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Benzyltri-n-butylammonium bromide, 99%, Thermo Scientific Chemicals
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Catalog number B23941.18
also known as B23941-18
Price (USD)/ Each
60.40
-
Quantity:
50 g
Price (USD)/ Each
60.40
Benzyltri-n-butylammonium bromide, 99%, Thermo Scientific Chemicals
Catalog numberB23941.18
Price (USD)/ Each
60.40
-
Chemical Identifiers
CAS25316-59-0
IUPAC Namebenzyltributylazanium bromide
Molecular FormulaC19H34BrN
InChI KeyUDYGXWPMSJPFDG-UHFFFAOYSA-M
SMILES[Br-].CCCC[N+](CCCC)(CCCC)CC1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder or fused solid
Appearance (Color)White
Assay (Titration ex Bromide)≥98.5 to ≤101.5%
Benzyltri-n-butylammonium bromide will react with N-vinyl-phthalimide to produce N-trans-cinnamyl-phthalimide.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Benzyltri-n-butylammonium bromide will react with N-vinyl-phthalimide to produce N-trans-cinnamyl-phthalimide.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Store under dry inert gas. It is hygroscopic in nature.
Benzyltri-n-butylammonium bromide will react with N-vinyl-phthalimide to produce N-trans-cinnamyl-phthalimide.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Store under dry inert gas. It is hygroscopic in nature.
RUO – Research Use Only
General References:
- Naotaka Yamada.; Eiichi Kuwano.; Masamichi Kikuchi.; Morifusa Eto. Synthesis and Bleaching Activity of 1,5-Disubstituted Imidazoles. Bioscience, Biotechnology, and Biochemistry. 1992, 56 (12), 1943-1948.
- J. Ståhlberg.; A. Furängen. An experimental verification of the electrostatic theory for ion pair chromatography. Chromatographia. 1987, 24 (1), 783-789.
- Quaternary salts undergo Heck-type coupling with activated alkenes: Synthesis, 245 (1995):