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4-Bromo-3-methyl-isothiazol-5-ylamine is a chemical compound that belongs to the class of isothiazole compounds. It is known for its potent antimicrobial properties, making it a widely used biocide and preservative in various industrial and consumer products.

85508-99-2

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85508-99-2 Usage

Uses

Used in Personal Care Products:
4-Bromo-3-methyl-isothiazol-5-ylamine is used as a preservative for personal care products to inhibit the growth of bacteria, fungi, and algae, thereby extending the shelf life and maintaining the quality of these products.
Used in Paints and Adhesives:
In the paint and adhesives industry, 4-Bromo-3-methyl-isothiazol-5-ylamine is used as a biocide to prevent microbial contamination, ensuring the stability and performance of the products during storage and application.
Used in Cooling Water Systems:
4-Bromo-3-methyl-isothiazol-5-ylamine is utilized as an algaecide and biocide in cooling water systems to control the growth of microorganisms, which can cause fouling, corrosion, and reduced heat transfer efficiency.
However, there have been concerns about the potential health hazards of 4-Bromo-3-methyl-isothiazol-5-ylamine, including its skin and respiratory irritant properties. As a result, regulations have been established to control its use and set maximum allowable concentrations in certain applications to ensure safety and minimize risks. Despite these concerns, 4-Bromo-3-methyl-isothiazol-5-ylamine remains an important and widely used chemical in various industries due to its effectiveness in preserving and protecting products from microbial contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 85508-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85508-99:
(7*8)+(6*5)+(5*5)+(4*0)+(3*8)+(2*9)+(1*9)=162
162 % 10 = 2
So 85508-99-2 is a valid CAS Registry Number.

85508-99-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (766372)  5-Amino-4-bromo-3-methylisothiazole  97%

  • 85508-99-2

  • 766372-500MG

  • 1,249.56CNY

  • Detail

85508-99-2SDS

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 4-bromo-3-methyl-1,2-thiazol-5-amine

1.2 Other means of identification

Product number -
Other names 4-Bromo-3-methyl-isothiazol-5-ylamine

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:85508-99-2 SDS

85508-99-2Relevant academic research and scientific papers

GPR40 AGONISTS FOR THE TREATMENT OF TYPE II DIABETES

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Page/Page column 90; 91, (2017/03/17)

Disclosed are compounds, compositions and methods for treating of disorders that are affected by the modulation of the GPR40 receptor. Such compounds are represented by Formula II.

GPR40 AGONISTS FOR THE TREATMENT OF TYPE II DIABETES

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Page/Page column 105; 106, (2017/03/08)

Disclosed are compounds, compositions and methods for treating of disorders that are affected by the modulation of the GPR40 receptor. Such compounds are represented by Formula (I), as follows: wherein R1, R2, R4, W, X, Y, and G, are defined herein.

GPR40 AGONISTS FOR THE TREATMENT OF TYPE II DIABETES

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Page/Page column 101; 102, (2017/03/08)

Disclosed are compounds, compositions and methods for treating of disorders that are affected by the modulation of the GPR40 receptor. Such compounds are represented by Formula (III); wherein R1c, R2C, R4C, Wc, Yc, Zc and Gc, are defined herein.

Methods for inhibiting protein kinases

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Page/Page column 150-151, (2010/11/27)

The present invention provides methods for inhibiting protein kinases selected from the group consisting of AKT, Checkpoint kinase, Aurora kinase, Pim-1 kinase, and tyrosine kinase using imidazo[1,2-a]pyrazine compounds and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with protein kinases using such compounds.

Imidazopyrazines as protein kinase inhibitors

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Page/Page column 76-77, (2010/11/27)

In its many embodiments, the present invention provides a novel class of imidazopyrazine compounds as inhibitors of protein and/or checkpoint kinases, methods of preparing such compounds, pharmaceutical compositions including one or more such compounds, methods of preparing pharmaceutical formulations including one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the protein or checkpoint kinases using such compounds or pharmaceutical compositions.

ANTICANCER COMPOUNDS

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Page 39-40; 42, (2008/06/13)

This invention features compounds having formula (I): wherein, R1, R 2,R3, R4, R6, R7, T, X, and Y are as defined herein. This invention also features a method for treating cancer. The method includes administrating to a subject in need thereof a compound of formula (I).

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