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2,6-DIBROMODIPHENYL ETHER, also known as a polybrominated diphenyl ether, is an organobromine compound characterized by the presence of bromine atoms at the 2nd and 6th positions on the diphenyl ether molecule. It exhibits properties such as flame retardancy and chemical stability, making it a valuable compound for various applications.

51930-04-2

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51930-04-2 Usage

Uses

Used in Flame Retardancy:
2,6-DIBROMODIPHENYL ETHER is used as an additive in the plastics and textiles industry for its flame retardant properties. The addition of 2,6-DIBROMODIPHENYL ETHER to materials enhances their resistance to ignition and slows down the spread of fire, making them safer for consumer use.
Used in Electronic Components:
In the electronics industry, 2,6-DIBROMODIPHENYL ETHER is used as a flame retardant in the manufacturing of electronic components and casings. Its incorporation into these materials helps to reduce the risk of fire hazards and improve the overall safety of electronic devices.
Used in Environmental Remediation:
Although 2,6-DIBROMODIPHENYL ETHER is a flame retardant, it is also recognized as an environmental pollutant. As a result, it is used in environmental remediation efforts to mitigate the negative impacts of 2,6-DIBROMODIPHENYL ETHER on ecosystems and human health. This includes the development of strategies for its safe disposal and the reduction of its release into the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 51930-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51930-04:
(7*5)+(6*1)+(5*9)+(4*3)+(3*0)+(2*0)+(1*4)=102
102 % 10 = 2
So 51930-04-2 is a valid CAS Registry Number.

51930-04-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dibromo-2-phenoxybenzene

1.2 Other means of identification

Product number -
Other names InChI=1/C12H8Br2O/c13-10-7-4-8-11(14)12(10)15-9-5-2-1-3-6-9/h1-8H

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51930-04-2 SDS

51930-04-2Downstream Products

51930-04-2Relevant academic research and scientific papers

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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