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112364

Sigma-Aldrich

Ethyl heptanoate

ReagentPlus®, 99%

Sinónimos:

Ethyl enanthate

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About This Item

Fórmula lineal:
CH3(CH2)5COOC2H5
Número de CAS:
106-30-9
Peso molecular:
158.24
Beilstein/REAXYS Number:
1752311
EC Number:
203-382-9
MDL number:
MFCD00009538
UNSPSC Code:
12352100
eCl@ss:
39022453
PubChem Substance ID:
24847090
NACRES:
NA.22

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

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

165.2 °F - closed cup

flash_point_c

74 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificados de análisis (COA)

Lot/Batch Number
SHBS3707
SHBQ5662
SHBQ9552
SHBP7808
SHBP6565

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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
Monographs on fragrance raw materials.
D L Opdyke
Food and cosmetics toxicology, 19(2), 237-254 (1981-04-01)
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
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