5711-29-5

Basic information

• Product Name: OLEIC ACID (9,10-D2)
• Synonyms: OLEIC-9,10-D2 ACID;OLEIC ACID (9,10-D2)
• CAS NO: 5711-29-5
• Molecular Formula: C₁₈H₃₄O₂
• Molecular Weight: 284.47
• Product Categories: Fatty AcidsStable Isotopes;Alphabetical Listings;N-O;Stable Isotopes
• Mol File: 5711-29-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 13.4 °C(lit.)
• Boiling Point: 192-195 °C/1.2 mmHg(lit.)
• Appearance: /
• Density: 0.896 g/mL at 25 °C
• Storage Temp.: -20°C
• CAS DataBase Reference: OLEIC ACID (9,10-D2)(CAS DataBase Reference)
• NIST Chemistry Reference: OLEIC ACID (9,10-D2)(5711-29-5)
• EPA Substance Registry System: OLEIC ACID (9,10-D2)(5711-29-5)

Safety Data

• Hazardous Substances Data: 5711-29-5(Hazardous Substances Data)

Upstream product

• 35356-36-6 methyl <9,10-(2)H2>octadec-9Z-enoate 
• 1120-32-7 stearolic acid methyl ester 
• 506-24-1 Stearolic acid 

Downstream Products

• 15456-69-6 2(3H)-furanone, dihydro-5-(2-octenyl)-, (Z)- 
• 107797-26-2 (R)-5-Hexyl-dihydro-furan-2-one 

Relevant articles and documents

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Biosynthesis of (R)-γ-decanolactone in the yeast Sporobolomyces odorus

Addition of [9,10-2H2]oleic acid to cultures of the yeast Sporobolomyces odorus led to the formation of labeled (R)-γ-decanolactone and both enantiomers of (Z)-6-γ-dodecenolactone and γ-dodecanolactone. The labeling patterns of these lactones were estimated by a quantitative gas chromatography/mass spectrometry method, suitable for ring-labeled lactones. For the first time, there is strong evidence of oleic acid being a genuine precursor of the important aroma compound (R)-γ-decanolactone. On the basis of the presented and former results, a new biosynthetic pathway of this compound is proposed. Starting with a strict enantioselective (R)-12-hydroxylation of oleic acid as an initial step, the following β-oxidation led to the lactone. In addition, biosynthetic aspects of the formation of (Z)-6-γ-dodecenolactone and γ-dodecanolactone in S. odorus are discussed.