112364
Ethyl heptanoate
ReagentPlus®, 99%
Sinônimo(s):
Ethyl enanthate
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About This Item
Fórmula linear:
CH3(CH2)5COOC2H5
Número CAS:
Peso molecular:
158.24
Beilstein:
1752311
Número CE:
Número MDL:
Código UNSPSC:
12352100
eCl@ss:
39022453
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
linha de produto
ReagentPlus®
Ensaio
99%
índice de refração
n20/D 1.412 (lit.)
p.e.
188-189 °C (lit.)
pf
−66 °C (lit.)
densidade
0.87 g/mL at 25 °C (lit.)
grupo funcional
ester
cadeia de caracteres SMILES
CCCCCCC(=O)OCC
InChI
1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3
chave InChI
TVQGDYNRXLTQAP-UHFFFAOYSA-N
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Descrição geral
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.
Aplicação
Ethyl heptanoate was used in a nickel nanoparticles-catalysed, transfer hydrogenation of olefins.
Informações legais
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
165.2 °F - closed cup
Ponto de fulgor (°C)
74 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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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
Monographs on fragrance raw materials.
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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
J Enrique Cometto-Muñiz et al.
Behavioural brain research, 156(1), 115-123 (2004-10-12)
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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