推荐产品
等級
ACS reagent
品質等級
化驗
≥98.0%
形狀
powder
雜質
≤0.5% trimethylamine hydrobromide
≤0.5% trimethylamine
mp
>300 °C (lit.)
SMILES 字串
[Br-].C[N+](C)(C)C
InChI
1S/C4H12N.BrH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
InChI 密鑰
DDFYFBUWEBINLX-UHFFFAOYSA-M
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一般說明
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.
應用
Tetrabutylammonium bromide (TBAB) 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).
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 2 Oral
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
其他客户在看
Heat capacities and thermodynamic properties of two tetramethylammonium halides.
J. Chem. Phys. , 36(9), 2420-2423 (1962)
Some physical properties of aqueous solutions of tetramethylammonium bromide and tetramethylammonium iodide
Australian Journal of Chemistry, 18(8), 1161-1170 (1965)
Viscosity of aqueous solutions. III. Tetramethylammonium bromide and the role of the tetraalkylammonium ions.
The Journal of Physical Chemistry, 66(5), 894-897 (1962)
Catalysis by ionic liquids: solvent-free efficient transthioacetalisation of acetals by molten tetrabutylammonium bromide.
Journal of the Chemical Society. Perkin Transactions 1, 13, 1520-1522 (2002)
Novel biobased polyurethanes synthesized from nontoxic phenolic diol containing l-tyrosine moiety under green media.
Journal of Polymers and the Environment, 18(4), 685-695 (2010)
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