The Chemistry of 1-Bromobutane: Properties, Synthesis, and Reactions
NINGBO INNO PHARMCHEM CO.,LTD. provides an in-depth look at 1-Bromobutane (CAS 109-65-9), exploring its fundamental chemical characteristics, synthesis routes, and the diverse reactions it participates in. This colorless, flammable liquid is a primary haloalkane, making it a reactive and versatile compound essential for many chemical processes.
Chemically, 1-Bromobutane (C4H9Br) is characterized by its molecular weight of 137.02 g/mol. It presents as a colorless, transparent liquid with a purity typically exceeding 99.5%. Its physical properties include miscibility with ethanol, ether, and chloroform, while exhibiting slight solubility in water. Understanding these attributes is crucial for chemists and manufacturers who buy 1-bromobutane online, ensuring optimal handling and application. The acidity and water content are typically kept to very low levels, as indicated by quality standards.
The synthesis of 1-Bromobutane commonly involves the reaction of butanol with hydrobromic acid or the free-radical addition of hydrogen bromide to butene, following anti-Markovnikov addition principles to yield the terminal bromide. These methods are well-established for producing this vital 1-bromobutane chemical intermediate. NINGBO INNO PHARMCHEM CO.,LTD. ensures that its product adheres to stringent quality standards, supporting consistent outcomes in downstream applications.
The reactivity of 1-Bromobutane is primarily driven by its structure as a primary haloalkane, making it highly susceptible to SN2 reactions. This makes it an excellent alkylating agent. Its reaction with magnesium metal to form the Grignard reagent is a classic example of its utility in forming carbon-carbon bonds. It also serves as a precursor for n-butyllithium and can be converted to 1-fluorobutane via reaction with potassium fluoride. For those seeking reliable uses of 1-bromobutane in synthesis, its predictable reactivity is a significant advantage. NINGBO INNO PHARMCHEM CO.,LTD. stands as a premier supplier of this critical chemical.
Perspectives & Insights
Quantum Pioneer 24
“The reactivity of 1-Bromobutane is primarily driven by its structure as a primary haloalkane, making it highly susceptible to SN2 reactions.”
Bio Explorer X
“Its reaction with magnesium metal to form the Grignard reagent is a classic example of its utility in forming carbon-carbon bonds.”
Nano Catalyst AI
“It also serves as a precursor for n-butyllithium and can be converted to 1-fluorobutane via reaction with potassium fluoride.”