Production Method 1

110-42-9

112-63-0

1731-88-0

1937-62-8

112-39-0

301-00-8

111-82-0

2734-47-6

1120-25-8

75190-82-8

124-10-7

112-62-9

2733-88-2

2390-09-2

90176-52-6

112-61-8

Reaction Conditions

1.1 Catalysts: Water ;  4 h, 22 bar, 175 °C

Reference

In situ biodiesel production from wet Chlorella vulgaris under subcritical condition

Tsigie, Yeshitila Asteraye; Huynh, Lien Huong; Ismadji, Suryadi; Engida, Adam Mekonnen; Ju, Yi-Hsu, Chemical Engineering Journal (Amsterdam, 2012, 213, 104-108

Methyl decanoate Preparation Products

• Methyl linoleate (112-63-0)
• Methyl tridecanoate (1731-88-0)
• Methyl Elaidate Standard (1937-62-8)
• Methyl palmitate (112-39-0)
• Methyl Linolenate (301-00-8)
• Methyl laurate (111-82-0)
• Methyl decanoate (110-42-9)
• Eicosapentaenoic acid methyl ester (2734-47-6)
• METHYL PALMITOLEATE (1120-25-8)
• (10Z)-10-Heptadecenoic Acid Methyl Ester (75190-82-8)
• Methyl myristate (124-10-7)
• Methyl oleate (112-62-9)
• Methyl Nervonate (2733-88-2)
• Methyl cis-11-Eicosenoate (2390-09-2)
• 10-Pentadecenoic acid,methyl ester, (10Z)- (90176-52-6)
• Methyl stearate (112-61-8)

• 1. Efficient ruthenium-catalysed oxidative cleavage of methyl oleate with hydrogen peroxide as oxidant
  Arno Behr,Nils Tenhumberg,Andreas Wintzer RSC Adv. 2013 3 172
• 2. Extraction optimization and pixel-based chemometric analysis of semi-volatile organic compounds in groundwater
  Peter Christensen,Giorgio Tomasi,Mette Kristensen,Peter E. Holm,Jan H. Christensen Anal. Methods 2017 9 5970
• 3. Microbial production of sebacic acid from a renewable source: production, purification, and polymerization
  Woo-Young Jeon,Min-Jeong Jang,Gyu-Yeon Park,Hye-Jeong Lee,Sung-Hwa Seo,Hee-Suk Lee,Changpyo Han,Heeun Kwon,Ho-Chang Lee,Jong-Hwa Lee,Yong-Taek Hwang,Myung-Ock Lee,Jeong-Gyu Lee,Hong-Weon Lee,Jung-Oh Ahn Green Chem. 2019 21 6491
• 4. Influence of Moringa oleifera biodiesel–diesel–hexanol and biodiesel–diesel–ethanol blends on compression ignition engine performance, combustion and emission characteristics
  Selvakumar Ramalingam,N. V. Mahalakshmi RSC Adv. 2020 10 4274
• 5. One-pot hydrodeoxygenation of biomass furan derivatives into decane under mild conditions over Pd/C combined with phosphotungstic acid
  Song Li,Long Yan,Qiying Liu,Jianguo Liu,Qiyu Liu,Wei Fan,Xuelai Zhao,Xinghua Zhang,Chenguang Wang,Longlong Ma,Qi Zhang Green Chem. 2020 22 2889

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid methyl esters
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid esters Fatty acid methyl esters
• Pesticide Chemicals Pesticide Active Ingredients Standard Substances
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Methyl Decanoate (CAS No. 110-42-9): Applications and Recent Research Developments

Methyl Decanoate, with the chemical formula C??H??O? and CAS number 110-42-9, is an ester derived from decanoic acid and methanol. This compound is widely recognized for its utility in various industrial and scientific applications, ranging from fragrances and solvents to pharmaceutical intermediates. The increasing interest in methyl decanoate stems from its unique chemical properties and its potential in advancing multiple fields of study.

The structural characteristics of methyl decanoate make it an attractive candidate for research in chemical synthesis and material science. Its linear aliphatic chain and ester functional group contribute to its solubility in organic solvents, making it a valuable component in formulating coatings, adhesives, and specialty chemicals. Moreover, the compound's relatively low volatility compared to other esters enhances its stability in formulations requiring prolonged shelf life.

In recent years, significant research has focused on the applications of methyl decanoate in pharmaceuticals. Studies have demonstrated its potential as a solvent and excipient in drug formulations, particularly for oral and topical medications. The compound's ability to enhance the bioavailability of certain active pharmaceutical ingredients (APIs) has been a subject of interest among medicinal chemists. For instance, research published in Journal of Pharmaceutical Sciences highlights the use of methyl decanoate in improving the solubility of poorly water-soluble drugs, thereby facilitating their absorption and efficacy.

The role of methyl decanoate in fragrance chemistry is another area where it has garnered attention. Its pleasant, fruity odor profile makes it a popular choice in perfumes, colognes, and personal care products. Researchers have been exploring ways to incorporate methyl decanoate into eco-friendly fragrance compositions, aligning with the growing demand for sustainable chemical products. A study published in Flavor and Fragrance Journal describes the synthesis of biodegradable fragrance blends that include methyl decanoate as a key component, demonstrating its versatility beyond traditional applications.

Advances in polymer science have also leveraged methyl decanoate as a monomer or modifier in the synthesis of novel polymers. Its incorporation into polymeric matrices can enhance thermal stability and mechanical properties, making it useful in high-performance materials. For example, researchers at the University of California have developed a series of thermoplastic elastomers that incorporate methyl decanoate to improve flexibility and durability. These findings were presented at the annual meeting of the American Chemical Society, showcasing the compound's potential in advanced material engineering.

The agricultural sector has not been left out of the benefits derived from methyl decanoate. Its use as a plant growth regulator has been investigated due to its ability to stimulate root development and stress resistance in crops. A recent study published in Plant Physiology suggests that methyl decanoate can enhance photosynthetic efficiency when applied as a foliar spray, potentially leading to higher yields in agricultural practices. This application aligns with global efforts to develop sustainable agricultural solutions that improve crop productivity without relying on synthetic chemicals.

The environmental impact of methyl decanoate has also been a focus of research. Studies have assessed its biodegradability and toxicity profiles to ensure its safe use in industrial processes. A comprehensive toxicological evaluation by the European Chemicals Agency (ECHA) has classified methyl decanoate as having low acute toxicity, reinforcing its suitability for widespread applications. Furthermore, efforts are underway to develop greener synthetic routes for producing methyl decanoate, reducing reliance on energy-intensive processes.

In conclusion, methyl decanoate (CAS No. 110-42-9) is a multifunctional compound with diverse applications across multiple industries. Its role in pharmaceuticals, fragrances, polymer science, agriculture, and environmental sustainability underscores its importance as a chemical intermediate. As research continues to uncover new uses for this compound, its significance is expected to grow further, driving innovation and sustainability across various scientific domains.

• 40710-36-9(Nonahexacontanoic acid methyl ester)
• 40710-34-7(Methyl pentacontanoate)
• 40710-35-8(Methyl hexacontanoate)
• 68052-55-1(Hexanedioicacid,dimethylester,polymerwithdimethylbutanedioate,dimethylpentanedioateand1,2-ethanediol)
• 52546-36-8(5-Methoxypentanoic acid methyl ester)
• 24397-43-1(Dimethyl triacontanedioate)
• 40710-33-6(Methyl hentetracontanoate)
• 55334-47-9(Octadecanoic acid, 18-methoxy-, methyl ester)
• 56599-84-9(METHYL OCTADECANOATE-13C18)
• 1931-69-7(Methyl 15-oxopentadecanoate)