51250-16-9

Basic information

• Product Name: (4-ammoniobutyl)dithiocarbamate
• CAS NO: 51250-16-9
• Molecular Formula: C₅H₁₂N₂S₂
• Molecular Weight: 164.2922
• Mol File: 51250-16-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 251.6°C at 760 mmHg
• Flash Point: 106°C
• Density: 1.152g/cm³
• Vapor Pressure: 0.0202mmHg at 25°C
• Refractive Index: 1.581
• CAS DataBase Reference: (4-ammoniobutyl)dithiocarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (4-ammoniobutyl)dithiocarbamate(51250-16-9)
• EPA Substance Registry System: (4-ammoniobutyl)dithiocarbamate(51250-16-9)

Safety Data

• Hazardous Substances Data: 51250-16-9(Hazardous Substances Data)

Usage

General Description

(4-ammoniobutyl)dithiocarbamate is a chemical compound that belongs to the dithiocarbamate family. It is often used as a chelating agent and in the production of rubber chemicals. The compound has been studied for its potential use as a corrosion inhibitor and as an antimicrobial agent. It is synthesized by reacting carbon disulfide with the amine group of 1,4-diaminobutane to form the dithiocarbamate moiety. The resulting compound is a yellowish solid with a pungent odor, and it is soluble in water. Due to its versatile properties, (4-ammoniobutyl)dithiocarbamate has potential applications in various industrial and agricultural processes.

Upstream product

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

Downstream Products

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

Relevant 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

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

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.