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rac Xanthophyll-d6_Molecular_structure_CAS_)
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rac Xanthophyll-d6

Catalog No. X742002 Name Toronto Research Chemicals
CAS Number Website http://www.trc-canada.com
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SYNONYMS

IUPAC name
4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl)-7,12-bis(2H3)methyl-3,16-dimethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol
IUPAC Traditional name
4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl)-7,12-bis(2H3)methyl-3,16-dimethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol
Synonyms
β,ε-Carotene-3,3'-diol-d6
6'-Hydro-4',5'-dehydro-β-carotene-3,3'-diol-d6
E 161b-d6
Oro Glo 7-d6
all-trans-(+)-Xanthophyll-d6
(all-E)-Lutein-d6
Bo-Xan-d6
E 161-d6
FloraGLO-d6
FloraGLO Lutein-d6
Lutein-d6
Lutein A-d6
Luteine-d6
OS 24-d6
Vegetable Lutein-d6

DATABASE IDS

PROPERTIES

Certificate of Analysis Download
MSDS Link Download

DETAILS

Description (English)
Labelled Xanthophyll. One of the most widespread carotenoid alcohols in nature. Originally isolated from egg yolk, also isolated by chromatography from nettles, algae, and petals of many yellow flowers.

REFERENCES

  • an het Hof, K., et al.: J. Nutr., 130, 503 (2000)
  • Cooper, D., et al.: J. Nutr., 134, 221S (2000)
  • Faulks, R., et al.: Biochim. Biophys. Acta, 1740, 95 (2000)
  • Rao, A., et al.: Pharmacol. Res., 55, 207 (2000)
  • Tuberoso, C., et al.: Food Chem., 103, 149 (2