CHEBI:83501 - acesulfame

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name acesulfame
Definition A sulfamate ester that is 1,2,3-oxathiazin-4(3H)-one 2,2-dioxide substituted by a methyl group at position 6.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C4H5NO4S
Net Charge 0
Average Mass 163.15200
Monoisotopic Mass 162.99393
InChI InChI=1S/C4H5NO4S/c1-3-2-4(6)5-10(7,8)9-3/h2H,1H3,(H,5,6)
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Biological Role(s): sweetening agent
Substance that sweeten food, beverages, medications, etc.
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
Application(s): sweetening agent
Substance that sweeten food, beverages, medications, etc.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing acesulfame (CHEBI:83501) has role environmental contaminant (CHEBI:78298)
acesulfame (CHEBI:83501) has role sweetening agent (CHEBI:50505)
acesulfame (CHEBI:83501) has role xenobiotic (CHEBI:35703)
acesulfame (CHEBI:83501) is a organic heteromonocyclic compound (CHEBI:25693)
acesulfame (CHEBI:83501) is a organonitrogen heterocyclic compound (CHEBI:38101)
acesulfame (CHEBI:83501) is a oxacycle (CHEBI:38104)
acesulfame (CHEBI:83501) is a sulfamate ester (CHEBI:48199)
6-methyl-1,2,3-oxathiazin-4(3H)-one 2,2-dioxide
INNs Sources
acesulfamo ChemIDplus
acesulfamum ChemIDplus
acesulfamum ChemIDplus
Manual Xref Database
HMDB0033585 HMDB
View more database links
Registry Numbers Types Sources
33665-90-6 CAS Registry Number ChemIDplus
510659 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
25046375 PubMed citation Europe PMC
25085815 PubMed citation Europe PMC
Last Modified
21 July 2015