_-CAROTENE 5,6-EPOXIDE

Code: 73342-1MG D2-231

General description

The 5,6-epoxy structure can give rise to a wide variety of carotenoid end-groups with the plausible biosynthetic transformations of the 5,6-epoxy-ß-...


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€900.63 1MG
€1,107.77 inc. VAT

General description

The 5,6-epoxy structure can give rise to a wide variety of carotenoid end-groups with the plausible biosynthetic transformations of the 5,6-epoxy-ß-ring to give diverse structures such as the cyclopentane carotenoids capsanthin and capsorubin, the retro-carotenoids eschscholtz- xanthin and rhodoxanthin, allenic carotenoids like the neoxanthin and fucoxanthin, 5,6-diols like the karpoxanthin and latoxanthin, 3,6-poxides as found in eutreptiellanone and cucurbitaxanthin, the 6-hydroxy-γ-ring structure found in prasinoxanthin and nigroxanthin, as well as the 5,6-seco-5,6-dione-end-group of semi-ß-carotenone.

λin hexane (with 2% dichloromethane)
assay≥85.0% (HPLC)
formpowder
InChI keyRVCRIPILOFSMFG-WWSVUWEKSA-N
InChI1S/C40H56O/c1-31(19-13-21-33(3)24-25-36-35(5)23-15-27-37(36,6)7)17-11-12-18-32(2)20-14-22-34(4)26-30-40-38(8,9)28-16-29-39(40,10)41-40/h11-14,17-22,24-26,30H,15-16,23,27-29H2,1-10H3/b12-11+,19-13+,20-14+,25-24+,30-26+,31-17+,32-18+,33-21+,34-22+
Quality Level100
SMILES stringCC(/C=C/C1=C(C)CCCC1(C)C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C=CC23C(C)(C)CCCC2(O3)C)C
storage temp.−20°C
UV absorptionλ: 443-447 nm Amax
Cas Number1923-89-3
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