Potassium carbonate ACS reagent 1 Kg
Potassium carbonate
ACS reagent, ≥99.0%
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CAS Number 584-08-7
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Linear Formula K2CO3
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Molecular Weight 138.21
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Beilstein/REAXYS Number 4267587
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EC Number 209-529-3
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MDL number MFCD00011382
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PubChem Substance ID 329752063
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NACRES NA.21
Properties
Related Categories | Adsorbents, Filter Aids and Drying Agents, Essential Chemicals, Other Drying Agents, Potassium Salts, Research Essentials, |
Quality Level | 200 |
grade | ACS reagent |
InChI Key | BWHMMNNQKKPAPP-UHFFFAOYSA
|
assay | ≥99.0% |
impurities | ≤0.004% S compounds as (SO42-) |
≤0.005% silica | |
≤0.01% insolubles | |
mp | 891 °C (lit.) |
anion traces | chloride (Cl-): ≤0.003% |
phosphate (PO43-): ≤0.001% | |
cation traces | Ca: ≤0.005% |
Fe: ≤5 ppm | |
Mg: ≤0.002% | |
Na: ≤0.02% | |
heavy metals: ≤5 ppm (by ICP-OES) |
Description
General description
Potassium carbonate is an inorganic base.[5] It participates as a base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene.[3] Addition of amino acids (glycine, sarcosine and proline) to K2CO3 (solvent) promotes the absorption of CO2.[7]
Application
Potassium carbonate has been used in the preparation of disulfonated bis[4-(3-aminophenoxy)phe
It may be used in the following studies:
• As a reagent in the synthesis of polysubstituted iodobenzene derivatives.[1]
• As a base for the synthesis of high molecular weight homopolymers and copolymers derived from various bisphenols.[2]
• As a base for the Suzuki coupling of aryl halides with aryl boronic acids.[4]
• The Heck reaction of styrene and bromobenzene.[5]
Packaging
100, 500 g in poly bottle
2.5, 12 kg in poly drum
Other Notes
Go to Redi-Dri™ Product Listing 791766
Legal Information
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