112364
Ethyl heptanoate
ReagentPlus®, 99%
Synonym(s):
Ethyl enanthate
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All Photos(3)
About This Item
Linear Formula:
CH3(CH2)5COOC2H5
CAS Number:
Molecular Weight:
158.24
Beilstein:
1752311
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39022453
PubChem Substance ID:
NACRES:
NA.22
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product line
ReagentPlus®
Assay
99%
refractive index
n20/D 1.412 (lit.)
bp
188-189 °C (lit.)
mp
−66 °C (lit.)
density
0.87 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CCCCCCC(=O)OCC
InChI
1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3
InChI key
TVQGDYNRXLTQAP-UHFFFAOYSA-N
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General description
Ethyl heptanoate, an aroma compound, was released from a series of sodium caseinate-stabilized, n-eicosane emulsions during the investigation of solid and liquid lipid droplet concentration.
Application
Ethyl heptanoate was used in a nickel nanoparticles-catalysed, transfer hydrogenation of olefins.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
165.2 °F - closed cup
Flash Point(C)
74 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Transfer hydrogenation of olefins catalysed by nickel nanoparticles.
Alonso F, et al.
Tetrahedron, 65(51), 10637-10643 (2009)
Supratim Ghosh et al.
Journal of agricultural and food chemistry, 54(5), 1829-1837 (2006-03-02)
Aroma compounds partition between the dispersed and the continuous phases in emulsions, and phase transitions in the lipid droplets profoundly affect the position of the equilibrium. In the present study, the release of ethyl butyrate, ethyl pentanoate, ethyl heptanoate, and
J Enrique Cometto-Muñiz et al.
Experimental brain research, 158(2), 196-206 (2004-04-28)
A series of experiments probed into the degree of chemosensory detection additivity exhibited by mixtures of ethyl propanoate and heptanoate in terms of their trigeminal detectability via nasal pungency (i.e., irritation) and eye irritation. Nasal pungency was tested in subjects
Mohammad Rafienia et al.
Current drug delivery, 6(2), 184-191 (2009-05-20)
In situ forming biodegradable polymeric systems were prepared from Poly (DL-lactide-co-glycolide), RG504H (50:50, lactide:glycolide), RG756 (75:25) and mixture of them. They were dissolved in N-methyl-2-pyrrolidone (33% w/w) and mixed with betamethasone acetate (BTMA, 5 and 10% w/w) and ethyl heptanoate
Monographs on fragrance raw materials.
D L Opdyke
Food and cosmetics toxicology, 19(2), 237-254 (1981-04-01)
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