40327-96-6

Basic information

• Product Name: 4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE
• Synonyms: 4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE;1,2,2,6,6-PENTAMETHYL-4-AMINOPIPERIDINE;1,2,2,6,6-PENTAMETHYL-4-PIPERIDINAMINE;4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE,98%;4-Amino-1,2,2,6,6-pentamethylpiperidine,99%;4-AMino-1,2,2,6,6-pentaMethylpiperidine, 99% 1GR;1,2,2,6,6-PentaMethylpiperidin-4-aMine
• CAS NO: 40327-96-6
• Molecular Formula: C₁₀H₂₂N₂
• Molecular Weight: 170.3
• Mol File: 40327-96-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 215-218 °C
• Flash Point: 65.5 °C
• Appearance: Clear colorless to pale yellow/Liquid
• Density: 0.9492 (rough estimate)
• Vapor Pressure: 1.09mmHg at 25°C
• Refractive Index: 1.4795-1.4815
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE(40327-96-6)
• EPA Substance Registry System: 4-AMINO-1,2,2,6,6-PENTAMETHYLPIPERIDINE(40327-96-6)

Safety Data

• Hazard Codes: C
• Statements: 34-22
• Safety Statements: 45-36/37/39-26
• Hazardous Substances Data: 40327-96-6(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless to pale yellow liquid

InChI:InChI=1/C10H22N2/c1-9(2)6-8(11)7-10(3,4)12(9)5/h8H,6-7,11H2,1-5H3/p+2

Downstream Products

• 66651-24-9 4-(β-cyanoethyl)-amino-1,2,2,6,6-pentamethyl-piperidine 
• 201929-00-2 SB 242784 
• 1562338-73-1 6-chloro-N-methyl-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyridazin-3-amine 
• 1562338-74-2 6-chloro-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyridazin-3-amine 
• 1562333-69-0 6-(benzo[b]thiophen-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyridazin-3-amine 

Relevant articles and documents

MODIFIED ZNO NANOPARTICLES

Process for the preparation of modified zinc oxide nanoparticles, which comprises reacting zinc oxide nanoparticles, which are dissolved in a solvent, in the presence of ammonia or amines with a tetraalkyl orthosilicate and optionally with an organosilane, with the proviso that the reaction takes place at a content of less than 5% by weight of water, based on the total amount of solvent and water. Modified zinc oxide nanoparticles which have Si—O-alkyl groups and are soluble in organic solvents, obtainable by this process for the preparation. Liquid or solid formulations which comprise modified ZnO nanoparticles. Inanimate organic materials, for example plastics or coatings, which comprise modified ZnO nanoparticles. Method of stabilizing inanimate organic materials against the effect of light, free radicals or heat, where modified ZnO nanoparticles, which optionally comprise UV absorbers and/or stabilizers as further additives, are added to the materials.