42418
D-Lactaldehyde solution
≥95.0% (TLC), liquid
Sinónimos:
(2R)-2-Hydroxypropanal solution, (R)-2-Hydroxypropionaldehyde solution
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| Tamaño de envase | SKU | Disponibilidad | Precio |
|---|---|---|---|
| 1 mL | Comprobar disponibilidad del carrito | US$ 293,00 | |
| 5 mL | Comprobar disponibilidad del carrito | US$ 1.140,00 |
Acerca de este artículo
Fórmula empírica (notación de Hill):
C3H6O2
Número CAS:
Peso molecular:
74.08
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.32
US$ 293,00
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Permítanos ayudarleNombre del producto
D-Lactaldehyde solution, 1 M in H2O
assay
≥95.0% (TLC)
Quality Level
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.
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Este artículo | |||
|---|---|---|---|
| assay ≥95.0% (TLC) | assay ≥95.0% (HPLC) | assay 85.0-90.0% | assay ≥98.0% (HPLC) |
| Quality Level 100 | Quality Level 100 | Quality Level 200 | Quality Level 100 |
| form liquid | form liquid | form - | form - |
| storage temp. −20°C | storage temp. −20°C | storage temp. - | storage temp. 2-8°C |
| optical purity enantiomeric ratio: ≥98.0:2.0 (HPLC) | optical purity - | optical purity - | optical purity - |
| concentration 1 M in H2O | concentration ~0.5 M in tert-butyl methyl ether | concentration ≥85%, 85.0-90.0% in H2O | concentration - |
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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)
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)
Número de artículo de comercio global
| SKU | GTIN |
|---|---|
| 42418-1ML | 04061838023346 |
| 42418-5ML | 04061838160577 |