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A2898 Aldrich

4-Aminobiphenyl

Synonym: 4-Aminodiphenyl, 4-Biphenylamine, 4-Biphenylylamine, 4-Phenylaniline, Biphenyl-4-ylamine, NSC 7660, Xenylamine

  • CAS Number 92-67-1

  • Linear Formula C6H5C6H4NH2

  • Molecular Weight 169.22

  •  Beilstein Registry Number 386533

  •  EC Number 202-177-1

  •  MDL number MFCD00007879

  •  PubChem Substance ID 57653839

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Properties

InChI Key   DMVOXQPQNTYEKQ-UHFFFAOYSA-N
autoignition temp.   842 °F
bp   191 °C/15 mmHg(lit.)
mp   52-54 °C(lit.)
Gene Information   human ... UGT1A4(54657)

Description

Biochem/physiol Actions

Hepatic tumor initiator in experimental animal model.

Packaging

1, 5, 25 g in glass bottle

Application

• Induces DNA damage (carcinogen) in human bladder carcinoma cells and bladder tissue in mouse
• Synthetic amine ligand for enrichment, depletion and one-step purification of leech proteins

Price and Availability

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 3077 9 / PGIII
WGK Germany 
3
RTECS 
DU8925000
Flash Point(F) 
235.4 °F
Flash Point(C) 
113 °C

Documents

Certificate of Analysis

Certificate of Origin

Protocols & Articles

Articles

Carcinogenesis and Epigenetics

Cancer research has revealed that the classical model of carcinogenesis, a three step process consisting of initiation, promotion, and progression, is not complete. The expansion of the carcinogenesi...
Vicki Caligur
BioFiles 2008, 3.5, 18.
Keywords: Acetylations, Adhesion, Alkylations, Apoptosis, Biofiles, Cancer, Carcinogens, Cell division, Cell proliferation, Cell signaling, DNA microarrays, Drug discovery, Environmental, Epigenetics, Events, Gene expression, Genetic, Hormones, Metabolism, Methylations, Microarray Analysis, Mutagens, PAGE, Recombination, Reductions, Sequences, Transcription, Type, transformation

Peer-Reviewed Papers
15

References

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