N-(2-AMINOETHYL)-2,2,4-TRIMETHYL-1-AZA-2-SILACYCLOPENTANE

Product Code: SIA0592.0
CAS No: 18246-33-8
SDS Sheets: EU | US
Pack Size
Quantity
Price
 
10 g
$110.00

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

  • HMIS

    3-2-1-X
  • Molecular Formula

    C8H20N2Si
  • Molecular Weight (g/mol)

    172.35
  • Boiling Point (˚C/mmHg)

    54-6° / 2
  • Density (g/mL)

    0.905
  • Refractive Index @ 20˚C

    1.4769

Additional Properties

  • Hydrolytic Sensitivity

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

  • Packaging Under

    Nitrogen
  • N-(2-Aminoethyl)-2,2,4-trimethyl-1-azasilacyclopentane, N-aminoethyl-aza-2,2-dimethyl-1-methylsilacyclopentane

  • Non-cross-linking cyclic azasilane
  • Cross-linking analog: SID3543.0
  • Used in vapor phase surface modification of nanoparticles
  • Primary amine and an internal secondary amine after deposition for UV cure and epoxy systems
  • Conventional analog available: SIA0587.2
  • 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.