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- |image=[[Image:Thionyl chloride.png|center|thumb|250px|{{#ifexist:Template:Thionyl chloride.png/credit|{{Cefaclor.jpg/credit}}<br/>|}}]] |molname=thionyl chloride1 KB (135 words) - 13:39, 28 November 2010
- 12 bytes (1 word) - 12:57, 28 November 2010
- | pagename = Thionyl chloride | abc = thionyl chloride812 bytes (65 words) - 12:57, 28 November 2010
- 96 bytes (12 words) - 12:58, 28 November 2010
- 827 bytes (133 words) - 12:58, 28 November 2010
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- |image=[[Image:Thionyl chloride.png|center|thumb|250px|{{#ifexist:Template:Thionyl chloride.png/credit|{{Cefaclor.jpg/credit}}<br/>|}}]] |molname=thionyl chloride1 KB (135 words) - 13:39, 28 November 2010
- | pagename = Thionyl chloride | abc = thionyl chloride812 bytes (65 words) - 12:57, 28 November 2010
- |[[Thionyl chloride]]5 KB (597 words) - 08:35, 24 January 2011
- ...] (PCl<sub>3</sub>) or other chlorinating agents including [[phosgene]], [[thionyl chloride]] or concentrated hydrochloride. An alternative approach, which was used t ...ng the production of mustard gas. While there are more applications for [[thionyl chloride]], both are in the least restrictive [[Chemical Weapons Convention/Schedule6 KB (979 words) - 11:49, 2 February 2023
- *[[Thionyl chloride]] – SOCl<sub>2</sub>26 KB (3,686 words) - 08:29, 5 May 2024
- ...m was reported to have exported thiodiglycol (a mustard gas precursor) and thionyl chloride (a nerve gas precursor) to Iraq in 1988 and 1989. <ref name=FT1991-07-29>{{28 KB (4,219 words) - 18:47, 3 April 2024