Key Documents

View All Documentation

42418

D-Lactaldehyde solution

Name: <SC>D</SC>-Lactaldehyde solution
Brand: SIGMA

≥95.0% (TLC), liquid

Synonym(s):

(2R)-2-Hydroxypropanal solution, (R)-2-Hydroxypropionaldehyde solution

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₃H₆O₂

CAS Number:

3946-09-6

Molecular Weight:

74.08

MDL number:

MFCD00870227

UNSPSC Code:

12352202

PubChem Substance ID:

329756223

NACRES:

NA.32

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Product Name

D-Lactaldehyde solution, 1 M in H₂O

assay

≥95.0% (TLC)

Quality Level

100

form

liquid

optical purity

enantiomeric ratio: ≥98.0:2.0 (HPLC)

concentration

1 M in H₂O

storage temp.

−20°C

SMILES string

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

InChI

1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3/t3-/m1/s1

InChI key

BSABBBMNWQWLLU-GSVOUGTGSA-N

Biochem/physiol Actions

D-Lactaldehyde is an intermediate in the pyruvate metabolic pathway. Pyruvaldehyde is irreversibly produced from D-lactaldehyde via the enzyme glyoxylate reductase.

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

BCCK0719

BCBP1882

BCBP1882V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Methylglyoxal, glyoxalases and the development of diabetic complications.

P J Thornalley

Amino acids, 6(1), 15-23 (1994-02-01)

The formation of the reactiveα,β-dicarbonyl metabolite, methylglyoxal, is increased during hyperglycaemia associated with diabetes mellitus. Methylglyoxal is metabolised to S-D-lactoylglutathione and D-lactate by the glyoxalase system and to hydroxyacetone (95%) and D-lactaldehyde by aldose reductase. Methylglyoxal and hydroxyacetone bind and

D-Fucose metabolism in a pseudomonad. IV. Cleavage of 2-keto-3-deoxy-D-fuconate to pyruvate and D-lactaldehyde by 2-keto-3-deoxy-L-arabonate aldolase.

A S Dahms et al.

The Journal of biological chemistry, 247(7), 2238-2241 (1972-04-10)

THE METABOLISM OF LACTALDEHYDE. VII. THE OXIDATION OF D-LACTALDEHYDE IN RAT LIVER.

S M TING et al.

Biochimica et biophysica acta, 97, 407-415 (1965-03-08)

Reduction of trioses by NADPH-dependent aldo-keto reductases. Aldose reductase, methylglyoxal, and diabetic complications.

D L Vander Jagt et al.

The Journal of biological chemistry, 267(7), 4364-4369 (1992-03-05)

The substrate specificities of human aldose reductase and aldehyde reductase toward trioses, triose phosphates, and related three-carbon aldehydes and ketones were evaluated. Both enzymes are able to catalyze the NADPH-dependent reduction of all of the substrates used. Aldose reductase shows

Global Trade Item Number

SKU	GTIN
42418-1ML	04061838023346
42418-5ML	04061838160577

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