What is the Ethyl heptanoate?

Ethyl heptanoate is clear colorless liquid, while it's Molecular Formula is C9H18O2. clear colorless liquid In the manufacture of liqueurs. Plays an important part in the formulation of raspberry, gooseberry, grape, cherry, apricot, currant, bourbon, and other artificial essences.

What is the CAS number for Ethyl heptanoate?

The CAS number of Ethyl heptanoate is 106-30-9.

What is the Ethyl heptanoate?

Ethyl heptanoate is clear colorless liquid, while it's Molecular Formula is C9H18O2. clear colorless liquid In the manufacture of liqueurs. Plays an important part in the formulation of raspberry, gooseberry, grape, cherry, apricot, currant, bourbon, and other artificial essences.

What is the CAS number for Ethyl heptanoate?

The CAS number of Ethyl heptanoate is 106-30-9.

Detailed introduction

Q: What is Ethyl heptanoate (106-30-9) used for?

Ethyl heptanoate is the ester resulting from the condensation of heptanoic acid and ethanol. It is used in the flavor industry because of its odor that is similar to grape.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

Manufacturer supply good quality Ethyl heptanoate 106-30-9 with stock

Molecular Formula:C9H18O2
Molecular Weight:158.241
Appearance/Colour:clear colorless liquid
Vapor Pressure:0mmHg at 25°C
Melting Point:-66 °C(lit.)
Refractive Index:n20/D 1.412(lit.)
Boiling Point:188.3 °C at 760 mmHg
Flash Point:66.1 °C
PSA：26.30000
Density:0.868 g/cm³
LogP:2.51990

Ethyl heptanoate(Cas 106-30-9) Usage

Preparation	By esterification of heptoic acid; by reacting the silver salt of the acid with ethyl-iodide or with ethyl alcohol in the presence of mineral acids.
Flammability and Explosibility	Notclassified
Safety Profile	Low toxicity by ingestion and skin contact. Flammable liquid when exposed to heat, sparks, or flame. When heated to decomposition it emits acrid smoke and irritating fumes.
Definition	ChEBI: The fatty acid ethyl ester of heptanoic acid.
Aroma threshold values	Detection: 2 ppb
Taste threshold values	Taste characteristics at 10 ppm: fruity and waxy with a green winey nuance.
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.

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

106-30-9 Relevant articles

The Pd3(dppm)3 (CO)2+ cluster: An efficient electrochemically assisted Lewis acid catalyst for the fluorination and alcoholysis of acyl chlorides

Lemaitre, Frederic,Lucas, Dominique,Mugnier, Yves,Harvey, Pierre D.

, p. 7537 - 7540 (2002)

The dicationic palladium cluster Pd3(dpp...

-

Takahashi,Y. et al.

, p. 339 - 340 (1978)

Immobilization of palladium acetate on ionic liquid copolymerized polystyrene: A way to eliminate inhibiting effect of imidazolium chloride and enhance catalytic performance

Sugimura, Rie,Kun, Qiao,Tomida, Daisuke,Kume, Yohei,Yokoyama, Chiaki

, p. 874 - 875 (2007)

Immobilization of palladium acetate on a...

Hydroethoxycarbonylation of α-olefins at low pressure of carbon(II) oxide in the presence of the PdCl2(PPh3)2–PPh3–AlCl3 system

Suerbaev, Kh. A.,Kudaibergenov, N. Zh.,Vavasori

, p. 707 - 712 (2017)

High catalytic activity of the PdCl2(PPh...

Sulphonic Acid-induced Fragmentation of Dialkyl Acylphosphonates, Formation of Alkyl Carboxylates and Alkyl Sulphonates

Breuer, Eli,Karaman, Rafik,Goldblum, Amiram,Leader, Haim

, p. 2029 - 2034 (1988)

Heating of dialkyl acylphosphonates with...

Oxidation of Diols and Ethers by NaBrO3/NaHSO3 Reagent

Sakaguchi, Satoshi,Kikuchi, Daisuke,Ishii, Yasutaka

, p. 2561 - 2566 (1997)

NaBrO3 combined with NaHSO3 was found to...

Hydroalkoxycarbonylation of olefins in the presence of palladium phosphine complexes: High activity and regioselectivity

Chepaikin,Bezruchenko,Suerbaev,Shalmagambetov

, p. 117 - 121 (2006)

Several types of catalyst systems were e...

Aldehydes α-iodes (I): preparation, constantes physico-chimiques et quelques proprietes chimiques

Riehl,Fougerousse,Lamy

, p. 4415 - 4416 (1968)

Palladium complexes with N-heterocyclic carbene ligands as catalysts for the alkoxycarbonylation of olefins

Roberts, Gina M.,Pierce, Philip J.,Woo, L. Keith

, p. 2033 - 2036 (2013)

Palladium catalysts, generated from Pd(O...

Cloning and expression of a Baeyer-Villiger monooxygenase oxidizing linear aliphatic ketones from Dietzia sp. D5

Bisagni, Serena,Smus?, Justyna,Chávez, Georgina,Hatti-Kaul, Rajni,Mamo, Gashaw

, p. 161 - 169 (2014)

A Baeyer-Villiger monooxygenase has been...

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Rogic,M.M. et al.

, p. 3848 - 3850 (1975)

Design, Synthesis, and Study of the Insecticidal Activity of Novel Steroidal 1,3,4-Oxadiazoles

Bai, Hangyu,Jiang, Weiqi,Li, Qi,Li, Tian,Ma, Shichuang,Shi, Baojun,Wu, Wenjun

, p. 11572 - 11581 (2021/10/12)

A series of novel steroidal derivatives ...

Alkoxydiaminophosphine Ligands as Surrogates of NHCs in Copper Catalysis

Pizarro, Juan Diego,Molina, Francisco,Fructos, Manuel R.,Pérez, Pedro J.

supporting information, p. 10330 - 10335 (2020/07/24)

A family of phosphine ligands containing...

Gold Complexes with ADAP Ligands: Effect of Bulkiness in Catalytic Carbene Transfer Reactions (ADAP = Alkoxydiaminophosphine)

Fructos, Manuel R.,Molina, Francisco,Pérez, Pedro J.,Pizarro, Juan Diego

supporting information, (2020/07/14)

A family of gold(I) complexes of composi...

Manganese-Catalyzed Electrochemical Deconstructive Chlorination of Cycloalkanols via Alkoxy Radicals

Allen, Benjamin D. W.,Hareram, Mishra Deepak,Seastram, Alex C.,McBride, Tom,Wirth, Thomas,Browne, Duncan L.,Morrill, Louis C.

supporting information, p. 9241 - 9246 (2019/11/19)

A manganese-catalyzed electrochemical de...

106-30-9 Process route

: 64-17-5
ethanol

: 111-26-2
hexan-1-amine

: 201230-82-2
carbon monoxide

: 123-66-0
Ethyl hexanoate

: 539-82-2
ethyl n-valerate

: 106-30-9
ethyl heptanoate

: 7451-47-0
N-hexylcarbamic acid ethyl ester

Conditions

Conditions	Yield
With oxygen; Sulfate; zirconium(IV) oxide; palladium dichloride; at 170 ℃; for 3h; under 45003.6 Torr; Further byproducts given. Title compound not separated from byproducts;	81%

: 925-78-0
3-nonanone

: 2445-76-3
n-hexyl propionate

: 106-30-9
ethyl heptanoate