Methyl octacosanoate

<strong>Methyl octacosanoate</strong>_x000D_ <strong>Catalog number:</strong> B2018012_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 438.77_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> RT_x000D_ <strong>Keywords:</strong> Octacosanoic acid methyl ester_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Lee H, Feakins SJ, Lu Z, Schimmelmann A, Sessions AL, Tierney JE, Williams TJ. Comparison of three methods for the methylation of aliphatic and aromatic compounds Rapid Commun Mass Spectrom. 2017 Oct 15;31(19):1633-1640._x000D_ 2: Shaari K, Zareen S, Akhtar MN, Lajis NH. Chemical constituents of Melicope ptelefolia Nat Prod Commun. 2011 Mar;6(3):343-8._x000D_ 3: Sonesson A, Jantzen E, Tangen T, Zähringer U. Chemical characterization of lipopolysaccharides from Legionella feeleii, Legionella hackeliae and Legionella jordanis Microbiology (Reading). 1994 Oct;140 ( Pt 10):2663-71._x000D_ 4: Dennis RD, Baumeister S, Geyer R, Peter-Katalinic J, Hartmann R, Egge H, Geyer E, Wiegandt H. Glycosphingolipids in cestodes. Chemical structures of ceramide monosaccharide, disaccharide, trisaccharide and tetrasaccharide from metacestodes of the fox tapeworm, Taenia crassiceps (Cestoda: Cyclophyllidea) Eur J Biochem. 1992 Aug 1;207(3):1053-62._x000D_ 5: Menéndez R, Más R, Amor AM, Rodeiros I, Gonzalez RM, Alfonso JL. Inhibition of cholesterol biosynthesis in cultured fibroblasts by D003, a mixture of very long chain saturated fatty acids Pharmacol Res. 2001 Oct;44(4):299-304._x000D_ 6: Li Y, Yang S, Bai S. [Studies on chemical constituents from roots of Angelica polymorpha] Zhongguo Zhong Yao Za Zhi. 2009 Apr;34(7):854-7._x000D_ 7: Yue JR, Feng DQ, Xu YK. A new triterpenoid bearing octacosanoate from the stems and roots of Clerodendrum philippinum var. simplex (Verbenaceae) Nat Prod Res. 2015;29(13):1228-34._x000D_ 8: Kuigoua GM, Kouam SF, Ngadjui BT, Schulz B, Green IR, Choudhary MI, Krohn K. Minor secondary metabolic products from the stem bark of Plumeria rubra Linn. displaying antimicrobial activities Planta Med. 2010 Apr;76(6):620-5._x000D_ 9: Liu XX, Wang L, Long Y, Sun LL, Wang Q. [Chemical constituents from Paris mairei] Zhongguo Zhong Yao Za Zhi. 2014 Aug;39(16):3107-11._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/11440139">10: Tomosaka H, Koshino H, Tajika T, Omata S. Lupeol esters from the twig bark of Japanese pear (Pyrus serotina Rehd.) cv. Shinko Biosci Biotechnol Biochem. 2001 May;65(5):1198-201. </a>_x000D_ _x000D_ <strong>Products Related to Methyl octacosanoate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>