Difference between revisions of "Strychnine"

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== Description ==
 
== Description ==
  
A highly toxic alkaloid derived from the seeds of the ''Strychnos nux-vomica'' tree and related species. Strychnine was first extracted in 1818 by French chemists Joseph-Bienaim Caventou and Pierre-Joseph Pelletier. The bitter tasting crystals are commercially used in rodent poisons.
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A highly toxic alkaloid derived from the seeds of the ''Strychnos nux-vomica'' tree and related species. Strychnine was first extracted in 1818 by French chemists Joseph-Bienaimé Caventou and Pierre-Joseph Pelletier. The bitter tasting crystals are commercially used in rodent poisons.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
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== Authority ==
 
== Authority ==
  
* Martha Windholz (ed.), ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 8724
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* ''The Merck Index'', Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983  Comment: entry 8724
  
* ''Encyclopedia Britannica'', ''Encyclopedia Britannica'', http://www.britannica.com  Comment: "strychnine" [Accessed March 26, 2002].
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* ''Encyclopedia Britannica'', http://www.britannica.com  Comment: "strychnine" [Accessed March 26, 2002].
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Revision as of 06:34, 24 July 2013

Description

A highly toxic alkaloid derived from the seeds of the Strychnos nux-vomica tree and related species. Strychnine was first extracted in 1818 by French chemists Joseph-Bienaimé Caventou and Pierre-Joseph Pelletier. The bitter tasting crystals are commercially used in rodent poisons.

Synonyms and Related Terms

strychnidin-10-one

Chemical structure

Strychnine.jpg


Other Properties

Soluble in chloroform, benzene, toluene, glycerols. Slightly soluble in ether, alcohols. Almost insoluble in water.

Composition C21H22N2O2
CAS 57-24-9
Density 1.35
Molecular Weight mol. wt. = 334.45
Boiling Point 270

Hazards and Safety

Highly toxic by ingestion. Causing cramps and convulsions within 20 minutes.

LINK: International Chemical Safety Card

Authority

  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 8724

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