104-50-7

  • Product NameGAMMA-OCTALACTONE
  • Molecular FormulaC8H14O2
  • Molecular Weight142.198
  • Purity99%
  • AppearanceColorless to yellowish oily shape liquid
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Product Details

Quick Details

  • CasNo: 104-50-7
  • Molecular Formula: C8H14O2
  • Appearance: Colorless to yellowish oily shape liquid
  • Purity: 99%

High Purity 99% Chinese Manufacturer Supply GAMMA-OCTALACTONE 104-50-7 Competitive Price

  • Molecular Formula:C8H14O2
  • Molecular Weight:142.198
  • Appearance/Colour:Colorless to yellowish oily shape liquid 
  • Vapor Pressure:0.0408mmHg at 25°C 
  • Melting Point:91 °C(Solv: ethanol (64-17-5)) 
  • Refractive Index:n20/D 1.444(lit.)  
  • Boiling Point:239.124 °C at 760 mmHg 
  • Flash Point:91.876 °C 
  • PSA:26.30000 
  • Density:0.981 g/cm3 
  • LogP:1.88220 

gamma-Octanoic lactone(Cas 104-50-7) Usage

Description

y-Octalactone has a strong, fruity odor reminiscent of coconut with a very sweet taste. This substance may be prepared synthetically from epoxy-1,2-hexane and sodio-malonic ester; after saponification the oxyacid is extracted with ether and is lactonized.

Chemical Properties

γ-Octalactone has a fruity odor reminiscent of coconut and a very sweet taste.

Occurrence

Reported found in apricot, peach, blue cheese, butter, cooked chicken and cooked pork, licorice, milk, raspberry, roasted barley, and roasted filbert.

Uses

4-Octanolide is one of the fine organic aerosol emitted from meat cooking operations that was examined by high-resolution gas chromatography.

Aroma threshold values

Detection: 7 ppb; aroma characteristics at 1.0%: sweet, fatty, creamy, coconut, lactonic and coumarinic.

Taste threshold values

Taste characteristics at 1 to 10 ppm: coconut, fatty, creamy, coumarinic, with a strong creamy and waxy mouthfeel.

Synthesis Reference(s)

Chemistry Letters, 23, p. 53, 1994The Journal of Organic Chemistry, 52, p. 4319, 1987 DOI: 10.1021/jo00228a032Tetrahedron Letters, 19, p. 419, 1978 DOI: 10.1016/S0040-4039(01)91443-1

General Description

γ--Octalactone is one of the flavor constituents of peaches, oranges and sweet fortified wines.

Flammability and Explosibility

Notclassified

Safety Profile

Mildly toxic by ingestion. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Synthesis

Prepared synthetically from epoxy-1,2-hexane and sodio-malonic ester; after saponification, the oxyacid is extracted with ether and is lactonized.

InChI:InChI=1/C8H14O2/c1-2-3-4-7-5-6-8(9)10-7/h7H,2-6H2,1H3/t7-/m0/s1

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Benzoyl peroxide-catalyzed free radical ...

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The benzoyl peroxide-catalyzed reaction ...

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A general synthesis of (+)-γ-substituted γ-butyrolactones using a kinetic alkylation-ozonolysis procedure

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Kabasakalian,Townley

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A mild biosynthesis of lactones via enantioselective hydrolysis of hydroxynitriles

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We have developed a biocatalytic method ...

OXIDATIVE ADDITION OF 1,3-DICARBONYL COMPOUNDS TO OLEFINS BY THE ACTION OF THE Mn(OAc)3/LiCl SYSTEM AND THE SYNTHESIS OF FUNCTIONALLY SUBSTITUTED CYCLOPROPANES

Vinogradov, M. G.,Dolinko, V. I.,Nikishin, G. I.

, p. 334 - 341 (1984)

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Calcium(II)- And Triflimide-Catalyzed Intramolecular Hydroacyloxylation of Unactivated Alkenes in Hexafluoroisopropanol

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We report an efficient intramolecular hy...

Photocatalytic Synthesis of γ-Lactones from Alkenes: High-Resolution Mass Spectrometry as a Tool to Study Photoredox Reactions

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A mild photocatalytic manifold for the s...

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104-50-7 Process route

Octanoic acid
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Octanoic acid

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6-propyl-tetrahydro-pyran-2-one

gamma-octalactone
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gamma-octalactone

1-Chloroheptane
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1-Chloroheptane

Conditions
Conditions Yield
With sodium persulfate; In water; at 85 - 90 ℃; for 5h;
30%
23%
12%
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89701-68-8

5-Acetoxyoctannitril

6-propyl-tetrahydro-pyran-2-one
698-76-0

6-propyl-tetrahydro-pyran-2-one

gamma-octalactone
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gamma-octalactone

Conditions
Conditions Yield
With sulfuric acid; at 130 ℃; Yields of byproduct given;
63%

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