Informatics Educational Institutions & Programs
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
3-Sulfanylpropane-1,2-diol[1] | |
| Other names
Thioglycerol
Monothioglycerol Thioglycerin Thiovanol 1-Thioglycerol Monothioglycerin Glycerol-1-thiol alpha-Thiolglycerol 3-Mercapto-1,2-propanediole | |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.002.269 |
| KEGG | |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C3H8O2S | |
| Molar mass | 108.16 g·mol−1 |
| Density | 1.25 g/mL |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
3-Mercaptopropane-1,2-diol, also known as thioglycerol, is a chemical compound and thiol that is used as a matrix in fast atom bombardment mass spectrometry and liquid secondary ion mass spectrometry.[2]
See also
References
- ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 697. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
The prefixes 'mercapto' (–SH), and 'hydroseleno' or selenyl (–SeH), etc. are no longer recommended.
- ^ Caldwell, G. W.; Reitz, A. B.; Masucci, J. A. (1990). "Application of dicyandiamide as a matrix additive in fast atom bombardment mass spectrometry". Organic Mass Spectrometry. 25 (6): 317–322. doi:10.1002/oms.1210250606.
