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13001-29-1

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13001-29-1 Usage

General Description

2-(2,4,6-trichloro phenoxy)chloroethane is a chemical compound used as a pesticide, specifically as an insecticide and acaricide. It belongs to the organochlorine group of chemicals, which are known for their persistent and toxic nature. Due to its potential health and environmental hazards, its use has been restricted in many countries. Exposure to this compound can lead to various health issues, including skin and eye irritation, respiratory problems, and damage to the liver and kidneys. It also poses a threat to aquatic life and other non-target organisms. Therefore, it is important to handle and dispose of this chemical with caution and adhere to safety regulations when using it.

Check Digit Verification of cas no

The CAS Registry Mumber 13001-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13001-29:
(7*1)+(6*3)+(5*0)+(4*0)+(3*1)+(2*2)+(1*9)=41
41 % 10 = 1
So 13001-29-1 is a valid CAS Registry Number.

13001-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trichloro-2-(2-chloroethoxy)benzene

1.2 Other means of identification

Product number -
Other names 2.4.6-Trichlor-1-(2-chlorethoxy)-benzol

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:13001-29-1 SDS

13001-29-1Relevant articles and documents

Method of preparing fungicidal intermediates

-

, (2008/06/13)

N-n-propyl-N-(2,4,6-trichlorophenoxy)-ethyl amine is prepared by reacting 2-phenoxy ethanol with thionyl chloride in the presence of a catalytic amount of tetraalkyl ammonium halide optionally in the presence of a solvent to form 2-phenoxy ethyl chloride; selectively chlorinating the 2-phenoxy ethyl chloride with chlorine at a temperature from 0° C. to 60° C. in the presence of a catalytic amount if urea to form 2-(2,4,6-trichlorophenoxy)-ethyl chloride; reacting the 2-(2,4,6-trichlorophenoxy)-ethyl chloride with n-propyl amine at a temperature of from 20° C. to 150° C., optionally in the presence of water; and recovering the N-n-propyl-N-2-(2,4,6-trichlorophenoxy)-ethyl amine formed.

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