Recommended Products
grade
for ion-selective electrodes
Quality Level
description
solvent for preparation of membranes
product line
Selectophore™
bp
212-218 °C
density
2.03 g/mL at 20 °C
SMILES string
FC1(F)C(F)(F)C(F)(F)C2(F)C(F)(C1(F)F)C(F)(F)C(F)(F)C3(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C23F
InChI
1S/C14F24/c15-1-2(16)4(18,10(29,30)14(37,38)12(33,34)6(2,21)22)8(25,26)7(23,24)3(1,17)9(27,28)13(35,36)11(31,32)5(1,19)20
InChI key
QKENRHXGDUPTEM-UHFFFAOYSA-N
Related Categories
General description
Visit our Sensor Applications portal to learn more.
Application
Perfluoroperhydrophenanthrene finds application as an intraoperative and postoperative surgical adjunct tool, during retinal operations and study.
Solvent for fluorous liquid phase in ion-selective electrodes
Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Ophthalmic surgery and lasers, 29(2), 144-146 (1998-03-21)
Perfluorocarbon liquids have gained wide acceptance as intraoperative tools that can simplify vitreoretinal surgical maneuvers. These low-viscosity liquids facilitate injection into the eye and removal from the eye during surgery. Tolerance to perfluoroperhydrophenanthrene and the development of proliferative vitreoretinopathy with
Retina (Philadelphia, Pa.), 17(2), 146-153 (1997-01-01)
Anterior and posterior segment changes of experimental vitreous and aqueous substitution with Perfluorophenanthrene were evaluated. In 28 rabbit eyes that underwent vitrectomy, tamponades of 1.2 cc Perfluorophenanthrene remained as long as 8 weeks under clinical and electrophysiologic control. Histologic examinations
International ophthalmology, 22(2), 89-96 (1999-09-03)
To evaluate the utility and efficacy of perfluoroperhydrophenanthrene in the management of retinal detachments secondary to severe proliferative diabetic retinopathy. Forty consecutive patients with proliferative diabetic retinopathy and retinal detachments were entered into the study at nine participating clinical centers.
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