26536-12-9 Usage
Uses
Used in Cosmetics Industry:
1,2,3-Tritridecanoyl glycerol is used as an ingredient in cosmetics for stimulating the growth of hair and skin. Its application in this industry is due to its ability to enhance hair and skin health, providing beneficial effects for consumers seeking improved hair and skin quality.
Used in Research and Analysis:
1,2,3-Tritridecanoyl glycerol is used as a standard for the relative quantification of triacylglycerols in C. elegans fat stores. This application is essential for accurate measurement and comparison of triacylglycerol levels in research studies.
Used in Medical Research:
In medical research, 1,2,3-Tritridecanoyl glycerol is used as an internal standard for the quantification of triacylglycerols in the serum and liver of adult rat offspring receiving dietary conjugated linoleic acids during and after gestation. This application aids in understanding the effects of dietary conjugated linoleic acids on triacylglycerol levels in offspring, which can have implications for human health and development.
Check Digit Verification of cas no
The CAS Registry Mumber 26536-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26536-12:
(7*2)+(6*6)+(5*5)+(4*3)+(3*6)+(2*1)+(1*2)=109
109 % 10 = 9
So 26536-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C42H80O6/c1-4-7-10-13-16-19-22-25-28-31-34-40(43)46-37-39(48-42(45)36-33-30-27-24-21-18-15-12-9-6-3)38-47-41(44)35-32-29-26-23-20-17-14-11-8-5-2/h39H,4-38H2,1-3H3
26536-12-9Relevant academic research and scientific papers
1H-Nuclear magnetic resonance spectroscopic studies of saturated, acetylenic and ethylenic triacylglycerols
Lie Ken Jie, Marcel S.F.,Lam
, p. 155 - 171 (2007/10/03)
The 1H-NMR spectroscopic properties of 15 synthetic homologous saturated triacylglycerols of type AAA and 16 mixed saturated triacylglycerols of type ABA and AAB have been studied. Triacylglycerols containing short-chain fatty acids (2:0-6:0) are readily identified. Triacylglycerols containing medium- and long-chain fatty acid components are not differentiated. From the analysis of 19 acetylenic triacylglycerols of type AAA, ABA and AAB (containing positional isomers of acetylenic fatty acids), it is only possible to characterize triacylglycerols with acyl groups containing the acetylenic bond at the Δ2-Δ5 position. 1H-NMR analysis could not confirm the positions (α- or β-acyl) of the acetylenic acids in mixed triacylglycerols. In the study of 22 ethylenic triacylglycerols of type AAA containing positional isomers of (Z)- or (E)-ethylenic acids, molecules containing an ethylenic bond in the Δ2 position of the acyl chains were readily characterized, as the ethylenic protons in the α- and β-acyl chains were fully resolved. Triacylglycerols containing an unsaturated center at the position were characterized by the shifts of the 2-H protons. The spectra of the remaining triacylglycerol molecules were very similar and the position of the ethylenic system could not be determined by this technique.
