Skip to Content
Merck
CN
All Photos(1)

Documents

G5001

Sigma-Aldrich

DL-Glyceraldehyde

≥90% (GC)

Sign Into View Organizational & Contract Pricing

Synonym(s):
α,β-Dihydroxypropionaldehyde, 2,3-Dihydroxypropanal
Empirical Formula (Hill Notation):
C3H6O3
CAS Number:
Molecular Weight:
90.08
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic

Quality Level

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

SMILES string

[H]C(=O)C(O)CO

InChI

1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2

InChI key

MNQZXJOMYWMBOU-UHFFFAOYSA-N

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.

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.

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.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
Kazuo Iwasa et al.
Journal of neuroimmunology, 301, 30-34 (2016-11-20)
Caveolin-3 is a muscle-specific membrane protein that localizes to the sarcolemma and T-tubule system. Caveolin-3 is needed for muscle repair and skeletal muscle development. The objective of this study was to compare caveolin-3 expression in myasthenia gravis (MG) and control
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service