1,1'-biphenyl]-4-yl-
NSC-65931NSC-227192DTXSID8039243RefChem:97635DTXCID3016N-(4-phenylphenyl)acetamideN-([1,1'-Biphenyl]-4-yl)acetamidep-Phenylacetanilide

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

Experimental & physicochemical properties

Chemical ClassesNitrogen Compounds -> Other Aromatics (Nitrogen)
SpringerMaterials Properties15N nuclear magnetic resonance spectrum
Color/FormCRYSTALS FROM DILUTED METHANOL
SolubilityVERY SOL IN ALC, ACETONE, METHANOL; INSOL IN WATER
Melting Point172 °C
Physical DescriptionSolid; [HSDB]

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

Safety & regulation

GHS classification

GHS Classification · 4 items

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

Hazards SummaryMutagen and tumorigen; [RTECS] See Biphenyl.
Hazard Classes and CategoriesAcute Tox. 4 (100%)

Toxicology

Non-Human Toxicity Excerpts · 3 items

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

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 3 items

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.

Absorption, Distribution and ExcretionTHE BINDING TO LIVER RNA & DNA WAS STUDIED 24 HR AFTER SINGLE IP INJECTION OF (3)H-LABELED COMPD.

Uses & manufacturing

Uses · 2 items

Not commercially used or produced in the US; [HSDB]

NO EVIDENCE OF CURRENT USE IN US

U.S. Exports · 2 items

(1977) No Data

(1979) No Data

U.S. Imports · 2 items

(1977) No Data

(1979) No Data

U.S. Production · 2 items

(1977) NOT PRODUCED COMMERCIALLY IN US

(1979) NOT PRODUCED COMMERCIALLY IN US

General Manufacturing InformationAcetamide, N-[1,1'-biphenyl]-4-yl-: INACTIVE

Applications

UsesN-Acetyl-4-aminobiphenyl is a metabolite of 4-Aminobiphenyl, a procarcinogenic agent.

Upstream & downstream products

Suppliers21 total

杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
上海陶素生化科技有限公司021-33632979 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
郑州康弗辰医药科技有限公司18210788515; 18210788515 · [email protected]
湖北昌玖新材料科技有限公司13407109540 · [email protected]

Additional notes

DefinitionChEBI: 4-Acetylaminobiphenyl is a member of biphenyls.

Related reactions

17 records

Compound notes

Loading…