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G5001

Sigma-Aldrich

DL-Glyceraldehyde

≥90% (GC)

Synonyme(s) :

α,β-Dihydroxypropionaldehyde, 2,3-Dihydroxypropanal

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About This Item

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

Source biologique

synthetic

Niveau de qualité

200

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 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.

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)

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In-Geun Ryoo et al.
Redox biology, 17, 246-258 (2018-05-08)
Cluster of differentiation 44 (CD44) is the most common cancer stem cell (CSC) marker and high CD44 expression has been associated with anticancer drug resistance, tumor recurrence, and metastasis. In this study, we aimed to investigate the molecular mechanism by
Jiarui Sun et al.
Research in veterinary science, 109, 135-141 (2016-11-29)
Several studies have found that melamine causes damage to the testes, epididymis and sperm. However, few studies have investigated the effect of melamine on the synthesis of testosterone, which plays an import role in testicular development and spermatogenesis. In present
René L Jacobs et al.
Molecular genetics and metabolism, 120(4), 325-336 (2017-03-16)
Classical homocystinuria (HCU) due to inactivating mutation of cystathionine β-synthase (CBS) is a poorly understood life-threatening inborn error of sulfur metabolism. A previously described cbs-/- mouse model exhibits a semi-lethal phenotype due to neonatal liver failure. The transgenic HO mouse
Yuka Hiroshima et al.
Journal of cellular biochemistry, 119(2), 1591-1603 (2017-08-05)
Accumulation of advanced glycation end-products (AGEs) in periodontal tissues of patients with diabetes mellitus aggravates periodontitis, but the mechanisms are unknown. Calprotectin, a heterocomplex of S100A8 and S100A9 proteins, is a constitutive cytoplasmic component of healthy gingival epithelial cells. This
Raman and infrared spectroscopy of carbohydrates: a review
Wiercigroch E, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 185(5), 317-335 (2017)
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