Skip to Content
Merck
All Photos(1)

Key Documents

23955

Sigma-Aldrich

Chlorodipyrrolidinocarbenium hexafluorophosphate

≥97.5% (CHN)

Synonym(s):

N,N,N′,N′-Bis(tetramethylene)chloroformamidinium hexafluorophosphate, Chloro-N,N,N′,N′-bis(tetramethylene)formamidinium hexafluorophosphate, PyClU

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C9H16N2Cl · PF6
CAS Number:
Molecular Weight:
332.65
Beilstein:
7898575
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97.5% (CHN)

form

solid

reaction suitability

reaction type: Coupling Reactions

mp

153-156 °C

application(s)

peptide synthesis

functional group

chloro

storage temp.

2-8°C

SMILES string

F[P-](F)(F)(F)(F)F.Cl\C(N1CCCC1)=[N+]2/CCCC2

InChI

1S/C9H16ClN2.F6P/c10-9(11-5-1-2-6-11)12-7-3-4-8-12;1-7(2,3,4,5)6/h1-8H2;/q+1;-1

InChI key

NHEGCUSBUWGOQM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Reactant for:
Enantioselective desymmetrization of meso-asiridines
Peptide coupling
Reagent for:
Heterocyclization of chloroformamidinium salts
Oxidative insertion for palladium and nickel catalyst synthesis

Other Notes

Crystalline and non-hygroscopic peptide coupling reagent, especially for N-methyl amino acids

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - 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

J. Coste et al.
Tetrahedron Letters, 32, 1967-1967 (1991)

Articles

Fluoroamidinium salts advance acid halogenation with greater stability and no oxazolones conversion compared to chlorides.

Fluoroamidinium salts advance acid halogenation with greater stability and no oxazolones conversion compared to chlorides.

Fluoroamidinium salts advance acid halogenation with greater stability and no oxazolones conversion compared to chlorides.

Fluoroamidinium salts advance acid halogenation with greater stability and no oxazolones conversion compared to chlorides.

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