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791784

Sigma-Aldrich

Tetrabutylammonium hydrogensulfate

anhydrous, free-flowing, Redi-Dri™, 97%

Synonyme(s) :

Tetrabutylammonium bisulfate

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About This Item

Formule linéaire :
(CH3CH2CH2CH2)4N(HSO4)
Numéro CAS:
32503-27-8
Poids moléculaire :
339.53
Numéro CE :
251-068-5
Numéro MDL:
MFCD00011637
Code UNSPSC :
12352100
ID de substance PubChem :
329768291
Nomenclature NACRES :
NA.21

Qualité

anhydrous
free-flowing

Niveau de qualité

100

Gamme de produits

Redi-Dri™

Pureté

97%

Forme

crystals

Pf

169-171 °C (lit.)

Chaîne SMILES 

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

InChI

1S/C16H36N.H2O4S/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-5(2,3)4/h5-16H2,1-4H3;(H2,1,2,3,4)/q+1;/p-1

Clé InChI

SHFJWMWCIHQNCP-UHFFFAOYSA-M

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Description générale

Tetrabutylammonium bisulfate(TBAHS), a quaternary ammonium salt, is a phase-transfer reagent. It severs as cocatalyst, additive, acid, also as ion-paring agent.

Application

Tetrabutylammonium hydrogensulfate is used as a cocatalyst in the synthesis of propionic acid and the ketones by hydrocarboxylation of ethylene.

Informations légales

Redi-Dri™ is a trademark of Sigma-Aldrich Co. LLC
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Pictogrammes

CorrosionExclamation mark
GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H314,H412

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

348.1 °F - closed cup

Point d'éclair (°C)

175.6 °C - closed cup

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCK3440
BCCH7923
BCCD2435
BCCF3917
BCCD2434

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Haji Bahadar et al.
Environmental toxicology and pharmacology, 39(3), 1161-1169 (2015-05-04)
Benzene (C6H6) is an organic compound used in petrochemicals and numerous other industries. It is abundantly released to our environment as a chemical pollutant causing widespread human exposure. This study mainly focused on benzene induced toxicity on rat pancreatic islets
K M Frankowski et al.
Journal of dairy science, 97(9), 5356-5370 (2014-07-16)
Many food companies are trying to limit the amount of sodium in their products. Permeate, the liquid remaining after whey or milk is ultrafiltered, has been suggested as a salt substitute. The objective of this study was to determine the
Hiroyuki Nakao et al.
Biochimica et biophysica acta, 1848(1 Pt A), 145-150 (2014-10-15)
KcsA is a pH-dependent potassium channel that is activated at acidic pH. The channel undergoes global conformational changes upon activation. We hypothesized that the open-close conformational changes of the transmem brane region could promote the flip-flop of phosphoiipids. Based on
Jia Bao et al.
Environmental science and pollution research international, 21(12), 7650-7655 (2014-03-14)
Severe perfluoroalkyl acid (PFAA) contamination resulting from the fast-growing semiconductor, electrochemical, and optoelectronic industries has been determined in the river water in the vicinity of the Taipei area, Taiwan, during recent years. However, little is known about body burdens of
Muhammet Uyanik et al.
Science (New York, N.Y.), 345(6194), 291-294 (2014-07-19)
The diverse biological activities of tocopherols and their analogs have inspired considerable interest in the development of routes for their efficient asymmetric synthesis. Here, we report that chiral ammonium hypoiodite salts catalyze highly chemo- and enantioselective oxidative cyclization of γ-(2-hydroxyphenyl)ketones
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