2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol
2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol Basic information
- Product Name:
- 2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol
- Synonyms:
-
- 2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol
- 2-(3,5-Dibromo-4-hydroxyphenyl)-2-(3-bromo-4-hydroxyphenyl)propane
- 2,2',6-Tribromo(4,4'-isopropylidenebisphenol)
- 2,2',6-Tribromo[4,4'-(dimethylmethylene)bis(phenol)]
- 2,6,6'-Tribromo-(4,4'-isopropylidenebisphenol)
- 3,3',5-Tri-Br-BPA
- C13621
- Phenol, 2,6-dibromo-4-1-(3-bromo-4-hydroxyphenyl)-1-methylethyl-
- CAS:
- 6386-73-8
- MF:
- C15H13Br3O2
- MW:
- 464.97
- EINECS:
- 228-988-0
- Mol File:
- 6386-73-8.mol
2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol Chemical Properties
- Melting point:
- 107-110 °C
- Boiling point:
- 413.1±40.0 °C(Predicted)
- Density
- 1.873±0.06 g/cm3(Predicted)
- solubility
- DMSO: Soluble: =10 mg/ml
Ethanol: Soluble: =10 mg/ml - pka
- 8.85±0.10(Predicted)
- EPA Substance Registry System
- Phenol, 2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]- (6386-73-8)
Safety Information
- RIDADR
- 3152
- HazardClass
- 9
- PackingGroup
- II
- Hazardous Substances Data
- 6386-73-8(Hazardous Substances Data)
2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol Usage And Synthesis
Uses
Tribromobisphenol A (Tri-BBPA; 2,2',6-Tribromobisphenol A) is a phenolic compound isolated from human breast milk[1].
Definition
ChEBI: 3,3',5-tribromobisphenol A is a bromobisphenol.
References
[1] Nakao T, et al. Levels of tetrabromobisphenol A, tribromobisphenol A, dibromobisphenol A, monobromobisphenol A, and bisphenol a in Japanese breast milk. Chem Res Toxicol. 2015 Apr 20;28(4):722-8. DOI:10.1021/tx500495j
[2] AIFENG LIU. Identification of Emerging Brominated Chemicals as the Transformation Products of Tetrabromobisphenol A (TBBPA) Derivatives in Soil[J]. Environmental Science and Technology, 2017, 51 10: 5434-5444. DOI: 10.1021/acs.est.7b01071
[3] ERIKA N. SEGRAVES. Probing the Activity Differences of Simple and Complex Brominated Aryl Compounds against 15-Soybean, 15-Human, and 12-Human Lipoxygenase§[J]. Journal of Medicinal Chemistry, 2004, 47 16: 4060-4065. DOI: 10.1021/jm049872s
[4] YAN YANG. Proliferation toxicity and mechanism of novel mixed bromine/chlorine transformation products of tetrabromobisphenol A on human embryonic stem cell.[J]. Journal of Hazardous Materials, 2023, 449 1: 131050. DOI: 10.2139/ssrn.4265415
[5] HONG-XUAN KUANG. Exposure to synthesized tribromobisphenol A and critical effects: Metabolic pathways, disease signature, and benchmark dose derivation[J]. Science of the Total Environment, 2024, 932: Article 173117. DOI: 10.1016/j.scitotenv.2024.173117
2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol (6386-73-8)Related Product Information
- 2,2',6,6'-TETRABROMO BISPHENOL ''A'' DIMETHACRYLATE
- 9,9-BIS(3',5'-DIBROMO-4'-HYDROXYPHENYL)FLUORENE
- Tetrabromobisphenol A bis(dibromopropyl ether)
- 4,4'-Isopropylidenebis[2-(2,6-dibromophenoxy)ethanol]
- TETRABROMOBISPHENOL A DIGLYCIDYL ETHER
- 4,4'-isopropylidenebis[2,6-dibromophenyl] diacetate
- GAMMA,GAMMA-BIS(3,5-DIBROMO-4-HYDROXY-PHENYL)VALERIC ACID
- 2,2',6,6'-TETRABROMO BISPHENOL ''A'' DIACRYLATE
- TETRABROMOBISPHENOL A DIMETHYL ETHER
- Tetrabromobisphenol A
- 2,6-dibromo-4-[1-(3-bromo-4-hydroxyphenyl)-1-methylethyl]phenol
- 2,2',6,6'-Tetrabromobisphenol A diallyl ether