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|Section2= | Section3 = |Section4= | Reference = 〔(【引用サイトリンク】title=QUINOLINE (BENZOPYRIDINE) )〕 }} Quinoline is a heterocyclic aromatic organic compound with the chemical formula C9H7N. It is a colorless hygroscopic liquid with a strong odor. Aged samples, especially if exposed to light, become yellow and later brown. Quinoline is only slightly soluble in cold water but dissolves readily in hot water and most organic solvents. Quinoline itself has few applications, but many of its derivatives are useful in diverse applications. A prominent example is quinine, an alkaloid found in plants. 4-Hydroxy-2-alkylquinolines (HAQs) are involved in antibiotic resistance. == Occurrence and isolation == Quinoline was first extracted from coal tar in 1834 by Friedlieb Ferdinand Runge. Coal tar remains the principal source of commercial quinoline.〔 Like other nitrogen heterocyclic compounds, such as pyridine derivatives, quinoline is often reported as an environmental contaminant associated with facilities processing oil shale or coal, and has also been found at legacy wood treatment sites. Owing to it relatively high solubility in water, quinoline has significant potential for mobility in the environment, which may promote water contamination. Quinoline is readily degradable by certain microorganisms, such as ''Rhodococcus'' species Strain Q1, which was isolated from soil and paper mill sludge. Quinolines are present in small amounts in crude oil within the virgin diesel fraction. It can be removed by the process called hydrodenitriification. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Quinoline」の詳細全文を読む スポンサード リンク
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