Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Beta-Carotene | HCID 5280489 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 9-Cis-Beta-Carotene | HCID 9828626 | — |
Reaction Steps
High purity beta-carotene from Example I was dissolved in a minimal amount of warm (about 40°-50° C.) hexane to achieve saturation. The solution was then chilled, typically to about -20° C., which caused the preferential crystallization of the trans-isomer of beta-carotene. The crystals were then separated from the supernatant solution by filtration through a hydrophobic 0.22 μ nylon membrane filter (Micron Separations, Inc., Cambridge, MA). Chromatograms of representative preparations of the supernatant enriched in the 9-cis isomer (approximately 75-80% 9-cis and 15-20% all-trans) and of the crystals containing the all-trans isomer (approximately 80-85% all-trans and 10-15% 9-cis) are shown in FIGS. 2B and 2C, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310554 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-ab9200a53bd244ffbd1c7a5b598f8f9f |
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| Source note | uspto-grants-1994_05 |
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