Description

2-(1-Benzyl-1H-1,2,3-Triazol-4-Yl)Ethanol is a versatile triazole derivative that serves as a critical building block in advanced organic synthesis. Its unique structure, featuring both a benzyl-protected triazole ring and a terminal ethanol group, makes it a valuable intermediate for constructing complex molecules with tailored properties. This compound is primarily sought after by research institutions and industrial R&D departments in the pharmaceutical, agrochemical, and material science sectors for developing new active ingredients and functional materials.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of novel drug candidates, particularly those targeting enzymes or receptors where the triazole moiety can act as a bioisostere.
• Agrochemical Research: Used in developing new fungicides, herbicides, and plant growth regulators, leveraging the biological activity of the 1,2,3-triazole scaffold.
• Ligand Synthesis: Serves as a starting material for creating chelating ligands in coordination chemistry and catalysis.
• Polymer & Material Science: Functional monomer for producing specialty polymers with enhanced thermal stability or specific surface properties.
• Click Chemistry: The benzyl-protected triazole, after deprotection or further modification, can be utilized in Huisgen cycloaddition reactions for bioconjugation.
• Chemical Biology Probes: Useful for synthesizing molecular probes to study biological processes and protein interactions.

Basic Information

Product Name	2-(1-Benzyl-1H-1,2,3-Triazol-4-Yl)Ethanol
CAS No.	808736-97-2
Molecular Formula	C11H13N3O
Molecular Weight	203.24 g/mol
Synonyms	4-(2-Hydroxyethyl)-1-benzyl-1H-1,2,3-triazole; 1-Benzyl-4-(2-hydroxyethyl)-1H-1,2,3-triazole; 2-(1-Benzyl-1H-1,2,3-triazol-4-yl)ethan-1-ol; 1-Benzyl-1H-1,2,3-triazole-4-ethanol; BTE; Benzyl-triazole-ethanol; N-Benzyl-4-(2-hydroxyethyl)triazole
EINECS	Contact for details

Quality Control

Our production of 2-(1-Benzyl-1H-1,2,3-Triazol-4-Yl)Ethanol adheres to stringent quality protocols to ensure batch-to-batch consistency and high purity for research and development applications. All materials are characterized using advanced analytical techniques, including NMR, HPLC, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with each shipment to support your quality assurance and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at room temperature (15-25°C). Keep the container tightly sealed to minimize exposure to atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Melting Point	Contact for details
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.