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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | ||
| StdInChIKey = WBHHMMIMDMUBKC-XLNAKTSKSA-N | | StdInChIKey = WBHHMMIMDMUBKC-XLNAKTSKSA-N | ||
| CASNo_Ref = {{cascite| |
| CASNo_Ref = {{cascite|correct|CAS}} | ||
| CASNo= |
| CASNo = 540-12-5 | ||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = 9O64E391KI | |||
| PubChem=445641 | | PubChem=445641 | ||
| ChEBI_Ref = {{ebicite|correct|EBI}} | | ChEBI_Ref = {{ebicite|correct|EBI}} |
Latest revision as of 15:41, 18 August 2022
Names | |
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Preferred IUPAC name (9E,12R)-12-Hydroxyoctadec-9-enoic acid | |
Other names (+)-(R)-Ricinelaidic acid | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChemSpider | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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Properties | |
Chemical formula | C18H34O3 |
Molar mass | 298.46 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Ricinelaidic acid or (+)-(R)-ricinelaidic acid is an unsaturated omega-9 trans fatty acid. It is the trans-isomer of the fatty acid ricinoleic acid.
External links
- Information about ricinelaidic acid in Organic Syntheses
- Wright, Amanda J.; Marangoni, Alejandro G. (2007). "Time, temperature, and concentration dependence of ricinelaidic acid-canola oil organogelation". Journal of the American Oil Chemists' Society. 84 (1): 3–9. doi:10.1007/s11746-006-1012-6. S2CID 96323666.
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