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49426

Sigma-Aldrich

DL-Lactaldehyde solution

~1 M in H2O

Sinónimos:

2-Hydroxypropanal solution, 2-Hydroxypropionaldehyde solution

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About This Item

Fórmula empírica (notación de Hill):
C3H6O2
Número de CAS:
598-35-6
Peso molecular:
74.08
Beilstein/REAXYS Number:
1719827
MDL number:
MFCD21662062
UNSPSC Code:
12352106
PubChem Substance ID:
329757448
NACRES:
NA.25

assay

≥95% (TLC)

Quality Level

100

concentration

~1 M in H2O

storage temp.

−20°C

SMILES string

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

InChI

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

InChI key

BSABBBMNWQWLLU-UHFFFAOYSA-N

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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. L-lactaldehyde is an intermediate metabolite in the pyruvate metabolism pathway and is irreversibly produced from pyruvaldehyde via the enzyme aldehyde reductase, which is then irreversibly converted to propylene glycol via aldehyde reductase.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Applied microbiology and biotechnology, 100(3), 1241-1251 (2015-10-12)
The pure stereoisomers of 1,2-propanediol (1,2-PDO) could be used as starting materials to synthesize high value-added specialty chemicals and chiral pharmaceutical products. As the stereoisomers of 1,2-PDO cannot be obtained by traditional chemical synthesis processes, biotechnological processes have gained increasing
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The Annals of pharmacotherapy, 39(10), 1732-1736 (2005-09-15)
To report a case of severe propylene glycol-induced lactic acidosis not attributable to renal dysfunction that was secondary to administration of high-dose intravenous lorazepam. A 24-year-old female with community-acquired pneumonia presented with severe acute respiratory distress syndrome. To maintain adequate
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