Ascorbyl Tetraisopalmitate

Ascorbyl Tetraisopalmitate

Product Name Ascorbyl Tetraisopalmitate
CAS Number 183476-82-6
Other Names Tetrahexyldecyl Ascorbate; Ascorbyl Tetraisopalmitate; VC-IP
Appearance Colorless to pale yellow clear oily liquid
Specifications ≥98.0% (HPLC)
Molecular Formula C62H114O8
Molecular Weight 1027.6 g/mol
Solubility Oil-soluble; miscible with most cosmetic oils; insoluble in water
Package 1 kg, 5 kg, 25 kg in aluminum bottles or drums

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Ascorbyl Tetraisopalmitate Structure

Synonyms: Tetrahexyldecyl Ascorbate, Ascorbyl Tetraisopalmitate, VC-IP, 183476-82-6

Ascorbyl Tetraisopalmitate (often abbreviated as VC-IP) is a high-performance oil-soluble derivative of L-ascorbic acid. Unlike its water-soluble parent, this molecule is engineered for stability and penetration. The synthesis involves esterifying the hydroxyl groups of ascorbic acid with isopalmitic acid, yielding a fully saturated branched-chain ester. This modification not only protects the labile enediol moiety from oxidative degradation but also renders the compound miscible with lipid-rich formulations, a critical advantage for anhydrous systems and emulsions.

In the personal care industry, VC-IP is recognized as a premium active for skin brightening, antioxidant defense, and collagen support. It is supplied as a clear, odorless oil that can be incorporated into creams, serums, and sunscreens without the need for special handling. Because it is non-irritating and compatible with a wide range of cosmetic ingredients, formulators frequently select VC-IP when aiming for high-efficacy vitamin C delivery with minimal formulation constraints.

Beyond its primary use in topical skincare, Ascorbyl Tetraisopalmitate is also investigated in pharmaceutical and nutraceutical research for its potential to modulate oxidative stress and inflammatory pathways. Its lipophilic nature allows for efficient cellular uptake, where it is enzymatically hydrolyzed to release ascorbic acid, thereby replenishing the skin’s antioxidant reservoir. This dual action—direct antioxidant activity and sustained release of ascorbate—makes it a valuable tool for studies on photoaging, pigmentation disorders, and barrier function.

Chemical Structure & Properties

The molecule consists of a central ascorbic acid core with four isopalmitate chains attached via ester linkages. This dense lipophilic shell confers exceptional oxidative stability, with a half-life significantly longer than that of ascorbic acid in solution. The branched C16 chains also contribute to a low melting point, ensuring the material remains liquid at room temperature. With a molecular weight exceeding 1000 Da, VC-IP is too large to penetrate intact through the stratum corneum; instead, it accumulates in the lipid bilayers and is gradually metabolized by esterases to liberate ascorbic acid. This slow-release mechanism provides prolonged antioxidant protection without the pro-oxidant risks associated with high-dose L-ascorbic acid.

Mechanism of Action

  • Antioxidant defense: Scavenges reactive oxygen species and regenerates alpha-tocopherol, interrupting lipid peroxidation chain reactions.
  • Collagen synthesis: Released ascorbic acid serves as a cofactor for prolyl and lysyl hydroxylases, stabilizing collagen triple-helix formation.
  • Melanin inhibition: Downregulates tyrosinase activity and interferes with melanosome transfer, reducing hyperpigmentation.
  • Barrier reinforcement: Stimulates ceramide production and promotes keratinocyte differentiation, improving skin barrier integrity.

Quality Specifications

Parameter Specification
Assay (HPLC) ≥98.0%
Appearance Colorless to pale yellow, clear oily liquid
Odor Practically odorless
Refractive Index (20°C) 1.450 – 1.470
Heavy Metals ≤10 ppm
Loss on Drying ≤0.5%

Supply & Documentation

  • Capacity: 100 kg per month
  • Lead time: 3-5 business days (stock items)
  • Documentation: COA, MSDS, TDS available upon request
  • Packaging: 1 kg, 5 kg, 25 kg in aluminum bottles or drums, custom packaging upon request

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