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3-Methylisothiazole-5-carboxylic acid is a chemical compound characterized by a five-membered heterocyclic ring with a carboxylic acid group attached. It is an isothiazole derivative known for its antimicrobial properties, which makes it a common preservative in a variety of consumer products, pharmaceuticals, and industrial applications.

66975-83-5

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66975-83-5 Usage

Uses

Used in Personal Care Products:
3-Methylisothiazole-5-carboxylic acid is used as a preservative to inhibit the growth of bacteria and fungi in personal care products, ensuring their safety and longevity by preventing microbial contamination.
Used in Pharmaceuticals:
In the pharmaceutical industry, 3-Methylisothiazole-5-carboxylic acid serves as a preservative for medicinal products, helping to maintain their sterility and potency by controlling microbial growth.
Used in Industrial Products:
3-Methylisothiazole-5-carboxylic acid is utilized as a preservative in various industrial products to protect them from microbial spoilage, thus extending their shelf life and ensuring their quality.
Used in Antimicrobial Agent Development:
3-Methylisothiazole-5-carboxylic acid is studied for its potential in the development of new antimicrobial agents and pharmaceuticals due to its biological activities, which could contribute to the creation of novel treatments for infections caused by resistant bacteria and fungi.

Check Digit Verification of cas no

The CAS Registry Mumber 66975-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,7 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66975-83:
(7*6)+(6*6)+(5*9)+(4*7)+(3*5)+(2*8)+(1*3)=185
185 % 10 = 5
So 66975-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NO2S/c1-3-2-4(5(7)8)9-6-3/h2H,1H3,(H,7,8)

66975-83-5SDS

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 3-methyl-1,2-thiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Carboxy-3-methylisothiazole

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:66975-83-5 SDS

66975-83-5Relevant academic research and scientific papers

Isothiazolecarboxylic acid derivatives, rice blast control agents containing the same as active ingredients, and rice blast control method applying the control agents

-

, (2008/06/13)

Application of a rice blast control agent containing an isothiazolecarboxylic acid derivative of the below-described formula, which shows excellent activity against rice blast (Pyricularia oryzae) in rice cultivation, to the water surface of a paddy rice field results in the absorption of the derivative through roots of rice plants, so that the resistance of the rice plants can be enhanced. STR1 wherein R1 and R2 independently mean a hydrogen or halogen atom or a particular group, and Y stands for an OR3 group (R3 being a hydrogen or alkali metal atom or a particular group), an NHR4 group (R4 being a hydrogen atom or a particular group), or a morpholino group.

VINYL MONOMERS CONTAINING 1,2-THIA-, -SELENA- AND -TELLURAZOLE SYSTEMS, THEIR POLYMERS AND COPOLYMERS

Lucchesini, Francesco,Bertini, Vincenzo,Munno, Angela de,Pocci, Marco,Picci, Nevio,Liguori, Michele

, p. 1587 - 1594 (2007/10/02)

3-Methyl-5-vinyl-1,2-tellurazole, -selenazole and -thiazole have been prepared by one pot reaction from 5-hexen-3-yn-2-one, hydroxylamine-O-sulphonic acid and the proper alkaline chalcogenide.Their radical homopolymeryzation and copolymerization with styrene have been investigated.

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