31582-45-3

Basic information

• Product Name: 2,2,6,6-TETRAMETHYL-4-PIPERIDYL METHACRYLATE
• Synonyms: 2,2,6,6-TETRAMETHYL-4-PIPERIDYL METHACRYLATE;METHACRYLIC ACID 2,2,6,6-TETRAMETHYL-4-PIPERIDYL ESTER;2-Propenoicacid,2-methyl-,2,2,6,6-tetramethyl-4-piperidinylester;2,2,6,6-Tetramethyl-4-piperidinyl methacrylate;2,2,6,6-Tetramethyl-4-piperidyl Methacrylate (stabilized with MEHQ);4-(Methacryloyloxy)-2,2,6,6-tetramethylpiperidine;4-Methacryloyloxy-2,2,6,6-tetramethylpiperidine;Fancryl FA-712HM
• CAS NO: 31582-45-3
• Molecular Formula: C₁₃H₂₃NO₂
• Molecular Weight: 225.33
• EINECS: 250-718-5
• Product Categories: Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 31582-45-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 61 °C
• Boiling Point: 273°Cat760mmHg
• Flash Point: 118.9°C
• Appearance: /
• Density: 0.97g/cm³
• Vapor Pressure: 0.006mmHg at 25°C
• Refractive Index: 1.474
• Storage Temp.: Refrigerator
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 10.13±0.10(Predicted)
• CAS DataBase Reference: 2,2,6,6-TETRAMETHYL-4-PIPERIDYL METHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,6,6-TETRAMETHYL-4-PIPERIDYL METHACRYLATE(31582-45-3)
• EPA Substance Registry System: 2,2,6,6-TETRAMETHYL-4-PIPERIDYL METHACRYLATE(31582-45-3)

Safety Data

• Hazardous Substances Data: 31582-45-3(Hazardous Substances Data)

Usage

Chemical Properties

White Waxy Solid

Uses

Different sources of media describe the Uses of 31582-45-3 differently. You can refer to the following data:
1. It is used as cholesterol-lowering agent.
2. 2,2,6,6-TetraMethyl-4-piperidyl Methacrylate is used as cholesterol-lowering agent.

InChI:InChI=1/C13H23NO2/c1-9(2)11(15)16-10-7-12(3,4)14-13(5,6)8-10/h10,14H,1,7-8H2,2-6H3

Upstream product

• 2403-88-5 4-hydroxy-2,2,6,6-tetramethylpiperidine 
• 920-46-7 Methacryloyl chloride 
• 97-63-2 methyl methacrylate 
• 760-93-0 methacryloyl anhydride 

Downstream Products

• 1126272-77-2 N-chloro-2,2,6,6-tetramethyl-4-piperidinyl methacrylate 

Relevant articles and documents

Reaction type hindered amine light stabilizer and preparation method thereof

The invention relates to a reaction type hindered amine light stabilizer and a preparation method of the reaction type hindered amine light stabilizer. The light stabilizer is prepared by dissolving tetramethyl-4-piperidinol and a derivative of the tetramethyl-4-piperidinol into a solvent, adding a polymerization inhibitor and alpha-beta unsaturated carboxylic ester, implementing an esterificationreaction under the action of a catalyst, washing with water, and desolventizing. According to the disclosed reaction type hindered amine light stabilizer and the preparation method of the reaction type hindered amine light stabilizer, the process is simple, the condition is mild, the purity of a produced product is high, and the yield is more than 90%. The synthesis method is simple to operate, the color of the product is light, and the light transmittance of the product is good.

Battery-inspired, nonvolatile, and rewritable memory architecture: A radical polymer-based organic device

A nonvolatile, bistable, and rewritable organic memory device based on radical polymers was prepared and tested. The excellent performance of a battery-inspired memory architecture with a configuration of p- and n-type charge-transporting radical polymers sandwiching a dielectric layer was characterized. The ON-OFF ratio was more than 4 orders of magnitude, and retention and endurance cycles of more than 104 and 103, respectively, were accomplished. Copyright

Phosphites and their production and use

Phosphites represented by the general formula (I): STR1 wherein R1, R2, R4 and R5 independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, an alkylcycloalkyl group having 6 to 12 carbon atoms, an aralkyl group having 7 to 12 carbon atoms or a phenyl group; R3 and R6 independently represent a hydrogen atom or an alkyl group having 1 to 8 carbon atoms; X1 is a dihydric alcohol residue, wherein HO--X1 --OH defines the corresponding dihydric alcohol from which residue X1, is obtained; and X2 is a direct bond or an alkylene group having 1 to 8 carbon atoms; and the phosphites are useful as stabilizers for organic materials.