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Mereiter, K.; Preisinger, A.; Mikenda, W.; Steidl, H. (1985). "Hydrogen bonds in sodium dialkylthiocarbamate hydrates. X-ray diffraction and vibrational spectroscopic study".
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can be prepared similarly from secondary amines and carbon disulfide. They are used as
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D. Coucouvanis (2007). "The
Chemistry of the Dithioacid and 1,1-Dithiolate Complexes".
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Sodium dimethyldithiocarbamate typically crystallizes from water as the diihydrate NaS
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O. The anhydrous salt and the trihydrate are often used interchangeably.
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Except where otherwise noted, data are given for materials in their
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Rüdiger
Schubart (2000). "Dithiocarbamic Acid and Derivatives".
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Sodium dimethyldithiocarbamate is obtained by treating
199:106–108 °C (223–226 °F; 379–381 K)
337:for transition metal ions and as precursors to
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246:. It is one of the simplest organic
394:nickel bis(dimethyldithiocarbamate)
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358:Iron tris(dimethyldithiocarbamate)
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18:Potassium dimethyldithiocarbamate
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486:Environmental Protection Agency
482:"Dimethyldithiocarbamate salts"
446:Progress in Inorganic Chemistry
209:(at 25 °C , 100 kPa).
28:Sodium dimethyldithiocarbamate
390:ferric dimethyldithiocarbamate
225:Sodium dimethyldithiocarbamate
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431:10.1016/s0020-1693(00)84914-2
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386:zinc dimethyldithiocarbamate
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229:organosulfur compound
396:. Oxidation gives
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213:Infobox references
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221:Chemical compound
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489:. Retrieved
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179:white solid
42:Identifiers
452:: 233–371.
258:Preparation
176:Appearance
123:Properties
78:100.004.434
611:Pesticides
600:Categories
525:3527306730
404:References
378:pesticides
345:reagents.
339:herbicides
252:fungicides
189:1.18 g/cm
164:Molar mass
49:CAS Number
491:July 26,
301:+ HN(CH
59:128-04-1
227:is the
185:Density
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398:thiram
392:, and
329:Other
169:143.20
555:is a
382:salts
360:(Fe(S
313:CN(CH
285:with
266:CN(CH
237:NN(CH
557:stub
520:ISBN
493:2016
462:ISBN
364:CNMe
349:Uses
341:and
321:+ H
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233:NaS
96:EPA
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154:S
148:N
145:6
142:H
139:3
136:C
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94:(
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