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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:16830 - methylamine
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ChEBI Name
methylamine
ChEBI ID
CHEBI:16830
Definition
The simplest of the methylamines, consisting of ammonia bearing a single methyl substituent.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:44374, CHEBI:6864, CHEBI:14595, CHEBI:25402
Supplier Information
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Read full article at Wikipedia
Formula
CH5N
Net Charge
0
Average Mass
31.05714
Monoisotopic Mass
31.04220
InChI
InChI=1S/CH5N/c1-2/h2H2,1H3
InChIKey
BAVYZALUXZFZLV-UHFFFAOYSA-N
SMILES
CN
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
methylamine (
CHEBI:16830
)
has role
mouse metabolite (
CHEBI:75771
)
methylamine (
CHEBI:16830
)
is a
methylamines (
CHEBI:25274
)
methylamine (
CHEBI:16830
)
is a
one-carbon compound (
CHEBI:64708
)
methylamine (
CHEBI:16830
)
is a
primary aliphatic amine (
CHEBI:17062
)
methylamine (
CHEBI:16830
)
is conjugate base of
methylammonium (
CHEBI:59338
)
Incoming
methylammonium (
CHEBI:59338
)
is conjugate acid of
methylamine (
CHEBI:16830
)
methylamino group (
CHEBI:44209
)
is substituent group from
methylamine (
CHEBI:16830
)
IUPAC Name
methanamine
Synonyms
Sources
aminomethane
NIST Chemistry WebBook
CH
3
‒NH
2
IUPAC
MeNH
2
ChEBI
Methanamine
KEGG COMPOUND
Methylamine
KEGG COMPOUND
METHYLAMINE
PDBeChem
MMA
Note: (2015-03-23) Ambiguous - has also been used as an abbreviation for methyl methacrylate and for methylmalonic acid
ChemIDplus
monomethylamine
NIST Chemistry WebBook
Manual Xrefs
Databases
C00218
KEGG COMPOUND
c0137
UM-BBD
DB01828
DrugBank
HMDB0000164
HMDB
Methylamine
Wikipedia
METHYLAMINE
MetaCyc
NME
PDBeChem
View more database links
Registry Numbers
Types
Sources
145
Gmelin Registry Number
Gmelin
74-89-5
CAS Registry Number
ChemIDplus
74-89-5
CAS Registry Number
NIST Chemistry WebBook
741851
Reaxys Registry Number
Reaxys
741851
Beilstein Registry Number
Beilstein
Citations
Types
Sources
11580915
PubMed citation
Europe PMC
11991665
PubMed citation
Europe PMC
18312416
PubMed citation
Europe PMC
Last Modified
20 November 2019