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2,2',4,4',5-Pentabromodiphenyl ether, a member of the polybrominated diphenyl ethers (PBDEs) family, is a highly brominated flame retardant chemical compound. It has been extensively utilized in various consumer products such as electronics, textiles, and plastics to mitigate fire hazards. However, due to its environmental persistence and bioaccumulation potential, there are significant concerns regarding its impact on human health and the environment. Studies have associated exposure to 2,2',4,4',5-PENTABROMODIPHENYL ETHER with detrimental effects like developmental and reproductive toxicity, neurological damage, and hormonal system disruption. Consequently, its usage has faced restrictions or bans in numerous countries, and there is an ongoing shift towards safer flame retardants.

60348-60-9

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60348-60-9 Usage

Uses

Used in Consumer Electronics:
2,2',4,4',5-Pentabromodiphenyl ether is used as a flame retardant in consumer electronics to reduce the risk of fire, ensuring the safety of users and prolonging the lifespan of electronic devices.
Used in Textile Industry:
In the textile industry, 2,2',4,4',5-Pentabromodiphenyl ether is used as a flame retardant for fabrics, enhancing their fire resistance and providing additional safety for consumers in various applications such as upholstery, carpets, and clothing.
Used in Plastics Manufacturing:
2,2',4,4',5-Pentabromodiphenyl ether is utilized as a flame retardant in the production of plastics, improving their fire safety characteristics and reducing the likelihood of fire incidents in various plastic products.
However, due to the growing awareness of the potential health and environmental risks associated with 2,2',4,4',5-Pentabromodiphenyl ether, there is a global trend towards the development and adoption of alternative, safer flame retardants in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 60348-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60348-60:
(7*6)+(6*0)+(5*3)+(4*4)+(3*8)+(2*6)+(1*0)=109
109 % 10 = 9
So 60348-60-9 is a valid CAS Registry Number.

60348-60-9 Well-known Company Product Price

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  • Sigma-Aldrich

  • (42235)  BDE No 99  analytical standard

  • 60348-60-9

  • 42235-10MG

  • 1,547.91CNY

  • Detail
  • Sigma-Aldrich

  • (33676)  BDE No 99 solution  50 μg/mL in isooctane, analytical standard

  • 60348-60-9

  • 33676-1ML

  • 4,182.75CNY

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60348-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2',4,4',5-PENTABROMODIPHENYL ETHER

1.2 Other means of identification

Product number -
Other names PBDE-99

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:60348-60-9 SDS

60348-60-9Downstream Products

60348-60-9Relevant academic research and scientific papers

Synthesis of polybrominated diphenyl ethers and their capacity to induce CYP1A by the Ah receptor mediated pathway

Chen,Konstantinov,Chittim,Joyce,Bols,Bunce

, p. 3749 - 3756 (2007/10/03)

Polybrominated diphenyl ethers (PBDEs) have become widely distributed as environmental contaminants due to their use as flame retardants. Their structural similarity to other halogenated aromatic pollutants has led to speculation that they might share toxicological properties such as hepatic enzyme induction. In this work we synthesized a number of PBDE congeners, studied their affinity for rat hepatic Ah receptor through competitive binding assays, and determined their ability to induce hepatic cytochrome P-450 enzymes by means of EROD (ethoxyre-sorufin-O-deethylase) assays in human, rat, chick, and rainbow trout cells. Both pure PBDE congeners and commercial PBDE mixtures had Ah receptor binding affinities 10-2-10-5 times that of 2,3,7,8-tetrachlorodibenzo-p-dioxin. In contrast with polychlorinated biphenyls, Ah receptor binding affinities of PBDEs could not be related to the planarity of the molecule, possibly because the large size of the bromine atoms expands the Ah receptor's binding site. EROD activities of the PBDE congeners followed a similar rank order in all cells. Some congeners, notably PBDE 85, did not follow the usual trend in which strength of Ah receptor binding affinity paralleled P-450 induction potency. Use of the gel retardation assay with a synthetic oligonucleotide indicated that in these cases the liganded Ah receptor failed to bind to the DNA recognition sequence.

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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