Jump to content
 







Main menu
    


Navigation  


●Main page
 ●Contents
 ●Current events
 ●Random article
 ●About Wikipedia
 ●Contact us
 ●Donate
  



Contribute  


●Help
 ●Learn to edit
 ●Community portal
 ●Recent changes
 ●Upload file
  







Search  

































●Create account

●Log in
 









●Create account
 ● Log in
  



Pages for logged out editors learn more  


●Contributions
 ●Talk
  


















Contents

   



(Top)
  


1 See also  




2 References  













3152 CT







Add links
  








●Article
 ●Talk
  
















●Read
 ●Edit
 ●View history
  







Tools
    


Actions  


●Read
 ●Edit
 ●View history
  



General  


●What links here
 ●Related changes
 ●Upload file
 ●Special pages
 ●Permanent link
 ●Page information
 ●Cite this page
 ●Get shortened URL
 ●Download QR code
 ●Wikidata item
  



Print/export  


●Download as PDF
 ●Printable version
  



In other projects  


●Wikimedia Commons
  















Appearance
    

 





From Wikipedia, the free encyclopedia
  

3152 CT
Identifiers

3D model (JSmol)

  • InChI=1S/C18H23N3O4.2HI/c1-21(2)18(22)25-17-11-14(20)10-16(12-17)24-8-4-7-23-15-6-3-5-13(19)9-15;;/h3,5-6,9-12H,4,7-8,19-20H2,1-2H3;2*1H

    Key: KDBKYZAHSYSXLC-UHFFFAOYSA-N

  • [NH3+]c(c1)cccc1OCCCOc(cc([NH3+])c2)cc2OC(=O)N(C)C.[I-].[I-]

Properties

Chemical formula

 C24H37I2N3O4
Molar mass 685.386 g·mol−1
Appearance Solid[1]
Melting point 182–184[1] °C (360–363 °F; 455–457 K)
Hazards
Lethal dose or concentration (LD, LC):

LD50 (median dose)

 16 μg/kg (intravenous, mice)[1]
8 μg/kg (intravenous, rabbits)[1]

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

3152 CT is an extremely toxic bisquaternary carbamate with powerful anticholinesterase action.[2]

See also[edit]

References[edit]

  1. ^ a b c d "Method for methylating and quaternizing".
  • ^ LEVIN, AP; JANDORF, BJ (February 1955). "Inactivation of cholinesterase by compounds related to neostigmine". The Journal of Pharmacology and Experimental Therapeutics. 113 (2): 206–11. PMID 13234044.
    • Stub icon

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  • t
  • e

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=3152_CT&oldid=1121753429"
    Categories: 
    ●Carbamate nerve agents
     ●Acetylcholinesterase inhibitors
     ●Quaternary ammonium compounds
     ●Phenol esters
     ●Phenol ethers
     ●Iodides
     ●Organic compound stubs
     Hidden categories: 
    ●Chemical articles without CAS registry number
     ●Chemicals without a PubChem CID
     ●Articles without InChI source
     ●Chemical pages without ChemSpiderID
     ●Articles without EBI source
     ●Articles without KEGG source
     ●Articles without UNII source
     ●Articles containing unverified chemical infoboxes
     ●Articles with short description
     ●Short description matches Wikidata
     ●All stub articles
      


    ●This page was last edited on 13 November 2022, at 23:40 (UTC).
    ●Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.


    ●Privacy policy
    ●About Wikipedia
    ●Disclaimers
    ●Contact Wikipedia
    ●Code of Conduct
    ●Developers
    ●Statistics
    ●Cookie statement
    ●Mobile view


    Wikimedia Foundation
    Powered by MediaWiki