Methyl myristelaidate
<strong>Methyl myristelaidate</strong>_x000D_ <strong>Catalog number:</strong> B2018085_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 240.38_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20℃_x000D_ <strong>Keywords:</strong> Methyl trans-9-tetradecenoate, Myristelaidic acid methyl ester_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Wu C, Wang Y, Sun H. Targeted and untargeted metabolomics reveals deep analysis of drought stress responses in needles and roots of Pinus taeda seedlings Front Plant Sci. 2023 Jan 31;13:1031466._x000D_ 2: Doma AO, Cristina RT, Muselin F, Dumitrescu E, Dégi J, Imre K, Boldea M, Vlad DC, Popescu R, Cimporescu A, Bratu DC. The Role of Methyl-(Z)-11-tetradecenoate Acid from the Bacterial Membrane Lipid Composition in Escherichia coli Antibiotic Resistance Biomed Res Int. 2022 Jun 13;2022:6028045._x000D_ 3: Choi MH, Yoon SC. Polyester Biosynthesis Characteristics of Pseudomonas citronellolis Grown on Various Carbon Sources, Including 3-Methyl-Branched Substrates Appl Environ Microbiol. 1994 Sep;60(9):3245-54._x000D_ 4: Watanabe H, Matsui A, Inomata S, Yamamoto M, Ando T. Biosynthetic Pathway for Sex Pheromone Components Produced in a Plusiinae Moth, Plusia festucae Front Endocrinol (Lausanne). 2011 Nov 14;2:74._x000D_ 5: Petkevicius K, Wenning L, Kildegaard KR, Sinkwitz C, Smedegaard R, Holkenbrink C, Borodina I. Biosynthesis of insect sex pheromone precursors via engineered β-oxidation in yeast FEMS Yeast Res. 2022 Sep 1;22(1):foac041._x000D_ 6: Hasan MM, Chowdhory SA, Rahman ASMS, Athanassiou CG. Development and diapause induction of the Indian meal moth, Plodia interpunctella (Hübner) (Lepidoptera: Pyralidae) at different photoperiods Sci Rep. 2020 Sep 7;10(1):14707._x000D_ 7: Ma PW, Roelofs WL. Sex pheromone gland of the female European corn borer moth, Ostrinia nubilalis (Lepidoptera, Pyralidae): ultrastructural and biochemical evidences Zoolog Sci. 2002 May;19(5):501-11._x000D_ 8: Miura Y, Fulco AJ. Omega-1, Omega-2 and Omega-3 hydroxylation of long-chain fatty acids, amides and alcohols by a soluble enzyme system from Bacillus megaterium Biochim Biophys Acta. 1975 Jun 23;388(3):305-17._x000D_ 9: Chao TH, Ehrman L, Permaul A, Vincent R, Sattaur L, Brandt D. Male-specific cuticular compounds of the six Drosophila paulistorum semispecies: structural identification and mating effect J Chem Ecol. 2010 Sep;36(9):933-42._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/9113629">10: Navarro I, Fabriàs G, Camps F. Possible fatty acyl pheromone precursors in Spodoptera littoralis. Search for 11- and 12-hydroxytetradecanoic acids in the pheromone gland Lipids. 1997 Apr;32(4):407-12. </a>_x000D_ _x000D_ <strong>Products Related to Methyl myristelaidate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals /"> Chemicals </a>
Product Specifications
Short Description
Catalog Number: B2018085 (50 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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