Molecular structure of Triethylamine hydrochloride, CAS Number: 554-68-7
Triethylamine hydrochloride (CAS 554-68-7)
CAS Number:
554-68-7
Purity:
98%
Molecular Weight:
137.65
Molecular Formula:
C6H15N•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Triethylamine hydrochloride exhibits solubility in water. This compound serves as an important intermediate in organic synthesis, finding diverse applications in the production of agrochemicals and various organic compounds. Moreover, it acts as a versatile catalyst in chemical reactions, a surfactant, and a solvent. In research and industry, Triethylamine hydrochloride plays a vital role in protein and biomolecule purification, as well as in peptide synthesis. Additionally, it aids in studying enzyme kinetics and contributes to the synthesis of peptide and carbohydrate derivatives.
Triethylamine hydrochloride (CAS 554-68-7) References
- Diazo preparation via dehydrogenation of hydrazones with 'activated' DMSO. | Javed, MI. and Brewer, M. 2007. Org Lett. 9: 1789-92. PMID: 17408280
- Multicomponent reactions for the synthesis of complex piperidine scaffolds. | Zhu, W., et al. 2009. Angew Chem Int Ed Engl. 48: 5880-3. PMID: 19308937
- Purification, recovery, and laser-driven fluorination of silicon from dissolved and particulate silica for the measurement of natural stable isotope abundances. | De La Rocha, CL., et al. 1996. Anal Chem. 68: 3746-50. PMID: 21619245
- Conferring flame retardancy on cotton using novel halogen-free flame retardant bifunctional monomers: synthesis, characterizations and applications. | Cheema, HA., et al. 2013. Carbohydr Polym. 92: 885-93. PMID: 23218381
- The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(II) and copper(II) complexes. | Sirbu, D., et al. 2015. Dalton Trans. 44: 14646-55. PMID: 26213204
- Identification of a new psychoactive substance in seized material: the synthetic opioid N-phenyl-N-[1-(2-phenethyl)piperidin-4-yl]prop-2-enamide (Acrylfentanyl). | Breindahl, T., et al. 2017. Drug Test Anal. 9: 415-422. PMID: 27476446
- Cathodic electrodeposited Cu-BTC MOFs assembled from Cu(II) and trimesic acid for electrochemical determination of bisphenol A. | Hu, P., et al. 2020. Mikrochim Acta. 187: 145. PMID: 31970521
- Sustainable and cost-effective ternary electrolyte Et3NHCl-AlCl3-Mg(DEP)2 for high-performance rechargeable magnesium batteries. | Prabhakar, S., et al. 2022. Phys Chem Chem Phys. 24: 1840-1848. PMID: 34988572
- Synthesis of trifluoromethylisoxazoloazines. | Tanaka, K. and Pedersen, EB. 1986. Acta Chem Scand B. 40: 760-3. PMID: 3825403
- Gel filtration and reactivity of sulphydryl groups of human hemoglobin in concentrated triethylamine hydrochloride solutions. | Spagnuolo, C., et al. 1972. Ital J Biochem. 21: 221-9. PMID: 4655510
- Lycopene accumulation induced by 2-(4-chlorophenylthio)-triethylamine hydrochloride. | Coggins, CW., et al. 1970. Science. 168: 1589-90. PMID: 5420543
- Studies on the relations between molecular and functional properties of hemoglobin. VIII. Equiliria and kinetics of the reactions of hemoglobin with ligands in concentrated solutions of triethylamine hydrochloride. | Amiconi, G., et al. 1971. J Biol Chem. 246: 1883-8. PMID: 5555558
- 1,2,3-triazole[4,5-d]pyridazines. III--Synthesis of new 4-amino derivatives and their affinity toward adenosine receptors. | Biagi, G., et al. 1994. Farmaco. 49: 357-62. PMID: 8080619
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Triethylamine hydrochloride, 50 g | sc-251324 | 50 g | $33.00 | |||
Triethylamine hydrochloride, 250 g | sc-251324A | 250 g | $43.00 |