30673-60-0

Usage

Uses

Used in Flavor and Fragrance Industry:
N-PROPYL DECANOATE is used as a flavoring agent for its mild, fruity odor, adding a pleasant aroma to various products such as perfumes, colognes, and other fragrances.
Used in Pharmaceutical Industry:
N-PROPYL DECANOATE is used as a solvent or excipient in the formulation of pharmaceutical products, particularly in the development of drug delivery systems. Its ability to dissolve various active ingredients makes it a valuable component in the production of medications.
Used in Cosmetics Industry:
N-PROPYL DECANOATE is used as an emollient, solvent, and viscosity-increasing agent in the cosmetics industry. It helps improve the texture, consistency, and stability of cosmetic products, providing a smooth and luxurious feel to the skin.
Used in Lubricants Industry:
N-PROPYL DECANOATE is used as a component in the formulation of lubricants, particularly in the production of personal lubricants. Its non-greasy texture and ability to reduce friction make it an ideal choice for this application.
Used in Plastics and Polymer Industry:
N-PROPYL DECANOATE is used as a plasticizer in the plastics and polymer industry, enhancing the flexibility and workability of various materials. It is particularly useful in the production of films, coatings, and adhesives.
Used in Research and Development:
N-PROPYL DECANOATE is used as a reagent and intermediate in the synthesis of various organic compounds, contributing to the advancement of research and development in the chemical and pharmaceutical industries.

InChI:InChI=1/C13H26O2/c1-3-5-6-7-8-9-10-11-13(14)15-12-4-2/h3-12H2,1-2H3

Upstream product

• 71-23-8 propan-1-ol 
• 334-48-5 1-decanoic acid 
• 112-13-0 n-decanoyl chloride 
• 1956-09-8 4-nitrophenyl decanoate 
• 124-11-8 non-1-ene 
• 201230-82-2 carbon monoxide 

Relevant academic research and scientific papers

Efficient microwave-assisted esterification reaction employing methanesulfonic acid supported on alumina as catalyst

A rapid and efficient protocol assisted by microwave irradiation for the synthesis of esters using methanesulfonic acid (CH3SO3H) supported on Al2O3 (AMA) as catalyst and free of solvent is described. The products were obtained in good yields and purity, with reduced reaction time, and the process is simple and environmentally benign. Copyright

Specific enzyme-catalyzed hydrolysis and synthesis in aqueous and organic medium using biocatalysts with lipase activity from Aspergillus niger MYA 135

In the present study, the specific hydrolytic activity of three biocatalysts such as the constitutive mycelium-bound lipase, the induced mycelium-bound lipase and the lyophilized induced supernatant from A. niger MYA 135 was evaluated in both aqueous and organic media.A direct correlation between activity in water and n-hexane was not observed for the same hydrolytic reaction. The n-hexane/water activity ratio (RO/A) was applied to characterize the activity in organic medium. The three biocatalysts showed RO/A values higher than 1 for hydrolysis of long-chain fatty acid esters, demonstrating a higher specific hydrolytic activity in organic solvent than in water. A different behavior was observed during hydrolysis of middle-chain fatty acid esters, which was higher in aqueous medium (R O/Adw) observed in a reaction mixture containing propanol and p-nitrophenyl laurate. Finally, both p-nitrophenyl caprate (C10) and p-nitrophenyl laurate (C12) were preferentially methanolized by the lyophilized induced supernatant, being this lipase activity the most specific biocatalyst preparation under transesterification conditions. A selectivity-based analysis of each lipase preparation toward transesterification or hydrolysis in organic medium was evaluated as well. Springer Science+Business Media, LLC 2012.

Synthesis, antimicrobial evaluation, QSAR and in silico ADMET studies of decanoic acid derivatives

Various derivatives of decanoic acid (CD) have been synthesized and evaluated against Gram positive B. subtilis, S. aureus and Gram negative E. coli bacteria as well as against fungi C. albicans and A. niger. Quantitative structure activity relationship (QSAR) models for antimicrobial activities were developed using multiple linear regression and cross validated by leave one out (LOO) approach. QSAR studies indicated that activity against Gram positive bacteria was governed by lipophilicity of the compounds while topological steric nature of the molecule was deciding factor for antifungal activity. Further, in silico ADMET studies showed that compounds CD12, 19, 20 and 23 could be explored further for other activities.