70424-62-3 Usage
Uses
Used in Sunscreen Industry:
2-Octanoyloxybenzoic acid is used as a UVB absorber for its sun-protective properties, helping to shield the skin from harmful ultraviolet radiation.
Used in Skincare Products:
2-Octanoyloxybenzoic acid is used as an ingredient in skincare products for its ability to protect the skin from sun damage while providing a non-greasy texture and light feeling on the skin.
Used in Cosmetics:
2-Octanoyloxybenzoic acid is used as a component in cosmetics for its sun-protective properties and favorable skin-feel, making it a popular choice in the beauty and skincare industry.
Overall, 2-octanoyloxybenzoic acid is a widely used chemical in the beauty and skincare industry for its sun-protective properties and favorable skin-feel, and is considered safe for use in skincare products, approved by regulatory bodies such as the FDA and the European Union's Cosmetics Directive.
Check Digit Verification of cas no
The CAS Registry Mumber 70424-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,2 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70424-62:
(7*7)+(6*0)+(5*4)+(4*2)+(3*4)+(2*6)+(1*2)=103
103 % 10 = 3
So 70424-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O4/c1-2-3-4-5-6-11-14(16)19-13-10-8-7-9-12(13)15(17)18/h7-10H,2-6,11H2,1H3,(H,17,18)
70424-62-3Relevant academic research and scientific papers
Low-energy collision-induced fragmentation of negative ions derived from diesters of aliphatic dicarboxylic acids made with hydroxybenzoic acids
Nishshanka, Upul,Attygalle, Athula B.
experimental part, p. 1502 - 1511 (2009/10/10)
Diesters of ortho-hydroxybenzoic acid (salicylic acid) made with glutaric, adipic, and pimelic acids are the monomers of some potential drug candidates for aspirin patches. Collision-induced dissociation (CID) spectra of negative ion derived from these compounds show a 120-Da 'neutral loss' specific to the ortho isomers. In contrast, the anions derived from diesters of meta- and para-hydroxybenzoic acids show a 138-Da loss for an elimination of elements of hydroxybenzoic acid by a charge-remote mechanism. Deuterium labeling studies confirmed that the hydrogen atom transferred for hydroxybenzoic acid loss originates specifically from the α position of the dicarboxylic acid moiety. Although all spectra showed a peak at m/z 137, a charge-mediated process specific for the ortho compounds renders it the most prominent peak in the spectra of ortho compounds. Appropriate deuterium labeling experiments demonstrated that the hydrogen atom transferred for the formation of the m/z 137 ion in ortho compounds is specifically derived from the α position of the dicarboxylic acid moiety. Copyright
