Thermo Scientific Chemicals

Dithiooxamide, 98%, Thermo Scientific Chemicals

Catalog number: B24866.06
5 g, Each
Thermo Scientific Chemicals

Dithiooxamide, 98%, Thermo Scientific Chemicals

Catalog number: B24866.06
5 g, Each
Quantity
Catalog number: B24866.06
also known as B24866-06
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Chemical Identifiers

CAS
79-40-3
IUPAC Name
ethanedithioamide
Molecular Formula
C2H4N2S2
InChI Key
OAEGRYMCJYIXQT-UHFFFAOYSA-N
SMILES
NC(=S)C(N)=S
Form
Crystals or powder or crystalline powder
Identification (FTIR)
Conforms
Elemental Analysis
C: 19.49-20.48% (Theory: 19.98(5)%)
Appearance (Color)
Orange to dark orange to red
Elemental Analysis
N: 22.72-23.89% (Theory: 23.31%)

Description

Dithiooxamide acts as a chelating agent and used in the determination of copper(II), nickel(II) and cobalt(II). It is used as a building block in the synthesis of cyclen. It is involved in the preparation of thiazolothiazole-linked porous organic polymers and N,N'-disubstituted dithiooxamides. It is also employed as a modifier to prepare the modified glassy carbon electrode which is used to investigate the electrochemical properties of quercetin, an important flavonoid derivative. Further, it is involved in the preparation of chelating resin with formaldehyde, which finds application in separation and concentration of silver ions.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Dithiooxamide acts as a chelating agent and used in the determination of copper(II), nickel(II) and cobalt(II). It is used as a building block in the synthesis of cyclen. It is involved in the preparation of thiazolothiazole-linked porous organic polymers and N,N′-disubstituted dithiooxamides. It is also employed as a modifier to prepare the modified glassy carbon electrode which is used to investigate the electrochemical properties of quercetin, an important flavonoid derivative. Further, it is involved in the preparation of chelating resin with formaldehyde, which finds application in separation and concentration of silver ions.

Solubility
Soluble in acetone and chloroform. Insoluble in water.

Notes
Incompatible with oxidizing agents.
RUO – Research Use Only

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