|
|
| | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid Basic information |
| Product Name: | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid | | Synonyms: | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid;Galactonic acid | | CAS: | 13382-27-9 | | MF: | C6H12O7 | | MW: | 196.16 | | EINECS: | | | Product Categories: | | | Mol File: | 13382-27-9.mol |  |
| | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid Chemical Properties |
| Melting point | 147.5 °C | | Boiling point | 673.6±55.0 °C(Predicted) | | density | 1.763±0.06 g/cm3(Predicted) | | pka | 3.35±0.35(Predicted) |
| | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid Usage And Synthesis |
| Uses | Galactonic acid is a sugar acid that is a metabolic breakdown product of galactose. Galactose dehydrogenase is responsible for converting galactose to galactonolactone, which then spontaneously or enzymatically converts to galactonic acid[1]. | | Definition | ChEBI: D-galactonic acid is a galactonic acid compound having D-configuration. It is a conjugate acid of a D-galactonate. It is an enantiomer of a L-galactonic acid. | | IC 50 | Microbial Metabolite | | References | [1] Liu P, et al. Valorization of Gelidium amansii for dual production of D-galactonic acid and 5-hydroxymethyl-2-furancarboxylic acid by chemo-biological approach. Microb Cell Fact. 2020 May 14;19(1):104. DOI:10.1186/s12934-020-01357-6 |
| | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanoic acid Preparation Products And Raw materials |
|