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Alpha Lipoic Acid, α-Lipoic Acid, DL-Thioctic Acid, ALA, 1077-28-7

Alpha Lipoic Acid, α-Lipoic Acid, DL-Thioctic Acid, ALA, 1077-28-7

Alpha Lipoic Acid 

1. Product Identity

Property Details
Product Name Alpha Lipoic Acid (α-Lipoic Acid)
CAS Number 1077-28-7
Molecular Formula C₈H₁₄O₂S₂
Molecular Weight 206.32 g/mol
Purity ≥ 95%

2. Synonyms and Other Names

Name Context / Notes
DL-Thioctic Acid Racemic form
DL-6,8-Dithiooctanoic acid Chemical description
1,2-Dithiolane-3-valeric acid Systematic name
Lipoic Acid Common name
Thioctic Acid Pharmaceutical name
α-Lipoic Acid Scientific designation
LA Abbreviation
ALA Abbreviation

3. Product Description

Alpha lipoic acid (ALA), also known as lipoic acid (LA), α-lipoic acid, and thioctic acid, is an organosulfur compound derived from octanoic acid. ALA is normally produced in animals and is necessary for aerobic metabolism. It is a coenzyme similar to vitamins found in mitochondria and eliminates free radicals that accelerate aging and cause diseases.

Alpha lipoic acid enters cells after being absorbed from the intestinal tract and has both fat-soluble and water-soluble properties. It is produced and available as a dietary supplement in some countries where it is marketed as an antioxidant and is available as a pharmaceutical drug in other countries.

Key Characteristics:

  • Naturally occurring fatty acid found in every cell of the body

  • Essential for energy production in normal body functions

  • Converts glucose (blood sugar) into energy

  • Functions as an antioxidant in both water and fat environments

  • Can recycle other antioxidants (vitamin C, glutathione)

  • Increases glutathione formation

4. Biological Functions

Function Description
Metabolic Antioxidant Regulates NF-κB signal transduction and protects against oxidative injury
Enzyme Cofactor Required for the activity of pyruvate dehydrogenase, glycine decarboxylase, and other enzyme complexes
Radical Scavenging Acts as a non-specific scavenger of reactive oxygen species (ROS)
Antioxidant Recycling Recycles vitamin C and glutathione after they are used
GSH Synthesis Accelerates glutathione synthesis
Transcription Factor Regulation Regulates NF-κB activity

5. Mechanism of Action

Process Description
Intracellular Reduction The exogenous compound is reduced intracellularly by enzymes
Reduced Form Activity Involved in radical scavenging, recycling of other antioxidants, accelerating GSH synthesis, and regulating transcription factor activity

6. Pharmacological Effects

Effect Description
Renal Protection Prevents decrease in renal antioxidant defense system
Lipid Peroxidation Prevents increase in lipid peroxidation
Platinum Accumulation Reduces platinum content in tissues
Plasma Creatinine Prevents increase in plasma creatinine concentrations
Macrophage Activity Decreases phagocytosis of myelin by macrophages

7. Stereoisomerism

Isomer Property
Dextral (R-isomer) Limited physical activity
Lipoic Acid (S-isomer) Basically no physical activity and no side effects

8. Applications and Uses

8.1. Pharmaceutical Applications

Application Description
Acute and Chronic Hepatitis Therapeutic agent
Liver Cirrhosis Hepatoprotective
Hepatic Coma Adjunctive therapy
Fatty Liver Treatment support
Diabetes Management of diabetic complications
Alzheimer's Disease Neuroprotective effects
Antioxidant Health Product Dietary supplement

8.2. Animal Feed Applications

Application Function
Growth Performance Improves growth performance and meat quality to increase economic benefits
Metabolism Regulation Coordinates sugar, fat, and amino acid metabolism to improve animal immune function
Feed Antioxidant Protects and promotes the absorption and transformation of VA, VE, and other oxidation nutrients in feed
Heat Stress Protection Ensures and improves livestock and poultry production performance and egg production in heat stress environments

9. Research Findings

Study Area Findings
Renal Antioxidant Defense Prevents decrease in renal antioxidant defense system
Lipid Peroxidation Inhibits lipid peroxidation
Platinum Content Reduces platinum accumulation in tissues
Plasma Creatinine Maintains normal plasma creatinine levels
Myelin Phagocytosis Decreases phagocytosis of myelin by macrophages

10. Summary

Alpha Lipoic Acid (CAS: 1077-28-7, Molecular Formula: C₈H₁₄O₂S₂, Molecular Weight: 206.32 g/mol, Purity: ≥95%) is an organosulfur compound derived from octanoic acid. It is a metabolic antioxidant that regulates NF-κB signal transduction and protects against oxidative injury.

Key Properties:

  • Naturally occurring in every cell of the body

  • Essential for energy production and glucose conversion

  • Unique antioxidant that functions in both water and fat environments

  • Recycles other antioxidants (vitamin C, glutathione)

  • Increases glutathione synthesis

  • Both fat-soluble and water-soluble

Main Application Areas:

  • Pharmaceutical: Treatment of hepatitis, liver cirrhosis, hepatic coma, fatty liver, diabetes, Alzheimer's disease; antioxidant health products

  • Animal Feed: Growth promoter, metabolism regulator, feed antioxidant, heat stress protector

Biological Functions:

  • Metabolic antioxidant regulating NF-κB signal transduction

  • Cofactor for pyruvate dehydrogenase and glycine decarboxylase

  • Free radical scavenger

  • Antioxidant recycling agent

  • Transcription factor regulator

Pharmacological Effects:

  • Renal protection

  • Prevention of lipid peroxidation

  • Reduction of platinum accumulation

  • Maintenance of normal plasma creatinine levels

  • Decreased myelin phagocytosis by macrophages

Alpha lipoic acid is a vitamin-like compound with limited physical activity in its dextral form, while its other isomer has minimal physical activity and no side effects. It is widely used in both pharmaceutical and veterinary applications for its antioxidant and metabolic regulatory properties.

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