CAS 106-30-9
:Heptanoato de etilo
Descripción:
Heptanoato de etilo, con el número CAS 106-30-9, es un éster formado a partir de la reacción del ácido heptanoico y el etanol. Se caracteriza por su aroma afrutado, a menudo reminiscentes de manzanas o peras, lo que lo convierte en un agente saborizante común en la industria alimentaria. Heptanoato de etilo es un líquido incoloro a temperatura ambiente y es ligeramente soluble en agua, pero más soluble en disolventes orgánicos como el etanol y el éter. Su fórmula molecular es C9H18O2, y tiene un punto de ebullición relativamente bajo, lo que contribuye a su volatilidad y propiedades fragantes. La sustancia se utiliza no solo en saborizantes alimentarios, sino también en perfumería y como disolvente en diversas aplicaciones químicas. Heptanoato de etilo se considera generalmente seguro para su uso en productos alimenticios, aunque debe manejarse con cuidado debido a su naturaleza inflamable. Su estructura química incluye una larga cadena de hidrocarburos, que contribuye a sus características hidrofóbicas e influye en su comportamiento en diferentes entornos.
Fórmula:C9H18O2
InChI:InChI=1/C38H72N2O12/c1-15-27-38(10,46)31(42)24(6)40(13)19-20(2)17-36(8,45)33(52-35-29(41)26(39(11)12)16-21(3)48-35)22(4)30(23(5)34(44)50-27)51-28-18-37(9,47-14)32(43)25(7)49-28/h20-33,35,41-43,45-46H,15-19H2,1-14H3/t20-,21-,22+,23-,24-,25+,26+,27-,28+,29-,30+,31-,32+,33-,35+,36-,37-,38-/m1/s1
Clave InChI:InChIKey=TVQGDYNRXLTQAP-UHFFFAOYSA-N
SMILES:C(CCCCCC)(OCC)=O
Sinónimos:- (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-2-ethyl-3,4,10-trihydroxy-3,5,6,8,10,12,14-heptamethyl-15-oxo-11-{[3,4,6-trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranosyl]oxy}-1-oxa-6-azacyclopentadecan-13-yl 2,6-dideoxy-3-C-methyl-3-O-methyl-alpha-L-ribo-hexopyranoside
- Aether oenanthicus
- Ai3-24251
- Brn 1752311
- Ccris 1344
- Cognac oil
- Enanthic acid, ethyl ester
- Enanthylic ether
- Ethyl enantate
- Ethyl enanthate
- Ethyl heptanoate (natural)
- Ethyl heptoate
- Ethyl heptylate
- Ethyl n-heptanoate
- Ethyl oenanthate
- Ethyl oenanthylate
- FEMA No. 2437
- Grape oil
- Heptanoic acid, ethyl ester
- Nsc 8891
- Oenanthic ether
- Oleum vitis viniferae
- Wine oil
- 4-02-00-00960 (Beilstein Handbook Reference)
- RARECHEM AL BI 0165
- ethylenantate
- enanthylicether
- Ethyl ester of heptanoic acid
- N-HEPTANOIC ACID ETHYL ESTER
- OENANTHIC ACID ETHYL ESTER
- FEMA 2441
- FEMA 2437
- Ver más sinónimos
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Encontrado 14 productos.
Ethyl Heptanoate
CAS:Fórmula:C9H18O2Pureza:>98.0%(GC)Forma y color:Colorless to Almost colorless clear liquidPeso molecular:158.24Ethyl heptanoate, 98+%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Fórmula:CH3(CH2)5CO2CH2CH3Pureza:98+%Forma y color:Liquid, Clear colorlessPeso molecular:158.24Ethyl heptanoate
CAS:Ethyl heptanoate is a RIFM spice that is produced and volatilized by the fermentation of eight packets of tempeh.Fórmula:C9H18O2Forma y color:SoildPeso molecular:158.24Ethyl Heptanoate(Heptanoic Acid Ethyl Ester)
CAS:Producto controladoFórmula:C9H18O2Forma y color:NeatPeso molecular:158.24Heptanoic Acid Ethyl-d5 Ester
CAS:Producto controladoFórmula:C9H13D5O2Forma y color:NeatPeso molecular:163.27Ethyl Heptanoate(Heptanoic Acid Ethyl Ester)
CAS:Ethyl Heptanoate is a colorless liquid that has a strong odor. It is used as a chemical intermediate in the production of ethyl decanoate, which is an ester. Ethyl Heptanoate is soluble in glycol ether and insoluble in water. It has been shown to be chemically stable under normal conditions, but can decompose at temperatures above 300°C. Ethyl Heptanoate has been used in studies to identify signal pathways that are involved in the regulation of cell growth and proliferation by inhibiting the activity of dibutyltin oxide (DBTO). This study was conducted on K562 cells, which were grown in microcapsules with ethyl heptanoate as the only source of oxygen. The results showed that DBTO inhibited cell proliferation by decreasing the activity of sodium carbonate (NaCO) and inhibiting the formation of ethyl decanoate from ethyl heptanoate and caproic acid (C6Fórmula:C9H18O2Pureza:Min. 95%Peso molecular:158.24 g/mol











