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Ethylammonium ethyldithiocarbamate is a chemical compound with the molecular formula C6H14N2S2. It is an organosulfur compound that belongs to the class of dithiocarbamates, which are known for their wide range of applications in various industries. ethylammonium ethyldithiocarbamate is characterized by its ability to form chelates with metal ions, making it useful in agriculture as a fungicide and in the rubber industry as an accelerator. It is also used in the synthesis of other chemicals and as a stabilizer in various formulations. Ethylammonium ethyldithiocarbamate is typically a white crystalline solid and is soluble in water and organic solvents. Its chemical structure consists of an ethyl group attached to a dithiocarbamate moiety, which includes a nitrogen atom bonded to two sulfur atoms and a carbon atom.

3063-20-5

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3063-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3063-20-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3063-20:
(6*3)+(5*0)+(4*6)+(3*3)+(2*2)+(1*0)=55
55 % 10 = 5
So 3063-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NS2.C2H7N/c1-2-4-3(5)6;1-2-3/h2H2,1H3,(H2,4,5,6);2-3H2,1H3

3063-20-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethanamine,ethylcarbamodithioic acid

1.2 Other means of identification

Product number -
Other names N-Aethyl-dithiocarbamidsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3063-20-5 SDS

3063-20-5Downstream Products

3063-20-5Relevant academic research and scientific papers

Trimethylplatinum(iv) complexes of dithiocarbamato ligands: An experimental NMR study on the barrier to C-N bond rotation

Heard, Peter J.,Kite, Kenneth,Nielsen, Julie Sogaard,Tocher, Derek A.

, p. 1349 - 1356 (2000)

The trimethylplatinum(iv) complexes of a number of dithiocarbamato ligands have been prepared. The complexes are dimeric in the solid state and in solution, with the ligands acting in both a bridging and chelating fashion. Restricted rotation about the ligand C-N bonds in solution leads to the formation of four rotomers. The kinetics of the restricted rotation was measured by a variety of dynamic NMR techniques in the slow and intermediate exchange regimes. Two distinct processes are observed, namely the independent rotation about each C-N bond and correlated rotation about both C-N bonds. The free energies of activation, which are strongly dependent on the nature of the ligand substituents, are in the range 65-88 kJ mol"1 at 298 K. The origins of the barrier to rotation and the effects of the nitrogen substituents are discussed. The crystal structures of/ac-[PtMe3(Me2NCS2)]2 and /ac-[PtMe3(Ph(H)NCS2)]2 are reported. The Royal Society of Chemistry 2000.

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