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Tetrabutylammonium iodide

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For Research Use Only | Not For Clinical Use
CATAP311284
CAS311-28-4
Structure
MDL NumberMFCD00011636
Molecular Weight369.37
EC Number206-220-5
InChI KeyDPKBAXPHAYBPRL-UHFFFAOYSA-M
REAXYS Number3916152
Descriptionfor electrochemical analysis, ≥99.0%
Solubilityacetonitrile: 0.1 g/mL, clear, colorless
Assay≥99.0% (AT); ≥99.0%
Gradefor electrochemical analysis
Linear Formula(CH3CH2CH2CH2)4N(I)
MP141-143 °C (lit.); 144-146 °C
Size5G
1

Charge-Transfer-to-Solvent Reaction in a Hydrophobic Tetrabutylammonium Iodide Molecular Layer in Aqueous Solution

Shutaro Karashima, Toshinori Suzuki

J Phys Chem B. 2019 May 2;123(17):3769-3775.

PMID: 30827113

1

Combination of Tetrabutylammonium Iodide (TBAI) With tert-Butyl Hydroperoxide (TBHP): An Efficient Transition-Metal-Free System to Construct Various Chemical Bonds

Rongxiang Chen, Jijun Chen, Jie Zhang, Xiaobing Wan

Chem Rec. 2018 Sep;18(9):1292-1305.

PMID: 29513383

1

Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of Baylis-Hillman Acetates With Sulfonylhydrazides in Water

Xiaoqing Li, Xiangsheng Xu, Yucai Tang

Org Biomol Chem. 2013 Feb 13;11(10):1739-42.

PMID: 23381111

1

Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of α-methyl Styrene Derivatives With Sulfonylhydrazides

Xiaoqing Li, Xiangsheng Xu, Can Zhou

Chem Commun (Camb). 2012 Dec 28;48(100):12240-2.

PMID: 23147597

1

Tetrabutylammonium Iodide-Promoted Thiolation of Oxindoles Using Sulfonyl Chlorides as Sulfenylation Reagents

Xia Zhao, Aoqi Wei, Xiaoyu Lu, Kui Lu

Molecules. 2017 Aug 1;22(8):1208.

PMID: 28763049

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