Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%, Thermo Scientific Chemicals
Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%, Thermo Scientific Chemicals
Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate, 98%, Thermo Scientific Chemicals

Have Questions?
Catalog NumberQuantity
ALFH54910.031 g
Catalog number ALFH54910.03
View Price:Sign in to see your account pricing. Need an account? Register with us today.
Quantity:
1 g
Request bulk or custom format
Specifications
Chemical Name or MaterialFluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate
CAS164298-23-1
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
View more
Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate is used as a reagent for synthesis of cationic antimicrobial β-2,2-amino acid derivatives, philanthotoxin analogues for inhibition of the ionotropic glutamate receptor, small β-peptidomimetics for antimicrobials and hydrazone ligation to assemble multifunctional viral nanoparticles.

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
Fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate is used as a reagent for synthesis of cationic antimicrobial β-2,2-amino acid derivatives, philanthotoxin analogues for inhibition of the ionotropic glutamate receptor, small β-peptidomimetics for antimicrobials and hydrazone ligation to assemble multifunctional viral nanoparticles.

Solubility
Soluble in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Terkel Hansen.; Dominik Ausbacher.; Gøril E Flaten.; Martina Havelkova.; Morten B Strom. Synthesis of cationic antimicrobial β(2,2)-amino acid derivatives with potential for oral administration. Journal of medicinal and pharmaceutical chemistry. 2011, 54 (3), 858-868.
  2. Sidsel Frolund.; Angelo Bella.; Anders S Kristensen.; Hanne L Ziegler.; Matthias Witt.; Christian A Olsen.; Kristian Stromgaard.; Henrik Franzyk.; Jerzy W Jaroszewski. Assessment of structurally diverse philanthotoxin analogues for inhibitory activity on ionotropic glutamate receptor subtypes: discovery of nanomolar, nonselective, and use-dependent antagonists. Journal of medicinal and pharmaceutical chemistry. 2010, 537 (20), 7441-7451.