CHEBI:22472 - ametryn

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ChEBI Name ametryn
ChEBI ID CHEBI:22472
Definition A methylthio-1,3,5-triazine that is 2-(methylsulfanyl)-1,3,5-triazine substituted by an ethylamino and an isopropylamino group at positions 4 and 6 respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C9H17N5S
Net Charge 0
Average Mass 227.33098
Monoisotopic Mass 227.12047
InChI InChI=1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)
InChIKey RQVYBGPQFYCBGX-UHFFFAOYSA-N
SMILES CCNc1nc(NC(C)C)nc(SC)n1
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): herbicide
A substance used to destroy plant pests.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing ametryn (CHEBI:22472) has role environmental contaminant (CHEBI:78298)
ametryn (CHEBI:22472) has role herbicide (CHEBI:24527)
ametryn (CHEBI:22472) is a diamino-1,3,5-triazine (CHEBI:38170)
ametryn (CHEBI:22472) is a methylthio-1,3,5-triazine (CHEBI:38174)
IUPAC Name
N-ethyl-6-(methylsulfanyl)-N'-(propan-2-yl)-1,3,5-triazine-2,4-diamine
Synonyms Sources
2-(methylthio)-4-(ethylamino)-6-(isopropylamino)-s-triazine NIST Chemistry WebBook
2-ethylamino-4-isopropylamino-6-methylmercapto-s-triazine ChemIDplus
2-methylthio-4-ethylamino-6-isopropylamino-s-triazine ChemIDplus
Ametrex ChemIDplus
ametryn UM-BBD
ametryne ChemIDplus
Evik ChemIDplus
Gesapax ChemIDplus
N-ethyl-N'-(1-methylethyl)-6-(methylthio)-1,3,5-triazine-2,4-diamine NIST Chemistry WebBook
N-ethyl-N'-(1-methylethyl)-6-(methylthio)-2,4-diaminetriazine UM-BBD
N-ethyl-N'-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine ChEBI
Manual Xrefs Databases
27 PPDB
c0260 UM-BBD
C18700 KEGG COMPOUND
RYN PDBeChem
View more database links
Registry Numbers Types Sources
613099 Beilstein Registry Number Beilstein
613099 Reaxys Registry Number Reaxys
834-12-8 CAS Registry Number NIST Chemistry WebBook
834-12-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
21626650 PubMed citation Europe PMC
23566464 PubMed citation Europe PMC
24413480 PubMed citation Europe PMC
24579518 PubMed citation Europe PMC
24757962 PubMed citation Europe PMC
Last Modified
28 July 2014