51250-16-9 Usage
Description
(4-Ammoniobutyl)dithiocarbamate is a chemical compound belonging to the dithiocarbamate family, characterized by its yellowish solid appearance, pungent odor, and solubility in water. It is synthesized by reacting carbon disulfide with the amine group of 1,4-diaminobutane, resulting in the formation of the dithiocarbamate moiety.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 51250-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51250-16:
(7*5)+(6*1)+(5*2)+(4*5)+(3*0)+(2*1)+(1*6)=79
79 % 10 = 9
So 51250-16-9 is a valid CAS Registry Number.
51250-16-9Relevant articles and documents
Novel bridgehead nitrogen heterocycles: Facile synthesis and antimicrobial activity of 2,3-diaryl-3,3a,6,7,8,9-hexahydro-2H-pyrazolothiazolodiazepines
Mohan, Jag,Singh, Virender,Malik, Nirmal
, p. 1105 - 1106 (2007/10/03)
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.
Synthesis and radioprotective effects of disodium alkanebisdithiocarbamates, ω aminoalkyldithiocarbamic acids and their N,N dimethyl derivatives
Barnes,Fatome,Esslemont,et al.
, p. 619 - 622 (2007/10/04)
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.
