Essential Guide azelaic acid
Several other non-restricted glycol ethers may be used as solvents for Azelaic acid, although the solubility of Azelaic acid is markedly lower compared to ethoxydiglycol and butoxydiglycol. These products are commercially made available by DOW Chemical under the trademark Dowanol®. Some examples are: Triglycol Ethyl Ether Common name: ethoxytriglycol. CAS: 112-50-5. No INCI name assigned. Excellent solvent for Azelaic acid. Cosmetic limitations: none. Dipropylene Glycol Monomethyl Ether Acetate INCI name: PPG-2 Methyl Ether Acetate. CAS: 88917-22-0. Cosmetic limitations: none. 1-Butoxy-2-propanol INCI name: Propylene Glycol Butyl Ether. CAS: 5131-66-8. Cosmetic limitations: none. 1-Propoxypropan-2-ol Common name: Propylene Glycol Propyl Ether. CAS: 1569-01-3. Cosmetic limitations: none. There is a massive set of other glycol ethers available, many of those are used in large quantities in chemical/technical applications, and some of those are suitable for use in personal care & cosmetic products. Attention shall be given to the residual monomer concentration (ethylene oxide/propylene oxide) and [substituted] p-dioxanes. If the formulator is working to obtain a gel based on Azelaic acid, the addition of a rheology modifier should also be considered. In addition, to thicken a high concentrated Azelaic acid solution, it must have high resistance to electrolytes. For example, polyacrylate crosspolymer-6 is characterized by a high resistance to electrolytes. Such a polymer is, for example, commercialized by Seppic with the trade name Sepimax ZEN. One possible formula to be used as a starting point for an R&D process to adjust a 10% Azelaic acid gel is reported below. According to the final use and to the claims to be reported on the label, other ingredients (soluble in this environment, to maintain the translucent aspect of the gel) can be added to this raw formulation. In this case, only propylene glycol (available worldwide, with a lower smell and also a better toxicological profile than the more efficient Azelaic acid solubilizers such as ethoxydiglycol and butoxydiglycol) is to be used to solubilize Azelaic acid. This is only a starting point, some small changes in terms of percentages could be required in case of different ingredients added, or in case other actives, fragrances or other ingredients in general have
PHASE
INREDIENT
% (BY WEIGHT)
A
1,3-PROPYLENE GLYCOL
35
Azelaic acid
10
B
Water
27
Sepimax ZEN
2
1,3-propylene glycol
20
C
Salycilic acid
1
1,3-propylene glycol
5
TABLE 13: Formulation Azelaic acid gel
35
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