Date published: 2025-10-19

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Methyl hexanoate (CAS 106-70-7)

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Alternate Names:
Caproic acid methyl ester; Methyl caproate
CAS Number:
106-70-7
Molecular Weight:
130.18
Molecular Formula:
C7H14O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl hexanoate, bearing the CAS number 106-70-7, is an ester formed from the reaction of hexanoic acid and methanol. Characterized by its fruity odor, often compared to that of apples and pineapples, it is prominently used in the flavor and fragrance industries to enhance the aroma profile of various products. Beyond its commercial utility, methyl hexanoate is an important subject in chemical research, especially in studies focused on esterification reactions, a fundamental aspect of organic chemistry. This ester exemplifies the process whereby carboxylic acids react with alcohols in the presence of an acid catalyst to yield esters and water, providing a simple system for investigating reaction mechanisms, kinetics, and catalyst effects. In research settings, methyl hexanoate is utilized to study the dynamics of ester formation and breakdown, offering insights into the stability and reactivity of ester bonds under different environmental conditions and in various solvents. Additionally, due to its volatile nature, methyl hexanoate is used in the field of analytical chemistry as a standard compound for developing and refining techniques in gas chromatography and mass spectrometry, aimed at detecting and quantifying organic compounds with precision. This makes it particularly valuable in studies related to environmental emissions of volatile organic compounds and their impact on air quality.


Methyl hexanoate (CAS 106-70-7) References

  1. Modeling of the oxidation of methyl esters-Validation for methyl hexanoate, methyl heptanoate, and methyl decanoate in a jet-stirred reactor.  |  Glaude, PA., et al. 2010. Combust Flame. 157: 2035-2050. PMID: 23710076
  2. Volatile compounds from thermally oxidized methyl oleate.  |  Withycombe, DA., et al. 1971. Lipids. 6: 758-62. PMID: 27519208
  3. The aroma volatile repertoire in strawberry fruit: a review.  |  Yan, JW., et al. 2018. J Sci Food Agric. 98: 4395-4402. PMID: 29603275
  4. Engineered P450 BM3 and cpADH5 coupled cascade reaction for β-oxo fatty acid methyl ester production in whole cells.  |  Ensari, Y., et al. 2020. Enzyme Microb Technol. 138: 109555. PMID: 32527525
  5. Extreme Low-Temperature Combustion Chemistry: Ozone-Initiated Oxidation of Methyl Hexanoate.  |  Rousso, AC., et al. 2020. J Phys Chem A. 124: 9897-9914. PMID: 33174431
  6. Aromatypicity of Austrian Pinot Blanc Wines.  |  Philipp, C., et al. 2020. Molecules. 25: PMID: 33287238
  7. Biosynthesis and emission of methyl hexanoate, the major constituent of floral scent of a night-blooming water lily Victoriacruziana.  |  Jiang, Y., et al. 2021. Phytochemistry. 191: 112899. PMID: 34481346
  8. Strawberry fruit FanCXE1 carboxylesterase is involved in the catabolism of volatile esters during the ripening process.  |  Martínez-Rivas, FJ., et al. 2022. Hortic Res. 9: uhac095. PMID: 35795396
  9. Evaluation of FAU-type Zeolite Membrane Stability in Transesterification Reaction Conditions.  |  Ikeda, A., et al. 2023. Membranes (Basel). 13: PMID: 36676875
  10. Effect of drainage ratio during strawberry cultivation:The volatilomics-based shelf-life indicators for strawberry fruit.  |  Cho, JY., et al. 2023. Front Plant Sci. 14: 1124827. PMID: 37025137

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl hexanoate, 1 kg

sc-215354
1 kg
$85.00

Methyl hexanoate, 4 kg

sc-215354A
4 kg
$242.00