D-α-Tocopherol
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D-α-Tocopherol
structure -
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CAS No:
59-02-9
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Formula:
C29H50O2
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Chemical Name:
D-α-Tocopherol
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Synonyms:
2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4R,8R)-4,8,12-trimethyltridecyl-, (2R)-;covirel;E-vitamin succinate;Pheryl-E;Vita plus E;(+)-ALPHA-TOCOPHEROL TYPE V;D-PROFECUNDIN;D-PHYTOGERMINE
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CAS No:
Description
(+)-α-Tocopherol is a vitamin E derivative. vitamin E is a fat-soluble antioxidant.
α-Tocopherol (phenyl-5,7-dimethyl-d6) is the most bioactive form of fat-soluble vitamin E, which has a stable deuterium label, can be used as an internal standard for chromatographic methods with a tandem mass spectrometric detector.
light yellow liquid
VITAMIN E is sometimes referred to as the antisterility vitamin, factor X (an earlier designation), chemically vitamin E is alphatocopherol. Active analogues and related compounds include: dl-α-Tocopherol; 1-α-tocopherol; esters (succinate, acetate, phosphate), and β, ζ 1, ζ 2- tocopherols. The principal physiological forms are D-a-tocopherol, tocopheronolactone, and their phosphate esters.
ChEBI: An alpha-tocopherol that has R,R,R configuration. The naturally occurring stereoisomer of alpha-tocopherol, it is found particularly in sunflower and olive oils.
Characteristics
29.46000
10.7
clear yellow oil
0.95 g/mL at 25 °C(lit.)
2.5-3.5 °C
200-220 °C0.1 mm Hg(lit.)
253 °C
n20/D1.505(lit.)
INSOLUBLE
2-8°C
1.4X10-8 mm Hg at 25 deg C (est)
24 º (c=2, in isooctane 25 ºC)
lt. yel. to red visc. oil, nearly odorless
Little or no taste
11.40±0.40(Predicted)
-20°C
Safety Information
NONH for all modes of transport
1
Xi
23-24/25-37/39-26
DJ2900000
Xi
Stable. Combustible. May be sensitive to light and air. Incompatible with strong oxidizing agents.
P261, P272, P280, P302+P352, P321, P333+P313, P363, P501
36/37/38
Drug Information
The physiological functions of vitamin E substances include: (1) bio logical antioxidant; (2) normal growth maintenance; (3) protects unsaturated fatty acids and membrane structures; (4) aids intestinal absorption of unsaturated fatty acids; (5) maintains normal muscle metabolism; (6) maintains integrity of vascular system and central nervous system; (7) detoxifying agent; and (8) maintains kidney tubules, lungs, genital structures, liver, and red blood cell membranes.In livestock and laboratory animals, a deficiency of vitamin E substances may cause degeneration of reproductive tissues, muscular dystrophy, encephalomalacia, and liver necrosis. Considerable research is required to fully determine supplementation of livestock diets unless typical symptoms of a deficiency appear. Symptoms have appeared where there are selenium deficiencies in the soil and where there are excessive levels of nitrates in the soil. “White muscle” is the term used to describe a condition of muscular dystrophy in cattle.
D-α-Tocopherol Use and Manufacturing
α-Tocopherol is the most bioactive of the naturally occurring forms of Vitamin E. Richest sources are green vegetables, grains, and oils, particularly palm, safflower and sunflower oils.
vitamin E, antioxidant
Use in insect cell culture applications as an antioxidant.
Computed Properties
Molecular Weight:430.7
XLogP3:10.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:12
Exact Mass:430.381080833
Monoisotopic Mass:430.381080833
Topological Polar Surface Area:29.5
Heavy Atom Count:31
Complexity:503
Defined Atom Stereocenter Count:3
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Price Analysis
Drug Function and Efficacy
Extract the name, type (main ingredient or excipient), content, unit, and pharmacological action of the raw material from the above information
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