G5001

DL-Glyceraldehyde

≥90% (GC)

• Synonyme(s) : α,β-Dihydroxypropionaldehyde, 2,3-Dihydroxypropanal
• Formule empirique (notation de Hill): C₃H₆O₃
• Numéro CAS: 56-82-6
• Poids moléculaire : 90.08
• Numéro CE : 200-290-0
• Numéro MDL: MFCD00064379
• Code UNSPSC : 12352201
• ID de substance PubChem : 24895192
• Nomenclature NACRES : NA.25

Propriétés

• Source biologique: synthetic
• Pureté: ≥90% (GC)
• Forme: powder
• Couleur: white to off-white
• Pf: 145 °C ((293 °F ))
• Solubilité: water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
• Température de stockage: room temp
• Chaîne SMILES: [H]C(=O)C(O)CO
• InChI: 1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2
• Clé InChI: MNQZXJOMYWMBOU-UHFFFAOYSA-N

Description

Description générale

Glyceraldehyde is a simple monosaccharide. Based on the number of carbon atoms and the type of carbonyl group present, glyceraldehyde belongs to subgroup triose. It is a colourless and sweet compound.

Application

DL-Glyceraldehyde has been used:

• as modifying reagent in the preparation of crystallization solution
• as a substrate to measure aldose reductase activity
• in the preparation of d/l-glyceraldehyde stock to determine the specific activity of GAPDH (glyceraldehyde 3-phosphate dehydrogenase)

Actions biochimiques/physiologiques

Glyceraldehyde serves as an efficient cross-linking agent and is considered non-toxic. It is an intermediate of a number of metabolic such as glycolysis and pentose phosphate pathway.

Autres remarques

DL-Glyceraldehyde is a substrate for the enzyme aldose reductase.

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

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)