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25279-26-9

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25279-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25279-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,7 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25279-26:
(7*2)+(6*5)+(5*2)+(4*7)+(3*9)+(2*2)+(1*6)=119
119 % 10 = 9
So 25279-26-9 is a valid CAS Registry Number.

25279-26-9Relevant academic research and scientific papers

Method for production of rare carotenoids from commercially available lutein

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Page/Page column 16, (2008/06/13)

Disclosed are processes for conversion of (3R,3′R,6′R)-lutein to (3R,6′R)-α-cryptoxanthin, (3R)-β-cryptoxanthin, anhydroluteins I, II, and III (dehydration products of lutein), and a method for separating and purifying the individual carotenoids including the unreacted (3R,3′R)-zeaxanthin. The invention also includes two methods that transform (3R,3′R,6′R)-lutein into (3R,6′R)-α-cryptoxanthin in excellent yields.

Separation and identification of carotenoids and their oxidation products in the extracts of human plasma

Khachik, Frederick

, p. 2111 - 2122 (2007/10/02)

Eighteen carotenoids as well as vitamin A and two forms of vitamin E (γ- and α-tocopherol) have been separated from extracts of human plasma by high-performance liquid chromatography (HPLC) on reversed-phase and silica-based nitrile-bonded columns. In the order of chromatographic elution on a C18 reversed-phase column, the carotenoids were identified as (3R,3′R,6′R)-β,ε-carotene-3,3′-dlol [(3R,3′R,6′R)-lutein], (3R,3′R)-β,β-carotene-3,3′-dlol [(3R,3′R)-zeaxanthin], 5,6-dihydroxy-5,6-dihydro-ψ,ψ-carotene,3-hydroxy-2′,3′- didehy-dro-β,ε-carotene,β,ε-caroten-3-ol,3-hydroxy-β- carotene,ψ,ψ-carotene, 7,8-dihydro-ψ,ψ-carotene, β,ψ-carotene, 7,8,7′,8′-tetrahydro-′,′-carotene, β,ε-carotene, β,β-carotene, 7,8,11,12,7′,8′-hexahydro-ψ,ψ-carotene, and 7,8,11,12,7′,8′,-11′,12′-octahydro-ψ,ψ-carotene. The polar carotenoids, which eluted in the vicinity of lutein and were unresolved on the C18 column, have been separated on a nitrile-bonded column employing isocratic HPLC conditions. In the order of elution, the carotenoids were ε,ε-carotene-3,3′-dione, 3′-hydroxy-ε,ε-caroten-3-one, 5,6-dihydroxy-5,6-dihydro-ψ,ψ-carotene, 3-hydroxy-β,ε-caroten-3′-one, (all-E,3r,3′R,6′R)-lutein, (all-E,3R,3′R)-zeaxanthin, and (all-E,3R,3′S,6′R)-β,ε-carotene-3,3′-diol (3′-epilutein) followed by several geometrical isomers of lutein and zeaxanthin.

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