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Dimethyldithiocarbamate

Base Information Edit
  • Chemical Name:Dimethyldithiocarbamate
  • CAS No.:137-30-4
  • Molecular Formula:C6H12N2S4Zn
  • Molecular Weight:305.829
  • Hs Code.:2930.20
  • European Community (EC) Number:205-288-3
  • ICSC Number:0348
  • UN Number:2771,3077
  • Nikkaji Number:J473.557I
  • Wikipedia:Zinc_bis(dimethyldithiocarbamate),Dimethyldithiocarbamate
  • Wikidata:Q27157659
  • Mol file:137-30-4.mol
Dimethyldithiocarbamate

Synonyms:Dimethyldithiocarbamate

Suppliers and Price of Dimethyldithiocarbamate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Zinc Dimethyldithiocarbamate
  • 1g
  • $ 80.00
  • TCI Chemical
  • Zinc Dimethyldithiocarbamate >97.0%(T)
  • 500g
  • $ 52.00
  • TCI Chemical
  • Zinc Dimethyldithiocarbamate >97.0%(T)
  • 25g
  • $ 18.00
  • Sigma-Aldrich
  • Ziram PESTANAL
  • 250mg
  • $ 28.00
  • Sigma-Aldrich
  • Zinc dimethyldithiocarbamate 97%
  • 1kg
  • $ 145.00
  • Medical Isotopes, Inc.
  • Zinc Dimethyldithiocarbamate
  • 1 g
  • $ 610.00
  • Chem-Impex
  • Zincdimethyldithiocarbamate,97%(Assaybytitration) 97%(Assaybytitration)
  • 500G
  • $ 54.88
  • Chem-Impex
  • Zincdimethyldithiocarbamate,97%(Assaybytitration) 97%(Assaybytitration)
  • 25G
  • $ 13.44
  • American Custom Chemicals Corporation
  • ZINC DIMETHYLDITHIOCARBAMATE 95.00%
  • 500G
  • $ 37900.00
  • AK Scientific
  • Ziram
  • 1g
  • $ 14.00
Total 100 raw suppliers
Chemical Property of Dimethyldithiocarbamate Edit
Chemical Property:
  • Appearance/Colour:Odorless white powder 
  • Vapor Pressure:<1 x 10-6 Pa 
  • Melting Point:248-257 °C(lit.) 
  • Boiling Point:129.4 °C at 760 mmHg 
  • Flash Point:32 °C 
  • PSA:134.68000 
  • Density:1.66 g/cm3 
  • LogP:1.52290 
  • Storage Temp.:APPROX 4°C 
  • Water Solubility.:0.0065 g/100 mL 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:119.99416654
  • Heavy Atom Count:6
  • Complexity:54.3
  • Transport DOT Label:Poison
Purity/Quality:

99% *data from raw suppliers

Zinc Dimethyldithiocarbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s): VeryT+,Dangerous
  • Hazard Codes:T+,N 
  • Statements: 22-26-37-41-43-48/22-50/53 
  • Safety Statements: 22-26-28-36/37/39-45-60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Pesticides -> Dithiocarbamates (Pesticide)
  • Canonical SMILES:CN(C)C(=S)[S-]
  • Inhalation Risk:A harmful concentration of airborne particles can be reached quickly when dispersed.
  • Effects of Short Term Exposure:The substance is severely irritating to the eyes. The substance is irritating to the skin and respiratory tract.
  • Effects of Long Term Exposure:Repeated or prolonged contact may cause skin sensitization. Tumours have been detected in experimental animals but may not be relevant to humans.
  • Uses Ziram is a protective fungicide applied to foliage to control diseases on pome fruit, stone fruit, nuts, vines, vegetables and ornamentals. It is used to control scab in apples and pears and Monilia, Alternaria, Septoria, peach leaf curl, shot hole, rusts, black rot and anthracnose. It is also used as a wildlife repellent, smeared as a paste onto tree trunks or sprayed onto ornamentals, dormant fruit trees and other crops. Zinc Dimethyldithiocarbamate is a member of a class of dithiocarbamates, and has been used in agriculture as a fungicide and in the rubber industry as a vulcanization accelerator. Rubber vulcanization accelerator; agricultural fungicide.
Technology Process of Dimethyldithiocarbamate

There total 3 articles about Dimethyldithiocarbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In water; byproducts: NaCl; ZnCl2, the thiocarbamate in water, immediately pptn.; filtered hot to remove NaCl and any excess of unreacted thiocarbamate, dried (vac. at 80°C), recrystn. (boiling benzene);
DOI:10.1016/S0020-1693(00)83216-8
Guidance literature:
In acetonitrile; Electrolysis; 4 h, initial voltage 10 V, Zn anode; product was collected, washed with acetonitrile and then petroleum ether and dried in vacuo; elem. anal.;
Guidance literature:
In acetone; direct reaction of ZnCl2 with dimethylamine and carbon disulfide in acetone;
DOI:10.1007/s10973-005-0055-5
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