G5001
DL-Glyceraldehyde
≥90% (GC)
Synonyme(s) :
α,β-Dihydroxypropionaldehyde, 2,3-Dihydroxypropanal
Se connecter pour consulter les tarifs organisationnels et contractuels.
Sélectionner une taille de conditionnement
A propos de cet article
Formule empirique (notation de Hill) :
C3H6O3
Numéro CAS:
Poids moléculaire :
90.08
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
EC Number:
200-290-0
NACRES:
NA.25
Service technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderService technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderNom du produit
DL-Glyceraldehyde, ≥90% (GC)
InChI
1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2
InChI key
MNQZXJOMYWMBOU-UHFFFAOYSA-N
SMILES string
[H]C(=O)C(O)CO
biological source
synthetic
assay
≥90% (GC)
form
powder
color
white to off-white
mp
145 °C ((293 °F ))
solubility
water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
storage temp.
room temp
Quality Level
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)
Biochem/physiol Actions
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.
General description
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.
Other Notes
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.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
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)
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
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
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
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
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
Contacter notre Service technique