Duloxetine HCl

Duloxetine HCl

製品名 Duloxetine HCl
CAS番号 136434-34-9
分子式 C18H19NOS·HCl
分子量 333.88 g/mol
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) 98.0% – 102.0% (on dried basis)
乾燥減量 ≤ 0.5%
焼失残渣 ≤ 0.1%
重金属 ≤ 20 ppm
パッケージ 25 kg fiber drum with double polyethylene bags

Duloxetine HCl Structure

同義語: (S)-N-Methyl-3-(1-naphthyloxy)-3-(2-thienyl)propan-1-amine hydrochloride, LY248686, Duloxetine hydrochloride, Cymbalta, Yentreve, Ariclaim, Xeristar

Duloxetine HCl is a dual serotonin and norepinephrine reuptake inhibitor (SNRI) that has become a cornerstone in the treatment of major depressive disorder, generalized anxiety disorder, and neuropathic pain. As a hydrochloride salt, it offers improved aqueous solubility and stability compared to the free base, making it the preferred form for oral solid dosage formulations. The compound was originally developed by Eli Lilly and received FDA approval in 2004 under the brand name Cymbalta.

Chemically, duloxetine HCl is a naphthalenyloxy-substituted thiophene propanamine. Its structure features a chiral center, and the active pharmaceutical ingredient is the (S)-enantiomer, which is significantly more potent than the (R)-enantiomer. The molecule’s lipophilic naphthalene and thiophene rings facilitate blood-brain barrier penetration, while the secondary amine side chain is responsible for its interaction with serotonin and norepinephrine transporters. This dual mechanism distinguishes it from selective serotonin reuptake inhibitors (SSRIs) and contributes to its broader efficacy profile.

From a manufacturing perspective, duloxetine HCl is synthesized through a multi-step process that typically starts from 1-naphthol and 2-acetylthiophene, followed by a resolution step to isolate the desired (S)-enantiomer. The final hydrochloride salt is crystallized to high purity, with particle size distribution carefully controlled to ensure consistent dissolution and bioavailability in finished dosage forms. Our material is produced under cGMP conditions and is supported by a comprehensive regulatory package, including DMF and CEP where applicable.

機能

  • SNRI activity: Inhibits serotonin and norepinephrine reuptake, enhancing neurotransmitter availability in the synaptic cleft.
  • Antidepressant effect: Improves mood and reduces anxiety symptoms in major depressive disorder and generalized anxiety disorder.
  • Analgesic properties: Effective in managing chronic musculoskeletal pain, diabetic peripheral neuropathic pain, and fibromyalgia.
  • Anxiolytic action: Reduces excessive worry and tension through modulation of serotonergic and noradrenergic pathways.
  • Stability and solubility: The hydrochloride salt ensures consistent dissolution and shelf-life in oral formulations.

Source & Standardization

  • 出典: Synthetic chemical synthesis, starting from 1-naphthol and 2-acetylthiophene.
  • Standardization: Assay 98.0% – 102.0% (HPLC, on dried basis), with strict control of chiral purity.
  • Forms: White to off-white crystalline powder, milled to a defined particle size range.
  • 用途: Antidepressant and analgesic medications, generic drug development, and clinical research.

仕様

パラメータ 仕様
分析(HPLC) 98.0% – 102.0%
識別 IR and HPLC retention time match reference standard
乾燥減量 ≤ 0.5%
焼失残渣 ≤ 0.1%
重金属 ≤ 20 ppm
Microbial Limits Total aerobic count ≤ 1000 CFU/g; Yeast & mold ≤ 100 CFU/g; E. coli absent

資料・供給

  • 月間処理能力: 10 metric tons
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS, DMF (where applicable), and CEP upon request
  • パッケージ: 25 kg fiber drum with double polyethylene bags, or as per customer requirements

見積依頼

  • リブバイオ株式会社. — メールアドレス: info@lyvbio.com

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