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17352-16-8

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17352-16-8 Usage

General Description

2,4,6-tris(dichloromethyl)-1,3,5-trioxane is a synthetic chemical compound that consists of a six-membered ring with three oxygen atoms and three dichloromethyl groups attached to it. It is a highly toxic and potentially carcinogenic substance commonly used as a pesticide and as a fumigant for agricultural products and stored grains. Exposure to this chemical can cause severe respiratory irritation, skin burns, and damage to the nervous system, kidneys, and liver. Due to its hazardous nature, it is strictly regulated and its use is restricted in many countries to prevent harm to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 17352-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17352-16:
(7*1)+(6*7)+(5*3)+(4*5)+(3*2)+(2*1)+(1*6)=98
98 % 10 = 8
So 17352-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6Cl6O3/c7-1(8)4-13-5(2(9)10)15-6(14-4)3(11)12/h1-6H

17352-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(dichloromethyl)-1,3,5-trioxane

1.2 Other means of identification

Product number -
Other names Dichlor-acetaldehyd-trimer

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:17352-16-8 SDS

17352-16-8Upstream product

17352-16-8Downstream Products

17352-16-8Relevant articles and documents

Preparation of dichloroacetaldehyde cyclic trimer and its depolymerization

Wakasugi,Miyakawa,Suzuki,Itsuno,Ito

, p. 1289 - 1294 (1993)

Dichlorination of paraldehyde followed by hydration gave white crystals of dichloroacetaldehyde(DCA) hydrate which were treated with concd sulfuric acid at 0°C to afford a cyclic trimer of DCA as a quite stable precursor of DCA.

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