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243982-83-4

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243982-83-4 Usage

Description

2,23,4,46Hexabromodiphenyl ether, also known as PBDE 140, is a polybrominated diphenyl ether, which is an organobromine compound. It is a related compound of PBDE 37 (P215200) and is characterized by its flame retardant properties.

Uses

Used in Consumer Products Industry:
2,23,4,46Hexabromodiphenyl ether is used as a flame retardant for enhancing the fire resistance of various consumer products, such as electronics, textiles, and plastics. Its application helps to reduce the risk of fire-related accidents and damage.
However, it is essential to note that PBDE 37, a related compound, has been identified as an environmental pollutant that may lead to pregnancy failure. This information serves as a reminder of the potential environmental and health risks associated with the use of such compounds, and the need for careful consideration and regulation in their application.

Check Digit Verification of cas no

The CAS Registry Mumber 243982-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,9,8 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 243982-83:
(8*2)+(7*4)+(6*3)+(5*9)+(4*8)+(3*2)+(2*8)+(1*3)=164
164 % 10 = 4
So 243982-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H4Br6O/c13-5-3-7(15)12(8(16)4-5)19-9-2-1-6(14)10(17)11(9)18/h1-4H

243982-83-4Upstream product

243982-83-4Downstream Products

243982-83-4Relevant articles and documents

Synthesis and characterization of 32 polybrominated diphenyl ethers

Marsh, Goeran,Hu, Jiwei,Jakobsson, Eva,Rahm, Sara,Bergman, Aeke

, p. 3033 - 3037 (2007/10/03)

Polybrominated diphenyl ethers (PBDEs) are widely used as additive flame retardants in, for example, textiles, computers, television sets, and other electrical appliances. present also in humans. The environmental levels of the PBDEs are, however, still in general lower than those of polychlorinated biphenyls (PCBs). However, while the levels of PCBs generally are decreasing, those of the PBDEs are increasing in, for example, human milk. In the present study 32 individual PBDE congeners were synthesized and characterized. Physicochemical parameters including melting points and UV, 1H NMR, and mass spectra are reported Twenty-nine monobrominated to heptabrominated diphenyl ethers were synthesized by the couping between four diphenyliodonium salts and nine phenolates. One tetrabromodiphenyl ether and two hexabromodiphenyl ethers were synthesized by bromination of two different PBDEs. Twenty-one of the PBDEs and two of the iodonium salts, 2,2′,4,4′-tetrabromodiphenyliodonium chloride and 3,3′,4,4′-tatrabromodiphenyliodonium chloride, are to the authors' knowledge described for the first time. These synthesized reference compounds will aid in the identification and quantification of PBDEs present in environmental samples and will allow further assessment of PBDE toxicity.

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