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| D-Glyceraldehyde Basic information |
| D-Glyceraldehyde Chemical Properties |
| Melting point | 127-129 C | | alpha | D25 +8.7° (c = 2 in H2O); D15 +21.2° (c = 18) | | Boiling point | bp17 127-129°; bp10 123-126° | | density | 1.272±0.06 g/cm3(Predicted) | | refractive index | n20/D 1.494 | | Fp | 112 °C | | storage temp. | 2-8°C | | solubility | DMSO, Methanol (Slightly), Water (Slightly) | | pka | 12.60±0.20(Predicted) | | form | liquid (viscous) | | color | Clear Colourless to Light Brown | | Merck | 13,4494 | | BRN | 1720474 | | CAS DataBase Reference | 453-17-8(CAS DataBase Reference) | | NIST Chemistry Reference | Propanal, 2,3-dihydroxy-, (r)-(453-17-8) |
| D-Glyceraldehyde Usage And Synthesis |
| Description | D-(+)-Glyceraldehyde is an intermediate in carbohydrate metabolism. It is phosphorylated by triose kinase to produce D-glyceraldehyde 3-phosphate, an intermediate in glycolysis, gluconeogenesis, photosynthesis, and other metabolic pathways. | | Chemical Properties | CLEAR ORANGE SYRUP | | Uses | D-Glyceraldehyde is the simplest of all aldoses and have been shown to be the one of the carbonyl metabolite of dietary fructose. | | Uses | D-(+)-Glyceraldehyde can be utilized as a reactant in the synthesis of: - (S)-homophenylalanine by ruthenium oxidation of a 3-amino-1,2-diol generated via coupling of an amine, and α-hydroxyaldehyde.
- β- and γ-allenols via metal-catalyzed cyclization. Allenols are used as a key precursor for the preparation of enantiopure dihydropyrans and tetrahydrooxepines.
- Isopropylidene D-glyceraldehyde intermediate, which controls the chirality in the total synthesis of prostaglandins (PGE1).
| | Definition | ChEBI: The D-enantiomer of glyceraldehyde. | | Purification Methods | enantiomer [453-17-8] is a syrup (70 + % H2O) with [] D +14o (c 2, H2O) and the dimethyl acetal has b 124-127 o/14mm and []15 +21o (c 18, H2O). [Beilstein 1 H 845, 1 IV 4114.] |
| D-Glyceraldehyde Preparation Products And Raw materials |
| Raw materials | L-Fructose, 1-(dihydrogen phosphate)-->1,2-Propanediol, 3,3-dimethoxy-, (R)- (9CI)-->Triose phosphate-->1-hydroxy-3-(phosphonooxy)acetone-->DL-GLYCERALDEHYDE-->(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde-->L-Glyceraldehyde-->Methylglyoxal-->1,2:5,6-Bis-O-(1-methylethylidene)-D-mannitol-->Formaldehyde-->GLYCOLALDEHYDE-->1,3-Dihydroxyacetone | | Preparation Products | (R)-Lactate-->D-Ribose-->Furfural |
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