3-O-Ethyl Ascorbic Acid

3-O-Ethyl Ascorbic Acid

Nom du produit 3-O-Ethyl Ascorbic Acid
Numéro CAS 86404-04-8
Apparence Poudre cristalline blanche à blanc cassé
Caractéristiques techniques ≥98.0% (HPLC)
Formule moléculaire C8H12O6
Poids moléculaire 204.18 g/mol
Solubilité Soluble in water, ethanol, propylene glycol
Perte au séchage ≤ 0,51 TP3T
Métaux lourds ≤ 10 ppm
Colis 25 kg fiber drum with inner polyethylene bag

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3-O-Ethyl Ascorbic Acid Structure

Synonymes : 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.

Structure chimique et propriétés

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.

Mécanisme d'action

  • Activité antioxydante: Scavenges reactive oxygen species (ROS) and regenerates α-tocopherol, protecting cellular lipids and proteins from oxidative damage.
  • Inhibition de la tyrosinase: 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.

Spécifications de qualité

Paramètre Spécifications
Assay (HPLC, dry basis) 98.0% – 102.0%
Apparence Poudre cristalline blanche à blanc cassé
Identification (IR) Conforms to reference spectrum
Perte au séchage ≤ 0,51 TP3T
Métaux lourds ≤ 10 ppm
Arsenic ≤2 ppm
Solvants résiduels ≤0.5% (ethanol)

Approvisionnement et documentation

  • Capacité: 20 metric tons per year
  • Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
  • Documentation: COA, MSDS, TDS, regulatory support (REACH, FDA, etc.)
  • Emballage: 25 kg fiber drum with double polyethylene liners; custom packaging available

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