W468501
δ-Tridecalactone
≥95%, FG
Synonym(s):
Tetrahydro-6-octyl-2H-pyran-2-one, 6-octyloxan-2-one
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About This Item
Empirical Formula (Hill Notation):
C13H24O2
CAS Number:
Molecular Weight:
212.33
FEMA Number:
4685
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
10.058
Recommended Products
biological source
synthetic
Quality Level
grade
FG
Halal
Kosher
reg. compliance
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 172.515
Assay
≥95%
application(s)
flavors and fragrances
Documentation
see Safety & Documentation for available documents
food allergen
no known allergens
Organoleptic
creamy; dairy; milk; musty; buttery
InChI
1S/C13H24O2/c1-2-3-4-5-6-7-9-12-10-8-11-13(14)15-12/h12H,2-11H2,1H3
InChI key
RZZLMGATMUAJPX-UHFFFAOYSA-N
Related Categories
General description
δ-Tridecalactone participates as an internal standard in a study on the conversion of linoleic acid to hydroxyl fatty acid by lactic acid bacterial strains. Its racemic form has been used in the synthesis of racemic-N-alkyl-5-acetoxyalkanamides.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
259.7 °F
Flash Point(C)
126.5 °C
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Yasutaka Shimotori et al.
Journal of oleo science, 64(11), 1213-1226 (2015-10-16)
A combination of Novozym 435-catalyzed methanolysis and amidation using racemic N-methyl-5-acetoxytridecan- and tetradecanamides as a substrate proceeded in good enantioselectivity to afford the corresponding (R)-N-methyl-5-acetoxyalkanamides, (S)-N-methyl-5-hydroxyalkanamides, and (S)-N-cyclohexyl-5-hydroxyalkanamides. Both enantiomers of δ-tri- and δ-tetradecalactones were synthesized in over 90% enantiomeric
Noriaki Kishimoto et al.
Lipids, 38(12), 1269-1274 (2004-02-12)
Twenty-three of 86 strains of lactic acid bacteria transformed linoleic acid into hydroxy FA. Two distinct conversion pathways were in operation. Two strains of Lactobacillus acidophilus and a strain of Pediococcus pentosaceus produced 13(S)-hydroxy-9-octadecenoic acid 113(S)-OH 18:11 and 10,13dihydroxyoctadecanoic acid
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