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158076-62-1

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158076-62-1 Usage

Description

2,2',3,3',4',5-Hexachloro-4-biphenylol is a chemical compound that belongs to the class of polychlorinated biphenyls (PCBs). It is characterized by its hexachlorinated structure, which consists of six chlorine atoms attached to a biphenyl molecule. 2,2',3,3',4',5-HEXACHLORO-4-BIPHENYLOL has been widely studied due to its environmental persistence and potential toxic effects on human health and the ecosystem.

Uses

Used in Environmental Testing and Research:
2,2',3,3',4',5-Hexachloro-4-biphenylol is used as a standard for environmental testing and research, particularly in the study of hydroxylated PCB metabolites. It serves as a reference compound to analyze and understand the presence and impact of PCBs in the environment, as well as their potential health risks.
Used in Historical Environmental Studies:
In the context of historical environmental studies, 2,2',3,3',4',5-Hexachloro-4-biphenylol has been utilized to investigate the presence of PCB metabolites in archived serum samples from California mothers in the 1950s and 1960s. This research helps to understand the historical exposure to PCBs and their potential long-term effects on human health and the environment.
Used in Analytical Chemistry:
2,2',3,3',4',5-Hexachloro-4-biphenylol is also used in analytical chemistry as a reference compound for the development and validation of analytical methods for the detection and quantification of PCBs and their metabolites in various environmental and biological samples.
Used in Toxicology and Risk Assessment:
2,2',3,3',4',5-HEXACHLORO-4-BIPHENYLOL is employed in toxicological studies to evaluate the potential toxic effects of PCBs on human health and the environment. The findings from these studies contribute to the development of risk assessment models and guidelines for the management and regulation of PCBs in the environment.
Used in Environmental Remediation:
Understanding the properties and behavior of 2,2',3,3',4',5-Hexachloro-4-biphenylol in the environment aids in the development of strategies and technologies for the remediation of contaminated sites, ensuring the protection of human health and the ecosystem.

Check Digit Verification of cas no

The CAS Registry Mumber 158076-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,0,7 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 158076-62:
(8*1)+(7*5)+(6*8)+(5*0)+(4*7)+(3*6)+(2*6)+(1*2)=151
151 % 10 = 1
So 158076-62-1 is a valid CAS Registry Number.

158076-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-trichloro-4-(2,3,4-trichlorophenyl)phenol

1.2 Other means of identification

Product number -
Other names (1,1'-Biphenyl)-4-ol,2,2',3,3',4',5-hexachloro

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:158076-62-1 SDS

158076-62-1Downstream Products

158076-62-1Relevant articles and documents

Synthesis and characterization of hydroxylated polychlorinated biphenyls (PCBs) identified in human serum

Safe,Safe, Stephen,Washburn,Washburn, Kent,Zacharewski,Zacharewski, Timothy,Phillips,Phillips, Timothy

, p. 3017 - 3023 (2007/10/03)

Hydroxylated polychlorinated biphenyls (PCBs) have been identified in wildlife and human samples. Most of these compounds are highly chlorinated (penta-hepatachloro) and contain a single meta- or para-hydroxyl group. Using the Cadogan coupling procedure, the following hydroxy-PCBs congeners were synthesized: 2,3,3',4',5-pentachloro-4-biphenylol, 2,3',4,4',5-pentachloro-3-biphenylol, 2',3,3',4',5-pentachloro-4-biphenylol, 2,2',3',4,4'-pentachloro-3-biphenylol, 2,2',3,3',4',5-pentachloro-4-biphenylol, 2,2',3',4,4',5-hexachloro-3-biphenylol, 2,2',3,4',5,5'-hexachloro-4-biphenylol, 2,2',3,3',4',5,5'-heptachloro-4-biphenyl 2,2',3',4,4',5,5'-heptachloro-3-biphenylol, 2,2',3,4',5,5',6-heptachloro-4-biphenylol. Many of these compounds have been detected as residues in human serum and current studies are investigating their activities as agonists and antagonists for several endocrine-mediated responses.

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