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345490

Sigma-Aldrich

Zinc p-toluenesulfonate hydrate

Sinónimos:

p-Toluenesulfonic acid zinc salt

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About This Item

Fórmula lineal:
(CH3C6H4SO3)2Zn·xH2O
Número de CAS:
13438-45-4
Peso molecular:
407.78 (anhydrous basis)
Beilstein/REAXYS Number:
4339837
EC Number:
236-576-7
MDL number:
MFCD00151013
UNSPSC Code:
12352302
PubChem Substance ID:
24861327
NACRES:
NA.23
assay:
≥98.5% (HPLC)
grade:
for analytical purposes
form:
powder

grade

for analytical purposes

assay

≥98.5% (HPLC)

form

powder

reaction suitability

reagent type: catalyst
core: zinc

concentration

≤15.7% Zn (EDTA titration)

SMILES string

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

InChI key

JCOXFVWERPVZPB-UHFFFAOYSA-L

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
75196KJ
10602ME
15802EA
13916PU
07614LI

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Sigma-Aldrich

337986

Magnesium trifluoromethanesulfonate

p-Toluenesulfonic acid monohydrate ACS reagent, ≥98.5%

Sigma-Aldrich

402885

p-Toluenesulfonic acid monohydrate

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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