CHEBI:82436 - decabromodiphenyl ether

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ChEBI Name decabromodiphenyl ether
Definition A polybromodiphenyl ether that is diphenyl ether in which all of the hydrogens have been replaced by bromines.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C12Br10O
Net Charge 0
Average Mass 959.164
Monoisotopic Mass 949.17830
InChI InChI=1S/C12Br10O/c13-1-3(15)7(19)11(8(20)4(1)16)23-12-9(21)5(17)2(14)6(18)10(12)22
SMILES C1(=C(C(=C(C(=C1Br)OC2=C(C(=C(C(=C2Br)Br)Br)Br)Br)Br)Br)Br)Br
Roles Classification
Chemical Role(s): persistent organic pollutant
Any environmental contaminant that is resistant to environmental degradation through photolytic, biological or chemical processes. Such substances can have significant impact on health and the environment, as they persist in the environment, bioaccumulate in animal tissue and so biomagnify in food chains.
(via polybromodiphenyl ether )
(via brominated flame retardant )
Biological Role(s): neurotoxin
A poison that interferes with the functions of the nervous system.
Application(s): endocrine disruptor
Any compound that can disrupt the functions of the endocrine (hormone) system
(via polybromodiphenyl ether )
flame retardant
Any compound that is added to manufactured materials to inhibit, suppress, or delay the production of flames and so prevent the spread of fire.
(via brominated flame retardant )
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ChEBI Ontology
Outgoing decabromodiphenyl ether (CHEBI:82436) has role neurotoxin (CHEBI:50910)
decabromodiphenyl ether (CHEBI:82436) is a polybromodiphenyl ether (CHEBI:134094)
bis(pentabromophenyl) ether
Synonyms Sources
1,1'-oxybis(2,3,4,5,6-pentabromobenzene) ChemIDplus
1,2,3,4,5-pentabromo-6-(pentabromophenoxy)benzene IUPAC
2,2',3,3',4,4',5,5',6,6'-decabrominated diphenyl ether ChemIDplus
2,2',3,3',4,4',5,5',6,6'-decabromobiphenyl ether ChemIDplus
2,2',3,3',4,4',5,5',6,6'-decabromodiphenyl ether ChEBI
BDE 209 ChemIDplus
BDE-209 ChemIDplus
decaBDE ChemIDplus
decabromodiphenyl oxide KEGG COMPOUND
pentabromophenyl ether NIST Chemistry WebBook
perbromodiphenyl ether ChEBI
Manual Xref Database
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Registry Numbers Types Sources
1163-19-5 CAS Registry Number KEGG COMPOUND
1163-19-5 CAS Registry Number NIST Chemistry WebBook
1163-19-5 CAS Registry Number ChemIDplus
2188438 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
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Last Modified
01 August 2017