CAS 207233-95-2
:Carbamodithioic acid, N,N-dimethyl-, sodium salt, hydrate (1:1:?)
Description:
Carbamodithioic acid, N,N-dimethyl-, sodium salt, hydrate (1:1:?) is a chemical compound characterized by its structure, which includes a carbamodithioic acid moiety with two methyl groups attached to the nitrogen atom, and a sodium salt form. This compound typically appears as a white to off-white solid and is soluble in water due to the presence of the sodium ion, which enhances its ionic character. The hydrate form indicates that it contains water molecules in its crystalline structure, which can influence its stability and solubility. As a sodium salt, it may exhibit properties typical of ionic compounds, such as conductivity in solution. The compound is likely to be used in various applications, including as a reagent in organic synthesis or in agricultural chemistry, although specific applications may vary. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C3H7NS2·xH2O·Na
InChI:InChI=1S/C3H7NS2.Na.H2O/c1-4(2)3(5)6;;/h1-2H3,(H,5,6);;1H2
InChI key:InChIKey=ITRGSMQEQGJHCF-UHFFFAOYSA-N
SMILES:C(N(C)C)(=S)S.[Na].O
Synonyms:- Carbamodithioic acid, N,N-dimethyl-, sodium salt, hydrate (1:1:?)
- Carbamodithioic acid, dimethyl-, sodium salt, hydrate
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Found 3 products.
Sodium dimethyldithiocarbamate hydrate
CAS:Formula:C3H8NNaOS2Purity:98%Color and Shape:SolidMolecular weight:161.2215N,N-Dimethyldithiocarbamate sodium hydrate
CAS:Controlled ProductFormula:C3H6NS2·Na·H2OColor and Shape:NeatMolecular weight:161.22Sodium dimethyldithiocarbamate hydrate
CAS:<p>Sodium dimethyldithiocarbamate hydrate is a salt of dimethyldithiocarbamic acid. It is used as an additive in paints and coatings to prevent corrosion of metal. Sodium dimethyldithiocarbamate hydrate is also used in the production of polyurethane and polyester resins, where it acts as a curing agent. Dimethyldithiocarbamic acid has been shown to be a ligand for the influenza virus, inhibiting viral activity by binding to the hemagglutinin protein. The crystal system of this substance is hexagonal; its salts exist in both acidic and basic forms. The functional theory explains the stabilization of this compound through coordination with nitrogen atoms on one side and phenyl substituents on the other side. Hexamethylenetetramine reacts with sodium chloride to form sodium dimethyldithiocarbamate hydrate, which can then react with methanol or eth</p>Formula:C3H6NNaS2·xH2OPurity:Min. 95%Color and Shape:White PowderMolecular weight:143.2 g/mol


