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Cosmetic grade : Derivative

Sodium Acetyl Hyaluronate

Shiseido developed sodium acetyl hyaluronate (AcHA), through partial substitution of hydroxyl groups of sodium hyaluronate (HA) by acetyl groups. The treatment let the sodium hyaluronate possess hydrophobicity in addition to the original hydrophilic nature. The new compound showed remarkably increased affinity to the skin surface and water holding capacity("anchoring humectant"). The high water holding capacity and corneum softening effect brought by the "anchoring" effect are the advantages of sodium acetyl hyaluronate.

Structure of sodium acetyl hyaluronate


Sodium acetyl hyaluronate

Mean molecular approximately 1.0 x 105
Degree of acetylation# 2.6-3.8
INCI code SODIUM ACETYLATED HYALURONATE
CAS No. 287390-12-9

(# of acetylated sites in the disaccharide unit)