Diethyldithiocarbamic acid ferric salt, with the CAS number 13963-59-2, is a coordination compound that typically appears as a solid. It is characterized by its dark color, often ranging from brown to black, due to the presence of iron in its structure. This compound is known for its chelating properties, where the dithiocarbamate ligands coordinate with iron ions, forming stable complexes. It is soluble in polar solvents, which enhances its utility in various chemical applications. Diethyldithiocarbamic acid ferric salt is primarily used in analytical chemistry, particularly in the extraction and determination of metal ions. Additionally, it exhibits fungicidal and herbicidal properties, making it relevant in agricultural chemistry. The compound's stability and reactivity can be influenced by factors such as pH and temperature, which are important considerations in its application. Safety data sheets indicate that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound serves as a significant agent in both industrial and research settings.

Diethyldithiocarbamicacidferricsalt; 95%

13963-59-2: (OC-6-11)-Tris(N,N-diethylcarbamodithioato-κS,κS′)iron, Diethyldithiocarbamic acid ferric salt, Iron diethyldithiocarbamate, Iron tris(diethyldithiocarbamate), Iron(3+) Tris(Diethylcarbamodithioate), Iron(III) diethyldithiocarbamate, Iron, tris(N,N-diethylcarbamodithioato-κS,κS′)-, (OC-6-11)-, Iron, tris(diethylcarbamodithioato-S,S′)-, (OC-6-11)-, Iron, tris(diethylcarbamodithioato-κS,κS′)-, (OC-6-11)-, Iron, tris(diethyldithiocarbamato)-, NSC 177698, Rhenogran TTFE 75, Tris(N,N-diethyldithiocarbamato)iron, Tris(diethyldithiocarbamato)iron

Iron, tris(N,N-diethylcarbamodithioato-κS,κS')-, (OC-6-11)-

Diethyldithiocarbamic acid ferric salt (DDTC) is a reactive metal immobilization agent that can be used in the synthesis of fatty acids. DDTC reacts with chlorine atoms from chlorinated solvents to form diethyldithiocarbamic acid chloride, which is then used to react with the desired fatty acid. This process results in a product that has an increased stability and decreased reactivity. DDTC can also be used as a catalyst for the production of hydrogen chloride, which is a reactive byproduct of hydrochloric acid. The liquid chromatography method is used to measure the optical properties of DDTC. The morphology of DDTC particles is dependent on their size and shape. Mammalian cells are sensitive to DDTC due to its ability to inhibit fatty acid metabolism and protein synthesis.

CAS 13963-59-2: Diethyldithiocarbamicacidferricsalt; 95%

Iron, tris(N,N-diethylcarbamodithioato-κS,κS')-, (OC-6-11)-

Ref: IN-DA001BF8

Diethyldithiocarbamic acid ferric salt

Ref: 3D-FD41218