3-O-Ethyl Ascorbic Acid

3-O-Ethyl Ascorbic Acid

Product Name 3-O-Ethyl Ascorbic Acid
CAS Number 86404-04-8
Appearance White to off-white crystalline powder
Specifications ≥98.0% (HPLC)
Molecular Formula C8H12O6
Molecular Weight 204.18 g/mol
Solubility Soluble in water, ethanol, propylene glycol
Loss on Drying ≤0.5%
Heavy Metals ≤10 ppm
Package 25 kg fiber drum with inner polyethylene bag

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3-O-Ethyl Ascorbic Acid Structure

Synonyms: 3-O-Ethyl Ascorbic Acid, 3-O-Ethyl-L-ascorbic acid, Ethyl Ascorbic Acid, EAC, Vitamin C Ethyl Ether, 3-O-Ethylascorbate

3-O-Ethyl Ascorbic Acid is a stable, lipophilic derivative of L-ascorbic acid (Vitamin C) where the hydroxyl group at the C-3 position is etherified with an ethyl group. This structural modification protects the enediol moiety—the key antioxidant pharmacophore—from rapid oxidation, while preserving the ability to release ascorbate upon enzymatic or chemical hydrolysis in vivo. The ethyl ether enhances lipophilicity, facilitating penetration through the stratum corneum and enabling delivery into deeper skin layers, where it acts as a reservoir for sustained Vitamin C activity.

Commercially, 3-O-Ethyl Ascorbic Acid is produced via a multi-step synthesis starting from L-ascorbic acid, involving selective protection and ethylation. It is supplied as a high-purity crystalline powder (≥98% HPLC) that remains stable under normal storage conditions, unlike ascorbic acid which degrades rapidly in aqueous formulations. This stability profile makes it a preferred active in anhydrous and emulsion-based cosmetic systems, as well as in topical pharmaceuticals where consistent dosing is critical.

In the B2B arena, 3-O-Ethyl Ascorbic Acid is utilized by formulators for skin-brightening, anti-aging, and antioxidant products. Its ability to inhibit tyrosinase and modulate collagen synthesis has been documented in peer-reviewed studies, driving demand in the personal care and dermatology sectors. Our material is manufactured under cGMP and is available with full regulatory documentation to support global product registrations.

Chemical Structure & Properties

The molecule retains the γ-lactone ring of ascorbic acid but carries an ethyl group at the C-3 hydroxyl, which blocks the primary site of oxidative degradation. The free C-2 hydroxyl still allows for antioxidant activity, though the ethyl group must be removed for full Vitamin C function. The compound is a white to off-white powder with a molecular weight of 204.18 g/mol. It is freely soluble in water (up to 10% w/v) and common glycols, and exhibits excellent stability in formulations with a pH below 6.0.

Mechanism of Action

  • Antioxidant activity: Scavenges reactive oxygen species (ROS) and regenerates α-tocopherol, protecting cellular lipids and proteins from oxidative damage.
  • Tyrosinase inhibition: Interferes with copper ions at the active site of tyrosinase, reducing melanin synthesis and thereby diminishing hyperpigmentation.
  • Collagen synthesis: Acts as a cofactor for prolyl and lysyl hydroxylases, enzymes essential for stabilizing the collagen triple helix, leading to improved skin firmness and elasticity.
  • Photoprotection: Reduces UV-induced erythema and thymine dimer formation, complementing sunscreen actives.

Quality Specifications

Parameter Specification
Assay (HPLC, dry basis) 98.0% – 102.0%
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Loss on Drying ≤0.5%
Heavy Metals ≤10 ppm
Arsenic ≤2 ppm
Residual Solvents ≤0.5% (ethanol)

Supply & Documentation

  • Capacity: 20 metric tons per year
  • Lead time: 3-5 business days (stock items)
  • Documentation: COA, MSDS, TDS, regulatory support (REACH, FDA, etc.)
  • Packaging: 25 kg fiber drum with double polyethylene liners; custom packaging available

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