2074-53-5 Usage
Physical properties
Vitamin E has demonstrated some success in the treatment of yellow nail syndrome when taken orally (600 EU to 1200 EU daily) for several months. Topically-applied vitamin E has also shown significant improvement in symptoms of yellow nail syndrome, as well as increased nail growth rates after six months.
Uses
Different sources of media describe the Uses of 2074-53-5 differently. You can refer to the following data:
1. Vitamin E supplement.
2. vitamin E (D-alpha-tocopherol; DL-alpha-tocopherol; tocopherol) is considered the most important oil-soluble anti-oxidant and freeradical scavenger. Studies indicate that vitamin e performs these functions when topically applied. It is also a photoprotectant, and it helps protect the cellular membrane from free-radical damage. In addition, vitamin e serves a preservative function given its ability to protect against oxidation. This benefits not only the skin, but also the product in terms of longevity. As a moisturizer, vitamin e is well-absorbed through the skin, demonstrating a strong affinity with small blood vessels and an ability to enhance blood circulation in the skin. It is also thought to improve the skin’s water-binding ability. In addition, vitamin e emulsions have been found to reduce transepidermal water loss, thereby improving the appearance of rough, dry, and damaged skin. This vitamin is also believed to help maintain the connective tissue. There is evidence that vitamin e is effective in preventing irritation owing to sun exposure: studies show that vitamin e topically applied prior to uV irradiation is protective against epidermal cell damage caused by inflammation. This indicates possible anti-inflammatory properties. Lipid peroxidation in tissues may be one cause of skin aging. Vitamin e, however, appears to counteract decreased functioning of the sebaceous glands and to reduce excessive skin pigmentation, which is found to increase almost linearly with age. It is available also as a tocopherol-polypeptide complex that delivers the vitamin in a waterdispersable form. In this way, when incorporated into cosmetic formulations, it does not need other compounds to assist in its solubilization. It is useful in anti-aging creams and lotions, and in uV protective products, tocopherol is a naturally occurring vitamin e found in a variety of cereal germ oils including wheat germ oil. It can also be produced synthetically.
Indications
Vitamin E is a potent antioxidant that is capable of protecting
polyunsaturated fatty acids from oxidative
breakdown.This vitamin also functions to enhance vitamin
A use.Although several other physiological actions
have been suggested, to date no unifying concept exists
to explain these actions. Vitamin E (α-tocopherol) is
found in a variety of foodstuffs, the richest sources being
plant oils, including wheat germ and rice, and the
lipids of green leaves.
Brand name
Aquasol E
(Astra); Eprolin (Lilly); Natopherol (Abbott).
Clinical Use
Deficiency of vitamin E is characterized by low
serum tocopherol levels and a positive hydrogen peroxide
hemolysis test.This deficiency is believed to occur in
patients with biliary, pancreatic, or intestinal disease
that is characterized by excessive steatorrhea. Premature
infants with a high intake of fatty acids exhibit a
deficiency syndrome characterized by edema, anemia,
and low tocopherol levels.This condition is reversed by
giving vitamin E.
Side effects
Prolonged administration of large dosages of vitamin
E may result in muscle weakness, fatigue, headache,
and nausea.This toxicity can be reversed by discontinuing
the large-dose supplementation.
Toxicology
α-Tocopherol is known as vitamin E and exists in many kind of plants, especially in lettuce and alfalfa. Its color changes from yellow to dark brown when exposed to sunlight. Natural vegetable oils are not readily oxidized due to the presence of
tocopherol. During refining processes, however, tocopherol may be removed
from oils; consequently, refined vegetable oils can become unstable toward
oxidation. In one experiment, vitamin E appeared to be relatively innocuous,
having been given to patients for months both orally and parenterally
at a dosage level of 300 mg/day without any observed ill effects. However,
in another experiment, 6 out of 13 patients given similar doses complained
of headache, nausea, fatigue, dizziness, and blurred vision.
Although the chronic toxicity of vitamin E has not been thoroughly
studied, WHO recommends 2 mg/kg/day as the maximum daily dose.
Check Digit Verification of cas no
The CAS Registry Mumber 2074-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2074-53:
(6*2)+(5*0)+(4*7)+(3*4)+(2*5)+(1*3)=65
65 % 10 = 5
So 2074-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C29H50O2/c1-20(2)12-9-13-21(3)14-10-15-22(4)16-11-18-29(8)19-17-26-25(7)27(30)23(5)24(6)28(26)31-29/h20-22,30H,9-19H2,1-8H3
2074-53-5Relevant articles and documents
Process of separating chiral isomers of chroman compounds and their derivatives and precursors
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Page/Page column 14, (2012/12/13)
The present invention relates to a process of separating chiral isomers of chroman compounds, particularly tocopherols and tocotrienols as well as the esters and intermediates thereof. It has been found that this process allows a separation of the desired isomer with a higher yield and enables the use of the non-desired isomers in a very efficient way. Said process is particularly useful when implemented in an industrial process. Furthermore, it has been found that this process allows using isomer mixtures as they result from traditional industrial synthesis.
Electron Transfer Reactions of Halothane-derived Peroxyl Free Radicals, CF3CHClO2.: Measurement of Absolute Rate Constants by Pulse Radiolysis
Moenig, Joerg,Asmus, Klaus-Dieter,Schaeffer, Michel,Slater, Trevor F.,Willson, Robin L.
, p. 1133 - 1138 (2007/10/02)
The halothane-derived peroxyl radical CF3CHClO2. has been generated in aqueous solutions by pulse radiolysis.Absolute rate constants for the reduction of halothane (2-bromo-2-chloro-1,1,1-trifluoroethane) by hydrated electrons, hydrogen atoms, and propan-2-ol free radicals have been determined to be k 1.4E10, 3.8E8, and 7.6E7 l mol-1 s-1, respectively.The predominant product radical CF3CHCl rapidly adds O2, and an estimate of k 1.3E9 l mol-1 s-1, has been obtained for the absolute rate constant of this reaction.The resulting peroxyl radical CF3CHClO2. has been found to react rapidly with a variety of nucleophilic compounds such as 2,2'-azinobis(3-ethylbenzthiazoline-6-sulphonate), the phenothiazines promethazine, chlorpromazine, and metiazinic acid, the vitamins C and E, and propyl gallate.The absolute rate constants for these reactions are found to be generally lower than for corresponding reactions of the carbon tetrachloride-derived radical, CCl3O2..
