26055-65-2

Basic information

• Product Name: Guanidine,N,N'''-1,4-phenylenebis-,dihydrochloride
• CAS NO: 26055-65-2
• Molecular Weight: 265.145
• Mol File: 26055-65-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Guanidine,N,N'''-1,4-phenylenebis-,dihydrochloride (CAS DataBase Reference)
• NIST Chemistry Reference: Guanidine,N,N'''-1,4-phenylenebis-,dihydrochloride (26055-65-2)
• EPA Substance Registry System: Guanidine,N,N'''-1,4-phenylenebis-,dihydrochloride (26055-65-2)

Safety Data

• Hazardous Substances Data: 26055-65-2(Hazardous Substances Data)

Usage

General Description

Guanidine, N,N'''-1,4-phenylenebis-, dihydrochloride is a chemical compound used primarily as a pharmaceutical intermediate and as a precursor for the synthesis of various organic compounds. It is commonly employed in the creation of polyurethane foams, epoxy resins, and pharmaceutical drugs. The dihydrochloride form of guanidine helps stabilize the molecule and enhance its solubility in water, making it easier to work with in various applications. It is important to handle this compound with care as it may be corrosive and harmful if not used properly. Overall, guanidine, N,N'''-1,4-phenylenebis-, dihydrochloride plays a valuable role in the production of a wide range of products and is an essential building block in organic chemistry.

Upstream product

• 624-18-0 benzene-1,4-diamine hydrochloride 
• 693-13-0 diisopropyl-carbodiimide 
• 420-04-2 CYANAMID 

Relevant articles and documents

TRICYCLIC AMINO CONTAINING COMPOUNDS FOR TREATMENT OR PREVENTION OF SYMPTOMS ASSOCIATED WITH ENDOCRINE DYSFUNCTION

The disclosure provides methods of use of certain compounds that are useful for treating certain symptoms of endocrine disturbances, and in particular those associated with hot flashes.

Synthesis, characterization and chemistry of the fluoronitramide anion

The fluoronitramide anion, as its potassium, tetraisopropyl p-phenylenediguanidinium, and tetraphenylphosphonium salts, have been synthesized. The latter salt was characterized in detail as it was by far the most stable. The free acid HN(F)(NO2) was found to be unstable, as was the ammonium salt of fiuoronitramide. The fluorine atom was shown to be capable of displacement by nucleophiles. In contrast to dinitramide, which at room temperature is unreactive towards aqueous alkali, fiuoronitramide reacts instantly with aqueous hydroxide. Single crystal X-ray diffraction data show an unusual degree of uncertainty in the position of the fluorine atom in all of the salts that were examined. Georg Thieme Verlag Stuttgart.