Gelest, Inc. PENTAFLUOROPHENOXYUNDECYLTRIMETHOXYSILANE SIP6716.0

Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Fluoroaromatic Silane - Conventional Surface Bonding Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure. Pentafluorophenoxyun decyltrimethoxysilan e; 1,2,3,4,5-Pentafluor o-6-[[11-(trimethoxy silyl)undecyl]oxy]-b enzene For non-covalent immobilization of proteins Trialkoxy silane
Datasheet
Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Fluoroaromatic Silane - Conventional Surface Bonding Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure. Pentafluorophenoxyun decyltrimethoxysilan e; 1,2,3,4,5-Pentafluor o-6-[[11-(trimethoxy silyl)undecyl]oxy]-b enzene For non-covalent immobilization of proteins Trialkoxy silane
Datasheet

Suppliers

Company
Product
Description
Supplier Links
PENTAFLUOROPHENOXYUNDECYLTRIMETHOXYSILANE - SIP6716.0 - Gelest, Inc.
Morrisville, PA, United States
PENTAFLUOROPHENOXYUNDECYLTRIMETHOXYSILANE
SIP6716.0
PENTAFLUOROPHENOXYUNDECYLTRIMETHOXYSILANE SIP6716.0
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Fluoroaromatic Silane - Conventional Surface Bonding Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure. Pentafluorophenoxyun decyltrimethoxysilan e; 1,2,3,4,5-Pentafluor o-6-[[11-(trimethoxy silyl)undecyl]oxy]-b enzene For non-covalent immobilization of proteins Trialkoxy silane

Additional Properties


  • Hydrolytic Sensitivity 7: reacts slowly with moisture/water
    Safety
  • Packaging Under Nitrogen
    Fluoroaromatic Silane - Conventional Surface Bonding
    Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.
    Pentafluorophenoxyundecyltrimethoxysilane; 1,2,3,4,5-Pentafluoro-6-[[11-(trimethoxysilyl)undecyl]oxy]-benzene
  • For non-covalent immobilization of proteins
  • Trialkoxy silane
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Inorganic Chemicals and Compounds
Product Number SIP6716.0
Product Name PENTAFLUOROPHENOXYUNDECYLTRIMETHOXYSILANE
Chemical Formula C 2 0 H 3 1 F 5 O 4 Si
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