Dazomet

Dazomet is a common soil fumigant that acts as a herbicide, fungicide, and nematicide.

Dazomet
Names
IUPAC name
3,5-Dimethyl-1,3,5-thiadiazinane-2-thione
Other names
Mylon; Basamid, Thiazone; Mylone; Tiazon; DMTT; Dimethylformocarbothialdine; Carbothialdin; Basamide; Nefusan
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.798
UNII
Properties
C5H10N2S2
Molar mass 162.27 g·mol−1
Appearance White solid
Density 1.29±0.1 g/mL[1]
Melting point 104 to 105 °C (219 to 221 °F; 377 to 378 K)
Boiling point 222.3±50.0 °C (predicted)[1]
Hazards
Flash point 156 °C (313 °F)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Applications

Dazomet is a chemical used to kill pests that inhibit plant growth through gaseous degradation. Dazomet is used as a soil sterilant on a variety of sites such as golf courses, nurseries, turf sites, and potting soils.[3] Dazomet is used for soil sterilization as an alternative to methyl bromide. Although less effective it is still used to kill pests because of its comparatively lower toxicity. Dazomet is applied to wet soil, which causes dazomet itself to decompose into a gaseous form, which is what actively controls pests. The decomposition of dazomet releases methyl isothiocyanate (MITC) a gas toxic to pests that would prevent or kill plant growth.

Synthesis

Dazomet is synthesized from carbon disulfide (CS2) and diluted methylamine (CH3NH2). After stirring for 1-2 hours, an oily substance is formed, which is the intermediate methylcarbamodithioic acid (HS2CNHCH3). Then, formaldehyde (CH2O) is added to the intermediate to form and precipitate out the dazomet .[4]

Toxicology and safety

Dazomet is irritating to the eyes[5] and its degradation product, MITC, is a dermal sensitizer. Dazomet is very toxic to aquatic organisms, and also acutely toxic to mammals. Exposure to dazomet can occur through several means; interaction with unincorporated granules, inhalation of it decomposition product, MITC, and/or water runoff.

Mass spectrum

The molecular ion peak of dazomet is at 162 m/z. There are two major fragment peaks, one at 89 m/z and one at 42 m/z. The fragment peak at 89 m/z represents the loss of MITC, which is the major, gaseous degrade of dazomet.[6]

Patents

Patent #US5989597

Ambrose Rajamannan was the inventor of the novel process of continuously and instantaneously sterilizing soil using a water-activated fumigant. Dazomet is one water-activated fumigant that could be used. This process ensures 100% activation of the fumigant. Therefore, less fumigant would be needed to ensure that the soil would be completely sterilized.[7]


Patent #CN1543787

See under "Synthesis".

gollark: The US has *much* mass surveillance, in some places apparently near-UK-level bizarre knife laws, insane and incoherent governance, and apparently bad policing.
gollark: It uses highly directed transcranial magnetic stimulation delivered by airborne nanobots to erase the concept of rules from people's minds temporarily.
gollark: Only the GTech™ experimental anarchy cube™ is free.
gollark: It was once exchanged for a trivial amount of euros.
gollark: They can pay in "krist", a "minecraft server" currency which is also cross-server and vaguely cryptocurrency.

References
  1. SciFinder.Dazomet.properties (accessed Oct. 5, 2014).
  2. "MSDS for Diazomet". Sigma-Aldrich.
  3. "RED Fact Sheet: Dazomet" (PDF). US Environmental Protection Agency, Office of Pesticide Programs. July 10, 2008. Archived from the original (PDF) on 2014-10-16. Cite journal requires |journal= (help)
  4. Cao, Y.; Lu, Y. Process for preparing dazomet dustless stable fine granules. CN1543787, Nov. 10, 2004.
  5. "Harmonised classification of dazomet in the C&L Inventory". ECHA. Retrieved 2019-02-11.
  6. NIST Chemistry WebBook. 2H-1,3,5-Thiadiazine-2-thione, tetrahydro-3,5-dimethyl-. http://webbook.nist.gov/ (accessed Oct. 5, 2014).
  7. Rajamannan, A. H. J. Process for sterilizing soil. US Patent 5989597, Nov. 23, 1999.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.