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DL-α-Tocopherol

$52

  • Brand : BIOFRON

  • Catalogue Number : BD-D1243

  • Specification : 95%(HPLC)

  • CAS number : 10191-41-0

  • Formula : C29H50O2

  • Molecular Weight : 430.717

  • Volume : 100MG

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Catalogue Number

BD-D1243

Analysis Method

HPLC,NMR,MS

Specification

95%(HPLC)

Storage

2-8°C

Molecular Weight

430.717

Appearance

Powder

Botanical Source

Structure Type

Other Phenolic Compounds

Category

SMILES

Synonyms

IUPAC Name

Applications

Density

0.9±0.1 g/cm3

Solubility

Flash Point

210.2±24.4 °C

Boiling Point

485.9±0.0 °C at 760 mmHg

Melting Point

2-4°C

InChl

InChl Key

WGK Germany

RID/ADR

HS Code Reference

2936280000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:10191-41-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

30156307

Title

Contact urticaria caused by tocopherol

Author

Tatiana Sanz-Sanchez 1, Beatriz NúNez Acevedo 2, Cristina Rubio Flores 1, Rosa M Diaz-Diaz 1

Publish date

2018 Dec;

PMID

15646369

Abstract

The non-steroidal anti-inflammatory drugs (NSAIDs) diclofenac (CAS 15307-79-6) and piroxicam (CAS 36322-90-4) were shown in previous works to induce bone marrow lymphopoiesis. The present work aimed at evaluating the extent to which lymphopoietic effects of the above mentioned drugs as well as their interactions with alpha-tocopherol (CAS 10191-41-0) may be reflected in changes in the tissue levels of norepinephrine (NE), dopamine (DA) and serotonin (5-HT). The study was performed in male adult mice. The doses were given once daily for 7 days. The evaluations were performed in 2 phases. First, dose-response relationships of each of diclofenac, piroxicam and alpha-tocopherol were evaluated using bone marrow lymphocytes counts and monoamines levels in plasma, brain and spleen. Then, interactions of alpha-tocopherol (10 mg/kg) with diclofenac (20 mg/kg) and piroxicam (3 mg/kg), respectively, were evaluated. The interaction evaluations included effects on bone marrow lymphocytes count, monoamines levels in plasma, brain, spleen and thymus, as well as spleen weight. The obtained findings revealed that diclofenac, piroxicam and alpha-tocopherol decreased NE and DA levels in plasma, brain and spleen. There was some correlation between the decrease in plasma NE and the bone marrow lymphopoiesis. Pre-administration of alpha-tocopherol failed to maintain monoamines levels at the range of normal values in plasma, brain and spleen of NSAIDs-treated mice except splenic DA levels. In addition, the decrease in NE level induced by administration of piroxicam or diclofenac, either alone or together with a-tocopherol, corresponded to the increase in bone marrow lymphopoiesis. The present work suggests that the diclofenac- and piroxicam-induced bone marrow lymphopolesis as well as their respective interactions with alpha-tocopherol are associated with parallel changes in monoamines levels, especially those of NE and 5-HT.

Title

Effects of diclofenac, piroxicam and alpha-tocopherol on monoaminelymphopoietic interfacing in mice

Author

Nahed M A Hassanein 1, Wafaa A Hasan, Mohamed Raouf Hamed

Publish date

2004

PMID

9706379

Abstract

The influence of vitamin E (tocopherol, CAS 10191-41-0) on stratum corneum hydration was tested in O/W and W/O emulsions. Additionally, the O/W emulsion was used in an in vivo/in vitro method to gravimetrically obtain evidence concerning the water-binding capacity of the stratum corneum. In the W/O emulsion, 2.5%, 5%, and 7.5% vitamin E were compared. With both types of emulsions, vitamin E increased the stratum corneum hydration statistically significantly (p = 0.0002). In addition, we could provide evidence of an enhanced water-binding capacity after treatment with vitamin E (p = 0.05). For the hydrating effect of vitamin E. its concentration is of importance. The optimum concentration turned out to be 5%.

Title

Influence of vitamin E acetate on stratum corneum hydration

Author

W Gehring 1, J Fluhr, M Gloor

Publish date

1998 Jul;