Skip to Content
Merck
All Photos(1)

Key Documents

520330

Sigma-Aldrich

Fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate

97%

Synonym(s):

TFFH

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
[FC[=N(CH3)2]N(CH3)2]PF6
CAS Number:
Molecular Weight:
264.12
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

reaction suitability

reaction type: Coupling Reactions

mp

104-109 °C (lit.)

application(s)

peptide synthesis

functional group

amine
fluoro

SMILES string

F[P-](F)(F)(F)(F)F.CN(C)\C(F)=[N+](/C)C

InChI

1S/C5H12FN2.F6P/c1-7(2)5(6)8(3)4;1-7(2,3,4,5)6/h1-4H3;/q+1;-1

InChI key

ZAVXOOLKAGPJPI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

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
Amine prodrugs of selective neuronal nitric oxide synthase inhibitors

Reagent for:
Selective cyclohexyl-derived imidazopyrazine insulin-like growth factor 1 receptor inhibitors
Hydrazone ligation to assemble multifunctional viral nanoparticles

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Anita K Kovács et al.
Frontiers in chemistry, 6, 120-120 (2018-05-05)
A general strategy for the synthesis of N-peptide-6-amino-D-luciferin conjugates has been developed. The applicability of the strategy was demonstrated with the preparation of a known substrate, N-Z-Asp-Glu-Val-Asp-6-amino-D-luciferin (N-Z-DEVD-aLuc). N-Z-DEVD-aLuc was obtained via a hybrid liquid/solid phase synthesis method, in which

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service