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Ethyl hypochlorite, also known as ethyl monochloroacetate or chloroacetic acid ethyl ester, is an organic compound with the chemical formula C4H7ClO2. It is a colorless, volatile liquid that is soluble in water and has a pungent odor. Ethyl hypochlorite is primarily used as a disinfectant and bleaching agent in various industrial applications, such as the production of paper, textiles, and detergents. It is also used in the synthesis of pharmaceuticals and agrochemicals. Due to its reactive nature, ethyl hypochlorite can be hazardous and requires proper handling and storage to prevent exposure and potential health risks.

624-85-1

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624-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 624-85-1 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 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 624-85:
(5*6)+(4*2)+(3*4)+(2*8)+(1*5)=71
71 % 10 = 1
So 624-85-1 is a valid CAS Registry Number.

624-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl hypochlorite

1.2 Other means of identification

Product number -
Other names Hypochlorigsaeure-aethylester

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:624-85-1 SDS

624-85-1Relevant academic research and scientific papers

Preparation of alkoxy halides

-

, (2008/06/13)

Alkyl-, aryl- or alkylaryl-alkoxy halides are prepared by reacting the corresponding alcohol, phenol or alkyl phenol with ethylene oxide and/or propylene oxide in the presence of an amine catalyst to form an alkoxy alcohol, and directly reacting the latter with a halogenating agent in the continuing presence of the amine catalyst. Neutralization of the product and/or catalyst removal from the first stage is no longer necessary and reaction rates and yields are increased in the second stage.

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