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11-Methyllauric acid (CAS 5681-98-1)

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Alternate Names:
11-Methyldodecanoic acid, Isotridecanoic acid
CAS Number:
5681-98-1
Molecular Weight:
214.34
Molecular Formula:
C13H26O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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11-Methyllauric acid is a compound often utilized in research focusing on the study of fatty acid metabolism and the elucidation of lipid biochemical pathways. It is employed by researchers to understand the specific roles of branched-chain fatty acids in cellular processes and their physical properties in comparison to straight-chain fatty acids. In addition, 11-Methyllauric acid is used to investigate the modification of lipid membranes and the impact of methyl branching on the fluidity and function of these biological structures. Studies involving 11-Methyllauric acid are also relevant in the context of microbial biosynthesis of fatty acids, as certain microorganisms produce branched-chain fatty acids as components of their cell membranes. The compound′s involvement in signaling mechanisms and its interactions with lipid-binding proteins are also areas of interest within biochemical research.


11-Methyllauric acid (CAS 5681-98-1) References

  1. Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis.  |  Mo, S., et al. 2008. Chem Biol. 15: 137-48. PMID: 18291318
  2. Structural and functional characterisation of the cytochrome P450 enzyme CYP268A2 from Mycobacterium marinum.  |  Child, SA., et al. 2018. Biochem J. 475: 705-722. PMID: 29343612
  3. A novel 1-acyl-sn-glycerol-3-phosphate O-acyltransferase homolog for the synthesis of membrane phospholipids with a branched-chain fatty acyl group in Shewanella livingstonensis Ac10.  |  Toyotake, Y., et al. 2018. Biochem Biophys Res Commun. 500: 704-709. PMID: 29678574
  4. Division of the role and physiological impact of multiple lysophosphatidic acid acyltransferase paralogs.  |  Ogawa, T., et al. 2022. BMC Microbiol. 22: 241. PMID: 36203164
  5. Heteroatom substitution shifts regioselectivity of lauric acid metabolism from omega-hydroxylation to (omega-1)-oxidation.  |  Alterman, MA., et al. 1995. Biochem Biophys Res Commun. 214: 1089-94. PMID: 7575514
  6. Fatty acid discrimination and omega-hydroxylation by cytochrome P450 4A1 and a cytochrome P4504A1/NADPH-P450 reductase fusion protein.  |  Alterman, MA., et al. 1995. Arch Biochem Biophys. 320: 289-96. PMID: 7625836
  7. Metabolic Profiling of Aliphatic, hydroxy, and Methyl-Branched Fatty Acids in Human Plasma by Gas Chromatography–Mass Spectrometry  |  Chan Seo, Youngbae Kim, Hyeon-Seong Lee, Sook Za Kim & Man-Jeong Paik. 2018. Analytical Letters. 51: 793-806.
  8. Elucidation of the Streptomyces coelicolor Pathway to 2-Undecylpyrrole, a Key Intermediate in Undecylprodiginine and Streptorubin B Biosynthesis  |  SJ Mo, PK Sydor, C Corre, MM Alhamadshe. 22 February 2008,. Chemistry & biology,. Volume 15, Issue 2,: Pages 137-148.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

11-Methyllauric acid, 10 mg

sc-213589
10 mg
$148.00