335991

Tetrabutylammonium acetate

97%

Manufacturer: Sigma Aldrich

CAS Number: 10534-59-5

Synonym(S): N,N,N-tributyl-1-butanaminium acetate, Tetra-n-butylammonium acetate

Select a Size

Pack Size SKU Availability Price
5 G 335991-5-G In Stock ₹ 10,543.55
10 G 335991-10-G In Stock ₹ 17,882.90
50 G 335991-50-G In Stock ₹ 47,261.95

335991 - 5 G

₹ 10,543.55

In Stock

Quantity

1

Base Price: ₹ 10,543.55

GST (18%): ₹ 1,897.839

Total Price: ₹ 12,441.389

Quality Level

200

Assay

97%

mp

95-98 °C (lit.)

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

Other Options

Image Product Name Manufacturer Price Range
50-179-7086
Sigma Aldrich Fine Chemicals Biosciences Tetrabutylammonium acetate solution 1.0 M in H2O | 10534-59-5 | MFCD00043208 | 50ML
Sigma Aldrich Fine Chemicals Biosciences ₹ 19,180.84
NC2315647
eMolecules​ Tetrabutylammonium acetate | 10534-59-5 | MFCD00043208 | 500g
eMolecules​ ₹ 6,801.16
50-179-7084
Sigma Aldrich Fine Chemicals Biosciences Tetrabutylammonium acetate 97% | 10534-59-5 | MFCD00043208 | 50G
Sigma Aldrich Fine Chemicals Biosciences ₹ 52,773.41
50-179-7083
Sigma Aldrich Fine Chemicals Biosciences Tetrabutylammonium acetate 97% | 10534-59-5 | MFCD00043208 | 10G
Sigma Aldrich Fine Chemicals Biosciences ₹ 20,438.57
86835
Tetrabutylammonium acetate
Supelco ₹ 61,475.18
401803
Tetrabutylammonium acetate solution
Sigma Aldrich ₹ 9,890.00
AR0036CO
Tetrabutylammonium acetate
Aaron Chemicals LLC ₹ 171.12 - ₹ 20,277.72
CS-W008039
Tetrabutylammonium acetate
ChemScene ₹ 855.60 - ₹ 10,096.08

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Description

  • General description: Tetrabutylammonium acetate (TBAA) is a phase transfer catalyst (PTC).
  • Application: Tetrabutylammonium acetate can be used: To catalyze the alkynylation of carbonyl compounds with trimethylsilylacetylenes providing good yields of propargylic alcohols.[1] Along with tetrabutylammonium bromide (TBAB) as a molten reaction medium in the synthesis of 4-aryl-2-quinolones.[2] As a promoter in the regioselective direct arylation of azoles (1-methylpyrazole, oxazole, and thiazole) with aryl bromides in presence of palladium acetate catalyst.[3]As an ionic liquid to dissolve cellulose in the presence of DMSO co-solvent.[4]As an activator in the synthesis of disubstituted alkynes through copper-free Sonogashira coupling reaction.[5]

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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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

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MCZDHTKJGDCTAE-UHFFFAOYSA-M

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1S/C8H12N2/c1-5-3-8(10)6(2)4-7(5)9/h3-4H,9-10H2,1-2H3

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