(N,N-DIMETHYLAMINOPROPYL)-AZA-2-METHYL-2-METHOXYSILACYCLOPENTANE, 95%

Product Code: SID3546.93
SDS Sheets: EU | US
Pack Size
Quantity
Price
 
10 g
$329.00

Prices listed are EXW price (Morrisville, PA US) in USD. Prices vary depending on currency and Incoterms.

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

  • HMIS

    3-3-1-X
  • Molecular Formula

    C10H24N2OSi
  • Molecular Weight (g/mol)

    216.39
  • Purity (%)

    95%
  • TSCA

    No
  • Boiling Point (˚C/mmHg)

    65-67/0.5
  • Density (g/mL)

    0.919
  • Density Temperature (˚C)

    25

Additional Properties

  • Hydrolytic Sensitivity

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

  • Packaging Under

    Nitrogen
  • (N,N-dimethylaminopropyl)-aza-2-methyl-2-methoxysilacyclopentane

  • Cross-linking cyclic azasilane
  • Monoalkoxy couplign agent for metals
  • Cyclic analog of SID3546.92
  • 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.

    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.