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2,2',4,4'-Tetrabromodiphenyl ether - 97%, high purity , CAS No.5436-43-1

    Grade & Purity:
  • ≥97%
In stock
Item Number
O303946
Grouped product items
SKU Size
Availability
Price Qty
O303946-50mg
50mg
3
$228.90
O303946-250mg
250mg
3
$698.90
O303946-1g
1g
3
$1,835.90
O303946-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$3,334.90

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

Taxonomy Tree

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

Associated Targets(Human)

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Homo sapiens (32628 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAPGEF4 Tchem Rap guanine nucleotide exchange factor 4 (11476 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

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)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
C2323772 Certificate of Analysis Mar 04, 2023 O303946
C2323810 Certificate of Analysis Mar 04, 2023 O303946
C2323793 Certificate of Analysis Mar 04, 2023 O303946
C2323783 Certificate of Analysis Mar 04, 2023 O303946

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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