Azelaic acid is normally infamous for being hard to dissolve. Azelaic acid is a dicarboxylic fatty acid: HOOC–(CH₂)₇–COOH That gives it; A hydrophobic middle (C9 chain) Two acidic heads (COOH) It behaves like a fatty acid organic acid hybrid, it hates plain water but loves: *Polar organic solvents *Hydrogen-bonding systems *Slightly ionic environments. Right? What if you place it in a hydrotrope ionic buffer. To partially converts to azelate salt: 😊 Azelaic acid ⇌ Azelate⁻ H⁺. Do you think it w
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