4-Aminomethyl-1-N-butylpiperidine

Base Information

• Chemical Name: 4-Aminomethyl-1-N-butylpiperidine
• CAS No.: 65017-57-4
• Molecular Formula: C10H22 N2
• Molecular Weight: 170.3
• Hs Code.: 2933399090
• European Community (EC) Number: 676-089-0
• DSSTox Substance ID: DTXSID10439903
• Wikidata: Q72514536

Synonyms:65017-57-4;4-Aminomethyl-1-N-butylpiperidine;4-(Aminomethyl)-1-(n-butyl)piperidine;(1-butylpiperidin-4-yl)methanamine;4-Aminomethyl-1-(n-butyl)piperidine;SCHEMBL2007745;DTXSID10439903;SXSSVNBOMMHRRB-UHFFFAOYSA-N;1-n-butyl-4-piperidinylmethylamine;(1-butyl-4-piperidinyl)methylamine;(1-n butyl-4-piperidyl)methylamine;MFCD02684339;[(1-butylpiperidin-4-yl)methyl]amine;1-(1-butyl-4-piperidinyl)methanamine;AKOS000210476;N-(1-butyl-4-piperidinyl)methylamine;N-(1-n butyl-4-piperidyl)methylamine;4-AMINOMETHYL-1-BUTYLPIPERIDINE;AB12630;AC-6751;AS-63444;A8852;FT-0654212;1-(1-BUTYLPIPERIDIN-4-YL)METHANAMINE;Q-103046

Chemical Property of 4-Aminomethyl-1-N-butylpiperidine

Chemical Property:

• Vapor Pressure: 0.0882mmHg at 25°C
• Refractive Index: 1.466
• Boiling Point: 225℃
• Flash Point: 88℃
• PSA: 29.26000
• Density: 0.883
• LogP: 2.09540
• Storage Temp.: 2-8°C
• Water Solubility.: Slightly soluble in water.
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 170.178298710
• Heavy Atom Count: 12
• Complexity: 106

Purity/Quality:

97% ^*data from raw suppliers

4-Aminomethyl-1N-butylpiperidine 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCN1CCC(CC1)CN

Technology Process of 4-Aminomethyl-1-N-butylpiperidine

There total 6 articles about 4-Aminomethyl-1-N-butylpiperidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%

1-bromo-butane (109-65-9) + 4-carboxamidopiperidine (39546-32-2) + aqueous potassium carbonate + LiAlH4.2 THF + 4-carboxamide-1-butylpiperidine (66073-48-1) → 1-(1-butyl-4-piperidinyl)methanamine (65017-57-4)

Guidance literature:

With sodium hydroxide; potassium carbonate; In toluene;

Reference yield: 51.0%

1-bromo-butane (109-65-9) + 4-Aminomethylpiperidine (7144-05-0) → 1-(1-butyl-4-piperidinyl)methanamine (65017-57-4)

Guidance literature:

In acetonitrile; at 0 - 20 ℃;

DOI:10.1016/S0968-0896(99)00172-8

Reference yield:

4-carboxamide-1-butylpiperidine (66073-48-1) → 1-(1-butyl-4-piperidinyl)methanamine (65017-57-4)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 45 ℃;

DOI:10.1016/S0223-5234(99)80083-X DOI:10.1016/S0223-5234(99)00158-0

upstream raw materials:

1-Butyl-piperidine-4-carbonitrile

4-carboxamide-1-butylpiperidine

1-bromo-butane

4-Aminomethylpiperidine

Downstream raw materials:

N-[(1-butyl-4-piperidinyl)methyl]-3,4-dihydro-7-benzyloxy-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide

4-amino-N-((1-butylpiperidin-4-yl)methyl)-3-methoxybenzamide

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