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3,4-anhydrolutein is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53783-01-0 Structure
  • Basic information

    1. Product Name: 3,4-anhydrolutein
    2. Synonyms:
    3. CAS NO:53783-01-0
    4. Molecular Formula:
    5. Molecular Weight: 550.868
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53783-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4-anhydrolutein(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-anhydrolutein(53783-01-0)
    11. EPA Substance Registry System: 3,4-anhydrolutein(53783-01-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 53783-01-0(Hazardous Substances Data)

53783-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53783-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53783-01:
(7*5)+(6*3)+(5*7)+(4*8)+(3*3)+(2*0)+(1*1)=130
130 % 10 = 0
So 53783-01-0 is a valid CAS Registry Number.

53783-01-0Downstream Products

53783-01-0Relevant articles and documents

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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