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Sodium 2-chloropropionate is a chemical compound derived from propionic acid, known for its antimicrobial properties and effectiveness against bacteria, yeast, and molds. It is used as a preservative in food and cosmetic products and as a stabilizer in pharmaceutical formulations. Although considered relatively safe for use in low concentrations, it should be used with caution due to its potential to cause skin and eye irritation and is regulated by health and safety guidelines.

16987-02-3

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16987-02-3 Usage

Uses

Used in Food and Cosmetic Industry:
Sodium 2-chloropropionate is used as a preservative for its antimicrobial properties, helping to prevent spoilage and extend the shelf life of various food and cosmetic products.
Used in Pharmaceutical Industry:
Sodium 2-chloropropionate is used as a stabilizer in pharmaceutical formulations to maintain the stability and effectiveness of the products during storage and use.
Used in Antimicrobial Applications:
Sodium 2-chloropropionate is used as an antimicrobial agent for its effectiveness against bacteria, yeast, and molds, providing protection against microbial contamination in various products.

Check Digit Verification of cas no

The CAS Registry Mumber 16987-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16987-02:
(7*1)+(6*6)+(5*9)+(4*8)+(3*7)+(2*0)+(1*2)=143
143 % 10 = 3
So 16987-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H5ClO2.Na/c1-2(4)3(5)6;/h2H,1H3,(H,5,6);/q;+1/p-1

16987-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium 2-chloropropionate

1.2 Other means of identification

Product number -
Other names 2-CHLOROPROPIONIC ACID SODIUM SALT

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:16987-02-3 SDS

16987-02-3Relevant academic research and scientific papers

Processes for producing phenoxy propionic acid derivatives

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, (2008/06/13)

PCT No. PCT/JP97/01711 Sec. 371 Date Dec. 3, 1998 Sec. 102(e) Date Dec. 3, 1998 PCT Filed May 21, 1997 PCT Pub. No. WO97/46538 PCT Pub. Date Dec. 11, 1997The present invention relates to processes for producing D(+)-2-[4-(6-chloro-2-quinoxalyloxy)phenoxy]propionic acid and ester derivatives thereof and which can be used as selective herbicides for foliage treatment for controlling gramineous weeds against broad leaf crop plants.

Process for the preparation and purification of D-hydroxyphenoxypropionic acid

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, (2008/06/13)

A process for the preparation of D-hydroxyphenoxypropionic acid and its purification from its reaction mixture containing the acid, together with inorganic salts and various organic impurities, by crystallization of D-hydroxyphenoxypropionic acid by cooling followed by washing the crystals of D-hydroxyphenoxypropionic acid by elution.

Process for preparing optically active 2-(4-hydroxy-phenoxy) propionic acid compounds

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, (2008/06/13)

A process for preparing an optically active 2-(4-hydroxyphenoxy)propionic acid compound, which comprises reacting an optically active compound having the formula: STR1 wherein X is a chlorine atom or a bromine atom, and M is a hydrogen atom or an alkali metal atom, with hydroquinone or an alkali metal salt of hydroquinone, in the presence of an alkali metal hydroxide and water, and precipitating optically active disodium 2-(4-hydroxyphenoxy)propionate.

Process for the preparation of dextrorotatory 2-phenoxypropionic acid derivatives

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, (2008/06/13)

Dextrorotatory 2-phenoxypropionic acids are made by heating an alkali metal salt of dextrorotatory 2-chloropropionic acid with an alkali metal phenate in an inert organic solvent of high boiling point under reflux.

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