ChemicalBook Product Catalog Chemical Reagents Organic reagents Silane 1H,1H,2H,2H-Perfluorodecyltrichlorosilane

1H,1H,2H,2H-Perfluorodecyltrichlorosilane

1H,1H,2H,2H-Perfluorodecyltrichlorosilane Basic information
Physicochemical Properties Application
Product Name:1H,1H,2H,2H-Perfluorodecyltrichlorosilane
Synonyms:PERFLUORODECYL-1H,1H,2H,2H-TRICHLOROSILANE;TRICHLORO-1H,1H,2H,2H-PERFLUORODECYLSILANE;1H,1H,2H,2H-PERFLUORODECYLTRICHLOROSILANE;(HEPTADECAFLUORO-1,1,2,2-TETRAHYDRODECYL)-1-TRICHLOROSILANE;(HEPTADECAFLUORO-1,1,2,2-TETRAHYDRODECYL)TRICHLOROSILANE;FDTS~Trichloro-1H,1H,2H,2H-perfluorodecylsilane;1H,1H,2H,2H-Perfluorodecyltrichlorosilane(Trichloro-1H,1H,2H,2H-perfluorodecylsilane);Silane, trichloro(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-
CAS:78560-44-8
MF:C10H4Cl3F17Si
MW:581.56
EINECS:
Product Categories:
Mol File:78560-44-8.mol
1H,1H,2H,2H-Perfluorodecyltrichlorosilane Structure
1H,1H,2H,2H-Perfluorodecyltrichlorosilane Chemical Properties
Melting point 10-11°C
Boiling point 224 °C
density 1.7
refractive index 1.349
Fp >110°C
solubility Miscible with tetrahydrofuran, tetrhydropyran, toluene and other organic solvents.
Specific Gravity1.7
Hydrolytic Sensitivity8: reacts rapidly with moisture, water, protic solvents
Sensitive Moisture Sensitive
BRN 5889653
Stability:Stable. Flammable. Incompatible with strong oxidizing agents.
InChIInChI=1S/C10H4Cl3F17Si/c11-31(12,13)2-1-3(14,15)4(16,17)5(18,19)6(20,21)7(22,23)8(24,25)9(26,27)10(28,29)30/h1-2H2
InChIKeyVIFIHLXNOOCGLJ-UHFFFAOYSA-N
SMILES[Si](Cl)(Cl)(Cl)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
CAS DataBase Reference78560-44-8(CAS DataBase Reference)
EPA Substance Registry SystemSilane, trichloro(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)- (78560-44-8)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR 3265
Hazard Note Corrosive/Moisture Sensitive
TSCA No
HazardClass 8
PackingGroup II
HS Code 29319090
MSDS Information
ProviderLanguage
ALFA English
1H,1H,2H,2H-Perfluorodecyltrichlorosilane Usage And Synthesis
Physicochemical Properties

1H,1H,2H,2H-Perfluorodecyltrichlorosilane, also known as FDTS, is a colorless liquid chemical with molecular formula C10H4Cl3F17Si. FDTS molecules form self-assembled monolayers. They bond onto surfaces terminated with hydroxyl (-OH) groups, such as glass, ceramics, or SiO2 forming a regular covalent bond. It anchors on oxide surfaces with its tricholoro-silane group and attaches covalently.

Application1H,1H,2H,2H-Perfluorodecyltrichlorosilane (FDTS) monolayer is often applied to movable microparts of microelectromechanical systems (MEMS). FDTS monolayer reduces surface energy and prevents sticking, so they are used to coat micro- and nano-features on stamps for a nanoimprint lithography which is becoming a method of choice for making electronics, organic photodiodes, microfluidics and other. Reduced surface energy is helpful for reduction of ejection force and demolding of polymer parts in an injection molding and 1H,1H,2H,2H-Perfluorodecyltrichlorosilane (FDTS) coating was applied onto some metallic injection molding molds and inserts. Further, it is used to coat micro-nano features on stamps for a nano imprint lithography. In addition, it is used in the preparation of other products by reacting with methanol.
Chemical Propertiescolourless to straw-coloured liquid with an odour of hydrogen chloride
Uses1H,1H,2H,2H-Perfluorodecyltrichlorosilane (CAS# 78560-44-8) is a useful compound used as part of antireflective coatings for solar cell efficiency improvement. The high level of hydrophobicity of 1H,1H,2H,2H-Perfluorodecyltrichlorosilane also makes it useful as coating for electrical insulators.
ApplicationDTS(FBTTh2)2 can be used as a conjugating polymer that forms a donor-acceptor system with acceptor molecules such as perylene diimide, PC71BM and other fullerenes for the fabrication of bulk-heterojunction based solar cells.
A tri-functional fluoro-carbon terminated silane (1H,1H,2H,2Hperfluorodecyltrichlorosilane, PFTCS) was used in solutions of hexane to create surfaces with teflon-like properties.
General DescriptionDTS(FBTTh2)2 is a conductive polymer that can be used as a donor molecule. It has a narrow band gap and shows a maximum power conversion efficiency of 7.0%. Its photostability is more than that of P3HT.
1H,1H,2H,2H-Perfluorodecyltrichlorosilane Preparation Products And Raw materials
Raw materials1H,1H,2H-Perfluoro-1-decene
1H,1H,2H,2H-Perfluorodecyltriethoxysilane (Perfluorohexyl)ethylene 1H,1H,2H,2H-PERFLUOROOCTYLTRICHLOROSILANE 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane Ethyltrichlorosilane N-DECYLTRICHLOROSILANE 1H,1H,2H,2H-Perfluorodecyltrichlorosilane 1-FLUORONONANE HEXYLDICHLOROSILANE HEXYLTRICHLOROSILANE Trichlorosilane Methyltrichlorosilane N-BUTYLTRICHLOROSILANE N-HEPTYLTRICHLOROSILANE DODECYLTRICHLOROSILANE Nonyl trichlorosilane Amyltrichlorosilane (mixed isomers)(Pentyltrichlorosilane) OCTYL DICHLOROSILANE
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