Dapoxetine HCl

Dapoxetine HCl

パラメータ 仕様
製品名 Dapoxetine HCl
CAS番号 129938-20-1
分子式 C21H23NO·HCl
分子量 341.87 g/mol
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) ≥99.0%
溶解度 Soluble in methanol, ethanol; slightly soluble in water
パッケージ 25 kg fiber drum with double PE bags

Dapoxetine HCl Structure

同義語: Dapoxetine hydrochloride, (S)-N,N-Dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride, LY210448, Priligy

Dapoxetine HCl is a selective serotonin reuptake inhibitor (SSRI) developed specifically for the treatment of premature ejaculation (PE). Unlike conventional SSRIs, dapoxetine has a rapid onset and short half-life, making it suitable for on-demand dosing. It was first synthesized by Eli Lilly and later licensed to Johnson & Johnson, receiving approval in Europe in 2009 under the brand name Priligy.

Chemically, dapoxetine is a naphthalenyloxy derivative of phenylpropylamine. The hydrochloride salt form is used in oral tablets, offering good stability and solubility. As a potent SSRI, it works by inhibiting the reuptake of serotonin, thereby delaying ejaculation. Its selectivity for the serotonin transporter over other monoamine transporters reduces side effects compared to older antidepressants.

Our Dapoxetine HCl is manufactured under strict GMP conditions and is available in high purity, suitable for pharmaceutical manufacturing and research. It is supplied as a white to off-white crystalline powder, with typical assay ≥99.0% by HPLC. The product is packaged in 25 kg fiber drums with double polyethylene bags for safe transport and storage.

Function & Mechanism

  • Serotonin reuptake inhibition: Blocks the serotonin transporter, increasing synaptic serotonin levels.
  • Rapid onset: Peak plasma concentration reached within 1-2 hours.
  • Short half-life: Eliminated quickly, reducing accumulation and side effects.
  • On-demand dosing: Suitable for intermittent use, improving patient compliance.
  • Selectivity: Minimal affinity for norepinephrine and dopamine transporters.

Source & Standardization

  • 出典: Synthetic chemical synthesis
  • Standardization: ≥99.0% (HPLC)
  • Forms: Crystalline powder
  • 用途: Pharmaceutical manufacturing, research

Quality Specifications (QC Tests)

Test Item 仕様
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
Organic Impurities ≤0.5% total, ≤0.1% individual
残留溶剤 Meets ICH Q3C limits

Bulk Supply & Documentation

  • 月間処理能力: 500 kg
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS
  • パッケージ: 25 kg fiber drum with double PE bags

よくある質問

What is the minimum order quantity (MOQ)?

Our standard MOQ is 1 kg. For larger quantities, please contact us for pricing and availability.

What is the delivery time?

For stock items, delivery time is 3-5 business days after order confirmation.

Do you provide COA and samples?

Yes, we provide a COA for each batch. Samples are available upon request, typically shipped within 1-2 days.

Contact & Ordering Information

  • Company: LyvBio Co., Ltd.
  • Address: Room 5-0203, Courtyard 205, Lianhu District, Xi’an, Shaanxi, China
  • Email: info@lyvbio.com
  • Phone: +86-29-65816888

send us your specification for a quotation.

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Room,5-0203, Unit 5, Beiyuanmen Street,Xi'an,Shaanxi,China

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