L1000

Lithium D-lactate

95-100%

• Sinónimos: (R)-2-Hydroxypropionic acid lithium salt, D-Lactic acid lithium salt
• Fórmula lineal: CH₃CH(OH)CO₂Li
• Número CAS: 27848-81-3
• Peso molecular: 96.01
• UNSPSC Code: 12352201
• NACRES: NA.25
• PubChem Substance ID: 24896268
• EC Number: 248-693-0
• Beilstein/REAXYS Number: 4823618
• MDL number: MFCD00013075

Propiedades

• assay: 95-100%
• storage temp.: −20°C
• SMILES string: [Li+].C[C@@H](O)C([O-])=O
• InChI: 1S/C3H6O3.Li/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m1./s1
• InChI key: GKQWYZBANWAFMQ-HSHFZTNMSA-M

Descripción

Application

Lactic acid is used as a reagent in organic synthesis (in the manufacture of adhesives). It is used in the leather, textile, and tanning industries. It may be used as a plasticizer, a catalyst, or an acidifying agent. Lactic acid has even been used as a flavoring agent in the manufacture of tobacco products.

Biochem/physiol Actions

In animals, lactic acid is a metabolic compound produced by proliferating cells and during anaerobic conditions such as strenuous exercise. Lactic acid can be oxidized back to pyruvate or converted to glucose via gluconeogenesis. Lactic acid is preferentially metabolized by neurons in several mammal species and during early brain development. D-lactate was utilized four times more slowly than L-lactate, but both isomers are absorbed at the same rate from the intestine.

Analysis Note

Assayed enzymatically using D(−)lactic dehydrogenase

Información de seguridad

• Clase de almacenamiento: 13 - Non Combustible Solids
• ¿Qué está pasando?: WGK 3
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• EPI (equipos de protección individual): Eyeshields, Gloves, type N95 (US)