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pyridine

American  
[pir-i-deen, -din] / ˈpɪr ɪˌdin, -dɪn /

noun

Chemistry.
  1. a colorless, flammable, liquid organic base, C 5 H 5 N, having a disagreeable odor, usually obtained from coal or synthesized from acetaldehyde and ammonia: used chiefly as a solvent and in organic synthesis.


pyridine British  
/ ˈpɪrɪˌdiːn /

noun

  1. a colourless hygroscopic liquid with a characteristic odour. It is a basic heterocyclic compound containing one nitrogen atom and five carbon atoms in its molecules and is used as a solvent and in preparing other organic chemicals. Formula: C 5 H 5 N

"Collins English Dictionary — Complete & Unabridged" 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012

pyridine Scientific  
/ pĭr′ĭ-dēn′ /
  1. Any of a class of organic compounds containing a six-member ring in which one of the carbon atoms has been replaced by a nitrogen atom. Pyridines include compounds used as water repellents, herbicides, and various drugs. The pyridine ring structure is also part of many larger compounds, including niacin and nicotine.

  2. The simplest of these compounds, a flammable, colorless or yellowish liquid base having a penetrating odor. It is used as a solvent and waterproofing agent and in the manufacture of various drugs and vitamins. Chemical formula: C 5 H 5 N.


Other Word Forms


Etymology

Origin of pyridine

First recorded in 1850–55; pyr- + -id 3 + -ine 2


Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

See Examples For:

In their latest study, which was published in Angewandte Chemie International Edition on 27 May 2024, they present a convenient methodology to access the pyridine side of quinolines and synthesize diverse 2D/3D frameworks.

From Science Daily ● Jun. 19, 2024

The researchers discovered that this boron-containing compound was extremely effective at inducing dearomative photocycloaddition almost exclusively on the pyridine side of quinoline.

From Science Daily ● Jun. 19, 2024

However, a panel of 12 experts said in January no definitive cause had been found, but they ruled out pyridine and concluded it was possible a disease or parasite new to UK waters was responsible.

From BBC ● May 19, 2023

“We just could not find evidence for high levels of pyridine in the coastal sea water,” said Lancaster University environmental chemist Crispin Halsall, who worked on the report.

From Seattle Times ● Jan. 20, 2023

By acting upon meconic acid with ammonia, comenamic acid is formed, and this latter, when heated with zinc dust, yields pyridine.

From Scientific American Supplement, No. 415, December 15, 1883 by Various

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