4104-44-3

Usage

Uses

Used in Agricultural Chemicals Production:
METHYL ISOAMYLAMINE is used as an intermediate for the synthesis of various agricultural chemicals, contributing to the development of products that enhance crop protection and yield.
Used in Pharmaceuticals Production:
In the pharmaceutical industry, METHYL ISOAMYLAMINE serves as an intermediate, playing a crucial role in the manufacturing process of different medicinal compounds, thereby aiding in the treatment and management of various health conditions.
Used in Rubber Chemicals Production:
METHYL ISOAMYLAMINE is utilized as an intermediate in the production of rubber chemicals, which are essential for improving the performance and durability of rubber products.
Used as a Corrosion Inhibitor:
METHYL ISOAMYLAMINE is employed as a corrosion inhibitor, helping to protect metal surfaces from degradation and extending the lifespan of industrial equipment and structures.
Used as a Flotation Agent:
In the mining industry, METHYL ISOAMYLAMINE is used as a flotation agent to enhance the separation of valuable minerals from waste materials, improving the efficiency of mineral processing operations.
Used as a Reagent in Organic Synthesis:
METHYL ISOAMYLAMINE is utilized as a reagent in organic synthesis, facilitating various chemical reactions that lead to the creation of new organic compounds for a wide range of applications.

InChI:InChI=1/C6H15N/c1-6(2)4-5-7-3/h6-7H,4-5H2,1-3H3

Upstream product

• 3060-46-6 N-methylleucine 
• 10285-87-7 N-isopentyl-formamide 
• 74-89-5 methylamine 
• 590-86-3 isovaleraldehyde 
• 107-85-7 1-amino-3-methylbutane 
• 74-88-4 methyl iodide 
• 110-88-3 1,3,5-Trioxan 
• 124-40-3 dimethyl amine 
• 115-11-7 isobutene 

Downstream Products

• 52317-69-8 3-(2,4-Dimethyl-phenyl)-1-methyl-1-(3-methyl-butyl)-thiourea 
• 52317-44-9 3-(4-Chloro-2-methyl-phenyl)-1-methyl-1-(3-methyl-butyl)-thiourea 
• 52317-95-0 3-(4-Fluoro-2-methyl-phenyl)-1-methyl-1-(3-methyl-butyl)-thiourea 
• 64796-61-8 3-[1-(3-Chloro-phenyl)-1-methyl-ethyl]-1-methyl-1-(3-methyl-butyl)-urea 
• 1224595-24-7 (S)-2-fluoro-6-(2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoethoxy)-N-isopentyl-N-methylbenzamide 
• 1450631-09-0 C₁₅H₂₀F₃NO₂ 

Relevant academic research and scientific papers

Competing Hydride Transfer and Ene Reactions in the Aminoalkylation of 1-Alkenes with N,N-Dimethylmethyleniminium Ions. A Literature Correction

A literature report that N,N-dimethylmethyleniminium ion (2) reacts with propylene and styrene to form unsaturated tertiary amines is shown to be incorrect.The major products are the secondary amines 1-(methylamino)butane and 1-(methylamino)-3-phenylpropane in which N-demethylation has occurred along with the saturation of the alkene.Analogous major products are formed with 1-butene, 1-hexene, 1-octene, 1-dodecene, 1-tetradecene, p-methylstyrene, and m-nitrostyrene as substrates.When the substrates are isobutylene, 2-ethyl-1-hexene, α-methylstyrene, and p-methoxystyrene, the major products are tertiary amines, but the secondary amines are also formed in smaller yields.The small yields of tertiary amines obtained in the cases of styrene and p-methylstyrene were increased by going from solvent acetic acid to acetonitrile and by increasing the branching of the alkyl groups on nitrogen.The internal olefins 5-decene and cyclohexene were far less reactive, giving only 3-4percent of amine products that were mainly tertiary in the former case and secondary in the latter.It is concluded that tertiary amine products are favored by an alkene structure and a solvent that favors the formation of a stable carbenium ion intermediate or a transition state with substantial carbenium ion character upon electrophilic attack of the iminium ion on the alkene.The secondary amine products are favored when a carbenium ion is of low stability and when the β-carbon atom of the olefin and/or the alkyl group attached to nitrogen is sterically unhindered; such hindrance decreases the rate of hydride ion transfer that is believed to occur in the production of secondary amines.