Trans-9,12-Octadecadienoic Acid Methyl ester
<strong>trans-9,12-Octadecadienoic Acid Methyl ester</strong>_x000D_ <strong>Catalog number:</strong> B2018150_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> N/A_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> N/A_x000D_ <strong>Keywords:</strong> N/A_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: Emken EA, Abraham S, Lin CY. Metabolism of cis-12-octadecenoic acid and trans-9,trans-12-octadecadienoic acid and their influence on lipogenic enzyme activities in mouse liver Biochim Biophys Acta. 1987 Jun 2;919(2):111-21._x000D_ 2: Janssen G, Parmentier G. Determination of double bond positions in fatty acids with conjugated double bonds Biomed Mass Spectrom. 1978 Jul;5(7):439-443._x000D_ 3: Emken EA, Rohwedder WK, Adlof RO, Rakoff H, Gulley RM. Metabolism in humans of cis-12,trans-15-octadecadienoic acid relative to palmitic, stearic, oleic and linoleic acids Lipids. 1987 Jul;22(7):495-504._x000D_ 4: Yurawecz MP, Roach JA, Sehat N, Mossoba MM, Kramer JK, Fritsche J, Steinhart H, Ku Y. A new conjugated linoleic acid isomer, 7 trans, 9 cis-octadecadienoic acid, in cow milk, cheese, beef and human milk and adipose tissue Lipids. 1998 Aug;33(8):803-9._x000D_ 5: Delmonte P, Roach JA, Mossoba MM, Morehouse KM, Lehmann L, Yurawecz MP. Synthesis and isolation of trans-7,cis-9 octadecadienoic acid and other CLA isomers by base conjugation of partially hydrogenated gamma-linolenic acid Lipids. 2003 May;38(5):579-83._x000D_ 6: Ando A, Ogawa J, Sugimoto S, Kishino S, Sakuradani E, Yokozeki K, Shimizu S. Selective production of cis-9,trans-11 isomer of conjugated linoleic acid from trans-vaccenic acid methyl ester by Delacroixia coronata J Appl Microbiol. 2009 May;106(5):1697-704._x000D_ 7: Ochin CC, Wilson T, Garelnabi M. Dietary Oxidized Linoleic Acids Modulate Fatty Acids in Mice J Lipid Atheroscler. 2022 May;11(2):197-210._x000D_ 8: Mosley EE, Shafii Dagger B, Moate PJ, McGuire MA. cis-9, trans-11 conjugated linoleic acid is synthesized directly from vaccenic acid in lactating dairy cattle J Nutr. 2006 Mar;136(3):570-5._x000D_ 9: Mosley EE, McGuire MK, Williams JE, McGuire MA. Cis-9, trans-11 conjugated linoleic acid is synthesized from vaccenic acid in lactating women J Nutr. 2006 Sep;136(9):2297-301._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/16475013">10: Kohno-Murase J, Iwabuchi M, Endo-Kasahara S, Sugita K, Ebinuma H, Imamura J. Production of trans-10, cis-12 conjugated linoleic acid in rice Transgenic Res. 2006 Feb;15(1):95-100. </a>_x000D_ _x000D_ <strong>Products Related to trans-9,12-Octadecadienoic Acid Methyl ester can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals /"> Chemicals </a>
Product Specifications
Short Description
Catalog Number: B2018150 (1 mL)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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