((addition))-(alpha)-Tocopherol

• CAT Number: I012970
• CAS Number: 59-02-9
• Molecular Formula: C₂₉H₅₀O₂
• Molecular Weight: 430.71
• Purity: ≥95%
• Target: Others
• Solubility: 10 mM in DMSO
• IUPAC Name: (2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol
• InChI: InChI=1S/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/t21-,22-,29-/m1/s1
• InChIKey: GVJHHUAWPYXKBD-IEOSBIPESA-N
• SMILES: CC1=C(C2=C(CC[C@@](O2)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=C1O)C)C

(α)-Tocopherol（Cat No.:I012970）, a form of vitamin E, is a potent antioxidant widely researched for its protective role against oxidative stress and cell damage. Naturally found in foods like nuts and seeds, it is crucial for maintaining immune function, skin health, and cardiovascular wellness. In research, (α)-Tocopherol is employed to study cellular aging, lipid peroxidation, and metabolic processes, as well as in developing skincare and dietary supplements. Its stability and bioavailability make it ideal for biochemical and pharmaceutical applications, advancing our understanding of antioxidant pathways and potential therapeutic uses.

Reference

[1]. Geissler RG, et al. In vitro improvement of bone marrow-derived hematopoietic colony formation in HIV-positive patients by alpha-D-tocopherol and erythropoietin. Eur J Haematol. 1994 Oct;53(4):201-6.