CHEBI:151129 - triethylenediamine

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ChEBI Name triethylenediamine
ChEBI ID CHEBI:151129
Definition An 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.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Mark Williams
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Formula C6H12N2
Net Charge 0
Average Mass 112.176
Monoisotopic Mass 112.10005
InChI InChI=1S/C6H12N2/c1-2-8-5-3-7(1)4-6-8/h1-6H2
InChIKey IMNIMPAHZVJRPE-UHFFFAOYSA-N
SMILES C1CN2CCN1CC2
Metabolite of Species Details
Escherichia coli (NCBI:txid562) Found in cell lysate (BTO:0004304). of strain Escherichia coli str. K-12 substr. DH10B [NCBITAXON:316385] See: MetaboLights Study
Roles Classification
Chemical Role(s): catalyst
A substance that increases the rate of a reaction without modifying the overall standard Gibbs energy change in the reaction.
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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 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 Sources
1,4-diaza[2.2.2]bicyclooctane NIST Chemistry WebBook
1,4-diazabicyclo-octane ChemIDplus
1,4-diazabicyclooctane ChemIDplus
1,4-ethylenepiperazine ChemIDplus
N,N'-endo-ethylenepiperazine ChemIDplus
Brand Names Sources
DABCO ChemIDplus
TED ChemIDplus
TEDA ChemIDplus
Manual Xrefs Databases
8882 ChemSpider
DABCO Wikipedia
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Registry Numbers Types Sources
103618 Reaxys Registry Number Reaxys
280-57-9 CAS Registry Number NIST Chemistry WebBook
280-57-9 CAS Registry Number ChemIDplus
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Last Modified
05 May 2021