Escitalopram Oxalate

Escitalopram Oxalate

製品名 Escitalopram Oxalate
CAS番号 219861-08-2
外観 白色からオフホワイトの結晶性粉末
仕様 ≥98.5% (HPLC)
分子式 C20H21FN2O · C2H2O4
分子量 414.43 g/mol

Escitalopram Oxalate Structure

同義語: (S)-1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile oxalate, S-Citalopram oxalate, Cipralex, Lexapro, Seroplex, Entact

Escitalopram oxalate is the oxalate salt of the S-enantiomer of citalopram, a selective serotonin reuptake inhibitor (SSRI). Its structure features a bicyclic isobenzofuran core with a 4-fluorophenyl substituent and a dimethylaminopropyl side chain, which confers high affinity and selectivity for the serotonin transporter (SERT).

As a second-generation antidepressant, escitalopram is widely prescribed for major depressive disorder and generalized anxiety disorder. The oxalate salt enhances aqueous solubility and stability, making it suitable for oral solid dosage forms. It is typically manufactured under cGMP conditions and meets pharmacopeial standards (USP/EP).

In research and pharmaceutical development, escitalopram oxalate serves as a reference standard and active pharmaceutical ingredient (API) for studying serotonin reuptake inhibition, neuropharmacology, and antidepressant efficacy.

化学構造と性質

Escitalopram oxalate is a white to off-white crystalline powder, freely soluble in methanol and water, with a molecular weight of 414.43 g/mol. It is the oxalate salt form, which improves solubility compared to the free base. The compound is optically active, with the S-enantiomer being the therapeutically active form.

作用機序

  • Serotonin transporter inhibition: Escitalopram binds with high affinity to the serotonin transporter (SERT), blocking reuptake of serotonin into presynaptic neurons.
  • Increased serotonergic neurotransmission: This leads to elevated extracellular serotonin levels, enhancing serotonergic signaling in the CNS.
  • Minimal effect on norepinephrine and dopamine: Unlike some other antidepressants, escitalopram has little effect on norepinephrine and dopamine reuptake, contributing to its favorable side effect profile.
  • Allosteric modulation: The S-enantiomer also interacts with an allosteric site on SERT, potentially enhancing its inhibitory effect.

品質仕様

パラメータ 仕様
分析(HPLC) 98.5% – 101.5% (on dried basis)
識別 IR, HPLC retention time conforms to standard
乾燥減量 ≤0.5%
焼失残渣 ≤0.11 TP3T
重金属 ≤20 ppm
Optical Purity ≥99.5% (S-enantiomer)

供給および書類

  • 容量: 5 MT per year
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS, cGMP, DMF available upon request
  • パッケージ: 1 kg, 5 kg, 25 kg fiber drums with double polyethylene liners

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