Skip to content

What is another name for vitamin E succinate? Exploring its synonyms and functions

3 min read

According to research, vitamin E succinate exhibits anticancer properties in certain cell cultures, a unique feature not typically shared by other common vitamin E forms like tocopherol. This powerful variant is also known by another key name, providing distinct benefits in both dietary supplements and topical applications.

Quick Summary

Vitamin E succinate is also known as alpha-tocopheryl succinate. The article details its chemical derivatives, unique properties compared to other vitamin E esters, and its diverse applications in health and cosmetics.

Key Points

  • Primary Synonym: The most common alternative name for vitamin E succinate is alpha-tocopheryl succinate.

  • Stable Powder: Unlike the oily free tocopherol, vitamin E succinate is a solid, stable powder, making it ideal for tablets.

  • Unique Action: In research, alpha-tocopheryl succinate has demonstrated unique pro-apoptotic effects on certain cancer cells, unlike other vitamin E esters.

  • Bioavailability: The body must cleave the succinate ester in the gut to absorb the active alpha-tocopherol, giving it a different bioavailability profile than other forms.

  • Diverse Uses: It is used in dietary supplements, cosmetics, and for its unique properties in pharmaceutical research.

In This Article

Understanding Vitamin E Succinate and Its Nomenclature

Vitamin E is a family of fat-soluble compounds with potent antioxidant properties. While most people are familiar with the common forms like tocopherol, derivatives like vitamin E succinate are engineered for specific purposes, such as enhanced stability or unique biological activities. The name of any given vitamin E compound can seem complex, but knowing the different names for a single variant, like vitamin E succinate, is key to identifying it on product labels.

The Most Common Alternative Name

The most widely accepted alternative name for vitamin E succinate is alpha-tocopheryl succinate. This name precisely describes its chemical structure: an ester created by attaching a succinic acid group to alpha-tocopherol, the most biologically active form of vitamin E.

Additional Synonyms and Derivatives

Because of variations in naming conventions, particularly in scientific literature and ingredient databases, several other synonyms also refer to this compound. Some of these include:

  • D-alpha-Tocopheryl acid succinate: This name specifies the naturally occurring, biologically superior isomer (D-alpha) and the acidic nature of the succinate ester.
  • D-alpha-Tocopherol succinate: A more simplified version of the above, also referencing the natural isomer.
  • RRR-alpha-tocopheryl succinate: A more technical, stereochemical name for the natural form.
  • d-alpha-tocopherol hemisuccinate: An older, but still referenced, name for the compound.

The Purpose of Esterification

Unlike free tocopherol, which is an oil, the esterified vitamin E succinate is a stable, powdered derivative. This stability is a primary reason for its use in applications such as tablets, where a solid, less-reactive form is preferable. The body's digestive enzymes then cleave the succinic acid, releasing the beneficial alpha-tocopherol.

Comparison of Vitamin E Forms

To better understand why vitamin E succinate is used, it helps to compare it to other common vitamin E forms found in supplements and topical products. Each has different properties and applications.

Feature Vitamin E Succinate (Alpha-Tocopheryl Succinate) Free Vitamin E (Alpha-Tocopherol) Vitamin E Acetate (Alpha-Tocopheryl Acetate)
Physical State Powder, solid at room temperature Oil, highly reactive Oil, stable
Stability Very stable, low susceptibility to degradation Less stable, prone to oxidation Very stable, good for cosmetics
Water Solubility Poorly soluble in water, but can be formulated as water-soluble TPGS Insoluble in water Insoluble in water
Key Application Dietary supplements (tablets), cosmetics, research Foods, direct skin application Cosmetics and supplements
Unique Property Promotes apoptosis in cancer cells in research Potent antioxidant, highly bioactive form Stable form for topical use

Health Benefits and Scientific Context

Beyond being a stable derivative, researchers have investigated vitamin E succinate for potential health benefits that extend beyond the general antioxidant function of vitamin E. The potential anticancer properties observed in some studies are a key area of interest. In vitro and animal studies have shown that alpha-tocopheryl succinate can inhibit the proliferation of certain cancer cells and induce apoptosis (programmed cell death), suggesting potential therapeutic applications. It is important to note that this is an area of ongoing research and not a proven treatment.

Additional research has explored its anti-inflammatory effects and ability to enhance the effectiveness of other therapies in certain contexts. However, the bioavailability of the succinate ester is generally lower than other forms, as it must first be cleaved in the gut to release the active alpha-tocopherol. For this reason, water-soluble variants like d-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS) have been developed for use in drug delivery systems.

Applications in Supplements and Cosmetics

In supplements, vitamin E succinate is favored for its powdered, solid form, which simplifies manufacturing and improves shelf-life. This makes it an ideal ingredient for tableting applications. In the cosmetic industry, tocopheryl succinate offers antioxidant benefits that help defend skin from environmental stressors. It is considered safe for use in cosmetics in low concentrations and helps stabilize other ingredients. For more detailed pharmaceutical research applications of tocopheryl succinate, a resource like DrugBank offers extensive information on its mechanism of action and properties.

Conclusion

Another name for vitamin E succinate is alpha-tocopheryl succinate, which is its most common chemical name. It also goes by other synonyms such as D-alpha-tocopheryl acid succinate. This derivative is a stable, powdered form of vitamin E that provides distinct advantages over free tocopherol in supplement and cosmetic manufacturing due to its enhanced stability. Furthermore, it has shown unique biological activity in preliminary cancer research, though it is not a cancer treatment. Recognizing its various names is crucial for understanding product labels and distinguishing its properties from other vitamin E compounds.

DrugBank provides extensive information on the therapeutic potential and chemical properties of alpha-tocopherol succinate.

Frequently Asked Questions

The primary alternative name for vitamin E succinate is alpha-tocopheryl succinate. This name refers to its chemical composition, an ester of succinic acid and alpha-tocopherol.

Vitamin E succinate can be either natural or synthetic. The natural form is labeled as d-alpha-tocopheryl succinate or RRR-alpha-tocopheryl succinate, while the synthetic version is often labeled with a dl-alpha prefix.

Unlike the free, oily form of vitamin E (tocopherol), the succinate ester is a stable powder. It also has unique properties in research, such as inducing apoptosis in certain cancer cell lines, a feature not typically seen in other vitamin E compounds.

Vitamin E succinate is used in supplements because its stable, powdered form is easier to handle and manufacture into tablets than the oil form of tocopherol, and it has an excellent shelf-life.

Vitamin E succinate is not naturally water-soluble. However, it can be formulated into water-soluble derivatives, such as the excipient TPGS, which is used in drug delivery systems.

In cosmetics, alpha-tocopheryl succinate acts as an antioxidant, helping to protect skin's lipids from environmental damage and stressors. It is also a stable ingredient that helps with product formulation.

After ingestion, digestive enzymes in the gut cleave the succinate group from the molecule, releasing the active alpha-tocopherol to be absorbed and utilized by the body.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.