4-(Isopropylamino)butanol: Properties and Synthesis Methods Explained
4-(Isopropylamino)butanol (CAS: 42042-71-7) is a bifunctional molecule possessing both an alcohol and a secondary amine group, which dictates its chemical reactivity and application potential. Physically, it is described as a colorless to light yellow transparent liquid, with a density of approximately 0.87 g/cm³. Its boiling point is noted at 193.546°C at 760 mmHg, and it has a flash point of 56.161°C, indicating moderate flammability. Solubility in water is also a key characteristic. Several synthesis methods are employed for its production. One common approach involves the reductive amination of 4-amino-1-butanol with acetone, often catalyzed by palladium on activated carbon under a hydrogen atmosphere. This method is generally efficient, yielding the product in good to quantitative yields. Another synthesis route described in patents involves reacting 4-chloro-1-butanol with isopropylamine. Optimizing reaction conditions, such as temperature, pressure, solvent, and catalyst, is crucial for achieving high yields and purity, especially for industrial-scale production. NINGBO INNO PHARMCHEM CO.,LTD. leverages these established synthesis methods, coupled with rigorous quality control, to ensure a reliable supply of high-purity 4-(Isopropylamino)butanol for both pharmaceutical and industrial clients. Understanding these properties and synthesis routes is vital for effective utilization and scale-up in various chemical processes.
Perspectives & Insights
Core Pioneer 24
“leverages these established synthesis methods, coupled with rigorous quality control, to ensure a reliable supply of high-purity 4-(Isopropylamino)butanol for both pharmaceutical and industrial clients.”
Silicon Explorer X
“Understanding these properties and synthesis routes is vital for effective utilization and scale-up in various chemical processes.”
Quantum Catalyst AI
“4-(Isopropylamino)butanol (CAS: 42042-71-7) is a bifunctional molecule possessing both an alcohol and a secondary amine group, which dictates its chemical reactivity and application potential.”