238732
Ammonium trifluoroacetate
98%
Synonym(s):
Trifluoroacetic acid ammonium salt
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About This Item
Linear Formula:
CF3CO2NH4
CAS Number:
Molecular Weight:
131.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
222-072-4
MDL number:
assay:
98%
form:
crystals
Product Name
Ammonium trifluoroacetate, 98%
InChI key
YCNIBOIOWCTRCL-UHFFFAOYSA-N
InChI
1S/C2HF3O2.H3N/c3-2(4,5)1(6)7;/h(H,6,7);1H3
SMILES string
N.OC(=O)C(F)(F)F
assay
98%
form
crystals
mp
123-125 °C (lit.)
functional group
carboxylic acid
fluoro
Quality Level
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Application
Used in the synthesis of hexafluoro-2-aminopentan-4-one ligand and in tuning and calibrating new liquid chromatography/mass spectrometry systems.
General description
Ammonium Trifluoroacetate is used as a catalyst in organic synthesis and as an additive in the mobile phase for chiral racemate separation.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Journal of Fluorine Chemistry, 27, 371-371 (1985)
Nimisha Thakur et al.
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
Jie Wang et al.
Biomedical chromatography : BMC, 33(3), e4438-e4438 (2018-11-18)
Tanshinol borneol ester (DBZ) is a potential drug candidate composed of danshensu and borneol. It shows anti-ischemic and anti-atherosclerosis activity. However, little is known about its metabolism in vivo. This research aimed to elucidate the metabolic profile of DBZ through
Ammonium Trifluoroacetate-Mediated Synthesis of 3, 4-dihydropyrimidin-2 (1H)-ones
Chandran R et al.
International Scholarly Research Network, 2011 (2011)
Garrett Hellinghausen et al.
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
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