N,2,2,6,6-Pentamethylpiperidin-4-amine

Base Information

• Chemical Name: N,2,2,6,6-Pentamethylpiperidin-4-amine
• CAS No.: 62995-79-3
• Molecular Formula: C10H22N2
• Molecular Weight: 170.298
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID20545988
• Nikkaji Number: J1.462.334E
• Wikidata: Q82423660
• Mol file: 62995-79-3.mol

Synonyms:62995-79-3;N,2,2,6,6-Pentamethylpiperidin-4-amine;4-METHYLAMINO-2,2,6,6-TETRAMETHYLPIPERIDINE;METHYL-(2,2,6,6-TETRAMETHYL-PIPERIDIN-4-YL)-AMINE;MFCD08059893;4-Piperidinamine, N,2,2,6,6-pentamethyl-;CHEMBRDG-BB 4012656;SCHEMBL1310223;DTXSID20545988;GMIARZNQLSJFCP-UHFFFAOYSA-N;AKOS006241785;SB38015;AS-36477;SY101566;N,2,2,6,6-Pentamethyl-4-piperidinamine;CS-0139570;2,2,6,6-tetramethyl-4-methylaminopiperidine;2,2,6,6-tetramethyl-4-(methylamino)piperidine;4-N-methyl amino-2,2,6,6-tetramethyl piperidine

Chemical Property of N,2,2,6,6-Pentamethylpiperidin-4-amine

Chemical Property:

• Vapor Pressure: 0.282mmHg at 25°C
• Boiling Point: 203.103oC at 760 mmHg
• PKA: 10.92±0.10(Predicted)
• Flash Point: 64.704oC
• PSA: 24.06000
• Density: 0.886g/cm3
• LogP: 2.23470
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 170.178298710
• Heavy Atom Count: 12
• Complexity: 145

Purity/Quality:

97% ^*data from raw suppliers

4-Methylamino-2,2,6,6-tetramethylpiperidine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(CC(CC(N1)(C)C)NC)C

Technology Process of N,2,2,6,6-Pentamethylpiperidin-4-amine

There total 6 articles about N,2,2,6,6-Pentamethylpiperidin-4-amine 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: 100.0%

2,2,6,6-Tetramethyl-4-piperidone (826-36-8) + methylamine hydrochloride (593-51-1) → 4-N-methylamino-2,2,6,6-tetramethylpiperidine (62995-79-3)

Guidance literature:

With C₈H₁₄BO₄^(1-)*Na⁽¹⁺⁾; triethylamine; In tetrahydrofuran; dichloromethane; at 20 ℃; for 6h;

DOI:10.1124/mol.118.112359

Reference yield: 50.0%

2,2,6,6-Tetramethyl-4-piperidone (826-36-8) + methylamine (74-89-5) → 4-N-methylamino-2,2,6,6-tetramethylpiperidine (62995-79-3)

Guidance literature:

With hydrogenchloride; sodium cyanoborohydride; In methanol; for 144h; Ambient temperature;

DOI:10.1021/jm00372a014

Reference yield:

C10H20N2 → 4-N-methylamino-2,2,6,6-tetramethylpiperidine (62995-79-3)

Guidance literature:

With sodium cyanoborohydride; In methanol; for 15h; Inert atmosphere;

DOI:10.1016/j.bmc.2010.11.049

upstream raw materials:

2,2,6,6-Tetramethyl-4-piperidone

methylamine

methylamine hydrochloride

4-AMINO-2,2,6,6-TETRAMETHYLPIPERIDINE

Downstream raw materials:

N-methyl-N-(2,2,6,6-tetramethyl-4-piperidyl)-α-(3,5-di-t-butyl-4-hydroxyphenyl)-α,α-pentamethylene acetamide

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