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Potassium Pyruvate, Potassium Oxopropanoate, Kalium Oxopropanoat, 4151-33-1

Potassium Pyruvate, Potassium Oxopropanoate, Kalium Oxopropanoat, 4151-33-1

(CAS No. 4151-33-1)

A) Physical and Chemical Properties

  • Chemical Name: Potassium 2-oxopropanoate

  • Molecular Formula: C₃H₃KO₃

  • Molecular Weight: 126.15 g/mol

  • Appearance: White to off-white crystalline powder

  • Melting Point: >175 °C (decomposes)

  • Solubility: Slightly soluble in water and methanol

  • Stability: Hygroscopic; store under inert atmosphere

  • LogP: ~ -1.24

  • Storage: Room temperature, dry, sealed container

B) Detailed Applications

  • Cell Culture: Energy source to enhance cell viability

  • Antioxidant: Scavenges ROS, protects against oxidative stress

  • Pharmaceuticals: Investigated for neuroprotective and metabolic support

  • Cosmetics: Used in UV-protective and anti-aging formulations

  • Nutritional Supplements: Supports energy metabolism and endurance

  • Biochemical Research: Substrate in glycolysis and TCA cycle studies

C) Synonyms

  • Potassium 2-oxopropanoate

  • Pyruvic Acid Potassium Salt

  • Propanoic acid, 2-oxo-, potassium salt

  • Kalium-2-oxopropanoat (German)

  • Potassiumpyruvate

  • Potassium pyruvate (1:1)

D) Production Method

  1. Neutralization of Pyruvic Acid with Potassium Hydroxide:

CH3COCOOH+KOH→CH3COCOOK+H2OCH₃COCOOH + KOH → CH₃COCOOK + H₂O

  1. Crystallization and vacuum drying

  2. Pyruvic acid may be sourced from microbial fermentation

E) Alternative Products

  • Sodium Pyruvate: Common but lacks potassium supplementation

  • Calcium Pyruvate: Used in sports nutrition

  • Lactic Acid Derivatives: Alternative carbon sources

  • Acetic Acid Derivatives: Simpler acids with limited bioactivity

F) Common Names

  • Potassium Salt of Pyruvate

  • Energy Salt (in supplements)

  • Muscle Support Salt (marketing term)

G) Reactions

  • Acidic Conditions: Converts back to pyruvic acid

  • Reduction: Forms lactic acid

  • Transamination: Precursor to alanine

  • Oxidative Decarboxylation: Forms acetyl-CoA for TCA cycle

  • UV Protection: Acts as a radical scavenger in skincare

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