693-97-0 Usage
Uses
Used in Industrial Water Treatment:
5-Methyl-isothiazole is used as a biocide for industrial water treatment to inhibit the growth of bacteria, fungi, and algae. Its effectiveness in controlling microbial populations helps maintain the efficiency and integrity of water systems.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 5-Methyl-isothiazole is used as a preservative to prevent the growth of microorganisms that could spoil the products or cause infections. Its antimicrobial properties help ensure the safety and longevity of these products.
Used in Household Cleaners:
5-Methyl-isothiazole is also utilized as a preservative in household cleaners to maintain their efficacy over time by preventing microbial contamination. This helps ensure that the cleaning products remain effective and safe for use.
It is important to handle 5-Methyl-isothiazole with care, as it can cause skin and eye irritation and may be harmful if ingested or inhaled. Proper safety measures should be taken during its use to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 693-97-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 693-97:
(5*6)+(4*9)+(3*3)+(2*9)+(1*7)=100
100 % 10 = 0
So 693-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H5NS/c1-4-2-3-5-6-4/h2-3H,1H3
693-97-0Relevant academic research and scientific papers
Phototransposition Chemistry of Methylisothiazoles and Methylthiazoles
Pavlik, James W.,Pandit, Chennagiri R.,Samuel, Christopher J.,Day, A. Colin
, p. 3407 - 3410 (2007/10/02)
Methylisothiazoles undergo phototransition in neutral solution to methylthiazoles by a single permutation process.Methylisothiazole -> methylisothiazole transpositions, previously reported to occur, were not detected in these reactions.In trifluoroacetic acid solvent, protonated methylisothiazoles and methylthiazoles phototranspose by P4 and P5 permutation pathways, respectively, resulting in a unique phototransposition cycle.
