Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos Principais

Visualizar Toda a Documentação

49426

Sigma-Aldrich

DL-Lactaldehyde solution

~1 M in H2O

Sinônimo(s):

2-Hydroxypropanal solution, 2-Hydroxypropionaldehyde solution

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(1)

About This Item

Fórmula empírica (Notação de Hill):
C3H6O2
Número CAS:
598-35-6
Peso molecular:
74.08
Beilstein:
1719827
Número MDL:
MFCD21662062
Código UNSPSC:
12352106
ID de substância PubChem:
329757448
NACRES:
NA.25

Ensaio

≥95% (TLC)

Nível de qualidade

100

concentração

~1 M in H2O

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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

InChI

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

chave InChI

BSABBBMNWQWLLU-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Ações bioquímicas/fisiológicas

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.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCBW7965
BCBQ6546V
BCBP1998V
BCBP1998

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 5

1 of 5

Methylglyoxal 1,1-dimethyl acetal ≥97%

Sigma-Aldrich

170216

Methylglyoxal 1,1-dimethyl acetal

4-Hydroxy-2-butanone 95%

Sigma-Aldrich

252557

4-Hydroxy-2-butanone

Pyruvic acid 98%

Sigma-Aldrich

107360

Pyruvic acid

Octanoic acid ≥99%

Sigma-Aldrich

C2875

Octanoic acid

DL-Lactic acid ~90% (T)

Sigma-Aldrich

69785

DL-Lactic acid

Lingfeng Zhu et al.
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
Manuela Centanni et al.
Applied and environmental microbiology, 85(7) (2019-01-27)
Infants fed breast milk harbor a gut microbiota in which bifidobacteria are generally predominant. The metabolic interactions of bifidobacterial species need investigation because they may offer insight into the colonization of the gut in early life. Bifidobacterium bifidum ATCC 15696
Bruce W Neale et al.
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
Robert H White et al.
Biochemistry, 45(40), 12366-12379 (2006-10-04)
A biosynthetic pathway is proposed for creating 6-deoxy-5-ketofructose-1-phosphate (DKFP), a precursor sugar for aromatic amino acid biosynthesis in Methanocaldococcus jannaschii. First, two possible routes were investigated to determine if a modified, established biosynthetic pathway could be responsible for generating 6-deoxyhexoses
Enzymic Synthesis of L-Fucose and Analogs
Wong, C.-H., et al.
The Journal of Organic Chemistry, 60, 7360-7363 (1995)
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica