| Identification | More | [Name]
1H,1H,2H,2H-Perfluorohexyl iodide | [CAS]
2043-55-2 | [Synonyms]
1,1,1,2,2,3,3,4,4-NONAFLUORO-6-IODOHEXANE
1H,1H,2H,2H-NONAFLUOROHEXYL IODIDE
1H,1H,2H,2H-PERFLUORO-1-IODOHEXANE
1H,1H,2H,2H-PERFLUOROHEXYL IODIDE
1-IODO-1H,1H,2H,2H-NONAFLUOROHEXANE
1-IODO-1H,1H,2H,2H-PERFLUOROHEXANE
2-(NONAFLUOROBUTYL)ETHYL IODIDE
2-(PERFLUOROBUTYL)ETHYL IODIDE
1,1,1,2,2,3,3,4,4-nonafluoro-6-iodo-hexan
1,1,2,2-Tetrahydroperfluorohexyliodide
1-Iodo-1H,1H,2H,2H-nonafluorohexane~1H,1H,2H,2H-Perfluorohexyl iodide
Hexane, 1,1,1,2,2,3,3,4,4-nonafluoro-6-iodo-
1H,1H,2H,2H-Perfluorohexyl iodide 95%
1H,1H,2H,2H-Perfluorohexyliodide95%
1H,1H,2H,2H-NONAFLUOROHEXYL IODIDE 99+%
3,3,4,4,5,5,6,6,6-Nonafluorohexyl iodide | [EINECS(EC#)]
218-055-6 | [Molecular Formula]
C6H4F9I | [MDL Number]
MFCD00039409 | [Molecular Weight]
373.99 | [MOL File]
2043-55-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
-25°C | [Boiling point ]
138 °C | [density ]
1.94 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.370
| [Fp ]
138-140°C | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Soluble), Methanol (Slightly) | [form ]
clear liquid | [color ]
Colorless to Light yellow to Light red | [Specific Gravity]
1.940 | [Sensitive ]
Light Sensitive | [BRN ]
1870862 | [InChIKey]
CXHFIVFPHDGZIS-UHFFFAOYSA-N | [CAS DataBase Reference]
2043-55-2(CAS DataBase Reference) | [EPA Substance Registry System]
2043-55-2(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [F ]
8 | [Hazard Note ]
Irritant | [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29037800 |
| Hazard Information | Back Directory | [Description]
1H,1H,2H,2H-Perfluorohexyl iodide is a polyfluorinated iodine alkane (PFI). This compound consists of an even-numbered hydrophobic alkyl chain (typically C4–C12), which is wholly or partially fluorinated and includes an iodine atom at one or both ends. PFIs are reaction products synthesized from the telomerization process by iodine pentafluoride reacting with unsaturated taxogen molecules such as tetrafluoroethylene and ethylene. PFIs are used as critical industrial intermediates for producing various PFCs, such as fluorotelomer alcohols, olefins, and acrylate monomers[1]. | [Chemical Properties]
Red liquid | [Uses]
1H,1H,2H,2H-Perfluorohexyl iodide has been used for the study for fluorinated phosphonium ionic liquids as a reagent, and in general is used as a reactant in organic reactions. | [References]
[1] Ruan, Ting , et al. "Trace determination of airborne polyfluorinated iodine alkanes using multisorbent thermal desorption/gas chromatography/high resolution mass spectrometry." Journal of Chromatography A 1217.26(2010):4439-4447. |
| Spectrum Detail | Back Directory | [Spectrum Detail]
1H,1H,2H,2H-Perfluorohexyl iodide(2043-55-2)MS
1H,1H,2H,2H-Perfluorohexyl iodide(2043-55-2)1HNMR
1H,1H,2H,2H-Perfluorohexyl iodide(2043-55-2)13CNMR
1H,1H,2H,2H-Perfluorohexyl iodide(2043-55-2)IR1
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