Chemodex

Tetrahexylammonium hydrogensulfate

CHF 77.00
In stock
CDX-T0610-G0055 gCHF 77.00
CDX-T0610-G02525 gCHF 258.00
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Product Details
Synonyms Tetra-n-Hexylammonium hydrogen sulfate; THAHS
Product Type Chemical
Properties
Formula C24H53NO4S
MW 451.75
CAS 32503-34-7
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (Titr.)
Appearance Colorless or white powder or crystals.
Solubility Soluble in methanol or DMSO.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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InChi Key RULHPTADXJPDSN-UHFFFAOYSA-M
Smiles OS([O-])(=O)=O.CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Keep under inert gas.
Very hygroscopic.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
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Product Specification Sheet
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Description

Tetrahexylammonium hydrogensulfate (THAHS) is a quaternary ammonium salt used in various chemical and biochemical applications. It consists of a tetracationic ammonium ion (C6H13)4N+ and a hydrogen sulfate anion (HSO4-). THAHS is used as a phase-transfer catalyst (PCT) and can facilitate various chemical reactions by aiding in the transfer of reactants between immiscible phases. Phase-transfer catalysis involves the transfer of reactants from one phase (usually an aqueous phase) to another phase (usually an organic phase) to facilitate a chemical reaction. THAHS can be employed in organic synthesis, particularly in reactions that involve the transfer of anions or reagents between organic and aqueous phases. Some common applications include, quaternization reactions, nucleophilic substitution reactions or halogenation reactions. It can also be used in processes that involve the extraction or separation of specific ions or compounds from one phase to another.

Product References

(1) R. Bar, et al.; J. Mol. Catal. 16, 175 (1982) | (2) D. Feldmann & M. Rabinovitz; J. Org. Chem. 53, 3779 (1988) | (3) L.G Sayers, et al.; Biochem. Soc. Trans. 21, 105S (1993) | (4) T.S. Straub; Tetrahedr. Lett. 36, 663 (1995) | (5) S. Amaratunga & H. Alper; J. Organometall. Chem. 488, 25 (1995) | (6) L.J. Csanyi & K. Jaky; Phys. Chem. Chem. Phys. 3, 2018 (2001) | (7) R.J. Fox & J. Qiu; Org. Process Res. Dev. 24, 235 (2020)

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