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Bis(3-chloropropyl) ether, with the chemical formula C6H12Cl2O, is a colorless liquid that exhibits a chloroform-like odor. It is recognized as an industrial solvent and a chemical intermediate, playing a significant role in various chemical processes. However, it is classified as a moderately hazardous substance and is potentially carcinogenic, necessitating careful handling to prevent skin and eye irritation. Moreover, it poses a risk to aquatic life, emphasizing the importance of proper disposal and adherence to safety protocols and regulations.

629-36-7

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629-36-7 Usage

Uses

Used in Industrial Applications:
Bis(3-chloropropyl) ether is utilized as an industrial solvent for its ability to dissolve a wide range of substances, facilitating various manufacturing processes. Its solvent properties make it a valuable component in the production of certain chemicals and materials.
Used in Chemical Synthesis:
As a chemical intermediate, bis(3-chloropropyl) ether is employed in the synthesis of other compounds, contributing to the development of new chemical products and innovations in the chemical industry.
Used in Regulatory Compliance:
Due to its toxic nature and potential carcinogenic effects, bis(3-chloropropyl) ether is subject to strict regulations. It is essential for industries using this chemical to adhere to safety protocols and environmental regulations to minimize its impact on human health and the environment.
Used in Safety Training and Procedures:
Given its potential hazards, bis(3-chloropropyl) ether necessitates the implementation of safety training and procedures for those handling the substance. This includes the use of appropriate personal protective equipment and the establishment of emergency response measures in case of accidental exposure or spills.

Check Digit Verification of cas no

The CAS Registry Mumber 629-36-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 629-36:
(5*6)+(4*2)+(3*9)+(2*3)+(1*6)=77
77 % 10 = 7
So 629-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Cl2O/c7-3-1-5-9-6-2-4-8/h1-6H2

629-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-(3-chloropropoxy)propane

1.2 Other means of identification

Product number -
Other names Propane, 1,1‘-oxybis[3-chloro-

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:629-36-7 SDS

629-36-7Relevant academic research and scientific papers

X-ray crystal structure of tris(11-crown-3)triphenylene

Buchanan, Gerald W.,Azad, Mastaneh,Yap, Glenn P. A.

, p. 145 - 151 (2001)

Benzo-11-crown-3 ether trimerizes in the presence of FeCl3 and aqueous H2SO4 to produce tris(11-crown-3)triphenylene. This compound crystallizes, along with a molecule of diethyl ether and CH2Cl2 in the triclinic P1? space group; a = 8.8913(9) ?, b = 13.5790(14) ?, c = 17.5244(17) ?, β = 91.026(2)°, with Z = 2. Two of the three 11-crown-3 ether units of the trimer possess essentially identical geometries, while the third has a significantly different conformation. These stereochemical results are compared to those calculated for benzo-11-crown-3 in the gas phase.

NONAQUEOUS SOLUTION OF HYPOCHLOROUS ACID AND CHLOROHYDRINATION REACTIONS OF CERTAIN LOWER ALKENES.

Bikbulatov,Valitov,Gromova,Stepanova,Martynova

, p. 2314 - 2317 (2007/10/02)

A study was made of the problems of preparing stable, highly concentrated nonaqueous solutions of hypochlorous acid and carrying out chlorohydrination reactions in them. The results on the chlorohydrination of alpha -alkenes showed that, in principle, it is possible and advisable to use solutions of hypochlorous acid in organic solvents, in particular, aliphatic and alicyclic ketones, ethyl acetate and tributyl phosphate. The use of organic solvents noticeably improves the stability of HOCl, so that the working concentrations of the acid can be increased, and the chlorohydrination reaction products can be more easily isolated.

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