89417-77-6

Basic information

• Product Name: 1-PROPYL-1,2,4-TRIAZOLE
• Synonyms: 1-PROPYL-1,2,4-TRIAZOLE;1-Propyl-1H-[1,2,4]triazole
• CAS NO: 89417-77-6
• Molecular Formula: C₅H₉N₃
• Molecular Weight: 111.15
• Mol File: 89417-77-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 203.9 °C at 760 mmHg
• Flash Point: 77.1 °C
• Appearance: /
• Density: 1.07 g/cm³
• Vapor Pressure: 0.27mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 1-PROPYL-1,2,4-TRIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PROPYL-1,2,4-TRIAZOLE(89417-77-6)
• EPA Substance Registry System: 1-PROPYL-1,2,4-TRIAZOLE(89417-77-6)

Safety Data

• Hazardous Substances Data: 89417-77-6(Hazardous Substances Data)

Usage

Molecular structure

A triazole derivative with a propyl group attached to the triazole ring

Molecular structure

A triazole ring with a propyl group attached

Industrial applications

Corrosion inhibitor in the oil and gas industry
Fungicide in agriculture
Stabilizer in the production of polymers

Pharmaceutical applications

Potential use in cancer treatment
Applicable for other disease treatments

Pharmaceutical applications

Use of a chemical compound in the development of medications for treating diseases

Research and development

Ligand in coordination chemistry
Chelating agent in metal ion removal processes

Triazole derivatives

A class of chemical compounds with various applications

Propyl group

A three-carbon alkyl group (-C3H7)

Corrosion inhibition

Prevention or reduction of corrosion in materials, such as metals

Fungicide

A chemical substance used to kill or inhibit the growth of fungi

Stabilizer

A substance that helps maintain the stability of a product, such as polymers

Cancer treatment

The use of a chemical compound to prevent or treat cancer

Coordination chemistry

A subfield of chemistry that studies the interaction between metal ions and ligands

Chelating agents

Substances that bind to metal ions, forming complexes and helping to remove them from a system

Metal ion removal

The process of removing metal ions from a solution or environment

InChI:InChI=1/C5H9N3/c1-2-3-8-5-6-4-7-8/h4-5H,2-3H2,1H3

Upstream product

• 288-88-0 1,2,4-Triazole 
• 106-94-5 propyl bromide 
• 107-08-4 1-iodo-propane 

Downstream Products

• 1435949-28-2 [(5-(diphenylphosphino)-1-propyl-1H-1,2,4-triazole)(triphenylphosphine)2Cu₂I₂] 
• 1401254-42-9 [3-(1-propyl-1H-1,2,4-triazolyl)]diphenylmethanol 

Relevant articles and documents

Functionalization of 1,3,4-Oxadiazoles and 1,2,4-Triazoles via Selective Zincation or Magnesiation Using 2,2,6,6-Tetramethylpiperidyl Bases

We report the metalation of the 1,3,4-oxadiazole and 1,2,4-triazole scaffolds via regioselective zincation or magnesiation using the TMP bases (TMP = 2,2,6,6-tetramethylpiperidyl) TMP2Zn·2LiCl, TMP2Zn·2MgCl2·2LiCl, TMPMgCl

Physicochemical and thermal properties for a series of 1-alkyl-4-methyl-1, 2,4-triazolium bis(trifluoromethylsulfonyl)imide ionic liquids

Physicochemical properties and long-term thermal stabilities are reported for a series of 1-alkyl-4-methyl-1,2,4-triazolium [NTf2] ionic liquids, and a Walden plot analysis was conducted in order to determine the ionicity of these materials. In general, viscosities were found to increase with increasing alkyl chain length while densities and molar conductivities were found to decrease. The 1,2,4-triazolium ionic liquids were classified as "good" ionic liquids after analysis of the Walden plot; however, they did not perform as well as the standard imidazolium ionic liquid [bmim][NTf 2]. Thermal properties from DSC and TGA experiments were also completed. 1,2,4-Triazolium ionic liquids with an alkyl chain length of octyl (C8) or less exhibited a single Tg transition below ?70 °C; however, the decyl (C10) and dodecyl (C12) systems exhibited a Tm value. No correlation between Tonset or Td5% and alkyl chain length was observed during short-term, temperature-ramped TGA experiments. However, long-term, isothermal TGA studies indicated a general increase in T0.01/10 value as the alkyl chain length increased. Both short- and long-term TGA studies indicated that the 1,2,4-triazolium ionic liquids were not as thermally stable as the model imidazolium ionic liquid [bmim][NTf 2].

Correlating structure with thermal properties for a series of 1-alkyl-4-methyl-1,2,4-triazolium ionic liquids

Thermal properties (Tm and Td) are reported for a series of 1-alkyl-4-methyl-1,2,4-triazolium ionic liquids where the alkyl chain length R and anion [X-] were varied. The highest melting transitions were observed when a lo