Chemistry:5-tert-Butyl-m-xylene
From HandWiki
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| Names | |
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| IUPAC name
1-tert-Butyl-3,5-dimethylbenzene
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| Other names
2,6-Dimethyl-4-tert-butyl-benzene
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| Identifiers[1] | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C12H18 | |
| Molar mass | 162.276 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.86 g/mL |
| Melting point | −22 °C (−8 °F; 251 K) |
| Boiling point | 207–209 °C (405–408 °F; 480–482 K) |
| Vapor pressure | 0.4 hPa (20 °C) |
| Hazards | |
| Main hazards | Irritant |
| Safety data sheet | Safety Data Sheet |
| GHS pictograms | 
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| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P280, P305+351+338, P304+340, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
5-tert-Butyl-m-xylene is a chemical compound from the family of alkylbenzenes and is a colorless liquid at room temperature.
It can be used for the synthesis of polyalkylated diaryl disulfides such as bis(4-tert-butyl-2,6-dimethylphenyl) disulfide and bis(2,4,6)-triisopropylphenyl) disulfide.[2]
It is also used as a precursor in the synthesis of xylometazoline.[3][4]
References
- ↑ "1-tert-Butyl-3,5-dimethylbenzene". 2013-10-25. https://www.alfa.com/de/catalog/A19220/.
- ↑ Sigma-Aldrich Co., 1-tert-Butyl-3,5-dimethylbenzene, 98%.
- ↑ "Synthetic method of xylometazoline hydrochloride compound". 2010-09-19. https://patents.google.com/patent/CN101928247B/en.
- ↑ Golander, Yechiel; DeWitte, Wayne J. (1985). "Xylometazoline Hydrochloride". Analytical Profiles of Drug Substances. 14. Elsevier. pp. 135–156. doi:10.1016/s0099-5428(08)60579-1. ISBN 978-0-12-260814-8.
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