1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluor-6-iodhexan Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-S?tze Betriebsanweisung:

S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
S24/25:Berührung mit den Augen und der Haut vermeiden.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Chemische Eigenschaften

liquid

Verwenden

Perfluorohexyl Iodide is an important intermediate in the synthesis of organic fluorides products. It also exhibits estrogenic activity in vitro. Perfluorohexyl Iodide is used in the screening assay for binding affinities of perfluoroalkyl iodide for estrogen receptor alpha and beta isoforms.

Allgemeine Beschreibung

Perfluorohexyl iodide forms 1:1 complexes with a variety of hydrogen-bond acceptors. It has been grafted onto the isocitronellene/propene copolymer by radical reaction yielding a poly(α-olefin) with fluorinated side chains. The radical addition of perfluorohexyl iodide to vinyl acetate, using azo-bis( isobutyronitrile) (AIBN) as an initiator, has been investigated.

Sicherheitsprofil

Explodes in contact with sodium when heated to the boiling point of the iodide. When heated to decomposition it emits toxic fumes of Fí and Ií.

Synthese

To an autoclave (stainless steel, volume:1L) equipped with a mixing tank and a stirrer, C4F9I which compound (1) flow rate 25mL/min, CF2=CF2 (tetrafluoroethylene) which compound (2) flow rate 0.37g/min, (C2F5COO)2 (10 and half hour life temperature: 31°C) which compound (4) flow rate 0.052 mmol/min were supplied, the mixture was prepared by mixing at stirrer. Temperature in the autoclave was 10°C, residence time of the mixture in the autoclave was 10 minutes. The molar ratio (C4F9I/CF2=CF2)of C4F9I and CF2=CF2 in the mixed solution was 41, the amount of (C2F5COO)2 with respect to C4F9I was 0.034 mol%. Only the mixture from the bottom of the autoclave was withdrawn in the absence of gas phase, the mixture was fed to the bottom of tubular reactor (Tankan-shiki, volume: 0.5L). The mixture was not seperated by gas-liquid separation, the mixture was flow towards the outlet from the inlet of the reaction tube in the tube reactor. The temperature of the reaction tube, and a 70°C, the residence time of the mixture in the tubular reactor was set to 20 minutes. The mixture containing a compound Perfluoro-1-iodohexane C6F13I was obtained.

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluor-6-iodhexan Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluor-6-iodhexan Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Henan Allgreen Chemical Co.,LTD	+86-37155567971 +86-13633837469	info@allgreenchem.com	China	5996	58
Hangzhou FandaChem Co.,Ltd.	+8615858145714	FandaChem@Gmail.com	China	8771	55
Shaanxi Dideu Medichem Co. Ltd	+86-029-81138252 +86-18789408387	1057@dideu.com	China	3889	58
Capot Chemical Co.,Ltd.	+86-（0）57185586718 +86-13336195806	sales@capot.com	China	29793	60
Shanghai Daken Advanced Materials Co.,Ltd	+86-371-66670886	info@dakenam.com	China	18940	58
Henan Tianfu Chemical Co.,Ltd.	+86-0371-55170693 +86-19937530512	info@tianfuchem.com	China	21634	55
career henan chemical co	+86-0371-86658258 +8613203830695	sales@coreychem.com	China	29879	58
Tianjin Huiren Chemtech Co., Ltd	+86-86-22-23707858 +86-86-13672008665	huirentech@foxmail.com	China	171	58
Chongqing Chemdad Co., Ltd	+86-023-6139-8061 +86-86-13650506873	sales@chemdad.com	China	39894	58
Wuhan Chemwish Technology Co., Ltd	027-67849912	sales@chemwish.com	CHINA	10821	58

355-43-1(1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluor-6-iodhexan)Verwandte Suche:

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• 1-IODOPERFLUOROHEXANE , STABILIZED WITH COPPER
• 1-IODOPERFLUOROHEXANE, 98+%, STAB. WITH COPPER
• 1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluorohexyl iodide
• 1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluoro-1-iodohexane, Tridecafluorohexyl iodide
• 1,1,2,2,3,3,4,4,5,5,6,6,6-Tridecafluorohexyl iodide
• Perfluoro-1-iodohexane, 98+%, stab. with copper
• 6-iodo-1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane
• Perfluorohexyliodide97%
• PERFLUOROHEXYL IODIDE 97%
• Perfluoro-1-iodohexane,99%
• Hexane, 1,1,1,2,2,3,3,4,4,5,5,6
• Perfluorohexyl iodide ,99%
• Perfluorohexyl iodide,1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluoro-1-iodohexane, Tridecafluorohexyl iodide
• Perfluorohexyl Iodide Tridecafluoro-1-iodohexane
• PERFLUOROHEXYL IODIDE FOR SYNTHESIS
• 1-Iodo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane, Perfluoro(1-iodohexane)
• Perfluoro-1-iodohexane, stabilized with copper
• 1-IODOTRIDECAFLUOROHEXANE
• 1-IODOPERFLUOROHEXANE
• PERFLUORO-1-IODOHEXANE
• PERFLUORO-N-HEXYL IODIDE
• 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodo-hexan
• Hexane, 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodo-
• TRIDECAFLUOROHEXYL IODIDE
• TRIDECAFLUORO-N-HEXYL IODIDE
• C1014NH5
• 1-[3-(2-piperidinylmethyl)-1-indolyl]ethanone
• Perfluorohexyl iodide, 98%, for synthesis
• Perfluorohexyliodide>98%
• uorohexyL
• TridecafL
• Perfluorohexyl Iodide Cas NO.: 355-43-1
• PERFLUOROHEXYL IODIDE
• TRIDECAFLUORO-1-IODOHEXANE
• 1,1,1,2,2,3,3,4,4,5,5,6,6-TRIDECAFLUORO-6-IODOHEXANE
• Perfluorohexyl iodine
• TI-6
• Perfluorohexyl iodoalkane
• 355-43-1
• CF3CF25I
• C6F3I
• Halogenated Hydrocarbons
• Organic Building Blocks
• Alkyl
• Building Blocks
• Fluorous Chemistry
• Fluorous Compounds
• Isoxazoles ,Oxazoles
• Organic Fluorides
• Fluorous Chemistry
• Fluorous Compounds
• Synthetic Organic Chemistry