113682-53-4

Basic information

• Product Name: 1-Acetyloxy-2,2,6,6-tetramethyl-4-oxopiperidine
• Synonyms: 1-Acetoxy-2,2,6,6-tetramethylpiperidin-4-one
• CAS NO: 113682-53-4
• Molecular Formula: C₁₁H₁₉NO₃
• Molecular Weight: 213.27
• Mol File: 113682-53-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 273.9°C at 760 mmHg
• Flash Point: 119.4°C
• Appearance: /
• Density: 1.06g/cm³
• Vapor Pressure: 0.00559mmHg at 25°C
• Refractive Index: 1.481
• CAS DataBase Reference: 1-Acetyloxy-2,2,6,6-tetramethyl-4-oxopiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Acetyloxy-2,2,6,6-tetramethyl-4-oxopiperidine(113682-53-4)
• EPA Substance Registry System: 1-Acetyloxy-2,2,6,6-tetramethyl-4-oxopiperidine(113682-53-4)

Safety Data

• Hazardous Substances Data: 113682-53-4(Hazardous Substances Data)

Usage

Chemical class

Piperidine derivatives

Molecular weight

227.3 g/mol

Application

Insect repellent

Mechanism of action

Creates a barrier that masks the user's smell, making them unattractive to insects

Effective against

Mosquitoes, ticks, fleas, and flies

Usage

Commonly used in lotions, sprays, and wipes

Purpose

Protection against insect bites and diseases they can transmit

Reputation

Highly effective and versatile insect repellent

Global usage

Widely used around the world

InChI:InChI=1/C11H19NO3/c1-8(13)15-12-10(2,3)6-9(14)7-11(12,4)5/h6-7H2,1-5H3

Upstream product

• 45985-26-0 4-oxo-2,2,6,6-tetramethylpiperidin-oxyl 
• 108-24-7 acetic anhydride 
• 3637-11-4 1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-one 
• 22963-71-9 1-hydroxy-4-oxo-2,2,6,6-tetramethylpiperidine hydrochloride 

Downstream Products

• 73645-92-8 p-bis(1-oxyl-2,2,6,6-tetramethyl-Δ³-4-piperidylethynyl)benzene 
• 198335-06-7 C₂₈H₃₆N₂O₂ 
• 198335-07-8 C₂₈H₃₆N₂O₂ 
• 198335-03-4 Acetic acid 4-[4-(1-acetoxy-2,2,6,6-tetramethyl-1,2,3,6-tetrahydro-pyridin-4-ylethynyl)-phenylethynyl]-2,2,6,6-tetramethyl-3,6-dihydro-2H-pyridin-1-yl ester 
• 198335-04-5 Acetic acid 4-[2-(1-acetoxy-2,2,6,6-tetramethyl-1,2,3,6-tetrahydro-pyridin-4-ylethynyl)-phenylethynyl]-2,2,6,6-tetramethyl-3,6-dihydro-2H-pyridin-1-yl ester 
• 137063-53-7 2',3'-O-(1-acetoxy-2,2,6,6-tetramethyl-4-piperidylidene)-5'-O-benzoyluridine 
• 198335-00-1 Acetic acid 4-[4-(1-acetoxy-4-hydroxy-2,2,6,6-tetramethyl-piperidin-4-ylethynyl)-phenylethynyl]-4-hydroxy-2,2,6,6-tetramethyl-piperidin-1-yl ester 
• 198335-02-3 Acetic acid 4-[3-(1-acetoxy-4-hydroxy-2,2,6,6-tetramethyl-piperidin-4-ylethynyl)-phenylethynyl]-4-hydroxy-2,2,6,6-tetramethyl-piperidin-1-yl ester 

Relevant articles and documents

Synthesis and properties of bicyclic aziridines, derivatives of triacetoneamine

Bicyclic aziridines, derivatives of 2,2,6,6-tetramethyl-4-piperidone (triacetoneamine), are synthesized, which by acids treatment undergo the N-C(1) or N-C(2) bonds cleavage to form the corresponding pyrrolines, pyrrolidines, and piperidines.

Conformationally Restricted Spin Labelled Nucleotides: a Model Study of the Synthesis and Properties of the 2',3'-O-Spiro Ketal of Uridine and 4-oxo-2,2,6,6-tetramethyl-1-piperidyloxy

The synthesis of 2',3'-O-(1-oxy-2,2,6,6-tetramethyl-4-piperidylidene)uridine 13 is described in a model study directed at the corresponding spin labelled spiro ketal derivative of ATP (adenosine triphosphate) 1 and of other nucleotides.The synthesis proce