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1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane

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

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

Transition metal complexes bearing NHC ligands substituted with secondary polyfluoroalkyl groups.

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...

The in vitro estrogenic activities of polyfluorinated iodine alkanes.

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 ...

Non-covalent interactions between iodo-perfluorocarbons and hydrogen bond acceptors.

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...


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