113682-53-4

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

• 137063-53-7 2',3'-O-(1-acetoxy-2,2,6,6-tetramethyl-4-piperidylidene)-5'-O-benzoyluridine 
• 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 
• 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 
• 198335-07-8 C₂₈H₃₆N₂O₂ 
• 198335-06-7 C₂₈H₃₆N₂O₂ 
• 73645-92-8 p-bis(1-oxyl-2,2,6,6-tetramethyl-Δ³-4-piperidylethynyl)benzene 
• 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 academic research and scientific papers

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.

Synthesis of terminal-biradical compounds consisting of two N-oxyl groups connected with conjugated π-systems

Terminal-biradical compounds 1 having two N-oxyl groups connected with conjugated π-systems were synthesized by (1) addition of magnesium acetylide to 4-oxo-TEMPO, followed by dehydration, or (2) cross-coupling between acetylene and vinyl triflate derived from 4-oxo-TEMPO.

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