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Propane-1,2,3-triyl tris(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) is a complex organic compound with the chemical formula C48H70O6. It is a type of antioxidant, specifically a hindered phenol, used to protect materials from oxidative degradation. propane-1,2,3-triyl tris(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) is characterized by its three propanoate groups attached to a propane backbone, with each propanoate group featuring a 3,5-di-tert-butyl-4-hydroxyphenyl moiety. The presence of the bulky tert-butyl groups enhances the molecule's steric hindrance, which is crucial for its effectiveness as an antioxidant by preventing radical reactions. propane-1,2,3-triyl tris(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoate) is commonly used in industrial applications, such as in the stabilization of polymers and lubricants, to extend their service life and improve their resistance to heat, light, and oxygen-induced degradation.

6386-64-7

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6386-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6386-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6386-64:
(6*6)+(5*3)+(4*8)+(3*6)+(2*6)+(1*4)=117
117 % 10 = 7
So 6386-64-7 is a valid CAS Registry Number.

6386-64-7Downstream Products

6386-64-7Relevant academic research and scientific papers

Synthesis, characterisation, and performance evaluation of tri-armed phenolic antioxidants

Higgins, Clare L.,Filip, Sorin V.,Afsar, Ashfaq,Hayes, Wayne

, (2020)

In this study, a series of core units (glycerol, triethanolamine and triisopropanolamine derivatives) were investigated for their use in tri-armed phenolic antioxidants. The antioxidant ability of these tri-armed phenolic compounds featuring different core units were then evaluated in a hydrocarbon lubricant using differential scanning calorimetry (DSC) and compared to the commercially available antioxidants Irganox L135 and Irganox L57. An impressive oxidation induction time of ca. 9–12 min was observed for the glycerol based antioxidants when compared to the commercial antioxidants (ca. 4–6 min), whereas in contrast in the case of triethanolamine and triisopropanolamine derived antioxidants, a solubilising unit was incorporated in order to provide appropriate solubility within the hydrocarbon medium and revealed an excellent oxidation induction time of ca. 11–12 min.

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