638-09-5

Basic information

• Product Name: 1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE
• Synonyms: 1,3,5-TRIAMINOBENZENE TRICHLORIDE;1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE;1,3,5-triaMine trihydrochloride;1,3,5-BenzenetriaMine, trihydrochloride;Benzene-1,3,5-triaMine trihydrochloride
• CAS NO: 638-09-5
• Molecular Formula: C₆H₉N₃*3ClH
• Molecular Weight: 232.54
• Mol File: 638-09-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 129 °C(Solv: chloroform (67-66-3))
• Boiling Point: 440.9 °C at 760 mmHg
• Flash Point: 220.5 °C
• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE(638-09-5)
• EPA Substance Registry System: 1,3,5-TRIAMINOBENZENE TRIHYDROCHLORIDE(638-09-5)

Safety Data

• Hazardous Substances Data: 638-09-5(Hazardous Substances Data)

Usage

General Description

1,3,5-Triaminobenzene trihydrochloride is a chemical compound with the molecular formula C6H9N3 ? 3HCl. It is a salt formed by the reaction of 1,3,5-triaminobenzene with hydrochloric acid. The compound is a white solid, soluble in water, and has a melting point of around 240°C. 1,3,5-Triaminobenzene trihydrochloride is used as a reagent in the synthesis of various organic compounds and as a corrosion inhibitor in metalworking fluids. It is also utilized in the production of dyes, pharmaceuticals, and polymers. Additionally, it has potential applications in the field of materials science, particularly in the synthesis of conductive polymers and coordination polymers. The compound's properties and its role as a building block in organic synthesis make it an important chemical in various industries.

Upstream product

• 618-87-1 3, 5-dinitroaniline 
• 7373-27-5 1,3,5-benzenetriisocyanate 

Downstream Products

• 165820-78-0 N¹,N³,N⁵-tris(4-tert-butylphenyl)benzene-1,3,5-triamine 
• 117882-61-8 N,N',N''-(2,4,6-trinitro-benzene-1,3,5-triyl)-tris-toluene-4-sulfonamide 
• 626-46-0 2,6-diamino-4-pyrimidinone 
• 111638-98-3 N,N',N''-benzene-1,3,5-triyl-tris-toluene-4-sulfonamide 

Relevant articles and documents

Modular Construction of Porous Hydrogen-Bonded Molecular Materials from Melams

Ordered materials with predictable structures and properties can be made by a modular approach, using molecules designed to interact with neighbors and hold them in predetermined positions. Incorporating 4,6-diamino-1,3,5-triazin-2-yl (DAT) groups in modules is an effective way to direct assembly because each DAT group can form multiple N?H???N hydrogen bonds according to established patterns. We have found that modules with high densities of N(DAT)2 groups can be made by base-induced double triazinylations of readily available amines. The resulting modules can form structures held together by remarkably large numbers of hydrogen bonds per molecule. Even simple modules with only 1–3 N(DAT)2 groups and fewer than 70 non-hydrogen atoms can crystallize to form highly open networks in which each molecule engages in over 20 N?H???N hydrogen bonds, and more than 70 % of the volume is available for accommodating guests. In favorable cases, guests can be removed to create rigorously porous crystalline solids analogous to zeolites and metal–organic frameworks.