Natural Sources of Vitamin E Oil
Natural vitamin E oil is fundamentally derived from plant sources, particularly vegetable oils and the by-products of their refining process. The term "vitamin E" actually refers to a family of eight fat-soluble compounds, divided into four tocopherols and four tocotrienols. These compounds are found in varying concentrations in different plants. For example, some common oils are particularly rich in specific vitamin E isoforms:
- Wheat germ oil: One of the richest dietary sources of alpha-tocopherol.
- Sunflower oil: Contains significant amounts of alpha-tocopherol.
- Soybean and Corn Oil: Characterized by higher levels of gamma-tocopherol compared to other forms.
- Palm Oil: Uniquely rich in tocotrienols, with gamma-tocotrienol being the major form.
During the manufacturing of cooking oils, the vitamin E compounds, known as tocochromanols, are concentrated in the deodorizer distillate, a sludge-like by-product created during the deodorization step. This distillate serves as the primary raw material for commercial natural vitamin E oil production.
The Commercial Extraction Process
Converting the raw oil by-product into a concentrated vitamin E oil is a multi-step process that refines and purifies the desired compounds. The main steps often include:
Molecular Distillation
This is a key industrial technique used to separate the tocopherols and tocotrienols from the fatty acid distillates. The process involves heating the crude mixture under a high vacuum. Because vitamin E has a different boiling point than other components like fatty acids and sterols, it can be collected as a distinct fraction. This results in a concentrate with a higher percentage of vitamin E.
Solvent Extraction and Chromatography
Some advanced purification methods may employ solvents and chromatographic separation. This allows for even greater purity and the isolation of specific isomers if desired. Ion-exchange chromatography, for instance, can help separate tocopherols from other substances and isolate specific homologues like delta-tocopherol.
Esterification
To improve its stability and shelf life, the natural vitamin E concentrate (d-alpha-tocopherol) is often converted into an ester form, such as d-alpha-tocopheryl acetate. The esterification protects the active site of the molecule from oxidation, which can degrade its potency over time. The body must then break down this ester to use the active vitamin E.
Synthetic Vitamin E: A Chemical Creation
In contrast to natural extraction, synthetic vitamin E is created entirely through a laboratory process. The standard industrial synthesis route involves the condensation of two main chemical intermediates: trimethylhydroquinone and isophytol. This chemical reaction results in a racemic mixture of eight different stereoisomers, labeled as dl-alpha-tocopherol. The 'dl' prefix denotes a combination of both 'd' (natural) and 'l' (synthetic) forms. While structurally similar to the natural version, only the 'd' isomers are recognized and utilized effectively by the human body.
Natural vs. Synthetic Vitamin E Oil: Key Differences
| Feature | Natural Vitamin E Oil | Synthetic Vitamin E Oil | 
|---|---|---|
| Origin | Extracted from plant sources, typically vegetable oil by-products. | Created chemically from petroleum-derived products. | 
| Form | Contains d-alpha-tocopherol and sometimes a mix of other tocopherols and tocotrienols. | A racemic mixture containing both d-alpha and l-alpha tocopherols, known as dl-alpha-tocopherol. | 
| Biological Activity | The body preferentially recognizes and utilizes the natural d-alpha-tocopherol form. | Contains less biologically active isomers; only about half of the synthetic form is utilized by the body. | 
| Labeling | Often labeled as d-alpha-tocopherol or with an RRR- prefix. | Typically labeled as dl-alpha-tocopherol or with an all-rac- prefix. | 
| Cost | Generally more expensive to produce due to reliance on natural plant sources and complex extraction. | Lower production cost due to large-scale chemical synthesis. | 
The Role of Vegetable Oils in the Global Vitamin E Supply Chain
Vegetable oil production, particularly from palm, soybean, and corn, is a cornerstone of the global vitamin E supply. The refining of these oils, a process that creates the deodorizer distillate rich in tocols, is a major economic driver for natural vitamin E extraction. For example, palm oil is the world's leading vegetable oil and a particularly rich source of tocotrienols, with an extraction process that can be economically viable for concentrating vitamin E. The increasing demand for natural products and awareness of bioavailability differences continues to drive innovation in extraction methods, including supercritical CO2 extraction, to maximize the yield and purity of natural vitamin E from these sources.
Conclusion
What is vitamin E oil made from depends entirely on whether it is a natural or synthetic product. Natural vitamin E oil is sourced from specific plants and vegetable oils, then extracted and purified through physical processes like molecular distillation. Synthetic vitamin E oil is created through a chemical reaction and is less biologically active than its natural counterpart. The production and properties of each form have distinct implications for consumers, affecting its cost, purity, and how the body utilizes it. Understanding these fundamental differences allows for informed decisions regarding vitamin E supplementation and use in products like skincare.
For more detailed information on vitamin E, including its various forms and metabolic pathways, the National Institutes of Health (NIH) Office of Dietary Supplements provides an excellent resource: Vitamin E - Health Professional Fact Sheet.