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138507-65-0

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138507-65-0 Usage

Description

2,3,4-Tribromophenol is an organic compound with the chemical formula C6H3Br3OH. It is a white crystalline solid and a known metabolite of polybrominated diphenyl ether (PBDE). 2,3,4-TRIBROMOPHENOL has gained attention due to its potential use as a biomarker for human exposure to polybrominated diphenyl ethers (PBDEs), which are a group of flame retardant chemicals.

Uses

Used in Environmental Monitoring and Human Health Assessment:
2,3,4-Tribromophenol is used as a biomarker for [detecting human exposure to polybrominated diphenyl ethers (PBDEs)] because of its association with these chemicals. The presence of 2,3,4-tribromophenol in human samples can indicate exposure to PBDEs, which are known to have adverse effects on human health and the environment.
Used in Chemical Research and Analysis:
2,3,4-Tribromophenol is used as a research compound for [studying the metabolism and toxicology of polybrominated diphenyl ethers (PBDEs)]. Understanding the metabolic pathways and potential health impacts of PBDEs is crucial for developing strategies to reduce human exposure and mitigate their environmental and health risks.
Used in Industrial Chemical Analysis:
In the chemical industry, 2,3,4-tribromophenol is used as an analytical compound for [identifying and quantifying the presence of polybrominated diphenyl ethers (PBDEs) in various products and materials]. This information is essential for compliance with regulations and guidelines related to the use and disposal of flame retardants and other materials containing PBDEs.
Used in Toxicology Studies:
2,3,4-Tribromophenol is used as a test compound in toxicology studies for [evaluating the potential health risks associated with exposure to polybrominated diphenyl ethers (PBDEs)]. These studies help to determine the safety of materials containing PBDEs and inform the development of safer alternatives.
Used in Environmental Remediation:
2,3,4-Tribromophenol can be used as a target compound in environmental remediation efforts for [cleaning up contaminated sites and reducing the release of polybrominated diphenyl ethers (PBDEs) into the environment]. By focusing on the removal of 2,3,4-tribromophenol and other related compounds, these efforts can help to mitigate the environmental impact of PBDEs.

Check Digit Verification of cas no

The CAS Registry Mumber 138507-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138507-65:
(8*1)+(7*3)+(6*8)+(5*5)+(4*0)+(3*7)+(2*6)+(1*5)=140
140 % 10 = 0
So 138507-65-0 is a valid CAS Registry Number.

138507-65-0SDS

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 2,3,4-TRIBROMOPHENOL

1.2 Other means of identification

Product number -
Other names 2,3,4-tribromo-phenol

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:138507-65-0 SDS

138507-65-0Relevant articles and documents

Polybrominated diphenyl ethers (BDEs); preparation of reference standards and fluorinated internal analytical standards

Liu, Huiling,Bernhardsen, Monica,Fiksdahl, Anne

, p. 3564 - 3572 (2007/10/03)

Four new difluorinated tetra- and pentabromo BDE internal standards for GC-MS/GC-ECD analysis, 2F-BDE 47, 2F-BDE 85, 2F-BDE 99 and 2F-BDE 119, have been prepared in 98-99.0% purity, mainly by coupling of the new tribromodifluorophenols (19-21) and symmetr

Identification of hydroxylated PCB metabolites and other phenolic halogenated pollutants in human blood plasma

Hovander,Malmberg,Athanasiadou,Athanassiadis,Rahm,Bergman,Wehler, E. Klasson

, p. 105 - 117 (2007/10/03)

A growing number of studies have reported phenolic halogenated compounds (PHCs) that are retained in the blood of humans and wildlife. These PHCs may be industrial chemicals; metabolites thereof, as in the case with polychlorobiphenylols (OH-PCBs); or of natural origin. The present study was aimed to identify hitherto unknown PHCs in human plasma with chemical structures that are consistent to PHCs known to possess endocrine-disrupting activity. For this purpose, samples of blood plasma from 10 randomly selected male blood donors from Sweden were pooled and analyzed by GC/ECD and GC/MS. Brominated, bromochlorinated, and chlorinated methyl derivatives of phenols and OH-PCBs were synthesized to be used as authentic reference standards. More than 100 PHCs were indicated in the plasma, and among those a total of 9 monocyclic brominated or chlorinated phenol-, guaiacol-, and/or catechol-type compounds were identified as their methylated derivatives. The two major compounds were 2,4,6-tribromophenol and pentachlorophenol. Thirty-eight OH-PCB congeners were structurally identified on two GC columns of different polarity. The origin of the OH-PCB metabolites in the context of their parent PCB congeners are suggested. Other PHCs identified in the male plasma were Triclosan (5-chloro-2-[2,4-dichlorophenoxy] phenol), a common bactericide; 4-hydroxy-heptachlorostyrene, a metabolite of octachlorostyrene; and 3,5-dibromo-2-(2,4-dibromophenoxy)phenol, a natural compound and a potential metabolite of polybrominated diphenyl ethers.

Agent for protecting sawn timber

-

, (2008/06/13)

The present invention relates to an agent or concentrate for protecting sawn timber against wood-discolouring fungi, containing a fungicide on phenol basis and a fungicide on organo-iodine basis, optionally fungicides and insecticides, dissolved in an organochemical solvent or solvent mixture or in a mixture of water and organochemical solvent or solvent mixture and at least one emulsifier.

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