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345490

Sigma-Aldrich

Zinc p-toluenesulfonate hydrate

Sinonimo/i:

p-Toluenesulfonic acid zinc salt

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About This Item

Formula condensata:
(CH3C6H4SO3)2Zn·xH2O
Numero CAS:
13438-45-4
Peso molecolare:
407.78 (anhydrous basis)
Beilstein:
4339837
Numero CE:
236-576-7
Numero MDL:
MFCD00151013
Codice UNSPSC:
12352302
ID PubChem:
24861327
NACRES:
NA.23

Saggio

≥98.5% (HPLC)

Forma fisica

powder

Impiego in reazioni chimiche

reagent type: catalyst
core: zinc

Concentrazione

≤15.7% Zn (EDTA titration)

Stringa SMILE

O.[Zn++].Cc1ccc(cc1)S([O-])(=O)=O.Cc2ccc(cc2)S([O-])(=O)=O

InChI

1S/2C7H8O3S.H2O.Zn/c2*1-6-2-4-7(5-3-6)11(8,9)10;;/h2*2-5H,1H3,(H,8,9,10);1H2;/q;;;+2/p-2
JCOXFVWERPVZPB-UHFFFAOYSA-L

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
75196KJ
10602ME
13916PU
07614LI
07529AS

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Magnesium trifluoromethanesulfonate 97%

Sigma-Aldrich

337986

Magnesium trifluoromethanesulfonate

acido p-toluenesolfonico ACS reagent, ≥98.5%

Sigma-Aldrich

402885

acido p-toluenesolfonico

Toratane Munegumi et al.
Chirality, 24(2), 188-192 (2011-12-17)
Preferential crystallization of amino acid derivatives by seeding a pure enantiomer into racemic amino acid solutions has been studied for many years. However, few examples of valine derivatives have been reported so far. Although there have been some reports using
Jhonny Azuaje et al.
ACS combinatorial science, 13(1), 89-95 (2011-01-21)
We document here the use of polymer-supported p-toluenesulfonic acid as a highly effective, robust, economical and eco-friendly isocyanide scavenger. The herein described strategy circumvent the intense and repulsive odor of volatile isocyanides, enabling simplified and odorless workup and purifications. The
Aditya Kulkarni et al.
Organic letters, 13(19), 5124-5127 (2011-09-10)
An environmentally benign procedure for the hydrogenation of unprotected indoles is described. The hydrogenation reaction is catalyzed by Pt/C and activated by p-toluenesulfonic acid in water as a solvent. The efficacy of the method is illustrated by the hydrogenation of
G Ozyilmaz et al.
Prikladnaia biokhimiia i mikrobiologiia, 47(2), 217-225 (2011-03-01)
Amperometric glucose biosensors have been developed based on entrapment on platinum (Pt) electrode using cyclic voltammetry technique in glucose oxidase (GOD) and pyrrole containing p-toluenesulfonic acid (pTSA) or sodium p-toluenesulfonate (NapTS) as supporting electrolyte solutions. Both of electrolyte solutions were
Koneni V Sashidhara et al.
Bioorganic & medicinal chemistry letters, 22(12), 3926-3930 (2012-05-23)
First synthesis of novel coumarin-trioxane hybrids is reported. The synthesis was achieved via condensation of β-hydroxyhydroperoxides with coumarinic-aldehydes in presence of p-toluenesulfonic acid in good yields and the novel hybrids were evaluated for their antimalarial activity both in vitro and
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