| Weight | 90.078 g/mol |
|---|---|
| Formula | C3H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
1,3-dihydroxyacetone (96-26-4)
Dihydroxyacetone · Vitadye · 1,3-Dihydroxy-2-Propanone
Score:
#667 in Biochemistry
,
#1873 in Biology
,
#2257 in Chemistry
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- GLYCEROLIPID BIOSYNTHESIS IN PEROXISOMES VIA THE ACYL DIHYDROXYACETONE PHOSPHATE PATHWAY (Annals of the New York Academy of Sciences, 1982)
- Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome (Biochemical and Biophysical Research Communications, 1984)
- Regulation of glucose uptake by muscle. 9. Effects of fatty acids and ketone bodies, and of alloxan-diabetes and starvation, on pyruvate metabolism and on lactate/pyruvate and l-glycerol 3-phosphate/dihydroxyacetone phosphate concentration ratios in rat heart and rat diaphragm muscles (Biochemical Journal, 1964)
- The Arabidopsis thaliana Dihydroxyacetone Phosphate Reductase Gene SUPPRESSOR OF FATTY ACID DESATURASE DEFICIENCY1 Is Required for Glycerolipid Metabolism and for the Activation of Systemic Acquired Resistance (The Plant Cell, 2004)
- Metabolic and regulatory changes associated with growth of Saccharomyces cerevisiae in 1.4 M NaCl. Evidence for osmotic induction of glycerol dissimilation via the dihydroxyacetone pathway (Journal of Biological Chemistry, 1997)
- Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies). (Journal of Biological Chemistry, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dihydroxyacetone
- Vitadye
- 1,3-Dihydroxy-2-Propanone
- Chromelin
- 1,3 Dihydroxy 2 Propanone
-
SMILESC(C(=O)CO)O
-
InChIKeyRXKJFZQQPQGTFL-UHFFFAOYSA-N
- Pubchem - 1,3-dihydroxyacetone
- Wikipedia - dihydroxyacetone
Dihydroxyacetone (listen), or DHA, also known as glycerone, is a simple saccharide (a triose) with formula C 3H 6O 3. DHA is primarily used as an ingredient in sunless tanning products. It is often derived from plant sources such as sugar beets and sugar cane, and by the fermentation of glycerin.
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1,3-dihydroxyacetone
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