51250-16-9

Usage

Uses

Used in Chelating Applications:
(4-Ammoniobutyl)dithiocarbamate is used as a chelating agent for its ability to form stable complexes with metal ions, which is crucial in various industrial processes to prevent unwanted reactions and facilitate the separation of components.
Used in Rubber Chemicals Production:
In the rubber industry, (4-ammoniobutyl)dithiocarbamate is used as a component in the production of rubber chemicals, contributing to the enhancement of rubber properties and performance.
Used in Corrosion Inhibition:
(4-Ammoniobutyl)dithiocarbamate has been studied for its potential use as a corrosion inhibitor, particularly in the protection of metal surfaces from degradation in various industrial applications.
Used as an Antimicrobial Agent:
(4-ammoniobutyl)dithiocarbamate has also been investigated for its antimicrobial properties, making it a potential candidate for use in the preservation and sanitation of materials in different industries, including agriculture and pharmaceuticals.
Used in Agricultural Processes:
(4-Ammoniobutyl)dithiocarbamate's antimicrobial and chelating properties make it a valuable compound for use in agricultural processes, where it can help protect crops from diseases and improve nutrient uptake.
Used in Industrial Processes:
Due to its versatile properties, (4-ammoniobutyl)dithiocarbamate has potential applications in various industrial processes, such as water treatment, where it can act as a chelating agent to remove heavy metals, and in the manufacturing of various chemicals and materials.

Upstream product

• 75-15-0 carbon disulfide 
• 110-60-1 1,4-diaminobutane 

Downstream Products

• 5700-04-9 1,3-diazacycloheptane-2-thione 
• 7783-06-4 hydrogen sulfide 
• 110-60-1 1,4-diaminobutane 
• 92897-50-2 2-[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene]-5,6,7,8-tetrahydro-thiazolo[3,2-a][1,3]diazepin-3-one 
• 173468-90-1 2-p-chlorobenzylidene-5,6,7,8-tetrahydrothiazolo<3,2-a><1,3>diazepin-3(2H)-one 
• 19055-93-7 1,3-diazepan-2-one 
• 5700-04-9 2-mercapto-4,5,6,7-tetrahydro-1H-1,3-diazepine 

Relevant academic research and scientific papers

Novel bridgehead nitrogen heterocycles: Facile synthesis and antimicrobial activity of 2,3-diaryl-3,3a,6,7,8,9-hexahydro-2H-pyrazolothiazolodiazepines

A facile synthesis of 2,3-diaryl-3,3a,6,7,8,9-hexahydro-2H-pyrazolothiazolodiazepines (3) has been achieved in a single-step by treating 2-arylidene-5,6,7,8-tetrahydrothiazolodiazepin-3(2H)-ones (2) with hydrazines.Compounds 2 is turn have been obtained in a single-step by condensing 4,5,6,7-tetrahydro-1H-1,3-diazepine-2-thiol (1) with ethyl chloroacetate and aldehydes in the presence of pyridine and piperidine.Compounds 3 represent a novel and hitherto unknown heterocyclic system.The antibacterial and antifungal activities of some of the compounds of this system have also been evaluated.

Cyclic Urea and Thiourea Derivatives as Inducers of Murine Erythroleukemia Differentiation

A series of derivatives of tetramethylurea, a known inducer of the differentiation of Friend erythroleukemia cells, has been synthesized and tested for its capacity to induce erythroid maturation, as measured by the synthesis of hemoglobin.Cyclic urea and thiourea derivatives consisting of five-, six-, and seven-membered ring systems containing N-alkyl substituents were prepared.Most of these agents were relatively effective inducers of differentiation, with N-alkyl substitution appearing to be essential for maximum response.The most potent agents developed wereN,N'-dimethyl cyclic ureas.Exposure to concentrations of 2 to 4 mM of these derivatives resulted in more than 90percent of the cell population achieving a differentiated state.Under these conditions, the parent compound, tetramethylurea, was slightly less efficacious, causing differentiation of only 68percent of the population at its maximum effective level of 4 mM.

Synthesis and radioprotective effects of disodium alkanebisdithiocarbamates, ω aminoalkyldithiocarbamic acids and their N,N dimethyl derivatives

The 12 compounds studied containing the dithiocarbamate group, 5 of which are new, showed remarkably low acute toxicity in mice, with LD50 values generally higher than 1,000 mg/kg by the intraperitoneal route. Most noteworthy was 2 aminoethyldithiocarbamic acid, which protected 100% of mice against an LD99 of whole body γ-radiation in dose of 750 mg/kg, while the LD50 exceeds 1,500 mg/kg: certain higher homologues and N-methylated derivatives were also radioprotective and the series may merit further study.