Perfluorobutyl iodide

Perfluorobutyl iodide
  • CAS No.:423-39-2
Other grades of this product :
Perfluorobutyl iodide Basic information
Product Name:Perfluorobutyl iodide
Synonyms:PERFLUOROBUTYL IODODE;Nonafluoro-1-iodobutane,1-Iodoperfluorobutane, Perfluorobutyl iodide;1-Iodoperfluorobutane, 1,1,1,2,2,3,3,4,4-Nonafluoro-4-iodobutane;1-Iodoperfluorobutane, Perfluorobutyl iodide;Perfluorobutyl iodide,99%;PERFLUOROBUTYL IODIDE (STABILISED WITH S;Nonafluoro-1-iodobutane 98%;Perfluorobutyl iodide (stabilised with silver platelets) for synthesis
CAS:423-39-2
MF:C4F9I
MW:345.93
EINECS:207-025-8
Product Categories:Alkyl;Building Blocks;Chemical Synthesis;Fluorinated Building Blocks;F-Tagged;Halogenated Hydrocarbons;Organic Fluorides;Fluorous Chemistry;Fluorous Compounds;Synthetic Organic Chemistry;Organic Building Blocks;Organic Fluorinated Building Blocks
Mol File:423-39-2.mol
Perfluorobutyl iodide Chemical Properties
Melting point -88 °C
Boiling point 66-67 °C
density 2.01 g/mL at 25 °C(lit.)
refractive index n20/D 1.3285(lit.)
Fp None
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form Liquid
Specific Gravity2.010
color Clear purple
Water Solubility immiscible
Sensitive Light Sensitive
BRN 1777546
Exposure limitsACGIH: TWA 0.01 ppm
Stability:Stable. Incompatible with bases.
InChIKeyPGRFXXCKHGIFSV-UHFFFAOYSA-N
CAS DataBase Reference423-39-2(CAS DataBase Reference)
NIST Chemistry Reference1-Iodononafluorobutane(423-39-2)
EPA Substance Registry SystemButane, 1,1,1,2,2,3,3,4,4-nonafluoro-4-iodo- (423-39-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
RIDADR 2810
WGK Germany 3
RTECS EK5360000
8
Hazard Note Irritant/Light Sensitive
TSCA T
HazardClass 6.1(b)
PackingGroup III
HS Code 29034700
MSDS Information
ProviderLanguage
1,1,1,2,2,3,3,4,4-Nonafluoro-4-iodobutane English
ACROS English
SigmaAldrich English
ALFA English
Perfluorobutyl iodide Usage And Synthesis
Chemical Propertiesclear colourless liquid with pungent odour
UsesPerfluorobutyl Iodide is used as an organocatalyst in some polymerization reactions.

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