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Archives of Dermatology, 1960
Dihydroxyacetone (DHA),*a degradation product of glucose, has recently created a great deal of interest in the cosmetic industry and among dermatologists because of its unique ability to "tan" the human skin. This preliminary report gives some of our experiences with it.
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Dihydroxyacetone (DHA),*a degradation product of glucose, has recently created a great deal of interest in the cosmetic industry and among dermatologists because of its unique ability to "tan" the human skin. This preliminary report gives some of our experiences with it.
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2013
(1,3-dihydroxy-2-propanone) [96-26-4] C3H6O3 (MW 90.08) InChI = 1S/C3H6O3/c4-1-3(6)2-5/h4-5H,1-2H2 InChIKey = RXKJFZQQPQGTFL-UHFFFAOYSA-N (1,3-dihydroxy-2-propanone dimer) [26776-70-5] C6H12O6 (MW 180.16) InChI = 1S/C6H12O6/c7-1-5(9)3-12-6(10,2-8)4-11-5/h7-10H,1-4H2 InChIKey = KEQUNHIAUQQPAC-UHFFFAOYSA-N trans-2,5 ...
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(1,3-dihydroxy-2-propanone) [96-26-4] C3H6O3 (MW 90.08) InChI = 1S/C3H6O3/c4-1-3(6)2-5/h4-5H,1-2H2 InChIKey = RXKJFZQQPQGTFL-UHFFFAOYSA-N (1,3-dihydroxy-2-propanone dimer) [26776-70-5] C6H12O6 (MW 180.16) InChI = 1S/C6H12O6/c7-1-5(9)3-12-6(10,2-8)4-11-5/h7-10H,1-4H2 InChIKey = KEQUNHIAUQQPAC-UHFFFAOYSA-N trans-2,5 ...
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A synthesis of dihydroxyacetone phosphate from dihydroxyacetone
Carbohydrate Research, 1967R.L. Colbran +3 more
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The structure of dihydroxyacetone in solution
Bioorganic Chemistry, 1973Abstract Nuclear magnetic resonance, infrared and ultraviolet spectral data for dihydroxyacetone are reported, together with a brief kinetic study of the dimer-monomer equilibrium. The results are interpreted in terms of a dimeric dioxan structure for solid dihydroxyacetone which dissociates into a mixture of free carbonyl and hydrated monomer upon ...
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Dihydroxyacetone Phosphate from Dihydroxyacetone
2011P. Clapés, W. -D. Fessner
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Contact allergy to dihydroxyacetone
Contact Dermatitis, 1991M, Morren +4 more
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