192449
4,4′-Isopropylidenebis(2,6-dichlorophenol)
98%
Synonym(s):
2,2′,6,6′-Tetrachloro-4,4′-isopropylidenediphenol
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About This Item
Linear Formula:
(CH3)2C[C6H2(Cl)2OH]2
CAS Number:
Molecular Weight:
366.07
EC Number:
201-237-4
UNSPSC Code:
12162002
MDL number:
assay
98%
mp
134-136 °C (lit.)
SMILES string
CC(C)(c1cc(Cl)c(O)c(Cl)c1)c2cc(Cl)c(O)c(Cl)c2
InChI
1S/C15H12Cl4O2/c1-15(2,7-3-9(16)13(20)10(17)4-7)8-5-11(18)14(21)12(19)6-8/h3-6,20-21H,1-2H3
InChI key
KYPYTERUKNKOLP-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Shigeyuki Kitamura et al.
Biochemical and biophysical research communications, 293(1), 554-559 (2002-06-11)
The thyroid hormonal-disrupting activity of the flame retardants tetrabromobisphenol A (TBBPA) and tetrachlorobisphenol A (TCBPA) was examined and compared with that of bisphenol A, a typical estrogenic xenobiotic. TBBPA and TCBPA, halogenated derivatives of bisphenol A, markedly inhibited the binding
Warm reception? Halogenated BPA flame retardants and PPARγ activation.
Julia R Barrett
Environmental health perspectives, 119(9), a398-a398 (2011-09-03)
Consuelo Sánchez-Brunete et al.
Journal of chromatography. A, 1216(29), 5497-5503 (2009-06-16)
In this work, an isotope dilution method for the determination, in agricultural and industrial soil samples, of tetrabromobisphenol-A, tetrachlorobisphenol-A and bisphenol-A by gas chromatography-mass spectrometry was developed. The compounds were extracted from soil by sonication assisted extraction in small columns
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 412392-1G | 04061837696893 |
| 412392-5G | 04061837696909 |