To search by structure, left click in the box below to display the chemdraw toolbar. Then, draw the chemical structure of interest in the box using the toolbar. When your structure is complete, click “Search by Name” or “Search by SMILES” to generate the product name or SMILES respectively. This feature will search within the Gelest product database for matching chemical names or SMILES. Note: In cases where Gelest uses alternate chemical names, it may be necessary to search for the product of interest by its CAS#.
- Einecs Number 218-222-3
- Synonyms TMSDMA, PENTAMETHYLSILANAMINE
- HMIS 3-4-1-X
- Molecular Formula C5H15NSi
- Molecular Weight (g/mol) 117.27
- TSCA Yes
- Delta H Vaporization (kJ/mol) 7.6 kcal/mole
- Boiling Point (˚C/mmHg) 85-86
- Density (g/mL) 0.741
- Flash Point (˚C) -19 °C
- Refractive Index @ 20˚C 1.3970
Selectively silylates equatorial hydroxyl groups in prostaglandin synthesis.1
Stronger silylation reagent than HMDS; silylates amino acids.2
Dialkylaminotrimethylsilanes are used in the synthesis of pentamethinium salts.3
With aryl aldehydes converts ketones to ?,?-unsaturated ketones.4
1. Yankee, E. et al. J. Am. Chem. Soc. 1972, 94, 3651.
2. Rühlman, K. Chem. Ber. 1961, 94, 1876.
3. Ko?ínek, M. et al. Synthesis 2009, 1291.
4. >Mojtahedi, M. M. et al. Synthesis, 2011, 3821.
Trimethylsilyl Blocking Agent
Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.
Alkyl Silane - Conventional Surface Bonding
Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.
Dimethylaminotrimethylsilane; Pentamethylsilanamine; Trimethylsilyldimethylamine; TMSDMA