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70362-48-0

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70362-48-0 Usage

Uses

2'',3,4,5-Tetrachlorobiphenyl is a polychlorinated biphenyl (PCB) congeners.

Check Digit Verification of cas no

The CAS Registry Mumber 70362-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70362-48:
(7*7)+(6*0)+(5*3)+(4*6)+(3*2)+(2*4)+(1*8)=110
110 % 10 = 0
So 70362-48-0 is a valid CAS Registry Number.

70362-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',3,4,5-Tetrachlorobiphenyl

1.2 Other means of identification

Product number -
Other names 1,2,3-trichloro-5-(2-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:70362-48-0 SDS

70362-48-0Downstream Products

70362-48-0Relevant articles and documents

Phototransformations of polychlorobiphenyls in brij 58 micellar solutions

Chu, Wei,Jafvert, Chad T.,Diehl, Claude A.,Marley, Karen,Larson, Richard A.

, p. 1989 - 1993 (2007/10/03)

Our purpose in conducting these studies was to examine photolysis as a destructive process for polychlorobiphenyls (PCBs) extracted from soils with surfactant solutions. Surfactants have shown promise as agents for removing free phase and sorbed contaminants from soils, yet information on ultimate disposal options and recycle/recovery strategies for the surfactants is generally lacking. For arylhalides, photodechlorination may result in decontamination, eliminating the need to physically separate these contaminants from the washing solution. Photochemical reactions of the PCB congener mixture, Aroclor 1254, and the specific congener, 2,3,4,5- tetrachlorobiphenyl (2,3,4,5-TeCB), were investigated in aqueous solutions containing surfactant micelles with UV light at 253.7 nm. Photoreduction through photodechlorination was shown to be the main decay pathway in which lesser chlorinated congeners were formed as intermediates. In experiments with 2,3,4,5-TeCB, final noncarbon-containing products included Cl- and H+, both produced nearly stoichiometrically from the starting materials. The quantum yield for decay of 0.1 μM 2,3,4,5-TeCB in 0.5 mM Brij 58 micellar solutions was over six times greater than in water alone. Sequential extraction from a soil and photoreduction of 2,3,4,5-tetrachlorobiphenyl by Brij 58 solutions proved to be limited by surfactant loss to the soil. Our purpose in conducting these studies was to examine photolysis as a destructive process for polychlorobiphenyls (PCBs) extracted from soils with surfactant solutions. Surfactants have shown promise as agents for removing free phase and sorbed contaminants from soils, yet information on ultimate disposal options and recycle/recovery strategies for the surfactants is generally lacking. For arylhalides, photodechlorination may result in decontamination, eliminating the need to physically separate these contaminants from the washing solution. Photochemical reactions of the PCB congener mixture, Aroclor 1254, and the specific congener, 2,3,4,5-tetrachlorobiphenyl (2,3,4,5-TeCB), were investigated in aqueous solutions containing surfactant micelles with UV light at 253.7 nm. Photoreduction through photodechlorination was shown to be the main decay pathway in which lesser chlorinated congeners were formed as intermediates. In experiments with 2,3,4,5-TeCB, final noncarbon-containing products included Cl- and H+, both produced nearly stoichiometrically from the starting materials. The quantum yield for decay of 0.1 μM 2,3,4,5-TeCB in 0.5 mM Brij 58 micellar solutions was over six times greater than in water alone. Sequential extraction from a soil and photoreduction of 2,3,4,5-tetrachlorobiphenyl by Brij 58 solutions proved to be limited by surfactant loss to the soil.

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