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Thermo Scientific Chemicals
1H-1,2,3-Triazole, 98%
CAS: 288-36-8 | C2H3N3 | 69.067 g/mol
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Catalog number A16999.03
also known as A16999-03
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52.65
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Quantity:
1 g
Price (USD)
52.65
Online Exclusive
58.60Save 5.95 (10%)
Each
Chemical Identifiers
CAS288-36-8
IUPAC Name2H-1,2,3-triazole
Molecular FormulaC2H3N3
InChI KeyQWENRTYMTSOGBR-UHFFFAOYSA-N
SMILESN1N=CC=N1
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Specifications
Specification Sheet
Specification SheetAssay (GC)≥97.5%
Appearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
FormLiquid
Refractive Index1.4960-1.5000 @ 20?C
It effectively promotes the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism. A useful triazole for proteomics research
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It effectively promotes the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism. A useful triazole for proteomics research
Solubility
Fully miscible in water.
Notes
Store away from oxidizing agents. Keep the container tightly sealed and store in cool, dry condition in well ventilated place.
It effectively promotes the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism. A useful triazole for proteomics research
Solubility
Fully miscible in water.
Notes
Store away from oxidizing agents. Keep the container tightly sealed and store in cool, dry condition in well ventilated place.
RUO – Research Use Only
General References:
- Zhen Zhou.; Siwen Li.; Yuelan Zhang.; Meilin Liu.; Wen Li. Promotion of proton conduction in polymer electrolyte membranes by 1H-1,2,3-triazole.J Am Chem Soc.,2005,127(31), 10824-10825.
- Kadir Dabak.; Özkan Sezer.; Ahmet Akar.; Olcay Anaç. Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazole derivatives.European Journal of Medicinal Chemistry,2003,38,(2), 215-218.
- In weakly alkaline (bicarbonate) solution, this and other azoles promote the Baylis Hillman reaction (see 1,4-Diazabicyclo[2.2.2]octane, A14003), giving high yields with short reaction times: Tetrahedron Lett., 45, 5171 (2006).