CHEBI:32506 - 4,4'-diaminodiphenylmethane

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ChEBI Name 4,4'-diaminodiphenylmethane
ChEBI ID CHEBI:32506
Definition An aromatic amine that is diphenylmethane substituted at the 4-position of each benzene ring by an amino group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:234513
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Formula C13H14N2
Net Charge 0
Average Mass 198.26374
Monoisotopic Mass 198.116
InChI InChI=1S/C13H14N2/c14-12-5-1-10(2-6-12)9-11-3-7-13(15)8-4-11/h1-8H,9,14-15H2
InChIKey YBRVSVVVWCFQMG-UHFFFAOYSA-N
SMILES Nc1ccc(Cc2ccc(N)cc2)cc1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): carcinogenic agent
A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.
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ChEBI Ontology
Outgoing 4,4'-diaminodiphenylmethane (CHEBI:32506) has parent hydride diphenylmethane (CHEBI:38884)
4,4'-diaminodiphenylmethane (CHEBI:32506) has role carcinogenic agent (CHEBI:50903)
4,4'-diaminodiphenylmethane (CHEBI:32506) is a aromatic amine (CHEBI:33860)
IUPAC Name
4,4'-methylenedianiline
Synonyms Sources
4,4'-Diaminodiphenylmethane KEGG COMPOUND
4,4'-Diaminodiphenylmethane ChemIDplus
4,4'-Diphenylmethanediamine ChemIDplus
4,4'-Methylenebis(benzeneamine) ChemIDplus
4,4'-methylenedianiline ChEMBL
4-(4-aminobenzyl)aniline ChEMBL
α-(p-aminophenyl)-p-toluidine NIST Chemistry WebBook
Bis(4-aminophenyl)methane ChemIDplus
Bis(p-aminophenyl)methane ChemIDplus
bis-p-aminophenylmethane ChEBI
DADPM NIST Chemistry WebBook
DAPM NIST Chemistry WebBook
DDM NIST Chemistry WebBook
di-(4-aminophenyl)methane ChEBI
di-(p-aminophenyl)methane ChEBI
Dianilinomethane ChemIDplus
p,p'-Diaminodiphenylmethane ChemIDplus
p,p'-Methylenedianiline ChemIDplus
Manual Xrefs Databases
1640 PPDB
4,4'-Methylenedianiline Wikipedia
C14288 KEGG COMPOUND
HMDB0041808 HMDB
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Registry Numbers Types Sources
101-77-9 CAS Registry Number NIST Chemistry WebBook
101-77-9 CAS Registry Number ChemIDplus
474706 Reaxys Registry Number Reaxys
474706 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
17061110 PubMed citation Europe PMC
17482318 PubMed citation ChEMBL
18844695 PubMed citation Europe PMC
22393703 PubMed citation Europe PMC
2607764 PubMed citation Europe PMC
7265110 PubMed citation ChEMBL
9022650 PubMed citation Europe PMC
Last Modified
28 July 2014