Saltar al contenido
Merck

73572

Sigma-Aldrich

L-(−)-Glyceraldehyde

≥90% (HPLC)

Sinónimos:

(2S)-2,3-Dihydroxypropanal

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula empírica (notación de Hill):
C3H6O3
Número de CAS:
Peso molecular:
90.08
Beilstein/REAXYS Number:
1720475
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32

Quality Level

assay

≥90% (HPLC)

optical activity

[α]/D -11.0±3.0°, c = 2 in H2O (after 24 h)

solubility

water: soluble 30 g/L at 18 °C

storage temp.

2-8°C

SMILES string

OC[C@H](O)C=O

InChI

1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m1/s1

InChI key

MNQZXJOMYWMBOU-GSVOUGTGSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Application


  • L-Glyceraldehyde Inhibits Neuroblastoma Cell Growth via a Multi-Modal Mechanism on Metabolism and Signaling.: This research highlights the inhibitory effects of L-Glyceraldehyde on neuroblastoma cell growth, revealing its impact through multiple pathways in metabolism and cell signaling (Forbes M et al., 2024).

Biochem/physiol Actions

L-(-)-Glyceraldehyde is an important intermediate in carbohydrate metabolism.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

233.6 °F - closed cup

flash_point_c

112 °C - closed cup


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Nina Richter et al.
Biotechnology and bioengineering, 106(4), 541-552 (2010-03-04)
A whole-cell catalyst using Escherichia coli BL21(DE3) as a host, co-expressing glycerol dehydrogenase (GlyDH) from Gluconobacter oxydans and glucose dehydrogenase (GDH) from Bacillus subtilis for cofactor regeneration, has been successfully constructed and used for the reduction of aliphatic aldehydes, such
Cancer biomarker AKR1B10 and carbonyl metabolism.
Balendiran, G. K., et al.
Chemistry & Biology, 178, 134-137 (2009)
David A Korasick et al.
Journal of molecular biology, 431(3), 576-592 (2018-12-24)
Heterokonts, Alveolata protists, green algae from Charophyta and Chlorophyta divisions, and all Embryophyta plants possess an aldehyde dehydrogenase (ALDH) gene named ALDH12. Here, we provide a biochemical characterization of two ALDH12 family members from the lower plant Physcomitrella patens and
Nina Richter et al.
Chembiochem : a European journal of chemical biology, 10(11), 1888-1896 (2009-07-07)
The acetic acid bacterium Gluconobacter oxydans has a high potential for oxidoreductases with a variety of different catalytic abilities. One putative oxidoreductase gene codes for an enzyme with a high similarity to the NADP+-dependent glycerol dehydrogenase (GlyDH) from Hypocrea jecorina.
Zhou Chen et al.
Enzyme and microbial technology, 133, 109456-109456 (2019-12-26)
Dihydroxyacetone phosphate (DHAP)-dependent aldolases demonstrate important values in the production of rare ketoses due to their unique stereoselectivities. As a specific example, we developed an efficient Escherichia coli whole-cell biocatalytic cascade system in which rare ketoses were produced from abundant

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico