2,2-DIMETHOXY-1,6-DIAZA-2-SILACYCLOOCTANE

Product Code: SID3543.0
CAS No: 182008-07-7
SDS Sheets: EU | US
Pack Size
Quantity
Price
 
25 g
$143.00

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

  • HMIS

    3-2-1-X
  • Molecular Formula

    C7H18N2O2Si
  • Molecular Weight (g/mol)

    190.32
  • TSCA

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

    71-73/2.5
  • Melting Point (˚C)

    61-2°

Additional Properties

  • Hydrolytic Sensitivity

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

  • Packaging Under

    Nitrogen
  • 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.

    2,2-Dimethoxy-1,6-diaza-2-silacyclooctane

  • Non-cross-linking analog: SIA0592.0
  • Primary amine and an internal secondary amine after deposition for UV cure and epoxy systems
  • Volatile coupling agent
  • Solid, available as a solution, 10% in cyclohexane: SID3543.1
  • Conventional analog available: SIA0591.0
  • Diamino Functional Dialkoxy Silane

    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.

    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, 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.