Heptatriacontanoic acid

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Heptatriacontanoic acid
Heptatriacontanoic acid.svg
Names
IUPAC name
Heptatriacontanoic acid
Identifiers
ChemSpider 4445724
Jmol-3D images Image
PubChem 5282597
Properties
C37H74O2
Molar mass 550.98 g·mol−1
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Heptatriacontanoic acid is a 37-carbon saturated fatty acid.

Sources[edit]

Heptatriacontanoic acid is present in Abelmoschus manihot and Alpinia nigra.[1][2] Heptatriacontanoic acid was also measured in zooplankton.[3]

Compounds[edit]

The compound 4,21-dimethyl-5,19-di-(trans)-enoyl-heptatriacontanoic acid is the "structure of the major homolog of free mycobacteric acids" of Mycobacterium brumae.[4]

Preparation[edit]

U.S. patent 5502226 covers a method of ω-hydroxy acid preparation that includes heptatriacontanoic acid.[5]

See also[edit]

References[edit]

  1. ^ Lai, X. Y.; Zhao, Y. Y.; Liang, H. (2006). "Studies on chemical constituents in flower of Abelmoschus manihot". China Journal of Chinese Materia Medica 31 (19): 1597–1600. PMID 17165583. 
  2. ^ Chunfeng, Qiao; Zhengtao, Wang; Hui, Dong; Luoshan, Xu; Xiaojiang, Hao (2000). "The Chemical Constituents of Blackfruit Galangal (alpinia nigra)". Chinese Traditional and Herbal Drugs 31 (6): 404–405. 
  3. ^ Brown, Paul B. "Food Webs in the 21st Century: Exploration of New Enabling Technologies to Understand and Predict Changes in Aquatic Food Webs and Impacts on Ecosystems" (PDF). Purdue College of Agriculture. Retrieved 2014-04-22. 
  4. ^ Rafidinarivo, Elie; Lanéelle, Marie-Antoinette; Montrozier, Henri; Pedro, Valero-Guillén; Astola, José; Luquin, Marina; Promé, Jean-Claude; Daffé, Mamadou (2008-09-04). "Trafficking pathways of mycolic acids: structures, origin, mechanism of formation, and storage form of mycobacteric acids" (PDF). The Journal of Lipid Research 50 (3): 477–490. doi:10.1194/jlr.M800384-JLR200. PMID 18772482. Retrieved 2014-04-22. Altogether these results established the structure of the major homolog of free mycobacteric acids of M. brumae as a 4,21-dimethyl-5,19-di-(trans)-enoyl-heptatriacontanoic acid. 
  5. ^ US 5502226, Cho, Suk H. & Victor DeFlorio, "Process of preparing ω-hydroxy acids", issued 1996-03-26 

External links[edit]

The dictionary definition of heptatriacontanoic acid at Wiktionary