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Sodium diethyldithiocarbamate


 Sodium diethyldithiocarbamate, DDTC

Sodium diethyldithiocarbamate

Properties:
Sodium diethyldithiocarbamate is the organosulfur compound with the formula NaS2CN(C2H5)2.

Oxidation of sodium diethyldithiocarbamate gives the disulfide, also called a thiuram disulfide (Et = ethyl):
2 NaS2CNEt2 + I2 → Et2NC(S)S-SC(S)NEt2 + 2 NaI
This disulfide is marketed as an anti-alcoholism drug under the labels Antabuse and Disulfiram. Chlorination of the above-mentioned thiuram disulfide affords the thiocarbamoyl chloride.


Grade:AR Grade

Purity:99.9% min

CAS Number :20624-25-3

EC Number:205-710-6

Molecular Formula:(C2H5)2NCSSNa · 3H2O


Technical Requirements:


ITEM

 Sodium diethyldithiocarbamate

Appearance White or colorless Powder
Copper Suitability Test Qualified
Solubility in H2O Qualified
ignition residue (w/%) 30.5--32.5%

Application:


Ligand bonding: The diethyldithiocarbamate ion chelates to many "softer" metals via the two sulfur atoms. Other more complicated bonding modes are known including binding as unidentate ligand and a bridging ligand using one or both sulfur atoms.

Spin trapping of nitric oxide radicals:Complexes of Dithiocarbamates with iron provide one of the very few methods to study the formation of nitric oxide (NO) radicals in biological materials. Although the lifetime of NO in tissues is too short to allow detection of this radical itself, NO readily binds to iron-dithiocarbamate complexes. The resulting mono-nitrosyl-iron complex (MNIC) is stable, and may be detected with Electron Paramagnetic Resonance (EPR) spectroscopy.

Antioxidant:Diethyldithiocarbamate inhibits superoxide dismutase, which can both have antioxidant and oxidant effects on cells, depending on the time of administration.


Packing:25g/bottle or according to your requirement.


How to buy  Sodium diethyldithiocarbamate


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