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2,3,3'-TRICHLOROBIPHENYL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38444-84-7

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38444-84-7 Usage

Uses

2,3,3''-Trichlorobiphenyl is a polychlorinated biphenyl (PCB) congeners.

Check Digit Verification of cas no

The CAS Registry Mumber 38444-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38444-84:
(7*3)+(6*8)+(5*4)+(4*4)+(3*4)+(2*8)+(1*4)=137
137 % 10 = 7
So 38444-84-7 is a valid CAS Registry Number.

38444-84-7SDS

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 2,3,3'-Trichlorobiphenyl

1.2 Other means of identification

Product number -
Other names 1,2-dichloro-3-(3-chlorophenyl)benzene

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:38444-84-7 SDS

38444-84-7Downstream Products

38444-84-7Relevant academic research and scientific papers

METHOD FOR SEPARATING AND CLEANING UP POLYHALOGENATED BIPHENYLS

-

Page/Page column 20-26, (2008/06/13)

The method for separating and cleaning up polyhalogenated biphenyls (PHBs) is characterized by comprising the following three steps: (1) the step of bringing a sample containing PHBs into contact with a fibrous activated carbon; (2) the step of washing the fibrous activated carbon with hexanes; and (3) the step of eluting PHBs from the fibrous activated carbon.

Synthesis of polychlorinated biphenyls (PCBs) using the Suzuki-coupling

Lehmler, Hans-Joachim,Robertson, Larry W

, p. 137 - 143 (2007/10/03)

An improved synthesis of polychlorinated biphenyls (PCBs) utilizing a palladium-catalyzed cross-coupling reaction (Suzuki-coupling) is described. The coupling of (chlorinated) aryl boronic acids 1-3 with bromochlorobenzenes 4 using the standard conditions of the Suzuki-coupling gave the desired PCB congeners 5-7 in good to excellent yields. The self-coupling product of the aryl boronic acids is the major impurity of this reaction. 3,4,5-trichlorophenyl derivatives such as 10 can be synthesized by coupling of an aryl boronic acid with the corresponding bromochloroaniline 8. The approach offers the advantage of high selectivity and good yields compared to conventional methods Such as the Cadogan reaction and allows the use of less toxic starting materials.

Physical, spectral and chromatographic properties of all 209 individual PCB congeners

Bolgar,et al.

, p. 2687 - 2705 (2007/10/03)

Through the use of two capillary GC columns: 40% octadecyl/ 15% phenyl methyl siloxane and 50% phenyl methyl siloxane, it was possible to separate 201 PCB congeners with only four unresolved pairs. The data compiled in this study for all 209 congeners will aid in the identification of selected individual components of these environmental pollutants. The use of this data also presents the opportunity for the improved quantification of the commercial PCB formulations. -from Authors

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