Chemistry:2-Methyl-2-heptanethiol
From HandWiki
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| Names | |
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| Preferred IUPAC name
2-Methylheptane-2-thiol | |
| Other names
2-Methyl-2-heptanethiol
tert-Octyl mercaptan tert-Octanethiol | |
| Identifiers | |
3D model (JSmol)
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PubChem CID
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| UNII | |
| UN number | 3023 |
CompTox Dashboard (EPA)
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| Properties | |
| C8H18S | |
| Molar mass | 146.29 g·mol−1 |
| Appearance | Straw-colored liquid |
| Density | 0.85 |
| Melting point | −74 °C (−101 °F; 199 K) |
| Boiling point | 155 °C (311 °F; 428 K) |
| Hazards | |
| Flash point | 46 °C (115 °F; 319 K) open cup |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
2-Methyl-2-heptanethiol is an organic compound classified as a thiol. It is a straw-colored liquid with a strong, obnoxious odor.[1][2]
It is used as a lubricant additive and in polymer modification.[1] The chemical is one of the tertiary aliphatic mercaptans (thiols) synthesized from petroleum, as described in a 1950 paper. Initial research postulated they could be used as lubricant additives, ore flotation collectors, vulcanization accelerators, fungicides, and nonionic detergents. [3]
References
- ↑ 1.0 1.1 "2-METHYL-2-HEPTANETHIOL". NOAA. http://cameochemicals.noaa.gov/chemical/24011.
- ↑ "ICSC: 1494, tert-OCTYL MERCAPTAN". International Programme on Chemical Safety. http://www.inchem.org/documents/icsc/icsc/eics1494.htm.
- ↑ Schulze, W.A. (1950). "Sulfur Compounds from Petroleum Hydrocarbons". Ind. Eng. Chem. 42 (5): 916–921. doi:10.1021/ie50485a043.
This article contains public domain text from the NOAA.
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