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Quality Level
Assay
98%
form
crystals
mp
123-125 °C (lit.)
SMILES string
N.OC(=O)C(F)(F)F
InChI
1S/C2HF3O2.H3N/c3-2(4,5)1(6)7;/h(H,6,7);1H3
InChI key
YCNIBOIOWCTRCL-UHFFFAOYSA-N
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General description
Ammonium Trifluoroacetate is used as a catalyst in organic synthesis and as an additive in the mobile phase for chiral racemate separation.
Application
Used in the synthesis of hexafluoro-2-aminopentan-4-one ligand and in tuning and calibrating new liquid chromatography/mass spectrometry systems.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Journal of pharmaceutical and biomedical analysis, 155, 70-81 (2018-04-07)
Core-shell particles (superficially porous particles, SPPs) have been proven to provide high-throughput and effective separations of a variety of chiral molecules. However, due to their limited commercialization, many separations have not been reported with these stationary phases. In this study
Chirality, 30(9), 1067-1078 (2018-07-04)
A modified macrocyclic glycopeptide-based chiral stationary phase (CSP), prepared via Edman degradation of vancomycin, was evaluated as a chiral selector for the first time. Its applicability was compared with other macrocyclic glycopeptide-based CSPs: TeicoShell and VancoShell. In addition, another modified
Ammonium Trifluoroacetate-Mediated Synthesis of 3, 4-dihydropyrimidin-2 (1H)-ones
International Scholarly Research Network, 2011 (2011)
European journal of mass spectrometry (Chichester, England), 26(2), 117-130 (2019-10-03)
A rapid and sensitive liquid chromatography-mass spectrometry method was developed, optimized, and validated for simultaneous quantification of empagliflozin and metformin in human plasma using empagliflozin D4and metformin D6 as an internal standard. Analytes and internal standard were extracted from plasma
Chirality, 31(9), 688-699 (2019-07-19)
The enantiomeric excess of chiral starting materials is one of the important factors determining the enantiopurity of products in asymmetric synthesis. Fifty-one commercially available chiral reagents used as building blocks, catalysts, and auxiliaries in various enantioselective syntheses were assayed for
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