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Vitamin E

CAS No.
59-02-9
Chemical Name:
Vitamin E
Synonyms
α-Tocopherol;VITAMIN E OIL;D-ALPHA-TOCOPHEROL;tocopheryl;VITAMINE E;D-α-Tocopherol;D-A-TOCOPHEROL;All-rac-alpha-tocopherol for peak identification CRS;verrol;covi-ox
CBNumber:
CB7132531
Molecular Formula:
C29H50O2
Molecular Weight:
430.71
MDL Number:
MFCD00072045
MOL File:
59-02-9.mol
Last updated:2024-11-20 11:41:24

Vitamin E Properties

Melting point 2.5-3.5 °C
Boiling point 200-220 °C0.1 mm Hg(lit.)
alpha 24 º (c=2, in isooctane 25 ºC)
Density 0.95 g/mL at 25 °C(lit.)
refractive index n20/D 1.505(lit.)
Flash point 253 °C
storage temp. -20°C
solubility Practically insoluble in water, freely soluble in acetone, in anhydrous ethanol, in methylene chloride and in fatty oils.
pka 11.40±0.40(Predicted)
form oil
color clear yellow
Odor lt. yel. to red visc. oil, nearly odorless
Water Solubility INSOLUBLE
Merck 14,9495
BRN 4712525
Stability Stable. Combustible. May be sensitive to light and air. Incompatible with strong oxidizing agents.
LogP 10.962 (est)
CAS DataBase Reference 59-02-9(CAS DataBase Reference)
NCI Dictionary of Cancer Terms alpha-tocopherol
FDA UNII N9PR3490H9
NCI Drug Dictionary alpha-tocopherol
NIST Chemistry Reference Vitamin e(59-02-9)
EPA Substance Registry System 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-, (2R)- (59-02-9)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  23-24/25-37/39-26
WGK Germany  1
RTECS  DJ2900000
8-10-23
HS Code  29362800
NFPA 704
1
0 0

Vitamin E price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T3634 (+)-α-Tocopherol from vegetable oil, Type V, ~1000?IU/g 59-02-9 10G $25.2 2023-06-20 Buy
Sigma-Aldrich T3634 (+)-α-Tocopherol from vegetable oil, Type V, ~1000?IU/g 59-02-9 100G $133 2023-06-20 Buy
Sigma-Aldrich T1539 (+)-α-Tocopherol Type VI, from vegetable oil, liquid (≥0.88M based on potency, density and molecular wt.), BioReagent, suitable for insect cell culture, ≥1000?IU/g 59-02-9 25G $54.9 2023-06-20 Buy
Sigma-Aldrich T1539 (+)-α-Tocopherol Type VI, from vegetable oil, liquid (≥0.88M based on potency, density and molecular wt.), BioReagent, suitable for insect cell culture, ≥1000?IU/g 59-02-9 100G $169 2023-06-20 Buy
TCI Chemical T2309 D-α-Tocopherol >97.0%(GC) 59-02-9 25g $92 2024-03-01 Buy
Product number Packaging Price Buy
T3634 10G $25.2 Buy
T3634 100G $133 Buy
T1539 25G $54.9 Buy
T1539 100G $169 Buy
T2309 25g $92 Buy

Vitamin E Chemical Properties,Uses,Production

Chemical Properties

light yellow liquid

Chemical Properties

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.

Originator

Doppelherz,Queisser Pharma,Germany

Uses

vitamin E, antioxidant

Uses

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.

Uses

Use in insect cell culture applications as an antioxidant.

Definition

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.

Manufacturing Process

Manufacturing process for Vitamin E, that is, α-tocopherol (5,7,8-trimethyltocol) in the past has been accomplished primarily by reacting trimethylhydroquinone (TMHQ) with isophytol (3,7,11,15-tetramethylhexadec-1-en-3-ol) or phytol (3,7,11,15-tetramethylhexadec-2-en-1-ol) in a condensation reaction. The reaction is well known and has been practiced for many years (StallaBourdillon, Ind. Chim. Belg., 35, 13 (1970); "The Vitamins" Vol. 5, pages 168- 223, Academic Press, New York, 1967). The Synthesis of Vitamin E includes these steps as follows: Rearrangement to C15 Acetylene; Saponification of the C20 Dienol Acetate to Dehydrophytol;Condensation of Dehydrophytol with TMHQ to yield Dehydro-Vitamin E.

Therapeutic Function

Antioxidant

General Description

α-Tocopherol is synthesized from γ-tocopherol by the action of enzyme γ-tocopherol methyltransferase. It is the major form of Vitamin E in human plasma. It is present in sunflower seed oil.

Health Hazard

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.

Biochem/physiol Actions

α-Tocopherol is essential for the photosynthesis in Synechocystis sp. strain PCC 6803. Supplementation with α-Tocopherol decreases lipid peroxidation and platelet aggregation. It inhibits protein kinase C and may play key role in gene regulation.

Safety Profile

Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Vitamin E is a viscous yellow oil which is distilled at high vacuum. It has max at 294nm (E1cm 1% 71). It is oxygen and light sensitive and is best stored as its stable D--acetate [58-95-7] which is purified by evaporative distillation at b 180-200o(bath temperature)/0.7mm, and has [] D 25 +3.3o (c 5.1, EtOH). It forms needles at -30o and has m 26.5-27.5o, [] D 25 +0.25o (c 10, CHCl3). [NMR: Cohen et al. Helv Chim Acta 6 4 1158 1981, Burton & Ingold Acc Chem Res 1 9 194 1986, Karrer et al. Helv Chim Acta 2 1 520 1938, Robeson J Am Chem Soc, 64 1487 1942, 65 1660 1943.] Of the eight isomers the D--isomer is the most active. [See W. Friedrich “Vitamins” Walter de Guyter Publ, Berlin 1988.] [Beilstein 17/4 V 168.]

110-19-0
505-32-8
700-13-0
59-02-9
Synthesis of Vitamin E from Isobutyl acetate and Isophytol and Trimethylhydroquinone
Global( 490)Suppliers
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Hebei Mojin Biotechnology Co., Ltd
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025-85710122 17714198479 sales@fine-chemtech.com CHINA 885 55

View Lastest Price from Vitamin E manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Vitamin E pictures 2024-11-22 Vitamin E
59-02-9
US $10.00 / kg 1kg 99% 50000KG/month Hebei Zhuanglai Chemical Trading Co.,Ltd
α-Vitamin E pictures 2024-11-19 α-Vitamin E
59-02-9
US $38.00 / mg 99.89% 10g TargetMol Chemicals Inc.
Vitamin E pictures 2024-11-14 Vitamin E
59-02-9
US $60.00 / KG 1KG 99% 1 ton Baoji Guokang Bio-Technology Co., Ltd.
  • Vitamin E pictures
  • Vitamin E
    59-02-9
  • US $10.00 / kg
  • 99%
  • Hebei Zhuanglai Chemical Trading Co.,Ltd
  • α-Vitamin E pictures
  • α-Vitamin E
    59-02-9
  • US $38.00 / mg
  • 99.89%
  • TargetMol Chemicals Inc.
  • Vitamin E pictures
  • Vitamin E
    59-02-9
  • US $60.00 / KG
  • 99%
  • Baoji Guokang Bio-Technology Co., Ltd.
phytogermine profecundin spavite syntopherol tokopharm vascuals viprimol vitaflexe vitaminealpha vitaplexe vitayonon viteolin viterrae VITAMIN E SYNTHETIC VITAMIN E (D-FORM) RRR-ALPHA-TOCOPHEROL (2r)-3,4-dihydro-2,5,7,8-tetramethyl-2-[(4r,8r)-4,8,12-trimethyltridecyl]-2h-1-benzopyran-6-ol (+)-2,5,7,8-TETRAMETHYL-2-(4',8',12'-TRIMETHYLTRIDECYL)-6-CHROMANOL 2,5,7,8-TETRAMETHYL-2-(4',8',12'-TRIMETHYLTRIDECYL)-6-CHROMANOL 5,7,8-TRIMETHYLTOCOL TOCOPHEROLCONCENTRATE,D-ALPHA- PALMVITAMINE ALPHA-D-TOCOPHEROLCONCENTRATE 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 (+)-ALPHA-TOCOPHEROL D-PROFECUNDIN D-PHYTOGERMINE D-VITAMIN E D-2,5,7,8-TETRAMETHYL-2-(4,8,12-TRIMETHYLTRIDECYL)-6-CHROMANOL D-5,7,8-TRIMETHYLTOCOL Vitamin E Natural Dl-alfa-tocophry acetate (+)-A-TOCOPHEROL TYPE VI FROM VEGETABLE OIL (+)-A-TOCOPHEROL TYPE V FROM VEGETABLE*O IL (+)-A-TOCOPHEROL TYPE VI: MIXED ISOMERS INSECT CELL VITAMIN E(D-ALPHA TYPE) NATURAL 1000-1400IU VITMIN E VitaminE1,000Iu(Natural) NaturalVitaminE VitaminEAcetate50% VitaminE(50%,Bp,Usp) D-Alpha Tocopheryl Acetate Oil 1200IU Water Soluble Natural Vitamin E D-alpha-Tocopherols D-alpha-Tocopheroloilnatural Tocopherolmixedpowder VitaminEpowdermixed D-ALFA-TOCOPHEROL (VITAMIN E) alpha-tocopherol (CAS ) a-VitaMin E D-α-Tocopherol, froM Trachycarpus fortunei MIXEDTOCOPHEROLS50%(BULK (2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chroman-6-ol