39705

D-Glyceraldehyde 3-phosphate solution

8-13 mg/mL in H₂O

• Synonym(s): (2R)-2-Hydroxy-3-phosphonooxypropanal, D-GAP, Triose phosphate
• Empirical Formula (Hill Notation): C₃H₇O₆P
• CAS Number: 591-57-1
• Molecular Weight: 170.06
• Beilstein: 1725007
• MDL number: MFCD23703755
• UNSPSC Code: 12352201
• PubChem Substance ID: 329755894
• NACRES: NA.25

Properties

• Assay: ≥97.0% (TLC)
• Quality Level: 100
• form: solution
• concentration: 8-13 mg/mL in H₂O
• color: colorless
• storage temp.: −20°C
• SMILES string: O[C@H](COP(O)(O)=O)C=O
• InChI: 1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8)/t3-/m0/s1
• InChI key: LXJXRIRHZLFYRP-VKHMYHEASA-N

Description

Application

• Enzymatic Assay Development with d-Glyceraldehyde 3-Phosphate: Demonstrated as a crucial reagent in enzymatic assays involving glycolysis pathways, specifically in the assessment of glyceraldehyde 3-phosphate dehydrogenase activities, which play a vital role in understanding cellular energy production and metabolic disorders (Li et al., 2022).

Biochem/physiol Actions

An important substance implicated in energy metabolism. It is a key node point linking other metabolic processes or pathways. Triosephosphate metabolism can be associated with many metabolic pathways, including glycolysis, pentose phosphate pathway, gluconeogenesis and lipid metabolism, and can also be involved in maintaining hemostasis. The metabolic abnormality of triosephosphate may be tied to many pathophysiological processes, such as triosephosphate isomerase deficiency, hyperglycemia and diabetic nephropathy; review and papers cited therein.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Safety Information

• Storage Class Code: 10 - Combustible liquids
• WGK: WGK 1
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable