• USA Home
  • 155071 - Azidotrimethylsilane

EMAIL THIS PAGE TO A FRIEND
155071 Aldrich

Azidotrimethylsilane

95%

Synonym: Trimethylsilyl azide

  • CAS Number 4648-54-8

  • Linear Formula (CH3)3SiN3

  • Molecular Weight 115.21

  •  Beilstein Registry Number 1903730

  •  EC Number 225-078-5

  •  MDL number MFCD00001986

  •  PubChem Substance ID 24849336

  •  eCl@ss 39100709

  • Popular Documents:  FTIR (PDF)  

Purchase

Properties

Related Categories Azidation/Diazo Transfer, Azide Sources, C-X Bond Formation (Non-Halogen), Chemical Biology, Chemical Synthesis,
InChI Key   SEDZOYHHAIAQIW-UHFFFAOYSA-N
assay   95%
refractive index   n20/D 1.414(lit.)
bp   52-53 °C/175 mmHg(lit.)
density   0.868 g/mL at 25 °C(lit.)
storage temp.   2-8°C

Description

Packaging

10, 50 g in glass bottle

Application

Versatile azidonation reagent for amines, amides, aldehydes, and ketones.

Price and Availability

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 1992 6.1(3) / PGII
WGK Germany 
3
Protocols & Articles

Articles

III-V Material Sources

At the forefront of optoelectronic, lighting and data storage applications, III-V semiconductor materials continue to generate exciting new applications. III-V quantum dot heterostructures can addres...
Chemfiles Volume 4 Article 3
Keywords: Applications, Automotive, Electronics, Inductively coupled plasma, Mass spectrometry, Semiconductor

Introduction of Terminal Azide and Alkyne Functionalities in Polymers

“Click” chemistry, and the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) in particular, is a powerful new synthetic tool in polymer chemistry and material science. Success of the CuAAC in th...
Dr. Joost A. Opsteen
Material Matters 2008, 3.3, 66.
Keywords: Building blocks, Catalysis, Cycloadditions, Esterifications, Materials Science, Nucleophilic substitutions, Polymer science, Polymerization reactions, Radical polymerization, Substitutions, transformation

Organic Azides and Azide Sources

Since the preparation of the first organic azide, phenyl azide, by Peter Griess in 1864 this energy-rich and versatile class of compounds has enjoyed considerable interest. In more recent years, comp...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 10.
Keywords: Combinatorial synthesis, Cycloadditions, Hydroazidations, Metathesis, Peptide synthesis

Related Content

Hydroazidation Catalyst in Chemical Synthesis

New Hydroazidation Catalyst for Facile Preparation of Organoazides The chemistry of organoazides is exceedingly rich, since the azide functionality reacts with electrophiles, nucleophiles, and dipola...
Keywords: Azide formation, Catalysis, Click chemistry, Cycloadditions, Hydroazidations, Ligands, Reductions, Substitutions, transformation

Peer-Reviewed Papers
15

References

Related Products

related product

Product #

Description

Add to Cart

08168 Timestrip Plus 8 °C

Technical Service:

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Bulk Ordering & Pricing:

Need larger quantities for your development, manufacturing or research applications?