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Merck
모든 사진(2)

주요 문서

P2522

Sigma-Aldrich

Potassium disulfite

≥98%

동의어(들):

Potassium metabisulfite, Potassium pyrosulfite

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About This Item

Linear Formula:
K2S2O5
CAS Number:
Molecular Weight:
222.32
EC Number:
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
NACRES:
NA.55
분석:
≥98%
양식:
powder

Quality Level

분석

≥98%

양식

powder

SMILES string

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

InChI

1S/2K.H2O5S2/c;;1-6(2)7(3,4)5/h;;(H,1,2)(H,3,4,5)/q2*+1;/p-2

InChI key

RWPGFSMJFRPDDP-UHFFFAOYSA-L

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관련 카테고리

일반 설명

Potassium disulfite (Potassium metabisulfite, PMB) is an inorganic salt with antimicrobial properties. It is a sulfiting agent that prevents browning of foods. Its genotoxic and cytotoxic effect has been assessed. PMB undergoes hydrolysis to form potassium bisulfite.

애플리케이션

Potassium disulfite has been used in a protocol for the modification of the polydimethylsiloxane (PDMS) polymer surfaces.
It may be used in the following processes:
  • Chemical etching of poly(vinylidene fluoride) in β-phase (β-PVDF) irradiated films.
  • Decolorization during the synthesis of 2-iodopyrimidine derivatives.
  • Palladium-catalyzed aminosulfonylation of aryl halides.

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Eye Dam. 1

보충제 위험성

Storage Class Code

11 - Combustible Solids

WGK

WGK 1


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시험 성적서(COA)

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문서 라이브러리 방문

Nanoporous β-PVDF membranes with selectively functionalized pores.
Cuscito O, et al.
Nucl. Instrum. Methods Phys. Res. Sect. B, 265(1), 309-313 (2007)
A palladium-catalyzed reaction of aryl halides, potassium metabisulfite, and hydrazines.
Ye S and Wu J.
Chemical Communications (Cambridge, England), 48(80), 10037-10039 (2012)
Amperometric quantification of sodium metabisulfite in pharmaceutical formulations utilizing tetraruthenated porphyrin film modified electrodes and batch injection analysis.
Quintino MSM, et al.
Talanta, 68(4), 1281-1286 (2006)
Biofunctionalization and self-interaction chromatography in PDMS microchannels.
Deshpande KS, et al.
Biochemical Engineering Journal, 67, 111-119 (2012)
Gábor Vlád et al.
The Journal of organic chemistry, 67(18), 6550-6552 (2002-08-31)
A high-yield synthesis was developed for the preparation of 2,2'-bipyrimidine (1) using the Ullmann coupling of 2-iodopyrimidine. The new procedure was also used for the preparation of 4,4',6,6'-tetramethyl-2,2'-bipyrimidine (2) and 5,5'-dibromo-2,2'-bipyrimidine (3).

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