(1-(3-TRIETHOXYSILYL)PROPYL)-2,2-DIETHOXY-1-AZA-2-SILACYCLOPENTANE, tech

Product Code: SIT8187.2
CAS No: 1184179-50-7
SDS Sheets: EU | US
Pack Size
Quantity
Price
 
25 g
$156.00

Product data and descriptions listed are typical values, not intended to be used as specification.

  • HMIS

    3-2-1-X
  • Molecular Formula

    C16H37NO5Si2
  • Molecular Weight (g/mol)

    379.64
  • TSCA

    Yes (L)
    Low Volume Exemption
  • Boiling Point (˚C/mmHg)

    136-138/1
  • Density (g/mL)

    0.974
  • Refractive Index @ 20˚C

    1.4322

Additional Properties

  • Hydrolytic Sensitivity

    8: reacts rapidly with moisture, water, protic solvents
  • Safety

  • Packaging Under

    Nitrogen
  • 1-(3-triethoxysilyl)propyl-2,2-diethoxy-1-aza-2-silayclopentane

  • Used for metal oxide films and microparticle surface modification
  • Advanced silane in Sivate A610 Activated silane blend
  • Dipodal analog: SIB1824.5
  • Cross-Linking Cyclic Azasilane

    Cyclic azasilanes react rapidly, less than one minute, with any and all surface hydroxyl groups is therefore of unique interest for surface modification. Volatile cyclic azasilanes afford high functional density monolayers on inorganic surfaces such as nanoparticles and other nanofeatured substrates without a hydrolysis step or the formation of byproducts. They exploit the Si–N and Si–O bond energy differences affording a thermodynamically favorable ring-opening reaction with surface hydroxyls at ambient temperature.

    Amine Functional Silane Coupling Agent

    Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials.

    Dipodal Silane

    Dipodal silanes are a series of adhesion promoters that have intrinsic hydrolytic stabilities up to ~10,000 times greater than conventional silanes and are used in applications such as plastic optics, multilayer printed circuit boards and as adhesive primers for ferrous and nonferrous metals. They have the ability to form up to six bonds to a substrate compared to conventional silanes with the ability to form only three bonds to a substrate. Many conventional coupling agents are frequently used in combination with 10-40% of a non-functional dipodal silane, where the conventional coupling agent provides the appropriate functionality for the application, and the non-functional dipodal silane provides increased durability. Also known as bis-silanes additives enhance hydrolytic stability, which impacts on increased product shelf life, ensures better substrate bonding and also leads to improved mechanical properties in coatings as well as composite applications.

    Silicon Chemistry, Applied Technology

    Cyclic Azasilanes and Cyclic Thiasilanes for Nano-Surface Modification

    How cyclic azasilanes and cyclic thiasilanes, a new class of silane coupling agents, modify nanoparticles and create nano-scale features.

    Silicon Chemistry, Articles

    Dipodal Silanes – Zazyczny et al.

    Manufacturing growth opportunities exist in the United States for alternative energy (photovoltaic modules, fuel cells, wind turbines) and medical and healthcare (surgical devices, dental implants and drug delivery) applications. More traditional markets where growth is expected include automotive, construction and specialty packaging.

    Applied Technology

    Emerging Molecular and Atomic Level Techniques for Nanoscale Applications

    This overview provides an introduction and comparison of emerging processing technologies that represent the best contenders to satisfy future demands for ultrathin film applications.

    Silicon Chemistry, Applied Technology

    Single-Molecule Orthogonal Double-Click Chemistry – Inorganic to Organic Nanostructure Transition – Arkles et al.

    Thiasilacyclopentane (TSCP) and azasilacyclopentane (ASCP) heteroatom cyclics reagents can be extended to “simultaneous doubleclicking” when both inorganic and organic substrates are present at the onset of the reaction. The simultaneous double-click depends on a first ring-opening click with an inorganic substrate that is complete in ~1 s at 30 °C and results in the reveal of a cryptic mercaptan or secondary amine group, which can then participate in a second click with an organic substrate.