195758
Bromure de tétraméthylammonium
98%
Synonyme(s) :
TMAB
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About This Item
Formule linéaire :
(CH3)4N(Br)
Numéro CAS:
Poids moléculaire :
154.05
Numéro Beilstein :
3620955
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.21
Produits recommandés
Niveau de qualité
Pureté
98%
Forme
solid
Pf
>300 °C (lit.)
Chaîne SMILES
[Br-].C[N+](C)(C)C
InChI
1S/C4H12N.BrH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
Clé InChI
DDFYFBUWEBINLX-UHFFFAOYSA-M
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Catégories apparentées
Description générale
Tetrabutylammonium bromide is a quaternary ammonium compound that is widely used as a phase transfer catalyst. Absolute viscosities of its aqueous solutions have been measured at various temperatures (20,25 and 30°C). Various physical properties (activity coefficient up to saturation, conductance, density and solubility in water) of TMABr have been evaluated.
Tetramethylammonium bromide (TMABr) is a quaternary ammonium salt that is widely used as a phase transfer catalyst. Absolute viscosities of its aqueous solutions have been measured at various temperatures (20,25 and 30°C). Various physical properties (activity coefficient up to saturation, conductance, density and solubility in water) of TMABr have been evaluated. Its impact on the first order rate constant values for the base hydrolysis of the following Fe(II) chelates has been investigated:
- bis(naphthylidene alanate) (nali)
- bis(naphthylidene phenylalanate) (nphali)
- bis(naphthylidene aspartate) (nasi)
- (naphthylidene histidinate) (nhi)
- bis(naphthylidenearginate) (nari)
Application
Tetrabutylammonium bromide may be used in the molten state in the following processes:
- Synthesis of (2S)-5-(3-phenyl-2-phthalimidylpropanoylamino)isophthalic acid.
- Synthesis of alkyl-substituted pyrroles in the absence of catalyst and organic solvent.
- Synthesis of dithioacetals from acetals by transthioacetalisation in a solvent free environment.
- Synthesis of polyamides (PAs) by the polymerization of terephthalic acid and diisocyanates.
- Catalyze the addition of thiols to conjugated alkenes.
- Dehydrochlorination of poly(vinyl chloride).
Tetramethylammonium bromide may be used as a template in the synthesis of small colloidal zeolite Y nanocrystals.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 2 Oral
Code de la classe de stockage
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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Les clients ont également consulté
Dehydrochlorination of poly (vinyl chloride) by aqueous sodium hydroxide solution under two-phase conditions.
Kise H.
Journal of Polymer Science, 20(11), 3189-3197 (1982)
Viscosity of aqueous solutions. III. Tetramethylammonium bromide and the role of the tetraalkylammonium ions.
Nightingale Jr ER.
The Journal of Physical Chemistry, 66(5), 894-897 (1962)
Controlling size and yield of zeolite Y nanocrystals using tetramethylammonium bromide.
Holmberg BA, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 59(1), 13-28 (2003)
Some physical properties of aqueous solutions of tetramethylammonium bromide and tetramethylammonium iodide
Levien BJ.
Australian Journal of Chemistry, 18(8), 1161-1170 (1965)
Kinetic study of the base-catalyzed hydrolysis of novel high-spin hydrophobic Fe(II)-azomethine amino acid chelates: Salt and structure effects on the reactivity
Russian Journal of General Chemistry, 85, 168-172 (2015)
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