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345865

Sigma-Aldrich

Ammonium trifluoromethanesulfonate

99%

Sinónimos:

Ammonium triflate

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About This Item

Fórmula lineal:
CF3SO3NH4
Número de CAS:
38542-94-8
Peso molecular:
167.11
MDL number:
MFCD00075332
UNSPSC Code:
12352302
PubChem Substance ID:
24861356
NACRES:
NA.23

assay

99%

form

crystals and lumps

mp

224-226 °C (lit.)

SMILES string

N.OS(=O)(=O)C(F)(F)F

InChI

1S/CHF3O3S.H3N/c2-1(3,4)8(5,6)7;/h(H,5,6,7);1H3

InChI key

BMWDUGHMODRTLU-UHFFFAOYSA-N

General description

Ammonium trifluoromethanesulfonate is a white crystalline solid that is highly soluble in water. It is thermally stable and widely used in the field of catalysis, batteries, and organic synthesis.

Application

Ammonium trifluoromethanesulfonate can be used:
  • As an electrolyte additive in aqueous metal ion batteries. It is used to enhance the ionic conductivity of electrolyte and widens the electrochemical stability window of the battery.
  • As a precursor to prepare solid polymer electrolytes and gel polymer electrolytes via solution casting by method.
  • As a co-catalyst to prepare Poly(p-phenylenediamine) and their derivatives. These conductive polymers are used in sensors and organic photovoltaic cells.
  • A dopant in the preparation of flexible poly(vinylidene fluoride-co-hexafluoropropylene)/polyethyl methacrylate ammonium triflate (PVDf-HFP/PEMA-NH4CF3SO3)polymer electrolyte films.
  • A cathode additive in proton exchange membrane (PEM) fuel cells to increase the local oxygen concentration near the Pt catalyst, which enhances single-cell performance.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCQ3727
MKCN8381
MKCM8329
MKCM1149
MKCL3826

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Journal of inorganic biochemistry, 210, 111154-111154 (2020-08-11)
Twenty-four novel organometallic osmium(II) phenylazopyridine (AZPY) complexes have been synthesised and characterised; [Os(η6-arene)(5-RO-AZPY)X]Y, where arene = p-cym or bip, AZPY is functionalized with an alkoxyl (O-R, R = Me, Et, nPr, iPr, nBu) or glycolic (O-{CH2CH2O}nR*, n = 1-4, R* = H, Me, or Et) substituent on the

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