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Merck

P5833

Sigma-Aldrich

Potassium carbonate

BioXtra, ≥99.0%

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About This Item

Fórmula lineal:
K2CO3
Número de CAS:
Peso molecular:
138.21
Beilstein/REAXYS Number:
4267587
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

product line

BioXtra

assay

≥99.0%

form

powder

impurities

≤0.0005% Phosphorus (P)
≤0.1% Insoluble matter

pH

11-13 (25 °C, 138 g/L)

mp

891 °C (lit.)

solubility

H2O: 1 M, clear, colorless

anion traces

chloride (Cl-): ≤0.005%
sulfate (SO42-): ≤0.02%

cation traces

Al: ≤0.0005%
Ca: ≤0.001%
Cu: ≤0.0005%
Fe: ≤0.0005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.5%
Pb: ≤0.001%
Zn: ≤0.0005%

SMILES string

[K+].[K+].[O-]C([O-])=O

InChI

1S/CH2O3.2K/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2

InChI key

BWHMMNNQKKPAPP-UHFFFAOYSA-L

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General description

Potassium carbonate is an inorganic base that is used in the alkylation of phenols and 1,3-dicarbonyl compounds, as well as the generation of sulfur and phosphorus ylides. It is also used to dry organic solvents.

Application

Potassium carbonate can be used as a catalyst in the:
  • Markovnikov addition reactions.
  • Suzuki cross-coupling reactions.
It can also be used as a base for the N-arylation of benzamides via C-N coupling reaction.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Potassium carbonate as a green catalyst for Markovnikov addition of azoles to vinyl acetate in PEG
Kidwai M, et al.
Green Chemistry Letters and Reviews, 6, 63-68 (2013)
Potassium Carbonate
Deshayes K
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Potassium Carbonate Promoted C-N Coupling Reaction between Benzamides and Aryl Iodides
Huang F, et al.
Synthesis, 50, 1090-1096 (2018)
Application of experimental design and multivariate analysis in the on-line reaction monitoring of a Suzuki cross-coupling reaction by Raman spectroscopy and multivariate analysis
Hetemi D, et al.
Vibrational Spectroscopy, 100, 93-98 (2019)
Carlos Arroniz et al.
Organic letters, 15(4), 910-913 (2013-02-05)
ortho-Arylation of ortho-substituted benzoic acids is a challenging process due to the tendency of the reaction products toward Pd-catalyzed protodecarboxylation. A simple method for preventing decarboxylation in sterically hindered benzoic acids is reported. The method described represents a reliable and

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