900501
Potassium carbonate
anhydrous, free-flowing, Redi-Dri™, ReagentPlus®, 99%
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About This Item
Linear Formula:
K2CO3
CAS Number:
Molecular Weight:
138.21
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
209-529-3
Beilstein/REAXYS Number:
4267587
MDL number:
Assay:
99%
Grade:
anhydrous
Form:
powder
InChI key
BWHMMNNQKKPAPP-UHFFFAOYSA-L
InChI
1S/CH2O3.2K/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
SMILES string
[K+].[K+].[O-]C([O-])=O
grade
anhydrous
product line
ReagentPlus®, Redi-Dri™
assay
99%
form
powder
quality
free-flowing
pH
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
Quality Level
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Related Categories
Application
- Improved 2-pyridyl reductive homocoupling reaction using biorenewable solvent: A detailed examination of using potassium carbonate in an enhanced reductive homocoupling of 2-pyridyl compounds in a biorenewable solvent, showcasing a sustainable approach to chemical synthesis (Webb et al., 2023).
- Fe(3)O(4)@void@C-Schiff-base/Pd yolk-shell nanostructures as a nanocatalyst for Suzuki coupling reaction: Discusses the development of a palladium-based nanocatalyst supported by potassium carbonate for improved Suzuki coupling reactions, an important reaction in organic chemistry (Barzkar et al., 2023).
- Enhanced LC-ESI-MS/MS Sensitivity by Cationic Derivatization of Organophosphorus Acids: Study on enhancing liquid chromatography-electrospray ionization tandem mass spectrometry sensitivity using potassium carbonate, improving the detection of organophosphorus acids (Shamai Yamin et al., 2023).
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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)
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)
Heck reaction using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
K Y Foo et al.
Bioresource technology, 102(20), 9814-9817 (2011-08-30)
Rice husk (RH), an abundant by-product of rice milling, was used for the preparation of activated carbon (RHAC) via KOH and K(2)CO(3) chemical activation. The activation process was performed at the microwave input power of 600 W for 7 min.
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