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18495-30-2

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18495-30-2 Usage

General Description

1,1,2,3-Tetrachloropropane is a highly toxic and potentially carcinogenic chemical compound. It is a chlorinated hydrocarbon with the chemical formula C3H4Cl4, and is used as a solvent and a chemical intermediate in the production of pesticides and other industrial chemicals. Exposure to 1,1,2,3-Tetrachloropropane can result in adverse health effects, including damage to the liver, kidneys, and central nervous system. It is also known to be harmful to aquatic organisms and may cause long-term environmental damage. Due to its potential health and environmental risks, the use and handling of 1,1,2,3-Tetrachloropropane is heavily regulated in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 18495-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18495-30:
(7*1)+(6*8)+(5*4)+(4*9)+(3*5)+(2*3)+(1*0)=132
132 % 10 = 2
So 18495-30-2 is a valid CAS Registry Number.

18495-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,3-TETRACHLOROPROPANE

1.2 Other means of identification

Product number -
Other names propane,1,1,2,3-tetrachloro

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:18495-30-2 SDS

18495-30-2Relevant articles and documents

PROCESSES FOR PREPARING PENTACHLOROPROPANE AND TETRACHLOROPROPENE FROM DICHLOROPROPENE

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Paragraph 0093, (2022/04/03)

A processes for preparing 1,1,2,3-tetrachloropropene, 2,3,3,3-tetrachloropropene, or a mixture thereof from 1,3-dichloropropene. The process may include a two successive chlorination and dehydrochlorination reactions. In a first chlorination reaction 1,3-dichloropropene is reacted with a chlorination agent to form a first chlorination reaction product including 1,1,2,3-tetrachloropropane. This first chlorination reaction product is reacted with a dehydrochlorination reagent in a first dehydrochlorination reaction to form a first dehydrochlorination reaction product including a trichloropropene. The trichloropropene containing reaction product is reacted with a chlorination agent in a second chlorination reaction to form a second chlorination reaction product including at least one of 1,1,1,2,3-pentachloropropane or 1,1,2,2,3-pentachloropropane. This reaction product is reacted with a dehydrochlorination reagent in a second dehydrochlorination reaction to form a second dehydrochlorination reaction product having 1,1,2,3-tetrachloropropene or a 2,3,3,3-tetrachloropropene.

SULFURYL CHLORIDE AS CHLORINATING AGENT

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Paragraph 0098-00100, (2013/07/05)

The use of sulfuryl chloride, either alone or in combination with chlorine, as a chlorinating agent is disclosed.

PROCESS FOR THE PRODUCTION OF CHLORINATED ALKANES

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Paragraph 0047; 0048, (2013/06/27)

Processes for the production of chlorinated alkanes are provided. The present processes comprise catalyzing the chlorination of a feedstream comprising one or more alkanes and/or alkenes with a catalyst system comprising one or more inorganic iodine salts and/or lower than conventional levels of elemental iodine and at least one Lewis acid. The processes are conducted in a nonaqueous media, and so, the one or more inorganic iodine salts are recoverable and/or reusable, in whole or in part.

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