R-Citalopram Oxalate

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Reagent Code: #229001
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CAS Number 219861-53-7

science Other reagents with same CAS 219861-53-7

blur_circular Chemical Specifications

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Weight 414.43 g/mol
Formula C₂₂H₂₃FN₂O₅
badge Registry Numbers
MDL Number MFCD06407825
inventory_2 Storage & Handling
Storage -20°C

description Product Description

R-Citalopram Oxalate is the R-enantiomer of citalopram oxalate. Unlike the S-enantiomer (escitalopram), which is the active ingredient used in the treatment of depression and anxiety disorders due to its potent selective serotonin reuptake inhibition (SSRI), the R-enantiomer exhibits minimal SSRI activity. It is primarily utilized in pharmaceutical research and development as a reference standard, for studying stereospecific pharmacological effects, enantioselective synthesis, and the role of chirality in neurochemical pathways related to mood regulation. It may also serve as an intermediate in the synthesis of racemic citalopram or escitalopram.

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inventory 5mg
10-20 days ฿17,600.00

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R-Citalopram Oxalate
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R-Citalopram Oxalate is the R-enantiomer of citalopram oxalate. Unlike the S-enantiomer (escitalopram), which is the active ingredient used in the treatment of depression and anxiety disorders due to its potent selective serotonin reuptake inhibition (SSRI), the R-enantiomer exhibits minimal SSRI activity. It is primarily utilized in pharmaceutical research and development as a reference standard, for studying stereospecific pharmacological effects, enantioselective synthesis, and the role of chirality i

R-Citalopram Oxalate is the R-enantiomer of citalopram oxalate. Unlike the S-enantiomer (escitalopram), which is the active ingredient used in the treatment of depression and anxiety disorders due to its potent selective serotonin reuptake inhibition (SSRI), the R-enantiomer exhibits minimal SSRI activity. It is primarily utilized in pharmaceutical research and development as a reference standard, for studying stereospecific pharmacological effects, enantioselective synthesis, and the role of chirality in neurochemical pathways related to mood regulation. It may also serve as an intermediate in the synthesis of racemic citalopram or escitalopram.

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