Merck
All Photos(3)

L1750

Sigma-Aldrich

L-(+)-Lactic acid

≥98%

Synonym(s):
(S)-2-Hydroxypropionic acid, Sarcolactic acid
Empirical Formula (Hill Notation):
C3H6O3
CAS Number:
Molecular Weight:
90.08
Beilstein:
1720251
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.25

Nível de qualidade

200

teor

≥98%

espectro de atividade do antibiótico

Gram-negative bacteria

Modo de ação

cell membrane | interferes

temperatura de armazenamento

2-8°C

SMILES string

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

InChI

1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1

InChI key

JVTAAEKCZFNVCJ-REOHCLBHSA-N

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Descrição geral

L-(+)-Lactic acid is the only naturally occurring lactic acid in humans and mammals. Commercially, few bacteria like Lactobacillus casei, L. delbrueckii, Streptococcus lactis produces L-Lactic acid by fermentation process.[1] Lactic acid activates hydroxycarboxylic acid receptor, G-protein coupled receptor 81 (GPR81).[2]

Aplicação

Lactic acid has been used:
  • as a component in substrate solution II for lactate dehydrogenase reaction[3]
  • as an additive in storage solution A[4]
  • as a supplement in the artificial gastric juice preparation for evaluation of degree of resistance Lactobacillus to the gastric stresses[5]

Embalagem

10, 100 g in glass bottle

Ações bioquímicas/fisiológicas

L-(+)-Lactic acid is used as a substrate for lactic acid dehydrogenase and lactate oxidase.

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Eye Dam. 1 - Skin Corr. 1C

Perigos de suplementos

Código de classe de armazenamento

8A - Combustible, corrosive hazardous materials

WGK

WGK 1

Ponto de fulgor (ºF)

230.0 °F - closed cup

Ponto de fulgor (ºC)

110.00 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

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Certificate of Origin

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