Dapoxetine

Dapoxetine

Parametro Specifiche
Nome del prodotto Dapoxetine
Numero CAS 119356-77-3
Formula molecolare C21H23NO
Peso molecolare 305.41 g/mol
Aspetto Polvere cristallina di colore da bianco a bianco sporco
Analisi (HPLC) ≥99.0%
Solubilità Soluble in methanol, ethanol; slightly soluble in water
Confezione 25 kg net weight in fiber drums, two polyethylene inner liners

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Dapoxetine Structure

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

Dapoxetine is a selective serotonin reuptake inhibitor (SSRI) developed specifically for the treatment of premature ejaculation (PE). Unlike other SSRIs, dapoxetine has a rapid onset and short half-life, making it suitable for on-demand dosing. It is the first oral medication approved for PE in several countries and has gained significant attention in the pharmaceutical market.

Dapoxetine is synthesized through a multi-step chemical process, yielding a highly pure active pharmaceutical ingredient (API). It is available as the hydrochloride salt, which enhances its solubility and stability. The compound is typically manufactured under cGMP conditions to ensure consistent quality and compliance with pharmacopeial standards.

Product Overview & Composition

Dapoxetine is a chiral molecule with the (S)-configuration at the stereogenic center. It acts by inhibiting the reuptake of serotonin, thereby increasing serotonin levels in the synaptic cleft and delaying ejaculation. The hydrochloride salt is the predominant form used in commercial products due to its favorable physicochemical properties.

The API is characterized by high purity, typically ≥99.0% as determined by HPLC, and low levels of organic impurities. It is a white to off-white crystalline powder, freely soluble in methanol and ethanol, and slightly soluble in water.

Applications & Product Lines

  • Pharmaceutical formulations: Dapoxetine is formulated into immediate-release tablets for the treatment of premature ejaculation.
  • Research and development: Used as a reference standard in analytical laboratories and for studying serotonin reuptake inhibition.
  • Generic drug manufacturing: API for generic versions of dapoxetine hydrochloride tablets.
  • Contract manufacturing: Supplied to CDMOs for incorporation into finished dosage forms.

Quality Control Standards

Test Item Specifiche
Identificazione IR spectrum complies with reference standard
Perdita per essiccazione ≤0.5%
Metalli pesanti ≤20 ppm
Organic Impurities Any individual ≤0.1%; total ≤0.5%
Limiti microbiologici Total aerobic microbial count ≤1000 CFU/g; yeast and mold ≤100 CFU/g; absence of E. coli

Bulk Packaging & Supply

  • Confezionamento: 25 kg fiber drums with two polyethylene inner liners
  • MOQ: 1 kg
  • Tempi di consegna: 3-5 business days for stock items
  • Documentazione: COA, MSDS, TDS available upon request

Frequently Asked Questions

What is the minimum order quantity (MOQ) for Dapoxetine?

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

What is the delivery time?

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

Do you provide a Certificate of Analysis (COA) and samples?

Yes, we provide a COA for each batch. Samples are available upon request.

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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