추천 제품
Grade
ACS reagent
Quality Level
분석
≥99.0%
양식
powder or crystals
불순물
≤0.004% S compounds as (SO42-)
≤0.005% silica
≤0.01% insolubles
pH
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
음이온 미량물
chloride (Cl-): ≤0.003%
phosphate (PO43-): ≤0.001%
양이온 미량물
Ca: ≤0.005%
Fe: ≤5 ppm
Mg: ≤0.002%
Na: ≤0.02%
heavy metals: ≤5 ppm (by ICP-OES)
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Potassium carbonate is an inorganic base. It participates as a base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene. Addition of amino acids (glycine, sarcosine and proline) to K2CO3 (solvent) promotes the absorption of CO2.
애플리케이션
Potassium carbonate has been used in the preparation of disulfonated bis[4-(3-aminophenoxy)phenyl]sulfone, a disulfonated diamine monomer.
It may be used in the following studies:
It may be used in the following studies:
- As a reagent in the synthesis of polysubstituted iodobenzene derivatives.
- As a base for the synthesis of high molecular weight homopolymers and copolymers derived from various bisphenols.
- As a base for the Suzuki coupling of aryl halides with aryl boronic acids.
- The Heck reaction of styrene and bromobenzene.
법적 정보
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
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)
Chelating N-heterocyclic carbene ligands in palladium-catalyzed Heck-type reactions.
Herrmann WA, et al.
Journal of Organometallic Chemistry, 557(1), 93-96 (1998)
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.
Synthesis, kinetic observations and characteristics of polyarylene ether sulphones prepared via a potassium carbonate DMAC process.
Viswanathan R, et al.
Polymer, 25(12), 1827-1836 (1984)
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