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911062

Sigma-Aldrich

Hydroxyde de potassium

free-flowing, Redi-Dri, ACS reagent, ≥85%, pellets

Synonyme(s) :

Potasse caustique

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About This Item

Formule linéaire :
KOH
Numéro CAS:
Poids moléculaire :
56.11
Numéro MDL:
Code UNSPSC :
12352320
Nomenclature NACRES :
NA.21

Qualité

ACS reagent
free-flowing

Agence

suitable for EPA 1621
suitable for EPA 1633
suitable for SM 5210

Pression de vapeur

1 mmHg ( 719 °C)

Gamme de produits

Redi-Dri

Pureté

≥85%

Forme

pellets

Impuretés

≤0.001% N compounds
≤2.0% K2CO3
10-15% water

Pf

361 °C (lit.)

Traces d'anions

chloride (Cl-): ≤0.01%
phosphate (PO43-): ≤5 ppm
sulfate (SO42-): ≤0.003%

Traces de cations

Ca: ≤0.005%
Fe: ≤0.001%
Mg: ≤0.002%
Na: ≤0.05%
Ni: ≤0.001%
heavy metals: ≤0.001% (by ICP-OES)

Chaîne SMILES 

[OH-].[K+]

InChI

1S/K.H2O/h;1H2/q+1;/p-1

Clé InChI

KWYUFKZDYYNOTN-UHFFFAOYSA-M

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Description générale

Potassium hydroxide is an inorganic salt mainly used as a precursor to synthesize other potassium compounds such as potassium acetate, potassium bicarbonate and potassium carbonate. On a commercial scale, it is synthesized by the electrolysis of potassium chloride.

Application

Redi-Dri is an innovative packaging product line that helps eliminate clumping material by adding extra packaging process steps without any chemical additives, anti-clumping agents, or hydrophobic compounds. Redi-Dri offers a more convenient and safer way to handle the products.
Potassium hydroxide may be used in the following processes:
  • Conversion of nitriles to amide in tert-butanol.
  • Cross-coupling of aryl halides with different sulfur-, oxygen- and nitrogen-based nucleophiles in dimethyl sulfoxide.
  • As an activator for the preparation of activated carbons from corn cobs.
  • As a base for the N-alkylation of nitrogen heterocycles in polyethylene glycol-ether solvents.
  • Synthesis of (S)-1-(4-benzyl-2-thioxothiazolidin-3-yl)propan-1-one from (S)-phenylalaninol.
  • To catalyze the polymerization of propylene oxide.

Informations légales

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Pictogrammes

CorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Code de la classe de stockage

8B - Non-combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Rokas Drevinskas et al.
Optics express, 23(2), 1428-1437 (2015-04-04)
Surface texturing is demonstrated by the combination of wet etching and ultrafast laser nanostructuring of silica glass. Using potassium hydroxide (KOH) at room temperature as an etchant of laser modified glass, we show the polarization dependent linear increase in retardance
Yoshihiro Takemura et al.
Plant physiology and biochemistry : PPB, 86, 121-129 (2014-12-02)
Endodormancy is an important feature of perennial deciduous fruit trees that survive in the extreme climates brought about by seasonal variation. To acquire a comprehensive knowledge of the biochemical processes occurring just before endodormancy breaking, the buds collected in the
Chen-Ting Lee et al.
PloS one, 10(3), e0120327-e0120327 (2015-03-21)
Traditional treatments, including a variety of thermal therapies have been known since ancient times to provide relief from rheumatoid arthritis (RA) symptoms. However, a general absence of information on how heating affects molecular or immunological targets relevant to RA has
Hassan M Albishri et al.
Journal of chromatographic science, 53(7), 1123-1130 (2014-12-30)
Two cyclodextrin micellar liquid chromatographic methods were developed and applied to the simultaneous determination of bisoprolol/hydrochlorothiazide and atenolol/chlorthalidone combinations in urine matrices without sample pretreatment. These combined β-blockers and diuretics chemotherapies are commonly used in the treatment of hypertension and
Carlos H Niño et al.
Memorias do Instituto Oswaldo Cruz, 110(7), 890-897 (2015-11-13)
The intracellular parasite Trypanosoma cruzi is the aetiological agent of Chagas disease, a public health concern with an increasing incidence rate. This increase is due, among other reasons, to the parasite's drug resistance mechanisms, which require nicotinamide adenine dinucleotide (NAD+).

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