131229-60-2 Usage
Description
[butoxy-(4-methoxybenzoyl)amino] acetate is a chemical compound utilized in the pharmaceutical and cosmetic industries, known for its antiseptic, anti-inflammatory, and antimicrobial properties. It is recognized for its ability to treat various skin conditions and its potential as a preservative and UV protection ingredient.
Uses
Used in Pharmaceutical and Cosmetic Industries:
[butoxy-(4-methoxybenzoyl)amino] acetate is used as an active ingredient for its antiseptic, anti-inflammatory, and antimicrobial properties, which contribute to the treatment of skin conditions such as acne, eczema, and psoriasis.
Used in Skincare Products:
In creams, lotions, and ointments, [butoxy-(4-methoxybenzoyl)amino] acetate is used as a therapeutic agent to help treat and alleviate symptoms of various skin conditions.
Used as a Preservative in Cosmetic Formulations:
[butoxy-(4-methoxybenzoyl)amino] acetate is used as a preservative to prevent the growth of harmful bacteria and fungi, ensuring the safety and longevity of cosmetic products.
Used in Sunscreens and UV Protection Products:
Due to its ability to absorb and filter UV radiation, [butoxy-(4-methoxybenzoyl)amino] acetate is used as an ingredient in sunscreens and other UV protection products to provide protection against the harmful effects of ultraviolet rays.
Check Digit Verification of cas no
The CAS Registry Mumber 131229-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,2 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131229-60:
(8*1)+(7*3)+(6*1)+(5*2)+(4*2)+(3*9)+(2*6)+(1*0)=92
92 % 10 = 2
So 131229-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO5/c1-4-5-10-19-15(20-11(2)16)14(17)12-6-8-13(18-3)9-7-12/h6-9H,4-5,10H2,1-3H3
131229-60-2Relevant articles and documents
Solvolysis and mutagenesis of n-acetoxy-n-alkoxybenzamides - Evidence for nitrenium ion formation
Campbell, John J.,Glover, Stephen A.,Rowbottom, Colleen A.
, p. 5377 - 5380 (1990)
Mutagenic N-acetoxy-N-butoxybenzamides undergo acid catalysed solvolysis in acetonitrile/water. Kinetic data and a Hammett σ+ correlation (ρ=-1.4) indicate nitrenium ion formation in the rate determining step. Levels of mutagenicity mirror the rates of solvolysis suggesting nitrenium ion involvement.
