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Carbon disulfide (also spelled as carbon disulphide) is an inorganic compound with the chemical formula CS 2 and structure S=C=S. It is also considered as the anhydride of thiocarbonic acid . [ 8 ] It is a colorless, flammable, neurotoxic liquid that is used as a building block in organic synthesis.
The handling of this chemical may incur notable safety precautions. It is highly recommended that you seek the Material Safety Datasheet for this chemical from a reliable source such as SIRI, and follow its direction.
The VOC Solvents Emissions Directive was the main policy instrument for the reduction of industrial emissions of volatile organic compounds (VOCs) in the European Union. It covers a wide range of solvent-using activities, e.g. printing, surface cleaning, vehicle coating, dry cleaning and manufacture of footwear and pharmaceutical products.
The following is a list of chemicals published as a requirement of Safe Drinking Water and Toxic Enforcement Act of 1986, commonly known as California Proposition 65, that are "known to the state to cause cancer or reproductive toxicity" as of January 3, 2020. [1]
Both diethyl ether and carbon disulfide have exceptionally low autoignition temperatures which increase greatly the fire risk associated with these solvents. The autoignition temperature of carbon disulfide is below 100 °C (212 °F), so objects such as steam pipes, light bulbs , hotplates , and recently extinguished bunsen burners are able to ...
Carbon sulfide may refer to: Carbon disulfide; Carbon monosulfide; Carbon subsulfide; Sulflower; Cyclohexanehexathione This page was last edited on 16 June ...
carbon tetrachloride tetrachloromethane: 56-23-5 C(CN) 4: tetracyanomethane: 24331-09-7 CFCl 3: trichlorofluoromethane freon-11: 75-69-4 CFCl 2 CF 2 Cl: chlorotrifluoromethane freon-13: 75-72-9 CHCl 3: chloroform trichloromethane methyl trichloride: 67-66-3 CHClF 2: chlorodifluoromethane: 75-45-6 CH(CN) 3: cyanoform: 454-50-2 CHNO isocyanic ...
Dazomet is synthesized from carbon disulfide (CS 2) and diluted methylamine (CH 3 NH 2). After stirring for 1-2 hours, an oily substance is formed, which is the intermediate methyldithiocarbamic acid (HS 2 CNHCH 3). Then, formaldehyde (CH 2 O) is added to the intermediate to form and precipitate out the dazomet. [6]