Literature DB >> 29467339

Photoreactivities of the Antiseptics Dehydroacetic Acid and Sodium Dehydroacetate Used in Cosmetics.

Takuya Izawa1, Koji Nakayama1, Noritaka Uchida2, Kazuhiro Nojima1.   

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.

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Keywords:  antiseptic; cosmetic; dehydroacetic acid; photoepoxidation; photoisomerization; sodium dehydroacetate

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Year:  2018        PMID: 29467339     DOI: 10.1248/cpb.c17-00938

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Photolysis, tautomerism and conformational analysis of dehydroacetic acid and a comparison with 2-hydroxyacetophenone and 2-acetyl-1,3-cyclohexanodione.

Authors:  María Victoria Cooke; Guillermo M Chans; Gustavo A Argüello; Walter José Peláez
Journal:  Heliyon       Date:  2020-07-22
  1 in total

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