CHEBI:138065 - 2,4-dibromophenyl 2,4,6-tribromophenyl ether

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ChEBI Name 2,4-dibromophenyl 2,4,6-tribromophenyl ether
ChEBI ID CHEBI:138065
Definition A polybromodiphenyl ether that is diphenyl ether in which the hydrogens at the 2, 4, 6, 2', and 4' positions have been replaced by bromines.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C12H5Br5O
Net Charge 0
Average Mass 564.686
Monoisotopic Mass 559.62573
InChI InChI=1S/C12H5Br5O/c13-6-1-2-11(8(15)3-6)18-12-9(16)4-7(14)5-10(12)17/h1-5H
InChIKey NSKIRYMHNFTRLR-UHFFFAOYSA-N
SMILES O(C=1C(=CC(=CC1Br)Br)Br)C=2C=CC(=CC2Br)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 )
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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,4-dibromophenyl 2,4,6-tribromophenyl ether (CHEBI:138065) is a polybromodiphenyl ether (CHEBI:134094)
IUPAC Name
2,4-dibromophenyl 2,4,6-tribromophenyl ether
Synonyms Sources
1,3,5-tribromo-2-(2,4-dibromophenoxy)benzene ChemIDplus
2,2',4,4',6-brominated diphenyl ether ChemIDplus
BDE 100 ChemIDplus
BDE-100 ChemIDplus
BDE100 ChEBI
PBDE 100 ChemIDplus
PBDE-100 ChEBI
PBDE100 ChEBI
pentabrominated diphenyl ether 100 ChemIDplus
Manual Xref Database
HMDB0037516
Note: (2017-08-01) Link is to the HMDB entry for pentabromodiphenyl ethers.
HMDB
View more database links
Registry Numbers Types Sources
189084-64-8 CAS Registry Number ChemIDplus
8152285 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16507514 PubMed citation Europe PMC
21390402 PubMed citation Europe PMC
22884212 PubMed citation Europe PMC
23302053 PubMed citation Europe PMC
25629761 PubMed citation Europe PMC
26906616 PubMed citation Europe PMC
27068391 PubMed citation Europe PMC
27234317 PubMed citation Europe PMC
28395225 PubMed citation Europe PMC
28557710 PubMed citation Europe PMC
Last Modified
01 August 2017