(-)-Ibuprofenamide

≥98%

Reagent Code: #61664
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CAS Number 121839-78-9

science Other reagents with same CAS 121839-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.3 g/mol
Formula C₁₃H₁₉NO
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

(-)-Ibuprofenamide is primarily utilized in pharmaceutical research as a chiral intermediate for the synthesis of enantiomerically pure ibuprofen, a widely used nonsteroidal anti-inflammatory drug (NSAID). Its application is crucial in developing formulations with improved efficacy and reduced side effects, as the (-)-enantiomer of ibuprofen is known to exhibit higher biological activity compared to its (+)-counterpart. Additionally, it serves as a valuable compound in studying the stereoselective metabolism and pharmacokinetics of ibuprofen, aiding in the design of more targeted and efficient therapeutic agents.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,000.00

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(-)-Ibuprofenamide
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(-)-Ibuprofenamide is primarily utilized in pharmaceutical research as a chiral intermediate for the synthesis of enantiomerically pure ibuprofen, a widely used nonsteroidal anti-inflammatory drug (NSAID). Its application is crucial in developing formulations with improved efficacy and reduced side effects, as the (-)-enantiomer of ibuprofen is known to exhibit higher biological activity compared to its (+)-counterpart. Additionally, it serves as a valuable compound in studying the stereoselective metabo

(-)-Ibuprofenamide is primarily utilized in pharmaceutical research as a chiral intermediate for the synthesis of enantiomerically pure ibuprofen, a widely used nonsteroidal anti-inflammatory drug (NSAID). Its application is crucial in developing formulations with improved efficacy and reduced side effects, as the (-)-enantiomer of ibuprofen is known to exhibit higher biological activity compared to its (+)-counterpart. Additionally, it serves as a valuable compound in studying the stereoselective metabolism and pharmacokinetics of ibuprofen, aiding in the design of more targeted and efficient therapeutic agents.

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