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 References  













1,8-Dibromooctane






●Deutsch
 ●Português
 ●தமிழ்
 ●中文
  
Edit 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
  















Appearance
    

 





From Wikipedia, the free encyclopedia
  

1,8-Dibromooctane
Names
Preferred IUPAC name

1,8-Dibromooctane

Identifiers

CAS Number

3D model (JSmol)
ChemSpider
ECHA InfoCard 100.022.648 Edit this at Wikidata
EC Number
  • 224-912-5

PubChem CID
UNII

CompTox Dashboard (EPA)

  • InChI=1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2

    Key: DKEGCUDAFWNSSO-UHFFFAOYSA-N

  • C(CCCCBr)CCCBr

Properties

Chemical formula

 C8H16Br2
Molar mass 272.024 g·mol−1
Melting point 12–16 °C (54–61 °F; 285–289 K)
Boiling point 270–272 °C (518–522 °F; 543–545 K)
Hazards
GHS labelling:

Pictograms

 GHS07: Exclamation mark

Signal word

 Warning

Hazard statements

 H315, H319, H335

Precautionary statements

 P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

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

Infobox references

1,8-Dibromooctane is a chemical compound used in the synthesis of the carbamate nerve agents EA-3990 and octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide).[1][2] 1,8-Dibromooctane can be obtained by the hydrobromination of cyclooctene with sulfuric acid and catalysts.[3]

References[edit]

  1. ^ "Chemical agents". Google Patents.
  • ^ "Isoquinilinium chemical agents". Google Patents.
  • ^ US3624171A - Process for the production of 1,8-Dibromoctan - Google Patents23. August 2018.
    • Stub icon

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

  • t
  • e

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=1,8-Dibromooctane&oldid=1180300376"
    Categories: 
    ●Bromoalkanes
     ●Nerve agent precursors
     ●Organohalide stubs
     Hidden categories: 
    ●Articles without InChI source
     ●Articles without EBI source
     ●Articles without KEGG source
     ●ECHA InfoCard ID from Wikidata
     ●Chembox having GHS data
     ●Articles containing unverified chemical infoboxes
     ●Chembox image size set
     ●Articles with short description
     ●Short description matches Wikidata
     ●All stub articles
      


    ●This page was last edited on 15 October 2023, at 19:24 (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