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β-Tocotrienol

From Wikipedia, the free encyclopedia

β-Tocotrienol
Names
Preferred IUPAC name
(2R)-2,5,8-Trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-1-benzopyran-6-ol
Identifiers
3D model (JSmol)
ChEBI
ECHA InfoCard 100.007.008 Edit this at Wikidata
UNII
  • InChI=1S/C28H42O2/c1-20(2)11-8-12-21(3)13-9-14-22(4)15-10-17-28(7)18-16-25-24(6)26(29)19-23(5)27(25)30-28/h11,13,15,19,29H,8-10,12,14,16-18H2,1-7H3/b21-13+,22-15+/t28-/m1/s1
  • CC1=CC(=C(C2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)O
Properties
C28H42O2
Molar mass 410.642 g·mol−1
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

β-Tocotrienol is a tocotrienol, a member of vitamin E family.[1][2]

YouTube Encyclopedic

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  • The Benefits of Tocotrienols (Part of the Vitamin E) – Benefits Of Vitamin E – Dr.Berg
  • Tocotrienols- the New Vitamin E with Dr Barrie Tan
  • Tocotrienols Benefits in Perimenopause and Menopause: An Interview with Expert Dr. Barrie Tan

Transcription

References

  1. ^ Kamal-Eldin A, Appelqvist LA (July 1996). "The chemistry and antioxidant properties of tocopherols and tocotrienols". Lipids. 31 (7): 671–701. doi:10.1007/BF02522884. PMID 8827691. S2CID 4052785.
  2. ^ Clarke MW, Burnett JR, Croft KD (2008). "Vitamin E in human health and disease". Critical Reviews in Clinical Laboratory Sciences. 45 (5): 417–50. doi:10.1080/10408360802118625. PMID 18712629. S2CID 85991655.


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This page was last edited on 7 November 2023, at 19:42
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