Jump to content

Benzyltrimethylammonium hydroxide: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
categorization/tagging using AWB
categories
Line 31: Line 31:
* 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
* 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
*
*


[[Category:Bases]]
{{Uncategorized|date=November 2010}}
[[Category:Aromatic hydrocarbons]]

Revision as of 02:21, 30 November 2010

Benzyltrimethylammonium hydroxide
Skeletal formula of benzyltrimethylammonium hydroxide
Names
IUPAC name
N,N,N-trimethyl-1-phenylmethanaminium hydroxide
Other names
Triton B, Trimethylbenzylammonium hydroxide
Identifiers
ECHA InfoCard 100.002.632 Edit this at Wikidata
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).

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