| Weight | 167.252 g/mol |
|---|---|
| Formula | C10H17NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Benzyltrimethylammonium hydroxide (100-85-6)
benzyltrimethylammonium · benzyltrimethylammonium chloride · benzyltrimethylammonium iodide
Score:
#347 in Materials science
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#2189 in Physics
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#6769 in Chemistry
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- Anion-exchange membranes for alkaline polymer electrolyte fuel cells: comparison of pendent benzyltrimethylammonium- and benzylmethylimidazolium-head-groups (Energy and Environmental Science, 2012)
- Efficient Conversion of Substituted Aryl Thioureas to 2-Aminobenzothiazoles Using Benzyltrimethylammonium Tribromide (Journal of Organic Chemistry, 2003)
- Rearrangements of Benzyltrimethylammonium Ion and Related Quaternary Ammonium Ions by Sodium Amide Involving Migration into the Ring1,2,3 (Journal of the American Chemical Society, 1951)
- Halogenation Using Quaternary Ammonium Polyhalides. VII. Iodination of Aromatic Amines by Use of Benzyltrimethylammonium Dichloroiodate(1 (Bulletin of the Chemical Society of Japan, 1988)
- Electrodeposition of aluminium and aluminium/platinum alloys from AlCl3/benzyltrimethylammonium chloride room temperature ionic liquids (Journal of Applied Electrochemistry, 2001)
- Bromination of Phenols by Use of Benzyltrimethylammonium Tribromide (Chemistry Letters, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzyltrimethylammonium
- benzyltrimethylammonium chloride
- benzyltrimethylammonium iodide
- benzyltrimethylammonium formate
- benzyltrimethylammonium hexafluorophosphate (1-)
- benzyltrimethylammonium acetate
- benzyltrimethylammonium butanoate
- benzyltrimethylammonium pentanoate
- benzyltrimethylammonium propanoate
- benzyltrimethylammonium octanoate
- benzyltrimethylammonium heptanoate
- benzyltrimethylammonium methoxide
- benzyltrimethylammonium hexanoate
- benzyltrimethylammonium carbonate (2:1)
- benzyltrimethylammonium bromide
- benzyltrimethylammonium nonanoate
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SMILESC[N+](C)(C)CC1=CC=CC=C1.[OH-]
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InChIKeyNDKBVBUGCNGSJJ-UHFFFAOYSA-M
- Pubchem - Benzyltrimethylammonium hydroxide
- Wikipedia - benzyltrimethylammonium hydroxide
Benzyltrimethylammonium hydroxide, also known as Triton B or trimethylbenzylammonium hydroxide, is a quaternary ammonium salt that functions as an organic base. It is usually handled as a solution in water or methanol. The compound is colourless, although the solutions often appear yellowish.
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Benzyltrimethylammonium hydroxide
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