Skip to Content
Merck
All Photos(1)

Documents

564990

Sigma-Aldrich

N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine

Synonym(s):

Ishikawa’s Reagent

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CF3CHFCF2N(C2H5)2
CAS Number:
Molecular Weight:
223.16
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

refractive index

n20/D 1.3460 (lit.)

bp

56-57 °C (lit.)

density

1.230 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)C(F)(F)C(F)C(F)(F)F

InChI

1S/C7H11F6N/c1-3-14(4-2)7(12,13)5(8)6(9,10)11/h5H,3-4H2,1-2H3

InChI key

BNTFCVMJHBNJAR-UHFFFAOYSA-N

General description

GC analysis includes Et2NCF=CFCF3 (two isomers), both of which are active fluorinating agents.

Application

Reactant for:
  • Friedel-Crafts type arylation of hydrofluorocarbons
  • Microbial hydroxylation of antibiotics
  • Electrochemical fluorination of trialkylamines and tetraalkylammonium salts
  • Fluorination of pyrethroides

Reactant for synthesis of:
  • γ-Hydroxy-α-fluoro-α-trifluoromethylcarboxamide
  • Florfenicol and thiamphenicol
Demonstrates utility in fluorination.
Displays the ability to insert a fluoro(trifluoromethyl) methylene moiety in unsaturated alcohols.

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

104.0 °F - closed cup

Flash Point(C)

40 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Ogu, K-i et al
Tetrahedron Letters, 39, 305-305 (1998)
Koch, G. et al
Synlett, 693-693 (2004)

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