1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane
Suppliers
Names
[ CAS No. ]:
355-43-1
[ Name ]:
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane
[Synonym ]:
1,1,2,2-Tetrahydroperfluorohexyl iodide
1-Iodotridecafluorohexane
Tridecafluoro-1-iodohexane
Hexane, 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodo-
Perfluorohexyl iodide
1-iodo-tridecafluoro-hexane
1,1,2,2-tetrahydroperfluorohexyliodide
Perfluoro-1-iodohexane
Perfluorohexyliodide
1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-1-iodohexane
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane
1-Iodoperfluorohexane
MFCD00001063
Perfluoro-n-hexyl iodide
EINECS 206-586-6
TRIDECAFLUOROHEXYL IODIDE
Chemical & Physical Properties
[ Density]:
2.0±0.1 g/cm3
[ Boiling Point ]:
117.1±8.0 °C at 760 mmHg
[ Melting Point ]:
-45 °C
[ Molecular Formula ]:
C6F13I
[ Molecular Weight ]:
445.948
[ Flash Point ]:
45.0±5.6 °C
[ Exact Mass ]:
445.883698
[ LogP ]:
7.22
[ Vapour Pressure ]:
21.1±0.2 mmHg at 25°C
[ Index of Refraction ]:
1.333
[ Stability ]:
Stable.
[ Water Solubility ]:
insoluble
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S23-S24/25-S37/39-S26
[ RIDADR ]:
2810
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
6.1(b)
[ HS Code ]:
29034700
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2903799090
[ Summary ]:
2903799090 halogenated derivatives of acyclic hydrocarbons containing two or more different halogens。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%
Articles
Dalton Trans. 44 , 19663-73, (2015)
Using three different approaches, racemic 1-(perfluoroalkyl)ethylamines were synthesized from perfluoroalkyl iodides or perfluoroalkanoic acids, and further transformed to the corresponding N,N'-disub...
Environ. Health Perspect. 120(1) , 119-25, (2012)
Polyfluorinated iodine alkanes (PFIs) are important intermediates in the synthesis of organic fluoride products. Recently, PFIs have been detected in fluoropolymers as residual raw materials, as well ...
Chem. Commun. (Camb.) (15) , 2005-7, (2009)
Quantitative studies of the 1 : 1 complexes formed between perfluorohexyl iodide and a variety of hydrogen-bond acceptors have been used to probe the relationship between halogen bonding, hydrogen bon...