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2,2',4,4'-Tetrabromodiphenyl ether - 97%, high purity , CAS No.5436-43-1
Basic Description
Synonyms
PBDE No. 47 | 98WI44OHIQ | PBDE-47 | SMR000568461 | XYBSIYMGXVUVGY-UHFFFAOYSA-N | UNII-U8HTX2GK8J | CAS-5436-43-1 | SCHEMBL899494 | PBDE No. 47 1000 microg/mL in Methanol | NSC21724 | 0N97R5X10X | 2,4-dibromo-1-(2,4-dibromophenoxy)benzene | BDE No 47, ana
Specifications & Purity
≥97%
Storage Temp
Room temperature,Desiccated
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Diphenylethers
Intermediate Tree Nodes
Not available
Direct Parent
Bromodiphenyl ethers
Alternative Parents
Diarylethers Phenoxy compounds Phenol ethers Bromobenzenes Aryl bromides Organobromides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Bromodiphenyl ether - Diaryl ether - Phenoxy compound - Phenol ether - Halobenzene - Bromobenzene - Aryl halide - Aryl bromide - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as bromodiphenyl ethers. These are compounds that contain two benzene groups linked to each other via an ether bond, and where at least one ring is substituted with a bromo group.
External Descriptors
PBDEs
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
504756255
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504756255
IUPAC Name
2,4-dibromo-1-(2,4-dibromophenoxy)benzene
INCHI
InChI=1S/C12H6Br4O/c13-7-1-3-11(9(15)5-7)17-12-4-2-8(14)6-10(12)16/h1-6H
InChIKey
XYBSIYMGXVUVGY-UHFFFAOYSA-N
Smiles
C1=CC(=C(C=C1Br)Br)OC2=C(C=C(C=C2)Br)Br
Isomeric SMILES
C1=CC(=C(C=C1Br)Br)OC2=C(C=C(C=C2)Br)Br
Molecular Weight
485.82
Reaxy-Rn
3356883
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3356883&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Boil Point(°C)
395.5°C at 760 mmHg
Molecular Weight
485.790 g/mol
XLogP3
6.200
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
485.711 Da
Monoisotopic Mass
481.715 Da
Topological Polar Surface Area
9.200 Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
227.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Yingying Sun, Jie Chen, Wei Wang, Lizhong Zhu.
(2023)
α-Galactosidase interacts with persistent organic pollutants to induce oxidative stresses in rice (Oryza sativa L.).
ENVIRONMENTAL POLLUTION,
335
(122353).
2.
Cheng-Qiang Wang, Zou Su, Chun-Guang Dai, Jia-Le Song, Bo Qian.
(2023)
Multi-omics analysis reveals BDE47 induces depression-like behaviors in mice by interfering with the 2-arachidonoyl glycerol-associated microbiota-gut-brain axis.
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,
259
(115041).
3.
Yao Ma, Haoliang Li, Chunsheng Xie, Xiaodong Du, Xueqin Tao, Guining Lu.
(2022)
Treatment of PBDEs from Soil-Washing Effluent by Granular-Activated Carbon: Adsorption Behavior, Influencing Factors and Density Functional Theory Calculation.
Processes,
10
(9):
(1815).
4.
Junyao Yang, Kuang Wang, Chengjie Xue, Zhanqiang Fang.
(2025)
The mechanism of activity-controlled release of 2,2′,4,4′-tetrabromodiphenyl degradation by polystyrene microcapsulated nanoscale zero-valent iron.
ENVIRONMENTAL RESEARCH,
269
(120915).
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