426288

Tetrabutylammonium bromide

ACS reagent, ≥98.0%

Manufacturer: Sigma Aldrich

CAS Number: 1643-19-2

Synonym(S): N,N,N-tributyl-1-butanaminium bromide, TBAB, TBABr, tetra-n-butylammonium bromide

Select a Size

Pack Size SKU Availability Price
25 G 426288-25-G In Stock ₹ 2,920.00
100 G 426288-100-G In Stock ₹ 5,444.98

426288 - 25 G

₹ 2,920.00

In Stock

Quantity

1

Base Price: ₹ 2,920.00

GST (18%): ₹ 525.60

Total Price: ₹ 3,445.60

grade

ACS reagent

Quality Level

200

Assay

≥98.0%

form

solid

greener alternative product characteristics

CatalysisLearn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

impurities

≤0.5% tributylamine hydrobromide≤0.5% tributylamine

mp

102-106 °C (lit.)

greener alternative category

SMILES string

[Br-].CCCC[N+](CCCC)(CCCC)CCCC

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Description

  • General description: Tetrabutylammonium bromide (TBAB) is a quaternary ammonium compound.[1] It is the most widely used phase transfer catalyst.[2] Its interfacial properties have been studied in case of hydroxide initiated reactions. This may be applied in understanding the mechanism of phase transfer reactions.[1] TBAB is reported to decrease retention time and remove peak tailing by acting as an ion pair reagent during the chromatographic analysis of quaternary ammonium compounds.[2] In the molten state TBAB behaves like an ionic liquid which is a promising green alternative to organic solvents in organic synthesis.[3][4] Its molar heat capacity, entropy and free energy function have been determined.[5]
  • Application: Tetrabutylammonium bromide (TBAB) may be used in the molten state in the following processes:Synthesis of (2S)-5-(3-phenyl-2-phthalimidylpropanoylamino)isophthalic acid.[6]Synthesis of alkyl-substituted pyrroles in the absence of catalyst and organic solvent.[7]Synthesis of dithioacetals from acetals by transthioacetalisation in a solvent free environment.[8]Synthesis of polyamides (PAs) by the polymerization of terephthalic acid and diisocyanates.[4]Catalyze the addition of thiols to conjugated alkenes.[9]Dehydrochlorination of poly(vinyl chloride).[10]

SAFETY INFORMATION

Pictograms

GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H361fd,H412

Precautionary Statements

P202 - P273 - P301 + P312 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves