L1000
Lithium D-lactate
95-100%
Sinónimos:
(R)-2-Hydroxypropionic acid lithium salt, D-Lactic acid lithium salt
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About This Item
Fórmula lineal:
CH3CH(OH)CO2Li
Número de CAS:
Peso molecular:
96.01
Beilstein:
4823618
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
NACRES:
NA.25
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Ensayo
95-100%
temp. de almacenamiento
−20°C
cadena SMILES
[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
Clave InChI
GKQWYZBANWAFMQ-HSHFZTNMSA-M
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Aplicación
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.
Acciones bioquímicas o fisiológicas
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.
Nota de análisis
Assayed enzymatically using D(−)lactic dehydrogenase
Código de clase de almacenamiento
13 - Non Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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In this study, we aimed to develop a new enzymatic assay system of d-lactate with good precision, accuracy, and sensitivity for the determination of D-lactate concentrations in rat serum. D-Lactate dehydrogenase (D-LDH) was utilized to catalyze D-lactate and NAD(+) to
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