Potassium tert-butoxide

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Reagent Code: #78401
label
Alias Potassium tert-butoxide
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CAS Number 865-47-4

science Other reagents with same CAS 865-47-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 112.21 g/mol
Formula C₄H₉KO
badge Registry Numbers
EC Number 212-740-3
MDL Number MFCD00012162
thermostat Physical Properties
Melting Point 256-258 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2-8℃, dark, dry, sealed

description Product Description

Potassium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is commonly employed in the preparation of esters, ethers, and other organic compounds through nucleophilic substitution reactions. In the pharmaceutical industry, it plays a key role in the synthesis of active pharmaceutical ingredients (APIs) by facilitating condensation and elimination reactions. Additionally, it is utilized in polymerization processes, such as the production of polyesters and polycarbonates, where it acts as a catalyst. Its strong basicity also makes it useful in the preparation of organometallic compounds and in the Wittig reaction for synthesizing alkenes. In research laboratories, it is often used for its ability to promote efficient and selective transformations in complex organic molecules.

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Test Parameter Specification
KOH, K2CO3 as KOH 0%, <=0.05%
Purity (HCl Titration) 97.5-102.5
Appearance White to off-white powder, needles and/or chunks
Infrared Spectrum Conforms to structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿800.00
inventory 500g
10-20 days ฿2,480.00
inventory 2.5kg
10-20 days ฿10,460.00

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Potassium tert-butoxide
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Potassium tert-butoxide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is commonly employed in the preparation of esters, ethers, and other organic compounds through nucleophilic substitution reactions. In the pharmaceutical industry, it plays a key role in the synthesis of active pharmaceutical ingredients (APIs) by facilitating condensation and elimination reactions. Additionally, it is utilized in polymerization processes, such as the production of polyesters and polycarbonates, where it acts as a catalyst. Its strong basicity also makes it useful in the preparation of organometallic compounds and in the Wittig reaction for synthesizing alkenes. In research laboratories, it is often used for its ability to promote efficient and selective transformations in complex organic molecules.
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