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CAS-Nr. | 58-95-7 |
Bezeichnung: | α-Tocopherylacetat |
Englisch Name: | D-alpha-Tocopheryl acetate |
Synonyma: | α-Tocopherylacetat Econ;Gevex;Erevit;Juvela;D-ECON;Alfacol;Ecofrol;E-Ferol;Tofaxin;E-Toplex |
CBNumber: | CB5241875 |
Summenformel: | C31H52O3 |
Molgewicht: | 472.74 |
MOL-Datei: | 58-95-7.mol |
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α-Tocopherylacetat physikalisch-chemischer Eigenschaften |
Schmelzpunkt:: |
~25 °C(lit.)
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alpha : |
3 º (c=2, in ethanol 25 ºC) |
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Siedepunkt:: |
224 °C0.3 mm Hg(lit.)
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Dichte: |
0.953 g/mL at 25 °C(lit.)
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Brechungsindex: |
n20/D 1.496(lit.)
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Wasserlöslichkeit: |
<0.1 g/100 mL at 17 ºC |
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Stabilität:: |
Stable. Incompatible with strong oxidizing agents. |
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EPA chemische Informationen: |
2H-1-Benzopyran- 6-ol, 3,4-dihydro-2,5,7,8-tetramethyl- 2-[(4R,8R)-4,8,12-trimethyltridecyl]-, acetate, (2R)-(58-95-7) |
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α-Tocopherylacetat Chemische Eigenschaften,Einsatz,Produktion Methoden |
Chemische Eigenschaften off-white crystalline solid |
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Allgemeine Beschreibung Odorless off-white crystals. Darkens at 401° F. |
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Air & Water Reaktionen D-alpha-Tocopheryl acetate may be sensitive to prolonged exposure to light and air. . Insoluble in water. |
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Reaktivität anzeigen An ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. |
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Brandgefahr Flash point data for D-alpha-Tocopheryl acetate are not available. D-alpha-Tocopheryl acetate is probably combustible. |
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S-Sätze Betriebsanweisung: S24/25:Berührung mit den Augen und der Haut vermeiden. |
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α-Tocopherylacetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler. Global( 110)Lieferanten |
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Prenols
Lipids
VITAMIN E ACETATE (D-FORM)
VITAMIN E ALPHA TOCOPHEROL ACETATE
VITAMINE E-ACETATE
(2r,4’r,8’r)-alpha-tocopherylacetate
(2R,4’R,8’R)-O-Acetyl-α-tocopherol
(r,r,r)-alpha-tocopherylacetate
[2R-[2R*(4R8,8R*)]]-3,4-Dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol acetate
2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-,acetate,(+)-6-chromano
2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-chromen-6-yl acetate
2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, acetate, [2R-[2R*(4R*,8R*)]]-
3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-,acetate,[2R-[2R*(4R*,8R*)]]-2H-1-Benzopyran-6-ol
6-Chromanol, 2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-, acetate, (+)-
acetate,[2theta-[2theta(4theta,8theta)]]-yl)
aceticacid2,5,7,8-tetramethyl-2-(4,8,12-trimethyl-tridecyl)-chroman-6-ylester
Alfacol
Combinal E
combinale
Contopheron
dl-alpha-tocopheryl
Ecofrol
Econ
E-Ferol
Endo E Dompe
endoedompe
Ephynal acetate
ephynalacetate
Erevit
E-Toplex
E-vicotrat
Evipherol
Fertilvit
Gevex
Juvela
Spondyvit
Tocopherex
Tocophrin
Tofaxin
Tokoferol acetate
tokoferolacetate
α-Tocopherolacetate
Biochemicals and Reagents
BioChemical
(+)-ALPHA-TOCOPHEROL ACETATE
58-95-7
D-VITAMIN E ACETATE
D-TOCOPHEROL ACETATE
D-TOCOPHRIN
D-ECON
D-A-TOCOPHERYL ACETATE
D-CONTOPHERON
D-ALFACOL
D-ALPHA-TOCOPHEROL ACETATE
D-ALPHA-TOCOPHERYL ACETATE
D-2,5,7,8-TETRAMETHYL-2-(4,8,12-TRIMETHYLTRIDECYL)-6-CHROMANOL ACETATE
D-FERTILVIT
D-A-TOCOPHEROL ACETATE FROM NATURAL*A-TO COPHEROL IN
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