4122-04-7

Basic information

• Product Name: 2-Amino-1,3,5-triazine
• Synonyms: TIMTEC-BB SBB005530;2-AMINO-1,3,5-TRIAZINE;1,3,5-TRIAZIN-2-AMINE;2-AMINO-1,3,5-TRIAZINE 98%;1,3,5-Triazin-2(5H)-imine;s-Triazine-2-amine;2-Amino-1,3,5-triazine,98%;2-AMino-1,3,5-triazine, 98% 1GR
• CAS NO: 4122-04-7
• Molecular Formula: C₃H₄N₄
• Molecular Weight: 96.09
• EINECS: 223-920-6
• Mol File: 4122-04-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 219-224 °C
• Boiling Point: 169.59°C (rough estimate)
• Flash Point: 182.2 °C
• Appearance: White to light yellow/Crystalline Powder
• Density: 1.2170 (rough estimate)
• Vapor Pressure: 0.000132mmHg at 25°C
• Refractive Index: 1.7380 (estimate)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 3.08±0.10(Predicted)
• CAS DataBase Reference: 2-Amino-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-1,3,5-triazine(4122-04-7)
• EPA Substance Registry System: 2-Amino-1,3,5-triazine(4122-04-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 24/25
• HazardClass: IRRITANT
• Hazardous Substances Data: 4122-04-7(Hazardous Substances Data)

Usage

Description

2-Amino-1,3,5-triazine is a white to light yellow crystalline powder with distinct chemical properties. It is an organic compound that has been identified for its potential applications in various fields due to its unique characteristics.

Uses

Used in Pharmaceutical Industry:
2-Amino-1,3,5-triazine is used as an oral anti-inflammatory agent for its ability to suppress bladder hyperactivity in a rat model. This application highlights its potential in developing treatments for urinary disorders and improving the quality of life for patients suffering from such conditions.
Used in Chemical Research:
Given its unique chemical properties, 2-Amino-1,3,5-triazine may also be utilized in chemical research and development. Its crystalline structure and specific characteristics can be further explored for the synthesis of new compounds or as a component in various chemical reactions.

InChI:InChI=1/C3H4N4/c4-3-6-1-5-2-7-3/h1-2H,(H2,4,5,6,7)

Upstream product

• 290-87-9 1,3,5-Triazine 
• 50-01-1 guanidine hydrochloride 
• 2533-68-8 trichloroacetamidine 
• 4774-33-8 tris(formylamino)methane 
• 593-85-1 diguanidine carbonate 
• 4471-51-6 formylguanidine 
• 77287-34-4 formamide 
• 68-12-2 N,N-dimethyl-formamide 
• 1572-46-9 9-benzylfluorene 

Downstream Products

• 1572-46-9 9-benzylfluorene 
• 104691-55-6 7-(4-Methylsulphonyloxy-2-methoxy-phenyl)-imidazo[1,2-a][1,3,5]triazine 
• 1345956-71-9 4-(benzylamino)-2-[(2-hydroxyethyl)amino]-7-(1,3,5-triazinylamino)-pyrido[3,2-d]pyrimidine 
• 1570135-48-6 2-((1,3,5-triazin-2-yl)amino)-N-(2-(4,5-dihydrooxazol-2-yl)phenyl)benzamide 

Relevant articles and documents

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A novel synthetic route to 2-amino and 2-alkylamino-1,3,5-triazines based on nucleophilic aromatic substitution of hydrogen: The first reactions of 1,3,5-triazine with nucleophiles without ring decomposition

2-Amino- and 2-alkylamino-1,3,5-triazines were smoothly obtained by oxidative (alkyl)amination of 1,3,5-triazine in ammonia-ethanol or alkylamine-ethanol with bis(pyridine)silver(I)permanganate (AgPy 2MnO4) as the oxidant. These transformations are the first reactions of 1,3,5-triazine with nucleophiles without ring decomposition and the first examples of nucleophilic substitution of hydrogen on this substrate. Georg Thieme Verlag Stuttgart.