CHEBI:82388 - p-anisidine

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ChEBI Name p-anisidine
ChEBI ID CHEBI:82388
ChEBI ASCII Name p-anisidine
Definition A substituted aniline that is aniline in which the hydrogen para to the amino group has been replaced by a methoxy group. It is used as a reagent for the detection of oxidation products such as aldehydes and ketones in fats and oils.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C7H9NO
Net Charge 0
Average Mass 123.153
Monoisotopic Mass 123.06841
InChI InChI=1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
InChIKey BHAAPTBBJKJZER-UHFFFAOYSA-N
SMILES C1=C(C=CC(=C1)OC)N
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): genotoxin
A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
Application(s): reagent
A substance used in a chemical reaction to detect, measure, examine, or produce other substances.
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ChEBI Ontology
Outgoing p-anisidine (CHEBI:82388) has role genotoxin (CHEBI:50902)
p-anisidine (CHEBI:82388) has role reagent (CHEBI:33893)
p-anisidine (CHEBI:82388) is a methoxybenzenes (CHEBI:51683)
p-anisidine (CHEBI:82388) is a primary amino compound (CHEBI:50994)
p-anisidine (CHEBI:82388) is a substituted aniline (CHEBI:48975)
Incoming methacetin (CHEBI:139354) has functional parent p-anisidine (CHEBI:82388)
IUPAC Name
4-methoxyaniline
Synonyms Sources
1-amino-4-methoxybenzene ChemIDplus
4-aminoanisole ChemIDplus
4-anisidine ChemIDplus
4-methoxyaniline UniProt
4-methoxybenzenamine NIST Chemistry WebBook
4-methoxybenzeneamine ChemIDplus
p-aminoanisole ChemIDplus
p-anisidine ChemIDplus
p-anisylamine ChemIDplus
p-methoxyaniline ChemIDplus
p-methoxyphenylamine ChemIDplus
para-anisidine ChEBI
Manual Xrefs Databases
C19326 KEGG COMPOUND
FDB000339 FooDB
HMDB0029300 HMDB
P-Anisidine Wikipedia
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Registry Numbers Types Sources
104-94-9 CAS Registry Number NIST Chemistry WebBook
104-94-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12643317 PubMed citation Europe PMC
12929121 PubMed citation Europe PMC
18966208 PubMed citation Europe PMC
IND22044074 Agricola citation Europe PMC
IND500608564 Agricola citation Europe PMC
Last Modified
19 February 2019