541-69-5 Usage
Description
Benzene-1,3-diamine dihydrochloride is an organic compound with the chemical formula C6H10Cl2N2. It is a white to slightly red crystalline powder that is widely used in various applications due to its unique chemical properties.
Uses
1. Used in Chemical Synthesis:
Benzene-1,3-diamine dihydrochloride is used as a chemical intermediate for the synthesis of various compounds, such as bis(thiazolidone) and bis(thiohydantoin) derivatives. Its ability to form different chemical bonds makes it a versatile building block in the creation of a range of products.
2. Used in Material Fabrication:
In the field of material science, benzene-1,3-diamine dihydrochloride is utilized to increase the pore size in the fabrication of poly(aniline-co-1,3-phenylenediamine) cryogels. This application is particularly important in the development of materials with specific properties, such as improved adsorption or filtration capabilities.
3. Used in Pharmaceutical Industry:
Benzene-1,3-diamine dihydrochloride serves as a key component in the production of certain pharmaceuticals. Its chemical structure allows it to be a precursor to various drugs, contributing to its importance in the development of new medications.
4. Used in Dye and Pigment Industry:
Due to its chemical properties, benzene-1,3-diamine dihydrochloride is also used in the dye and pigment industry. It can be employed in the synthesis of various dyes and pigments, contributing to the vibrant colors and shades in textiles, plastics, and other materials.
5. Used in Analytical Chemistry:
Benzene-1,3-diamine dihydrochloride is utilized as a reagent in analytical chemistry for the detection and quantification of specific substances. Its unique chemical properties make it suitable for use in various analytical techniques, such as spectrophotometry and chromatography.
Safety Profile
Poison by intraperitoneal route. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits very toxic fumes of HCl and NOx. See also other phenylenediamine entries and AMINES
Check Digit Verification of cas no
The CAS Registry Mumber 541-69-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 541-69:
(5*5)+(4*4)+(3*1)+(2*6)+(1*9)=65
65 % 10 = 5
So 541-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2.2ClH/c7-5-2-1-3-6(8)4-5;;/h1-4H,7-8H2;2*1H
541-69-5Relevant articles and documents
Reduction of dinitrobenzenes by electron-carrying catalysts in the electrosynthesis of diaminobenzenes
Abakumov, M. V.,Leonova, M. Yu.,Mikhalchenko, L. V.,Novikov, V. T.,Zaplavin, A. P.
, p. 1927 - 1933 (2021/11/05)
The interaction of isomeric dinitrobenzenes (DNBs) with titanium(III), tin(II), and vanadium(II) chlorides, which are reducing agents used as electron carriers in the electrosynthesis of diaminobenzenes, has been studied. Rate constants of the reduction of isomeric DNBs and nitrophenylhydroxylamines by SnCl2 and TiCl3 in a 2 M water-alcohol solution (10 vol.% C2H5OH) of HCl were measured, and activation energies of the reduction of isomeric DNBs were determined. The rates of interaction of DNBs with the listed mediators increase in the series SnCl2 3 2. It is shown that the electrolysis of DNBs in the presence of an excess of these mediators makes it possible to obtain the corresponding diaminobenzenes with a yield of 60–90%.
