Icaridin

This MedLibrary.org supplementary page on Icaridin is provided directly from the open source Wikipedia as a service to our readers. Please see the note below on authorship of this content, as well as the Wikipedia usage guidelines. To search for other content from our encyclopedia supplement, please use the form below:

Icaridin
Picaridin
IUPAC name 1-piperidinecarboxylic acid

2-(2-hydroxyethyl)-1-­methylpropylester

PubChem 125098
Identifiers
CAS number [119515-38-7]
SMILES
Properties
Molecular formula C12H23NO3
Molar mass 229.3 g/mol
Boiling point

296 °C

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Icaridin, also known as picaridine, KBR 3023, under the INCI name hydroxyethyl isobutyl piperidine carboxylate, and under the old trade name Bayrepel and the current trade name Saltidin, is an insect repellent. It has a broad efficacy against different insects and is almost colorless and odorless.

The name picaridin was proposed as an International Nonproprietary Name (INN) to the World Health Organization (WHO), but the official name that has been approved by the WHO is icaridin. The compound was developed by the German chemical company Bayer and was given the name Bayrepel. In 2005, LANXESS AG, and its subsidiary Saltigo GmbH were spun-off of Bayer [1] and the compounds was renamed Saltidin in 2008 [2].

Contents

Empirical findings

Icaridin has been reported to be as effective as DEET without the irritation associated with DEET.[3] According to the WHO, icaridin “demonstrates excellent repellent properties comparable to, and often superior to, those of the standard DEET.” In the United States, the Centers for Disease Control and Prevention recommends using repellants based on icaridin, DEET, or oil of lemon eucalyptus (which may require more applications[4]), for effective protection against mosquitoes that carry the West Nile virus, Eastern Equine Encephalitis and other illnesses.

Unlike DEET, icaridin does not dissolve plastics.[5]

Chemistry

The INCI name for icaridin is hydroxyethyl isobutyl piperidine carboxylate[6]. This chemical name name is wrong as icaridin it is an sec-butyl ester, not an isobutyl ester. Icaridin contains the substructure R2N-C(=O)-O-R, formally making it a substituted carbamate.

See also

References

  1. ^ Bayer completes spin off of Lanxess AG
  2. ^ C&EN News: Saltigo renames insect repellant
  3. ^ Journal of Drugs and Dermatology (Jan-Feb 2004)
  4. ^ CDC Approves New Weapons Against West Nile Virus. WCVB TV, 3 May 2005.
  5. ^ Picaridin
  6. ^ WHO Specifications and evaluations for public health pesticides: Icaridin

External links

Wikipedia content modification information:

  • This page was last modified on 22 August 2008, at 18:41.

Wikipedia Authorship and Review

Wikipedia content provided here is not reviewed directly by MedLibrary.org. Wikipedia content is authored by an open community of volunteers and is not produced by or in any way affiliated with MedLibrary.org.

Wikipedia Usage Guidelines

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article on "Icaridin".

The URL for this specific entry is:

All Wikipedia text is available under the terms of the GNU Free Documentation License. (See Copyrights for details). Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc.