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Photoreactivities of the Antiseptics Dehydroacetic Acid and Sodium Dehydroacetate Used in Cosmetics
- Source :
- Chemical and Pharmaceutical Bulletin. 66:581-584
- Publication Year :
- 2018
- Publisher :
- Pharmaceutical Society of Japan, 2018.
-
Abstract
- Dehydroacetic acid (1) was found to induce photoisomerization, converting aldrin (3) and dieldrin (4) into photoaldrin (5) and photodieldrin (6), respectively, not only when irradiated with artificial light at wavelengths longer than 290 nm in air but also when exposed to sunlight in air. By contrast, sodium dehydroacetate (2) induced both photoisomerization, primarily converting 3 to 5 and photoepoxidation, partially forming 6. Thus, because 2 is usually used as a water-soluble antiseptic, photo-erethism might occur due to the isomerization and epoxidation properties of this compound. The difference between the photoreactivity of 1 and that of 2 might be attributed to the spin density of the odd electron on the carbon atom in the respective radicals that were formed after photo-excited 1 and 2 caused H-abstraction.
- Subjects :
- Free Radicals
Molecular Structure
Photoisomerization
010405 organic chemistry
Radical
Sodium dehydroacetate
Cosmetics
General Chemistry
General Medicine
Dehydroacetic acid
Photochemical Processes
010402 general chemistry
Photochemistry
01 natural sciences
0104 chemical sciences
Dieldrin
chemistry.chemical_compound
chemistry
Pyrones
Drug Discovery
Anti-Infective Agents, Local
Quantum Theory
Aldrin
Irradiation
Isomerization
Subjects
Details
- ISSN :
- 13475223 and 00092363
- Volume :
- 66
- Database :
- OpenAIRE
- Journal :
- Chemical and Pharmaceutical Bulletin
- Accession number :
- edsair.doi.dedup.....81ae316242a300b1411d96658c312608