Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Quinoline
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
== Applications == Quinolines are used in the manufacture of [[dye]]s and the preparation of [[hydroxyquinoline]] sulfate and [[niacin (substance)|niacin]]. It is also used as a solvent for [[resin]]s and [[terpene]]s. Quinoline is mainly used as in the production of other [[specialty chemicals]]. Approximately 4 [[tonne]]s were produced annually according to a report published in 2005.<ref name=Hoke/> Its principal use is as a precursor to [[8-hydroxyquinoline]], which is a versatile chelating agent and precursor to pesticides. Its [[quinaldine|2-]] and [[lepidine|4-methyl]] derivatives are precursors to [[cyanine dye]]s. Oxidation of quinoline affords [[quinolinic acid]] (pyridine-2,3-dicarboxylic acid), a precursor to the herbicide sold under the name "Assert".<ref name=Hoke>{{Ullmann | author1 = Gerd Collin | author2 = Hartmut HΓΆke | title = Quinoline and Isoquinoline | doi = 10.1002/14356007.a22_465}}</ref> The reduction of quinoline with [[sodium borohydride]] in the presence of [[acetic acid]] is known to produce [[Kairoline A]].<ref name="GRIBBLEHEALD1975">{{cite journal|last1=GRIBBLE|first1=Gordon W.|last2=HEALD|first2=Peter W.|title=Reactions of Sodium Borohydride in Acidic Media; III. Reduction and Alkylation of Quinoline and Isoquinoline with Carboxylic Acids|journal=Synthesis|volume=1975|issue=10|year=1975|pages=650β652|issn=0039-7881|doi=10.1055/s-1975-23871}}</ref> (Cf. [[Kairine]]) Several [[Antimalarial medication|anti-malarial]] drugs contain quinoline substituents. These include [[Antimalarial medication#Quinine and related agents|quinine]], [[Antimalarial medication#Chloroquine|chloroquine]], [[Antimalarial medication#Amodiaquine|amodiaquine]], and [[Antimalarial medication#Primaquine|primaquine]]. Quinoline is used as a solvent and reagent in organic synthesis.<ref>{{cite book |doi=10.1002/047084289X.rq002.pub2 |chapter=Quinoline |title=Encyclopedia of Reagents for Organic Synthesis |year=2001 |last1=Sherman |first1=Angela R. |last2=Caron |first2=Antoine |last3=Collins |first3=Shawn K. |pages=1β4 |isbn=9780470842898 }}</ref> Quinolinium compounds (e.g. salts) can also be used as corrosion inhibitors and intensifiers.
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)