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Thionyl chloride is an inorganic compound with the chemical formula SOCl 2.It is a moderately volatile, colourless liquid with an unpleasant acrid odour.Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes (50,000 short tons) per year being produced during the early 1990s, [5] but is occasionally also used as a solvent.
Aricell manufactures non-rechargeable lithium-thionyl chloride batteries. A 1986 Jet Propulsion Laboratory study titled Safety Considerations of Lithium-Thionyl Chloride Cells noted that "safety hazards have ranged from mild venting of toxic materials to violent explosions and fires." [3]
Occupational safety and health (OHS/OSH): Main hazards. Highly toxic, [2] corrosive ... although thionyl chloride generally gives better yields than PCl 3. ...
3,5-Dinitrobenzoyl chloride (C 7 H 3 ClN 2 O 5) is an organic compound with a melting point of 68–69 °C. [1] It is the acyl chloride of 3,5-dinitrobenzoic acid and like it is mainly used in the analysis of organic substances by derivatization .
For this application, thionyl chloride is commonly used instead of phosgene. ... due to safety concerns phosgene nowadays finds limited use in organic synthesis.
The best practice for preventing foodborne illnesses for all foods, including meat, is the CDC's four steps to food safety: clean, separate, cook, and chill. Wash hands, surfaces, utensils, and ...
In October, the FDA listed the drug as having serious risks or new safety information and that psychiatric disorders linked to the drug would require the agency to evaluate the "need for ...
The von Braun amide degradation is the chemical reaction of a monosubstituted amide with phosphorus pentachloride or thionyl chloride to give a nitrile and an organohalide. [1] It is named after Julius Jacob von Braun, who first reported the reaction. [2] [3] The von Braun amide degradation