Escitalopram Oxalate

Escitalopram Oxalate

제품명 Escitalopram Oxalate
CAS 번호 219861-08-2
외관 흰색에서 미백색의 결정성 분말
사양 ≥98.5% (HPLC)
분자식 C20H21FN2O · C2H2O4
분자량 414.43 g/mol

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Escitalopram Oxalate Structure

동의어: (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.

Chemical Structure & Properties

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.

작용 기전

  • 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.

Quality Specifications

매개변수 사양
분석법 (HPLC) 98.5% – 101.5% (on dried basis)
식별 IR, HPLC retention time conforms to standard
건조 손실 ≤0.5%
소각 잔류물 ≤0.1%
중금속 ≤20 ppm
Optical Purity ≥99.5% (S-enantiomer)

Supply & Documentation

  • Capacity: 5 MT per year
  • 리드 타임: 3-5 business days (stock items)
  • 문서: COA, MSDS, TDS, cGMP, DMF available upon request
  • 포장: 1 kg, 5 kg, 25 kg fiber drums with double polyethylene liners

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