Food-grade high-content lutein ester and preparation method thereof
A technology for lutein ester and food grade is applied in the field of separating and preparing food grade high-content lutein ester, which can solve the problems of long process time, low yield and high energy consumption, and achieves simple process steps and low solvent residue. , the effect of short time
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Embodiment 1
[0035] Weigh 20.0g of marigold extract with lutein ester UV content (UV detection content) of 31.2%, put it into a 250mL three-necked flask, add 80mL propanol, stir at 30°C for 4 hours, and filter to obtain filter cake I; filter cake Add 30mL of methanol to I, stir at 40°C for 1 hour and then filter to obtain filter cake II; filter cake II is dried at 30°C for 2.5 hours to obtain 4.7g of lutein ester product, wherein the UV content of lutein ester is 82.1%, The content of all-trans lutein ester determined by HPLC is 92.1%, and the n-hexane dissolved residue in the product is 0.3ppm.
[0036] The lutein ester product prepared in this example is an orange-red powder crystal with good looseness and fluidity.
Embodiment 2
[0038] Weigh 20.0g of marigold extract with lutein ester UV content of 29.5%, put it into a 250mL three-neck flask, add 100mL of recovered propanol once, stir at 40°C for 3 hours, filter to obtain filter cake I; add 40mL of Ethanol, stirred at 40°C for 0.5 hours and then filtered to obtain filter cake II; filter cake II was dried at 50°C for 1 hour to obtain 4.5g of lutein ester product, wherein the UV content of lutein ester was 84.4%, which was determined by HPLC The content of all-trans lutein ester is 92.0%, and the n-hexane dissolved residue in the product is 0.5ppm.
[0039] Described primary recovery propanol is the propanol that extracts marigold extract with the method of embodiment 1, the propanol that obtains through recovery.
[0040] The lutein ester product prepared in this example is an orange-red powder crystal with good looseness and fluidity.
Embodiment 3
[0042] Weigh 20.0g of marigold extract with lutein ester UV content of 29.5%, put it into a 250mL three-neck flask, add 120mL of n-butanol, and filter it after ultrasonic treatment at 35°C for 1 hour to obtain filter cake I; add 30mL of Ethanol, stirred at 30°C for 1 hour and filtered to obtain filter cake II; filter cake II was dried at 40°C for 2 hours to obtain 4.2 g of lutein ester product, wherein the UV content of lutein ester was 87.6%, and the crystal content was determined by HPLC. The content of all-trans lutein ester is 93.0%, and the residue in n-hexane is 0.3ppm.
[0043] The lutein ester product prepared in this example is an orange-red powder crystal with good looseness and fluidity.
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