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Supelco

Tetrabutylammonium acetate

for electrochemical analysis, ≥99.0%

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About This Item

Linear Formula:
(CH3CH2CH2CH2)4N(OCOCH3)
CAS Number:
10534-59-5
Molecular Weight:
301.51
Beilstein:
3599376
EC Number:
234-101-8
MDL number:
MFCD00043208
UNSPSC Code:
26111700
PubChem Substance ID:
329769490
NACRES:
NB.61

grade

for electrochemical analysis

Quality Level

100

Assay

≥99.0% (NT)
≥99.0%

form

powder

mp

95-98 °C (lit.)

solubility

acetonitrile: 0.1 g/mL, clear, colorless to very faintly brown

SMILES string

CC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC

InChI

1S/C16H36N.C2H4O2/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-2(3)4/h5-16H2,1-4H3;1H3,(H,3,4)/q+1;/p-1

InChI key

MCZDHTKJGDCTAE-UHFFFAOYSA-M

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General description

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Application


  • Improved Process for the Synthesis of 3-(3-Trifluoromethylphenyl)propanal for More Sustainable Production of Cinacalcet HCl.: This research outlines an enhanced synthetic route using tetrabutylammonium acetate, emphasizing efficiency and sustainability in pharmaceutical manufacturing processes (Rathod et al., 2023).

  • Anion-exchange Facilitated Selective Extraction of Sulfate and Phosphate by Overcoming the Hofmeister Bias.: The paper investigates selective extraction processes enhanced by tetrabutylammonium acetate, useful in environmental and analytical chemistry applications (Gogoi et al., 2023).

  • Synthesis of Enamines, Aldehydes, and Nitriles from CO2: Scope of the One-Pot Strategy via Formamides.: This study presents a novel one-pot synthesis strategy involving tetrabutylammonium acetate, demonstrating its versatility in organic synthesis (Nakaoka et al., 2023).

  • All-Inorganic Perovskite Solar Cells with Tetrabutylammonium Acetate as the Buffer Layer between the SnO2 Electron Transport Film and CsPbI3.: This research showcases the application of tetrabutylammonium acetate in improving the efficiency of perovskite solar cells, a significant advancement in renewable energy technologies (Zhong et al., 2022).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Michelle L Ingalsbe et al.
Bioorganic & medicinal chemistry letters, 19(17), 4984-4987 (2009-08-08)
Due to the increasing number of strains of drug-resistant bacteria, the development of new antibiotics has become increasingly important. The antibacterial properties of quaternary amines and their derivatives on both Gram-positive and Gram-negative bacteria are well known. However, an encompassing
Łukasz Orzeł et al.
Dalton transactions (Cambridge, England : 2003), 44(13), 6012-6022 (2015-02-28)
The nature of chlorophyll interactions with copper(II) ions varies considerably in organic solvents, depending on the dominant coordinative form. Besides formation of the metallo tetrapyrrolic complex, Cu(II) ions can cause oxidation of the pigment, reversible or irreversible, which can lead

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