15959-40-7 Usage
Description
N-butyldioctylamine, also known as octyldibutylamine, is a chemical compound belonging to the amine class. It is synthesized from the reaction of butanol with octylamine and is recognized for its capacity to form a protective layer on metal surfaces, thereby serving as an effective corrosion inhibitor. N-butyldioctylamine also functions as a catalyst and intermediate in the synthesis of other chemicals, such as surfactants and lubricants, showcasing its versatility and value in various industrial applications.
Uses
Used in Oil and Gas Production Industry:
N-butyldioctylamine is used as a corrosion inhibitor to protect metal surfaces from corrosion, thereby extending the lifespan of equipment and infrastructure. Its application in this industry is crucial for maintaining the integrity and efficiency of oil and gas production processes.
Used in Chemical Production:
N-butyldioctylamine serves as a catalyst and intermediate in the production of various chemicals, including surfactants and lubricants. Its role in these processes enhances the efficiency and effectiveness of chemical synthesis, contributing to the development of a range of industrial and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 15959-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,5 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15959-40:
(7*1)+(6*5)+(5*9)+(4*5)+(3*9)+(2*4)+(1*0)=137
137 % 10 = 7
So 15959-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H43N/c1-4-7-10-12-14-16-19-21(18-9-6-3)20-17-15-13-11-8-5-2/h4-20H2,1-3H3
15959-40-7Relevant articles and documents
Ruthenium-catalyzed direct amination of alcohols with tertiary amines
Luo, Jiaying,Wu, Mingyue,Xiao, Fuhong,Deng, Guojun
experimental part, p. 2706 - 2709 (2011/06/19)
A highly selective phosphine-based ruthenium catalyst system efficiently catalyzes the direct amination of alcohols with aliphatic tertiary amines, yielding unsymmetric tertiary amines in yields up to 87%. Ligand and solvent both affect the reaction yields significantly. The reaction can be performed with a wide variety of functionalities.
