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Hexahydrocurcumin's advantage over curcumin is rooted in its chemical structure. Through catalytic hydrogenation, the double bonds present in curcumin are saturated, leading to increased molecular stability. This structural modification significantly enhances its resistance to degradation, thereby improving its bioavailability and prolonging its activity in biological systems. For researchers looking to establish robust Hexahydrocurcumin in vitro and in vivo models, this enhanced stability is a critical factor.

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