| Identification | Back Directory | [Name]
RAC-TOCOL | [CAS]
119-98-2 | [Synonyms]
TOCOL
RAC-TOCOL
Vitamin E Related Compound 1
2-methyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydrochromen-6-ol
Vitamin E Related Compound (2-Methyl-2-(4,8,12-Trimethyltridecyl)-6-Chromanol)
Vitamin E Related Compound 1 (2-Methyl-2-(4,8,12-Trimethyltridecyl)-6-Chromanol)
(2R)-3,4-Dihydro-2-methyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-ol | [Molecular Formula]
C26H44O2 | [MDL Number]
MFCD08703020 | [MOL File]
119-98-2.mol | [Molecular Weight]
388.63 |
| Chemical Properties | Back Directory | [Melting point ]
<25 °C | [Boiling point ]
bp0.001 165-175° | [density ]
0.938±0.06 g/cm3(Predicted) | [solubility ]
Ethanol: soluble; Hexane: soluble; Methanol: soluble | [pka]
10.57±0.40(Predicted) |
| Hazard Information | Back Directory | [Description]
(±)-Tocol is a synthetic vitamin E derivative. Unlike (±)-α-tocopherol , (±)-tocol does not suppress retinol-induced erythrocyte hemolysis or increase microviscosity of rat liver phosphatidylcholine (PC) liposomes. [Matreya, LLC. Catalog No. 1797] | [Uses]
Tocol can be useful in the study of synergistic interaction between tocol and phenolic extracts from different tree nut species against human cancer cell line. | [References]
[1] S. URANO. Vitamin E: inhibition of retinol-induced hemolysis and membrane-stabilizing behavior.[J]. The Journal of Biological Chemistry, 1992, 42 1: 18365-18370. DOI: 10.1016/s0021-9258(19)36970-4 |
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