Printer Friendly
Dictionary, Encyclopedia and Thesaurus - The Free Dictionary
3,901,808,422 visitors served.
forum Join the Word of the Day Mailing List For webmasters
?
Dictionary/
thesaurus
Medical
dictionary
Legal
dictionary
Financial
dictionary
Acronyms
 
Idioms
Encyclopedia
Wikipedia
encyclopedia
?

Pyrrole

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.01 sec.
pyrrole [′pi‚rōl]
(organic chemistry)
C4H5N Water-insoluble, yellowish oil, with pungent taste; soluble in alcohol, ether, and dilute acids; boils at 130°C; polymerizes in light; used to make drugs.

Pyrrole 

a heterocyclic compound; colorless liquid that darkens rapidly upon exposure to air. Melting point, — 23.42°C; boiling point, 130°C; density, 0.9698 g/cm3 at 20°C. Moderately soluble in water. Pyrrole is a very weak acid; it forms a salt with potassium or anhydrous caustic potash. It resinifies under the influence of acids, and it oxidizes readily. It hydrogenates with H2 over Ni at 200°C to pyrrolidine.

Pyrrole was first isolated from coal tar. It is produced commercially

by dry distillation of the ammonia salt of mucic acid or by passing a mixture of furan and NH3 over Al2O3 at 400°–450°C. The pyrrole nucleus is a structural fragment of porphyrin molecules. Pyrrole is used in the production of pyrrolidine and in the synthesis of pharmaceuticals—for example, the antiseptic Iodol (2,3,4,5-tetraiodopyrrole).



Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content.
?Page tools
Printer friendly
Cite / link
Feedback
Mentioned in?  References in periodicals archive?   Encyclopedia browser?   Full browser?
No references found
 
I believe that caffeine and its metabolites disturb the excretion of porphyrins, the pyrrole color agent in hemoglobin.
Electrochemical impedance spectroscopic measurements and morphological analysis of electrocoated thin films of pyrrole derivatives (19), poly(N-vinylcarbazole) (20), polyaniline (21), and poly(N-methyl pyrrole) (22), (23) were studied previously.
It was reported that, during overoxidation, PPy loses its electroactivity due to the ejection of the dopant (dedoping), and oxygen-containing groups such as carbonyl and carboxyl are introduced to the pyrrole unit [36].
 
 
 
Encyclopedia
?

Terms of Use | Privacy policy | Feedback | Advertise with Us | Copyright © 2012 Farlex, Inc.
Disclaimer
All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.