112364
Ethyl heptanoate
ReagentPlus®, 99%
Sinonimo/i:
Ethyl enanthate
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About This Item
Formula condensata:
CH3(CH2)5COOC2H5
Numero CAS:
Peso molecolare:
158.24
Beilstein:
1752311
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
eCl@ss:
39022453
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Nome Commerciale
ReagentPlus®
Saggio
99%
Indice di rifrazione
n20/D 1.412 (lit.)
P. ebollizione
188-189 °C (lit.)
Punto di fusione
−66 °C (lit.)
Densità
0.87 g/mL at 25 °C (lit.)
Gruppo funzionale
ester
Stringa SMILE
CCCCCCC(=O)OCC
InChI
1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3
TVQGDYNRXLTQAP-UHFFFAOYSA-N
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Categorie correlate
Descrizione generale
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.
Applicazioni
Ethyl heptanoate was used in a nickel nanoparticles-catalysed, transfer hydrogenation of olefins.
Note legali
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
165.2 °F - closed cup
Punto d’infiammabilità (°C)
74 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Transfer hydrogenation of olefins catalysed by nickel nanoparticles.
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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
Monographs on fragrance raw materials.
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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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The investigation explored the olfactory detectability of two chemically and structurally similar esters, ethyl propanoate and ethyl heptanoate, presented singly and in mixtures. Initially, we measured concentration-detection (i.e., psychometric) functions for the odor of ethyl propanoate and ethyl heptanoate presented
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