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Potassium tert-butoxide / 25 G

Purity: 98 %
Synonym: Potassium tert-butylate; Potassium t-butoxide; Potassium tert-butanolate
Molecular Formula: (CH3)3COK
Molecular Weight: 112.21
SKU: MND-77439
CAS Number: 865-47-4
MDL number: MFCD00012162
EC Number: 212-740-3
Form: solid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 25 G  
161.70 EUR



Safety Information


Hazard Statements

H225
H302
H335
H314
H336
H351
H228
H252
H260

Precautionary Statements

P210
P280
P303 + P361 + P353
P305 + P351 + P338
P304 + P340 + P310
P260
P231 + P232

Pictograms



Properties

Signal WordDanger
Flash Point (C)Not available
Flash Point (F)Not available
Vapor Pressure1 mmHg ( 220 °C)
Melting Point256-258 °C (dec.) (lit.)

 Product Description

POTASSIUM TERT-BUTOXIDE is a strong base commonly used in organic synthesis reactions. It is valued for its ability to deprotonate various compounds and initiate reactions such as deprotonation, condensation, and elimination.

 

Application:

POTASSIUM TERT-BUTOXIDE finds application as a base in organic synthesis, particularly in reactions requiring strong basic conditions. It is utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.

 

 

Articles:

- Potassium tert-butoxide in synthesis

Publication Date: February 1, 1974

D. E. Pearson and Calvin A. Buehler

https://doi.org/10.1021/cr60287a004

 

- The super-basic butyllithium/potassium tert-butoxide mixture and other LICKOR reagents

Publication Date: 1984

Schlosser, Manfred; Strunk, Sven

https://doi.org/10.1016/S0040-4039(01)80014-9

 

- Potassium tert-Butoxide-Catalyzed Dehydrogenative SiO Coupling: Reactivity Pattern and Mechanism of an Underappreciated Alcohol Protection

Publication Date: 24 February 2009

Andreas Weickgenannt, Martin Oestreich Prof. Dr

https://doi.org/10.1002/asia.200800426