27689-95-8 Usage
Uses
Used in Pharmaceutical Industry:
TRIMETHYL 4-HYDROXYORTHOBENZOATE is used as a preservative for its ability to prevent the growth of bacteria and fungi, ensuring the safety and stability of pharmaceutical products.
Used in Personal Care Products:
In the personal care industry, TRIMETHYL 4-HYDROXYORTHOBENZOATE is used as a preservative to maintain the freshness and quality of products, such as creams, lotions, and shampoos, by inhibiting microbial contamination.
Used in Food Industry:
TRIMETHYL 4-HYDROXYORTHOBENZOATE is used as a preservative in the food industry to extend the shelf life of products by preventing spoilage caused by microbial growth.
Used as a Fragrance Ingredient:
TRIMETHYL 4-HYDROXYORTHOBENZOATE is used in the fragrance industry to enhance the scent of various products, contributing to their overall sensory appeal.
Used as a UV Filter in Sunscreen Products:
In the cosmetics industry, TRIMETHYL 4-HYDROXYORTHOBENZOATE is used as a UV filter in sunscreen products, providing protection against harmful ultraviolet radiation and helping to prevent skin damage.
Despite the widespread use of TRIMETHYL 4-HYDROXYORTHOBENZOATE, there is a growing awareness of potential health concerns associated with parabens, leading to a movement towards using alternative preservatives in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 27689-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,8 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27689-95:
(7*2)+(6*7)+(5*6)+(4*8)+(3*9)+(2*9)+(1*5)=168
168 % 10 = 8
So 27689-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c1-12-10(13-2,14-3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3
27689-95-8Relevant academic research and scientific papers
Ramig, Keith,Englander, Miriam,Kallashi, Florida,Livchits, Lilia,Zhou, Jessica
, p. 7731 - 7734 (2002)
The trifluoromethyl group of certain compounds containing one or two trifluoromethyl groups can be converted to the carbomethoxy group by treatment with sodium methoxide followed by aqueous acidic work-up. α-Trifluoromethyl esters can be obtained by selective methanolysis of the 1,1,1,3,3,3-hexafluoroisopropyl group in some cases. The structural requirements for the transformation are delineated, and a mechanistic study confirms the proposed mechanism, a dehydrofluorination-addition-elimination process.
