Dapoxetine HCl

Dapoxetine HCl

Parameter Technische Daten
Produktname Dapoxetine HCl
CAS-Nummer 129938-20-1
Molekülformel C21H23NO·HCl
Molekulargewicht 341.87 g/mol
Aussehen Weißes bis cremefarbenes kristallines Pulver
Analyse (HPLC) ≥99.0%
Löslichkeit Soluble in methanol, ethanol; slightly soluble in water
Verpackung 25 kg fiber drum with double PE bags

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Dapoxetine HCl Structure

Synonyme: 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

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

Quality Specifications (QC Tests)

Test Item Technische Daten
Identification IR, HPLC retention time conforms to standard
Trocknungsverlust ≤0,5%
Verbrennungsrückstand ≤0,1%
Schwermetalle ≤20 ppm
Organic Impurities ≤0.5% total, ≤0.1% individual
Residual Solvents Meets ICH Q3C limits

Bulk Supply & Documentation

  • Monthly capacity: 500 kg
  • Lieferzeit: 3–5 Werktage (Lagerware)
  • Dokumentation: COA, MSDS, TDS
  • Verpackung: 25 kg fiber drum with double PE bags

Häufig gestellte Fragen

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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