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CHEBI:151129 - triethylenediamine

ChEBI IDCHEBI:151129
ChEBI Nametriethylenediamine
Stars
DefinitionAn organic heterobicylic compound that is piperazine with an ethane-1,2-diyl group forming a bridge between N1 and N4. It is typically used as a catalyst in polymerization reactions.
Last Modified5 May 2021
Submittermwilliams
DownloadsMolfile
FormulaC6H12N2
Net Charge0
Average Mass112.176
Monoisotopic Mass112.10005
SMILESC1CN2CCN1CC2
InChIInChI=1S/C6H12N2/c1-2-8-5-3-7(1)4-6-8/h1-6H2
InChIKeyIMNIMPAHZVJRPE-UHFFFAOYSA-N
Wikipedia
Species of MetaboliteComponentSourceComments
Escherichia coli (ncbitaxon:562) cell lysate (BTO:0004304) MetaboLights (MTBLS1079) Strain: Escherichia coli str. K-12 substr. DH10B [NCBITAXON:316385]
Roles Classification
Chemical Roles:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
catalyst  A substance that increases the rate of a reaction without modifying the overall standard Gibbs energy change in the reaction.
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Application:
reagent  A substance used in a chemical reaction to detect, measure, examine, or produce other substances.
ChEBI Ontology
Outgoing Relation(s)
triethylenediamine (CHEBI:151129) has role antioxidant (CHEBI:22586)
triethylenediamine (CHEBI:151129) has role catalyst (CHEBI:35223)
triethylenediamine (CHEBI:151129) has role reagent (CHEBI:33893)
triethylenediamine (CHEBI:151129) is a bridged compound (CHEBI:35990)
triethylenediamine (CHEBI:151129) is a diamine (CHEBI:23666)
triethylenediamine (CHEBI:151129) is a saturated organic heterobicyclic parent (CHEBI:38419)
triethylenediamine (CHEBI:151129) is a tertiary amino compound (CHEBI:50996)
IUPAC Name 
1,4-diazabicyclo[2.2.2]octane
Synonyms  Source
N,N'-endo-ethylenepiperazineChemIDplus
1,4-diazabicyclooctaneChemIDplus
1,4-diazabicyclo-octaneChemIDplus
1,4-ethylenepiperazineChemIDplus
1,4-diaza[2.2.2]bicyclooctaneNIST Chemistry WebBook
Brand Names  Source
TEDChemIDplus
DABCOChemIDplus
TEDAChemIDplus
Manual XrefsDatabases
DABCOWikipedia
8882ChemSpider
Registry NumbersSources
Reaxys:103618Reaxys
CAS:280-57-9ChemIDplus
CAS:280-57-9NIST Chemistry WebBook
Citations