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310263

Sigma-Aldrich

Potassium carbonate

ReagentPlus®, 99%

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2.5 KG
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$821.00

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1 KG
$90.40
2.5 KG
$155.00
5 KG
$205.60
12 KG
$351.00
50 KG
$821.00

About This Item

Linear Formula:
K2CO3
CAS Number:
584-08-7
Molecular Weight:
138.21
Beilstein/REAXYS Number:
4267587
EC Number:
209-529-3
MDL number:
MFCD00011382
UNSPSC Code:
12352302
PubChem Substance ID:
329753617
NACRES:
NA.21
assay:
99%
form:
solid

$90.40

Available to ship onApril 29, 2025Details

Request a Bulk Order

Quality Level

100

product line

ReagentPlus®

assay

99%

form

solid

pH

11-13 (25 °C, 138 g/L)

mp

891 °C (lit.)

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.[1] It participates as a base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene.[2] Addition of amino acids (glycine, sarcosine and proline) to K2CO3 (solvent) promotes the absorption of CO2.[3]

Application

Potassium carbonate may be used in the following processes:
  • As a reagent in the synthesis of polysubstituted iodobenzene derivatives.[4]
  • As a base for the Suzuki coupling of aryl halides with aryl boronic acids.[5]
  • The Heck reaction of styrene and bromobenzene.[1]
  • Preparation of disulfonated bis[4-(3-aminophenoxy)phenyl]sulfone, a disulfonated diamine monomer.[6]

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2512
BCCL2951
BCCK7798
MKCR5476
BCCJ6920

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A kinetic study of CO2 capture with potassium carbonate solutions promoted with various amino acids: glycine, sarcosine and proline.
Thee H, et al.
International Journal of Greenhouse Gas Control, 20, 212-222 (2014)
Polyamide interfacial composite membranes prepared from m-phenylene diamine, trimesoyl chloride and a new disulfonated diamine.
Xie W, et al.
Journal of Membrane Science, 403, 152-161 (2012)
Robert Möckel et al.
Organic letters, 17(7), 1644-1647 (2015-03-21)
The cobalt-catalyzed Diels-Alder reaction of trimethylsilyl-substituted alkynes with 1,3-dienes led to dihydroaromatic intermediates which were transformed into iodobenzene derivatives. For this transformation, the dihydroaromatic intermediates had to be oxidized and the trimethylsilyl-substituted arene had to undergo a silicon-iodine exchange reaction.
Chelating N-heterocyclic carbene ligands in palladium-catalyzed Heck-type reactions.
Herrmann WA, et al.
Journal of Organometallic Chemistry, 557(1), 93-96 (1998)
Heck reaction using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
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