Method to produce stable anthocyanin for next-generation natural colorantsA method to efficiently produce pyranoanthocyanins using cyanidin-3-derivatives and pyruvic acid or caffeic acid was established to be healthy substitute for artificial colorants and unstable alternative anthocyanins.
The Need The demand for naturally derived food colorants has been steadily increasing due to consumer health concerns over synthetic dyes. Anthocyanins, which provide vibrant red, blue, and purple hues, are naturally derived pigments derived from fruits and vegetables. However, anthocyanins are prone to degradation under varying conditions, limiting their stability and application as food colorants. Pyranoanthocyanins, characterized by enhanced stability and resilience, offer a promising alternative, but their natural formation is time-consuming and limited in quantity. Therefore, there is a clear need for a technology that allows for the efficient synthesis of pyranoanthocyanins in larger quantities and shorter time periods. The Technology The disclosed technology presents innovative methods for the synthesis of pyranoanthocyanins in significantly reduced time frames compared to their natural formation. By utilizing specific reactions and temperature conditions, this technology enables the production of larger quantities of pyranoanthocyanins with improved stability and application potential as naturally derived pigments. Commercial Applications
Benefits/Advantages
In summary, the innovative technology for the synthesis of pyranoanthocyanins addresses the pressing commercial need for naturally derived and stable colorants, providing numerous applications across industries, along with notable benefits such as time efficiency, increased stability, and larger quantity production. |
Tech IDT2020-194 CollegeCollege of Food, Agricultural, and Environmental Sciences (CFAES) Licensing ManagerDahlman, Jason "Jay" InventorsCategoriesPublications |