38360-74-6

Usage

Uses

Used in Organic Synthesis:
N,N'-Diaminoguanidine monohydrochloride is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the production of a wide range of organic compounds.
Used in Pharmaceutical Production:
As an intermediate, N,N'-Diaminoguanidine monohydrochloride plays a crucial role in the manufacturing process of certain pharmaceuticals, aiding in the synthesis of active ingredients or other essential components of medications.
Used in Dye Manufacturing:
N,N'-Diaminoguanidine monohydrochloride is utilized in the production of dyes, where it serves as an intermediate or a key component in the synthesis of colorants used in various industries.
Used as a Corrosion Inhibitor:
N,N'-Diaminoguanidine monohydrochloride is employed as a corrosion inhibitor, protecting materials from the damaging effects of corrosion, thereby extending their service life and improving their performance.
Used as a Stabilizer in Nitroguanidine Production:
In the production of nitroguanidine, N,N'-Diaminoguanidine monohydrochloride acts as a stabilizer, ensuring the safe and consistent manufacturing process of this high-energy compound used in propellants and explosives.
Used in Antifungal Applications:
N,N'-Diaminoguanidine monohydrochloride has been investigated for its antifungal properties, showing potential in the treatment of various fungal infections. Its use in this area is still under research and development.

Upstream product

• 506-77-4 cyanogen chloride 
• 1937-19-5 1-aminoguanidine hydrochloride 

Downstream Products

• 21532-07-0 3,4-diamino-5-methyl-1,2,4-triazole 
• 3560-86-9 2,2'-bis(phenylmethylene)carbonimidic dihydrazide 
• 104025-82-3 5-(2-Phenoxy-ethyl)-[1,2,4]triazole-3,4-diamine; hydrochloride 
• 77874-58-9 (14C)-1,3-Bis(p-chlorobenzylideneamino)guadine 
• 98275-29-7 3-Butyl-4.5-diamino-1.2.4-triazol 
• 1206770-39-9 1,3-bis-((1-(3-pyridyl)ethylidene)amino)guanidine hydrochloride 
• 1262322-10-0 1,1'-carbonylbis(3-phenyl-5-trifluoromethyl-1H-pyrazole) 

Relevant academic research and scientific papers

A facile synthesis of energetic salts based on fully nitroamino-functionalized [1,2,4]triazolo[4,3-b] [1,2,4]triazole

A novel family of fully nitroamino-functionalized [1,2,4]triazolo[4,3-b][1,2,4]triazole-based energetic salts were synthesized. All salts were characterized by IR and multinuclear NMR spectroscopy, thermal analysis and elemental analysis. The crystal structures of salts 5, 6, and 7 were confirmed by single-crystal X-ray diffraction. The densities of these salts are between 1.65 (4) and 1.89 g cm-3 (3), whilst their oxygen balances are between -42.8% (7) and -11.3% (3). Theoretical performance calculations (Gaussian 09 and EXPLO 6.01) provided detonation pressures and velocities for salts 2-7 in the ranges of 27.6-41.1 GPa and 8519-9518 m s-1, respectively, which make them competitive energetic materials.

1,3-diaminoguanidine-2,4,5-trinitroimidazole salt and preparation method thereof

The invention discloses a 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt and a preparation method thereof, belongs to the technical field of organic energetic materials and aims at solving the problem in the prior art that a TNT-based melt-cast explosive harms the environment in the use process. The method comprises the steps of using imidazole as a reaction raw material to generate 2,4,5-trinitroimidazole through step-by-step nitrification; enabling a nitrification product to react with a potassium carbonate/potassium chloride solution to form a salt to prepare 2,4,5-trinitroimidazole potassium salt; and finally obtaining a target product 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt through double-decomposition reaction of 1,3-diamino guanidine hydrochloride and the 2,4,5-trinitroimidazole potassium salt. The preparation method is simple, low in preparation cost and good in security; and the final product 1,3-diaminoguanidine-2,4,5-trinitroimidazole salt is high in purity.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.