N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine CAS 309-88-6

Introduction:Basic information about N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine CAS 309-88-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

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

Product Name:N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine
Synonyms:SHIKAWA'S REAGENT;N,N-DIETHYL-1,1,2,3,3,3-HEXAFLUOROPROPYLAMINE;Ishikawa's Reagent, 1-(Diethylamino)-1,1,2,3,3,3-hexafluoropropane;N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine, 40% solution in THF;Ishikawa;Ishikawa's Reagent, technical, 90%;Ishikawa Reagent;MEC-81
CAS:309-88-6
MF:C7H11F6N
MW:223.16
EINECS:628-698-8
Product Categories:Fluorinated Building Blocks;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Fluorination;Halogenation;Synthetic Organic Chemistry;Chemical Synthesis;Fluorination Reagents;Synthetic Reagents
Mol File:309-88-6.mol

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

Boiling point 56-57 °C (lit.)
density 1.230 g/mL at 25 °C (lit.)
refractive index 1.3460
Fp 56-57°C/58mm
storage temp. Flammables area
solubility soluble in Acetone,Ether
pka1.50±0.70(Predicted)
form Liquid
color Clear colorless to yellow
Specific Gravity1.230
Merck 14,5108
InChI1S/C7H11F6N/c1-3-14(4-2)7(12,13)5(8)6(9,10)11/h5H,3-4H2,1-2H3
InChIKeyBNTFCVMJHBNJAR-UHFFFAOYSA-N
SMILESCCN(CC)C(F)(F)C(F)C(F)(F)F
CAS DataBase Reference309-88-6(CAS DataBase Reference)
EPA Substance Registry SystemN,N-Diethyl-2H-perfluoropropanamine (309-88-6)

Safety Information

Hazard Codes C
Risk Statements 10-34
Safety Statements 16-26-36/37/39-45
RIDADR 3267
WGK Germany 3
Hazard Note Corrosive
HazardClass 8
PackingGroup II
HS Code 29211999
Storage Class3 - Flammable liquids
Hazard ClassificationsFlam. Liq. 3
Skin Corr. 1B

N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine Usage And Synthesis

Chemical PropertiesClear colorless to yellow liquid
UsesDemonstrates utility in fluorination.7
UsesFluorinating agent.
UsesReactant 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
General DescriptionGC analysis includes Et2NCF=CFCF3 (two isomers), both of which are active fluorinating agents.
SynthesisN,N-diethyl-1,1,2,3,3,3-hexafluoropropylamine is prepared as follows: take 600-700 portions of dichloromethane, add 65-85 portions of diethylamine, lower the temperature to -5 ?? to -25 ??, pass 110 portions of -165 portions of hexafluoropropylene after the reaction for 1h. 165 portions of hexafluoropropylene, pass through the reaction after 1h, get fluoride reagent standby; the addition amount of diethylamine is preferably 75-80 portions, the addition amount of hexafluoropropylene is preferably 160-165 portions.

N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamine Preparation Products And Raw materials

Raw materials1-Propen-1-amine, N,N-diethyl-1,2,3,3,3-pentafluoro--->N,N-DIETHYL-2,3,3,3-TETRAFLUOROPROPIONAMIDE-->1,2-DIBROMOHEXAFLUOROPROPANE-->Diethylamine-->Hexafluoropropylene
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