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lactate

Catalog No.
M1355
A compound used for preparing polylactic acid polymers and exhibiting anti-proliferative activity.
Grouped product items
SizePriceStock Qty
Evaluation Sample
$30.00
In stock
10g
$50.00
In stock
50g
$175.00
In stock
100g
$240.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

lactate (CAS No.: 79-33-4) is an endogenous alpha hydroxy acid metabolite generated during anaerobic glycolysis through the reduction of pyruvate, and it plays a central role in cellular energy metabolism and redox balance. As a key intermediate in metabolic pathways, lactate participates in metabolic coupling between tissues and serves as both a carbon source and signaling molecule influencing processes such as hypoxia response, angiogenesis, and immune cell function, with reported involvement in pathways regulated by hypoxia-inducible factors and monocarboxylate transporters. In biochemical and cell-based research, lactate is widely utilized as a marker of metabolic stress and tissue hypoxia, and its accumulation is frequently monitored to assess mitochondrial function and glycolytic flux. Additionally, this compound has been reported to exhibit antiproliferative effects in certain in vitro systems, with activity generally observed across micromolar to millimolar concentration ranges depending on cell type and experimental conditions. Beyond its role in metabolic studies, lactate also serves as a precursor in the biosynthesis of poly-lactic acid and related biomaterials, supporting its relevance in bioengineering and materials science research. Experimental applications commonly include its use in cell culture models to investigate metabolic reprogramming, tumor microenvironment dynamics, and immune modulation, as well as in animal models to study systemic metabolic adaptations, with concentrations tailored to specific study designs and objectives.

Chemical Properties

Physical AppearanceA colorless liquid
Storage -20°C
M.Wt90.08
Cas No.79-33-4
FormulaC3H6O3
Solubility≥44.5 mg/mL in DMSO; ≥64.6 mg/mL in EtOH; ≥9 mg/mL in H2O
Chemical Name(S)-2-hydroxypropanoic acid
Canonical SMILESC[C@@](O)([H])C(O)=O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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