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77011
(S)-γ-Caprolactone
≥98.5% (GC)
Synonim(y):
(−)-γ-Hexalactone, (5S)-5-Ethyldihydro-2(3H)-furanone, (5S)-5-Ethyloxolan-2-one, (S)-γ-Ethyl-γ-butyrolactone, (S)-4-Hexanolide
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Informacje o tej pozycji
Numer CAS:
UNSPSC Code:
12352204
NACRES:
NA.32
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
41035-07-8
assay
≥98.5% (GC)
form
liquid
optical activity
[α]20/D -51±1°, c = 1 in methanol
optical purity
enantiomeric excess: ≥95.0% (GC)
storage temp.
2-8°C
SMILES string
CC[C@H]1CCC(O1)=O
InChI
1S/C6H10O2/c1-2-5-3-4-6(7)8-5/h5H,2-4H2,1H3/t5-/m0/s1
InChI key
JBFHTYHTHYHCDJ-YFKPBYRVSA-N
Biochem/physiol Actions
Metabolite produced by plants, as a component of aroma flavours and fragrances and aromas of fruits and vegetables. An intense aroma of caramel and liquorice, found in many fruits, but also in different foods and beverages, like butter, beer, brandy, tea, and added to tobacco as flavoring agent.
gamma-Caprolactone is occasionally found as a volatile component of human urine and has been found in the polar fraction of human blood. Biological fluids such as blood and urine have been shown to contain a large number of components apparently present in all individuals. It is a promotor of the growth of biocontrol bacteria and a metabolite of a new assimilative pathway.
gamma-Caprolactone is occasionally found as a volatile component of human urine and has been found in the polar fraction of human blood. Biological fluids such as blood and urine have been shown to contain a large number of components apparently present in all individuals. It is a promotor of the growth of biocontrol bacteria and a metabolite of a new assimilative pathway.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Klasa składowania
10 - Combustible liquids
wgk
WGK 2
flash_point_f
No data available
flash_point_c
No data available
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Stereoisomeric flavor compounds: structure and properties of gamma-lactone enantiomers.
Mosandl, A. and Gunther, C.
Journal of Agricultural and Food Chemistry, 37, 413-418 (1989)
Carlo Bicchi et al.
Journal of chromatography. A, 1212(1-2), 114-123 (2008-10-31)
The analysis of complex real-world samples of vegetable origin requires rapid and accurate routine methods, enabling laboratories to increase sample throughput and productivity while reducing analysis costs. This study examines shortening enantioselective-GC (ES-GC) analysis time following the approaches used in
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| 77011-100MG | 04061832405209 |
| 77011-500MG | 04061832405216 |
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