| Identification | More | [Name]
Perfluorooctyl iodide | [CAS]
507-63-1 | [Synonyms]
1-IODOPERFLUOROOCTANE
HEPTADECAFLUORO-1-IODOOCTANE
HEPTADECAFLUORO-N-OCTYL IODIDE
HEPTADECAFLUOROOCTYL IODIDE
PERFLUORO-N-OCTYL IODIDE
PERFLUOROOCTYL IODIDE
1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-8-iodo-octan
1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-Heptadecafluoro-8-iodooctane
1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-8-iodo-Octane
1-Iodoheptadecafluorooctane
1-iodoperfluorooctane98%
heptadecafluoro-1-iodo-octan
Octane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-8-iodo-
Octane, heptadecafluoro-1-iodo-
Perfluoro-1-iodooctane
PERFLUOROOCTYL IODIDE 97%
Perfluorooctyliodide98%
1-Iodoperfluorooctane, Heptadecafluorooctyl iodide, Perfluorooctyl iodide
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Heptadecafluoro-1-iodooctane | [EINECS(EC#)]
208-079-5 | [Molecular Formula]
C8F17I | [MDL Number]
MFCD00001064 | [Molecular Weight]
545.96 | [MOL File]
507-63-1.mol |
| Chemical Properties | Back Directory | [Appearance]
clear light pink liquid after melting | [Melting point ]
25 °C
| [Boiling point ]
160-161 °C(lit.)
| [density ]
2.067 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.329(lit.)
| [Fp ]
160-161°C | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
Chloroform, Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
Liquid After Melting | [color ]
Clear colorless to yellow or light pink | [Sensitive ]
Light Sensitive | [BRN ]
1717141 | [Exposure limits]
ACGIH: TWA 0.01 ppm | [InChIKey]
KWXGJTSJUKTDQU-UHFFFAOYSA-N | [CAS DataBase Reference]
507-63-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Perfluorooctyl iodide(507-63-1) | [Storage Precautions]
Light sensitive | [EPA Substance Registry System]
507-63-1(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 .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2922 | [WGK Germany ]
3
| [RTECS ]
RG9700050
| [F ]
8 | [Hazard Note ]
Harmful | [TSCA ]
T | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29037800 | [Toxicity]
LD50 ivn-mus: 7500 mg/kg MIVRA6 8,320,74 |
| Hazard Information | Back Directory | [Chemical Properties]
clear light pink liquid after melting | [Uses]
Perfluorooctyl Iodide is a perfluoroalkyl iodide used in organocatalysis via substrate activation by halogen bonding. Perfluorooctyl Iodide is a potential candidate substitute for banned Halon fire extinguishers. | [Cytotoxicity]
Exposure of H295R cells to Perfluorooctyl iodide (PFOI) (<100 μM) and Perfluorooctanoic acid (PFOA) (<100 μM) did not cause significant toxicity within the concentration ranges tested (p > 0.05). However, 125 μM PFOI and PFOA induced significant toxicity in H295R cells (p < 0.05). No obvious morphological alterations were observed in the cells treated with PFOI or PFOA at levels lower than 100 μM upon microscopic examination[1]. | [Safety Profile]
Slightly toxic by intravenous route. When heated to decomposition it emits toxic vapors of Fí and Ií. | [Environmental considerations]
Production of perfluorooctyl iodide (PFOI) has great commercial value. PFOI is a potential estrogenic compound. Studies have shown that the concentration of PFOI is relatively higher in the air and soil than the concentrations of the other derivatives of Perfluorinated iodine alkanes (PFIs). In addition, the degradation of PFIs can cause the formation of other Perfluorinated iodine alkanes (PFCs), thereby resulting in environmental behaviors similar to those of FTOHs. Release of PFIs may increase the environmental burden of PFCs[1-2].
| [References]
[1] Chang Wang. "Perfluorooctyl Iodide Stimulates Steroidogenesis in H295R Cells via a Cyclic Adenosine Monophosphate Signaling Pathway." Chemical Research in Toxicology 28 5 (2015): 848–854.
[2] WangYichen. "Estrogen-like response of perfluorooctyl iodide in male medaka (Oryzias latipes) based on hepatic vitellogenin induction." Environmental Toxicology 28 10 (2013): 571–8.
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