Hexamethyldisiloxane
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| Hexamethyldisiloxane | |
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| General | |
| Systematic name | Hexamethyldisiloxane |
| Other names | HMDS Bis(trimethylsilyl) ether Bis(trimethylsilyl) oxide |
| Molecular formula | C6H12OSi2 |
| SMILES | CSi(C)(C)OSi(C)(C)C |
| Molar mass | 162.38 g/mol |
| Appearance | colorless liquid |
| CAS number | [107-46-0] |
| Properties | |
| Density and phase | 0.764 g/cm3 |
| Solubility in water | low |
| Other solvents | all organic solvents |
| Melting point | −59 °C |
| Boiling point | 101 °C |
| Viscosity | ? cP at ? °C |
| Structure | |
| Dipole moment | ? D |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | flammable |
| NFPA 704 | |
| Flash point | ? °C |
| R/S statement | R: 11 S: 16 |
| RTECS number | JM9237000 |
| Supplementary data page | |
| Structure and properties |
n = 1.377 |
| Thermodynamic data |
Phase behaviour Solid, liquid, gas |
| Spectral data | 1H NMR ~0.49 (δ scale) |
| Related compounds | |
| Related compounds | Tetramethylsilane Dimethyl ether Bis(trimethylsilyl)amine |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Hexamethyldisiloxane is a chemical compound with the formula O[Si(CH3)3]2. This volatile liquid is used as a solvent and as a reagent. The species arises by the hydrolysis of trimethylsilyl chloride. The molecule is the protypical silyl ether and can be considered a subunit of polydimethylsiloxane.
Contents |
[edit] Uses
It is primarily used as source of the trimethylsilyl functional group (-Si(CH3)3) in organic synthesis. For example, in the presence of acid catalyst, it converts alcohols and carboxylic acids into the silyl ethers and silyl esters, respectively.[1]
[edit] Miscellaneous uses
HMDS is used as an internal standard for calibrating chemical shift in 1H NMR spectroscopy. It is more easily handled since it is less volatile than the usual standard tetramethylsilane but still displays only a singlet near 0 ppm.
HMDS has even poorer solvating power than alkanes. It is therefore sometimes employed to crystallize highly lipophilic compounds.
[edit] Safety
Like most siloxanes, hexamethyldisiloxane is fairly innocuous.
[edit] References
- ^ Pfeifer, J. "Hexamethyldisiloxane" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. DOI: 10.1002/047084289.
[edit] External links
- Links to external chemical sourcesTemplate:Lien AdQ
