Benzyltrimethylammonium hydroxide: Difference between revisions
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* http://www.chemcas.com/AnalyticalDetail.asp?pidx=1&id=19594&cas=100-85-6&page=490 |
* http://www.chemcas.com/AnalyticalDetail.asp?pidx=1&id=19594&cas=100-85-6&page=490 |
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* Chaturvedi, D., & Ray, S. (2006). Triton b catalyzed, efficient, one-pot synthesis of carbamate esters from alcoholic tosylates. Monatshefte fuer Chemie, 137. Retrieved from http://www.springerlink.com/content/m48703268m3qw323/fulltext.pdf doi: 10.1007/s00706-005-0452-2 |
* Chaturvedi, D., & Ray, S. (2006). Triton b catalyzed, efficient, one-pot synthesis of carbamate esters from alcoholic tosylates. Monatshefte fuer Chemie, 137. Retrieved from http://www.springerlink.com/content/m48703268m3qw323/fulltext.pdf doi: 10.1007/s00706-005-0452-2 |
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[[Category:Bases]] |
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{{Uncategorized|date=November 2010}} |
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[[Category:Aromatic hydrocarbons]] |
Revision as of 02:21, 30 November 2010
Names | |
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IUPAC name
N,N,N-trimethyl-1-phenylmethanaminium hydroxide
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Other names
Triton B, Trimethylbenzylammonium hydroxide
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Identifiers | |
ECHA InfoCard | 100.002.632 |
CompTox Dashboard (EPA)
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Properties | |
C10H17NO | |
Molar mass | 167.125 g/mol |
Appearance | Liquid, clear, slightly yellow |
Density | 0.95 g/mL |
Miscible in water | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Benzyltrimethylammonium Hydroxide, also known as Triton B or trimethylbenzylammonium hydroxide, is an organic base. It is used in Aldol Condensation reactions and base-catalyzed dehydration reactions.
Sources
- http://www.chemcas.com/AnalyticalDetail.asp?pidx=1&id=19594&cas=100-85-6&page=490
- Chaturvedi, D., & Ray, S. (2006). Triton b catalyzed, efficient, one-pot synthesis of carbamate esters from alcoholic tosylates. Monatshefte fuer Chemie, 137. Retrieved from http://www.springerlink.com/content/m48703268m3qw323/fulltext.pdf doi: 10.1007/s00706-005-0452-2