Product Name :
1,3-Dihydroxyacetone (CAS 96-26-4)

Synonym :
Bis(hydroxymethyl) Ketone; Chromelin; Dihydroxyacetone

Application :

CAS:
96-26-4

Purity:

Molecular Weight:
90.08

Formula :
C3H6O3

Physical state:
Solid

solubility :
Soluble in DMSO, methanol, and water.

Shipping Condition :
Desiccate at room temperature

Melting point:
72-75° C

SMILES:

References:
:Detailed investigation of the production of the bread flavor component 6-acetyl-1,2,3,4-tetrahydropyridine in proline/1,3-dihydroxyacetone model systems. | Adams, A., et al. 2004. J Agric Food Chem. 52: 5685-93. PMID: 15373410Molecular structure and conformational composition of 1,3-dihydroxyacetone studied by combined analysis of gas-phase electron diffraction data, rotational constants, and results of theoretical calculations. Ideal gas thermodynamic properties of 1,3-dihydroxyacetone. | Dorofeeva, OV., et al. 2007. J Phys Chem A. 111: 6434-42. PMID: 17595068[Progress in metabolic engineering of microbial production of 1,3-dihydroxyacetone]. | Sun, L., et al. 2010. Sheng Wu Gong Cheng Xue Bao. 26: 1218-24. PMID: 21141111Use of glycerol for producing 1,3-dihydroxyacetone by Gluconobacter oxydans in an airlift bioreactor. | Hu, ZC., et al. 2011. Bioresour Technol. 102: 7177-82. PMID: 21592784Enhancement of 1,3-dihydroxyacetone production by a UV-induced mutant of Gluconobacter oxydans with DO control strategy. | Hu, ZC. and Zheng, YG. 2011. Appl Biochem Biotechnol. 165: 1152-60. PMID: 21833510Improvement of 1,3-dihydroxyacetone production from Gluconobacter oxydans by ion beam implantation. | Hu, ZC., et al. 2012. Prep Biochem Biotechnol. 42: 15-28. PMID: 22239705Mechanistic studies on the cascade conversion of 1,3-dihydroxyacetone and formaldehyde into alpha -hydroxy- gamma -butyrolactone.20765-98-4 manufacturer | Yamaguchi, S., et al. 2015. ChemSusChem. 8: 853-60. PMID: 25648856Simultaneous Bioconversion of Xylose and Glycerol to Xylonic Acid and 1,3-Dihydroxyacetone from the Mixture of Pre-Hydrolysates and Ethanol-Fermented Waste Liquid by Gluconobacter oxydans. | Zhou, X., et al. 2016. Appl Biochem Biotechnol. 178: 1-8. PMID: 26378011Optimization of 1,3-dihydroxyacetone production from crude glycerol by immobilized Gluconobacter oxydans MTCC 904.33036-62-3 Computational Chemistry Data | Dikshit, PK.PMID:33478271 and Moholkar, VS. 2016. Bioresour Technol. 216: 1058-65. PMID: 26873288Gas-Phase Reactions of Glyceraldehyde and 1,3-Dihydroxyacetone as Models for Levoglucosan Conversion during Biomass Gasification. | Fukutome, A., et al. 2016. ChemSusChem. 9: 703-12. PMID: 26893057Conversion of glycerol to 1,3-dihydroxyacetone by glycerol dehydrogenase co-expressed with an NADH oxidase for cofactor regeneration. | Zhang, J., et al. 2016. Biotechnol Lett. 38: 1559-64. PMID: 27233513Enhancement of 1,3-Dihydroxyacetone Production from Gluconobacter oxydans by Combined Mutagenesis. | Lin, X., et al. 2016. J Microbiol Biotechnol. 26: 1908-1917. PMID: 27876710Detection of 1,3-dihydroxyacetone by tris(2,2′-bipyridine)ruthenium(II) electrochemiluminescence. | Sun, J., et al. 2018. Anal Bioanal Chem. 410: 2315-2320. PMID: 29430601Sustainable Co-Synthesis of Glycolic Acid, Formamides and Formates from 1,3-Dihydroxyacetone by a Cu/Al2 O3 Catalyst with a Single Active Sites. | Dai, X., et al. 2019. Angew Chem Int Ed Engl. 58: 5251-5255. PMID: 30715789Tautomer Structures in Ketose-Aldose Transformation of 1,3-Dihydroxyacetone Studied by Infrared Electroabsorption Spectroscopy. | Chen, SH. and Hiramatsu, H. 2019. J Phys Chem B. 123: 10663-10671. PMID: 31765151