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30603

Hydroxyde de potassium

pellets, reag. Ph. Eur., ≥85%

Synonyme(s) :

Potasse caustique

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A propos de cet article

Formule linéaire :
KOH
Numéro CAS:
Poids moléculaire :
56.11
PubChem Substance ID:
eCl@ss:
38100303
UNSPSC Code:
12352106
NACRES:
NA.21
EC Number:
215-181-3
MDL number:
Assay:
≥85%
Form:
pellets
Solubility:
water: soluble ((1,130 g/l (68 °F / 20 °C))
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Quality Level

agency

USP/NF, reag. Ph. Eur.

vapor pressure

1 mmHg ( 719 °C)

assay

≥85%

form

pellets

impurities

≤2.0% K2CO3

pH

~13.5 (25 °C, 5.6 g/L)

mp

361 °C (lit.)

solubility

water: soluble ((1,130 g/l (68 °F / 20 °C))

anion traces

chloride (Cl-): ≤0.02%, phosphate (PO43-): ≤0.01%, sulfate (SO42-): ≤0.02%

cation traces

Al: ≤0.001%, Ca: ≤0.001%, Fe: ≤0.001%, Na: ≤1.0%, Ni: ≤0.0005%

SMILES string

[OH-].[K+]

InChI

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

InChI key

KWYUFKZDYYNOTN-UHFFFAOYSA-M

General description

Potassium hydroxide is a strong alkali that can be used in nucleophilic substitution reactions, addition reactions, and basic hydrolysis reactions. It can also be used to catalyze aldol-type reactions.

Application

Potassium hydroxide can be used as a base:
  • In the Pd-catalyzed Heck reaction of aryl halides with alkenes.
  • To synthesize β-alkylated alcohols via pincer-Ni catalyzed Guerbet reaction.
  • For the hydroxylation of aryl or heteroarylboronic acids to corresponding phenols.
It can also be used as a catalyst for the:
  • Transesterification of triglycerides to prepare biodiesels.
  • Synthesis of β-phenylethylamines via intermolecular addition of arylamines to styrenes.
  • Claisen-Schmidt condensation reaction to synthesize chalcones.

Packaging

This product is also available in glass bottles.


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

Classe de stockage

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Potassium hydroxide catalyzed addition of arylamines to styrenes
Jaspers D, et al.
Synlett, 2011, 1444-1448 (2011)
Novel CuCl2-cryptand-[2.2. Benzo] complex: A base free and oxidant free catalyst for Ipso-Hydroxylation of aryl/heteroaryl-boronic acids in water at room temperature
Bora S, et al.
Journal of Organometallic Chemistry, 851, 52-56 (2017)
Yuewang Huang et al.
Optics express, 23(5), 6780-6786 (2015-04-04)
We demonstrate a novel technique to fabricate sub-micron silicon nitride waveguides using conventional contact lithography with MEMS-grade photomasks. Potassium hydroxide anisotropic etching of silicon facilitates line reduction and roughness smoothing and is key to the technique. The fabricated waveguides is



Numéro d'article de commerce international

RéférenceGTIN
30603-1KG04061826672716
30603-6X1KG04061826672730
30603-500G04061826672723
30603-5KG04061833458891