Azidotrimethylsilane (TMSN 3) is a a colorless and stable organosilane reagent. It shows very slow decomposition at high temperatures. It is a very commonly used azide source and has been used in the synthesis of aminotriazole ligands.

Trimethylsilyl azide is the organosilicon compound with the formula (CH 3) 3 SiN 3. A colorless liquid, it is a reagent in organic chemistry, serving as the equivalent of hydrazoic acid. [3]

Silanes can be used to prime metals, bind biomaterial, immobilize catalysts, provide crosslinking, and improve polymer and particle dispersions. They can also enhance adhesive bonding, increase electrical properties, maximize composite strength, and increase mechanical properties.

Silane-peg-azide | C14H31N5O5Si | CID 156598925 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Synonyms: trimethylsilyl azide Molecular Weight (g/mol): 115.21 Molecular Formula: C3H9N3Si

Trimethylsilyl azide: Does not have an individual approval but may be used under an appropriate group standard

Trimethylsilyl azide for synthesis; CAS Number: 4648-54-8; Synonyms: Trimethylsilyl azide,Azidotrimethylsilane; Linear Formula: (CH3)3SiN3 at Sigma-Aldrich

Silane-PEG-Azide, MW 1,000 is a PEG linker containing azido and triethoxysilane moieties. The azide can be used for copper-catalyzed Click Chemistry reactions with alkynes, DBCO and BCN. The triethoxysilane moiety is used for surface modification.

Silane PEG azide is one of Nanocs’ surface reactive Pegylation and silanization reagents that contain a terminal triethoxysilane silane and an azide on each PEG terminus.

Silane, azido- | H3N3Si | CID 139627 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.