1-(2-Aminoethyl)-1H-1,2,3-triazole

1-(2-Aminoethyl)-1H-1,2,3-triazole - Names and Identifiers

Name	2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE
Synonyms	1H-1,2,3-Triazole-1-ethanamine 2-[1,2,3]Triazol-1-ylethylamine 2-(1,2,4-triazol-1-yl)ethanamine 2-(1H-1,2,3-TRIAZOL-1-YL)ETHAMINE 1-(2-Aminoethyl)-1H-1,2,3-triazole 2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE [2-(1H-[1,2,3]Triazol-1-yl)ethyl]amine
CAS	4320-94-9

1-(2-Aminoethyl)-1H-1,2,3-triazole - Physico-chemical Properties

Molecular Formula	C4H8N4
Molar Mass	112.13
Density	1.31
Boling Point	241℃
Flash Point	100℃
pKa	7.38±0.10(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2–8 °C

1-(2-Aminoethyl)-1H-1,2,3-triazole - Introduction

2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE, chemical formula C3H6N4, is an aromatic cyclic compound containing three nitrogen atoms. It is in the solid state, colorless to pale yellow, and has special ammonia and azide groups.

The compound is commonly used as an intermediate in organic synthesis, and has a wide range of applications in the fields of drugs, dyes and pesticides. Specific uses include anti-infective drugs, anti-cancer drugs, anti-pain drugs, dyes and optical brighteners, etc. In addition, 2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE can also be used as a ligand for the silver catalyst.

There are many methods for preparing 2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE. The commonly used preparation methods include catalytic hydrogenation oxidation reaction, protective group conversion reaction and organic synthesis reaction.

Regarding safety information, the toxicity of 2-(1H-1,2,3-TRIAZOL-1-YL)ETHANAMINE to humans is unknown. However, like most organic compounds, prolonged contact and inhalation of the substance should be avoided. During the operation, appropriate protective measures should be used, such as wearing gloves, safety glasses and protective masks, and ensure that the operation is carried out in a well-ventilated environment. If ingestion or contact causes discomfort, seek medical attention immediately.

Last Update：2024-04-09 20:52:54