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2,2',4,4',5,5'-HEXABROMODIPHENYL ETHER, also known as BDE No 153, is a chemical compound that is primarily recognized as a contaminant. It is a brominated flame retardant that has been used commercially in various applications due to its ability to slow down the spread of fire.

68631-49-2

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68631-49-2 Usage

Uses

Used in Building Materials:
2,2',4,4',5,5'-HEXABROMODIPHENYL ETHER is used as a flame retardant additive in the building materials industry to enhance the fire resistance of materials such as insulation, construction panels, and other components.
Used in Textiles:
In the textile industry, 2,2',4,4',5,5'-HEXABROMODIPHENYL ETHER is used as a flame retardant to improve the fire safety of fabrics, particularly those used in upholstery, curtains, and other home furnishings.
Used in Plastics:
2,2',4,4',5,5'-HEXABROMODIPHENYL ETHER is utilized as a flame retardant in the plastics industry, where it is added to materials such as polyurethane foams, polystyrene, and other plastic products to reduce their flammability.
Used in Electronic Equipment:
In the electronics industry, 2,2',4,4',5,5'-HEXABROMODIPHENYL ETHER is used as a flame retardant additive in the production of electronic equipment, such as circuit boards and casings, to minimize the risk of fire and improve overall safety.

Check Digit Verification of cas no

The CAS Registry Mumber 68631-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,3 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68631-49:
(7*6)+(6*8)+(5*6)+(4*3)+(3*1)+(2*4)+(1*9)=152
152 % 10 = 2
So 68631-49-2 is a valid CAS Registry Number.

68631-49-2 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33683)  BDE No 153 solution  50 μg/mL in isooctane, analytical standard

  • 68631-49-2

  • 33683-1ML

  • 4,182.75CNY

  • Detail

68631-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-tribromo-5-(2,4,5-tribromophenoxy)benzene

1.2 Other means of identification

Product number -
Other names 2,2',3,4,5,6'-HEXACHLOROBIPHENYL

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:68631-49-2 SDS

68631-49-2Downstream Products

68631-49-2Relevant academic research and scientific papers

Solid-phase synthetic method and application of polybrominated diphenyl ether monomer

-

Paragraph 0051-0053, (2017/08/31)

The invention discloses a solid-phase synthetic method and application of a polybrominated diphenyl ether monomer. According to the solid-phase synthetic method and the application, the problems of an existing polybrominated diphenyl ether synthetic method that the reaction time is long, the reagent corrosivity is large, the postprocessing is complicated, and special equipment is required in the prior arts are solved. The solid-phase synthetic method has the beneficial effects that by utilizing a method of synthesizing polybrominated diphenyl ether through catalysis of solid superacid under a grinding condition, strong-base and strong-acid liquid reagents are not used, the safety is high, and the cleanness and the environmental protection are achieved; the synthesis time is 10-30 minutes, and compared with an ''iodonium salt-coupling two-step reaction method'', the reaction time is greatly shortened. According to the technical scheme, the solid-phase synthetic method comprises the step of enabling bromophenol to generate dehydration coupling reaction under the catalysis of solid superacid, so as to obtain the polybrominated diphenyl ether monomer.

Residues of polybrominated diphenyl ethers in honeys from different geographic regions

Wang, Jun,Kliks, Michael M.,Jun, Soojin,Li, Qing X.

experimental part, p. 3495 - 3501 (2011/07/07)

Polybrominated diphenyl ethers (PBDEs) are a class of widely used flame-retardants. Fifty honey samples labeled as being from different countries and regions were analyzed for 27 PBDE congeners. The concentrations of the 26 PBDEs, excluding BDE-209, ranged from 300 to 10,550 pg/g while the concentrations of BDE-209 ranged from nondetected to 9,260 pg/g. The honey samples labeled as originating In developed countries generally displayed higher concentrations of the total 27 PBDEs than those labeled as being from developing countries. Concentrations of 26 PBDEs ranged from 2,720 to 10,550 pg/g in honeys originating in developed countries and ranged from 1,030 to 3,470 pg/g in those from developing countries. BDE-209 was a dominant PBDE congener in all honey samples, on average accounting for 16% and 65% of the total 27 PBDEs in honeys from developed and developing countries, respectively. Honeys originating in developing countries, however, showed much higher BDE-209 levels and higher ratios of BDE-209 relative to the other PBDE congeners. In addition, some highly brominated PBDE congeners such as BDE196, -197, -206, and -207 showed elevated concentrations in honeys from developing countries. The findings were in agreement with the long, heavy historical uses of PBDE products in developed countries and the current, heavy uses of BDE-209 in developing countries. When BDE-209 was fortified in honey and incubated in the dark for four weeks at 25 or 60 °C, BDE-153, -183, -206, and -207 were detected as debromination products of BDE-209. Less brominated congeners in honeys may primarily come from the environment. Debromination of BDE-209 is also a source of less brominated congeners in honeys. The detection of PBDEs in honeys suggests that human exposure to PBDEs occurs as a result of honey consumption. 2010 American Chemical Society.

Synthesis and Characterization of Polybrominated Diphenyl Ethers - Unlabelled and Radiolabelled Tetra,- Penta- and Hexa-bromodiphenyl Ethers

Oern, Ulrika,Eriksson, Lars,Jakobsson, Eva,Bergman, Ake

, p. 802 - 807 (2007/10/03)

Diphenyl ether, 3-bromodiphenyl ether and 3,3'-dibromodiphenyl ether have been synthesized via coupling of the appropriate phenol and bromobenzene.Each of these compounds was subsequently brominated to (i) 2,2',4,4'-tetrabromodiphenyl ether, (ii) 2,2'3,4,

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