49840-60-0

Basic information

• Product Name: N,N-dimethylpiperidin-1-amine
• Synonyms: 1-piperidinamine, N,N-dimethyl-; N,N-Dimethylpiperidin-1-amine
• CAS NO: 49840-60-0
• Molecular Formula: C₇H₁₆N₂
• Molecular Weight: 128.2153
• Mol File: 49840-60-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 166.1°C at 760 mmHg
• Flash Point: 47.9°C
• Density: 0.92g/cm³
• Vapor Pressure: 1.82mmHg at 25°C
• Refractive Index: 1.49
• PKA: 10.04±0.20(Predicted)
• CAS DataBase Reference: N,N-dimethylpiperidin-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethylpiperidin-1-amine(49840-60-0)
• EPA Substance Registry System: N,N-dimethylpiperidin-1-amine(49840-60-0)

Safety Data

• Hazardous Substances Data: 49840-60-0(Hazardous Substances Data)

Upstream product

• 53779-90-1 dimethylaminopyrrolidine 
• 23337-88-4 1,2-Dipropyl-1,2-dimethylhydrazin 
• 116149-14-5 1,2-di-n-butyldimethylhydrazine 
• 126216-65-7 (2,6-Bis-benzotriazol-1-yl-piperidin-1-yl)-dimethyl-amine 
• 38704-89-1 1,2-dimethylpyrazolidine 
• 6415-12-9 tetramethylhydrazine cation radical 
• 111-30-8 Glutaraldehyde 
• 26163-37-1 N,N'-dimethylpiperidazine 
• 68970-05-8 N,N'-Di-sec-butyl-N,N'-dimethyl-hydrazine 
• 106376-59-4 1,2-di-n-pentyldimethylhydrazine 
• 68970-09-2 N,N'-Bis-(2,2-dimethyl-propyl)-N,N'-dimethyl-hydrazine 
• 6130-94-5 1-(piperidin-1-yl)piperidine 
• 18389-95-2 octahydro-[1,1']bipyrrolyl 

Downstream Products

• 106376-69-6 N,N'-Dipiperidin-Kation-Radikal 
• 106376-72-1 [1,1']Bipiperidinyl 
• 6415-12-9 tetramethylhydrazine 
• 106403-60-5 Dimethyl-pyrrolidin-1-yl-amine 
• 106376-68-5 N,N'-Bis-(2,2-dimethyl-propyl)-N,N'-dimethyl-hydrazine 
• 106376-61-8 1,2-di-n-propyldimethylhydrazine cation radical 
• 106376-65-2 1,2-di-n-butyldimethylhydrazine cation radical 
• 106376-60-7 1,2-di-n-pentyldimethylhydrazine cation radical 
• 38704-89-1 1,2-dimethylpyrazolidine cation radical 
• 106376-73-2 N,N'-Di-sec-butyl-N,N'-dimethyl-hydrazine 
• 26163-37-1 1,2-dimethylhexahydropyridazine cation radical 

Relevant articles and documents

A Novel and Versatile Synthesis of 1-Alkyl-, 1-Aryl-, 1-(Alkylamino)-, or 1-Amido-Substituted and of 1,2,6-Trisubstituted Piperidines from Glutaraldehyde and Primary Amines or Monosubstituted Hydrazines

Various primary amines and 1-mono- and 1,1-disubstituted hydrazines were converted into the corresponding N-substituted piperidines in good to excellent yields via the products of double condensations with benzotriazole and glutaraldehyde.Reduction of the 2,6-bis(benzotriazolyl) N-substituted piperidines 4 and 7 with sodium borohydride in tetrahydrofuran afforded N-substituted piperidines.The benzotriazole moieties were also replaced by alkyl groups by reaction with Grignard reagents to produce 1,2,6-trisubstituted piperidines.