• 1. Correlating supercritical fluid extraction parameters with volatile compounds from Finnish wild mushrooms (Craterellus tubaeformis) and yield prediction by partial least squares regression analysis
  Xiao Chen,Nghia Huynh,Heping Cui,Peng Zhou,Xiaoming Zhang,Baoru Yang RSC Adv. 2018 8 5233
• 2. Correlating supercritical fluid extraction parameters with volatile compounds from Finnish wild mushrooms (Craterellus tubaeformis) and yield prediction by partial least squares regression analysis
  Xiao Chen,Nghia Huynh,Heping Cui,Peng Zhou,Xiaoming Zhang,Baoru Yang RSC Adv. 2018 8 5233
• 3. Biosynthesis of insect spiroacetals
  Yvonne K. Booth,William Kitching,James J. De Voss Nat. Prod. Rep. 2009 26 490
• 4. Alteration of intermolecular interactions between units of asphaltene dimers exposed to an amide-enriched modifier
  Masoumeh Mousavi,Farideh Pahlavan,Daniel Oldham,Tahereh Abdollahi,Ellie H. Fini RSC Adv. 2016 6 53477
• 5. A diverse suite of spiroacetals, including a novel branched representative, is released by female Bactrocera tryoni (Queensland fruit fly)
  Yvonne K. Booth,Brett D. Schwartz,Mary T. Fletcher,Lynette K. Lambert,William Kitching,James J. De Voss Chem. Commun. 2006 3975

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Acetamides

N-(3-Methylbutyl)acetamide: A Comprehensive Overview

N-(3-Methylbutyl)acetamide, also known by its CAS number 13434-12-3, is a versatile organic compound with significant applications in various industries. This compound is a member of the acetamide family, characterized by its amide functional group and its ability to act as a solvent, plasticizer, and additive in different chemical processes. The molecular structure of N-(3-Methylbutyl)acetamide consists of an acetyl group attached to a 3-methylbutyl chain, making it a branched amide with unique physical and chemical properties.

The synthesis of N-(3-Methylbutyl)acetamide typically involves the reaction of acetyl chloride with 3-methylbutylamine in the presence of a base. This reaction yields a pure product that is widely used in industrial settings due to its stability and compatibility with various substrates. Recent studies have highlighted the potential of this compound in enhancing the performance of polymeric materials, particularly in terms of improving their thermal stability and mechanical properties.

One of the most notable applications of N-(3-Methylbutyl)acetamide is in the formulation of adhesives and coatings. Its ability to act as a plasticizer makes it an ideal additive for modifying the rheological properties of polymer-based systems. Researchers have demonstrated that incorporating N-(3-Methylbutyl)acetamide into polyurethane formulations can significantly improve their flexibility and resistance to environmental factors such as temperature fluctuations and UV exposure.

In addition to its industrial applications, N-(3-Methylbutyl)acetamide has also found relevance in the field of biotechnology. Recent advancements have explored its use as a solvent in protein crystallization studies, where its ability to dissolve hydrophobic molecules has proven beneficial for structural analysis. This compound's role in facilitating the crystallization process has opened new avenues for studying enzyme mechanisms and developing novel therapeutic agents.

The environmental impact of N-(3-Methylbutyl)acetamide has also been a subject of recent research. Studies have shown that this compound exhibits low toxicity to aquatic organisms, making it a safer alternative to traditional solvents in certain industrial processes. Furthermore, its biodegradability under aerobic conditions suggests that it can be effectively integrated into sustainable chemical practices.

Looking ahead, the demand for N-(3-Methylbutyl)acetamide is expected to grow as industries continue to seek eco-friendly alternatives for their chemical processes. Its unique combination of physical properties and compatibility with various materials positions it as a key player in the development of next-generation materials and technologies.

• 69131-12-0(Acetamide, N-[(2-methylcyclopentyl)methyl]-, trans- (9CI))
• 64317-66-4(Capsiamide)
• 855880-21-6(Acetamide,N-(3-ethylheptyl)-)
• 25651-96-1(Acetamide,N-(2-ethylhexyl)-)
• 5699-41-2(N-(4-Aminobutyl)Acetamide)
• 54824-90-7(N-(2-methylbutyl)acetamide)
• 1119-49-9(Acetamide, N-butyl-)
• 76526-42-6(N-butyl-3-methylbutanamide)
• 70924-83-3(N-[[4-(acetamidomethyl)cyclohexyl]methyl]acetamide)
• 69131-27-7(Acetamide, N-[(2-methylcyclopentyl)methyl]-, cis- (9CI))