sertraline hydrochloride

sertraline hydrochloride

Nazwa produktu Sertraline Hydrochloride
Numer CAS 79559-97-0
Wzór cząsteczkowy C17H17Cl2N
Masa cząsteczkowa 342.69 g/mol
Wygląd Biały lub prawie biały krystaliczny proszek
Oznaczenie (HPLC) ≥99%
Strata przy suszeniu ≤0,51 TP3T
Popiół po spaleniu ≤0,11 TP3T
Metale ciężkie ≤10 ppm
Temperatura topnienia 243-245°C
Współczynnik obrotowy [α]D20 = +30° to +34° (c=1, methanol)
Specyfikacja 99%HPLC

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sertraline hydrochloride Structure

  • Synonimy
  • Sertraline HCl, (1S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine hydrochloride, Zoloft, Lustral, Sertraline hydrochloride, Sertraline (as HCl), CP-51,974-1, Sertraline HCL

Sertraline hydrochloride is a well-established selective serotonin reuptake inhibitor (SSRI) widely used in the treatment of major depressive disorder, obsessive-compulsive disorder, panic disorder, and post-traumatic stress disorder. As a high-purity pharmaceutical intermediate, our sertraline hydrochloride (CAS 79559-97-0) meets the rigorous demands of formulation scientists and bulk manufacturers seeking a reliable, cost-effective source.

We supply sertraline hydrochloride in quantities ranging from research samples to full-scale production volumes. With a purity of ≥99% (HPLC), our product ensures consistent batch-to-batch quality, backed by comprehensive documentation and fast global shipping. Whether you are developing generic formulations or conducting bioequivalence studies, our sertraline HCl is the smart choice for your supply chain.

Funkcja

  • Antidepressant API: Sertraline hydrochloride is the active pharmaceutical ingredient in numerous approved antidepressant medications, offering proven efficacy in managing serotonin levels.
  • Research & Development: Ideal for R&D scale-up, clinical trial supplies, and formulation development, providing a stable and pure reference standard.
  • Generic Drug Manufacturing: Suitable for large-scale production of generic sertraline tablets and capsules, ensuring regulatory compliance and therapeutic equivalence.

Źródło i czystość

  • Źródło: Synthesized via a well-controlled chemical process, ensuring high enantiomeric purity and consistent quality.
  • Normalizacja: Each batch is tested for assay (HPLC ≥99%), loss on drying, residue on ignition, heavy metals, and specific rotation to meet international pharmacopoeial standards.
  • Formularze: Available as a white to off-white crystalline powder, packaged in sealed containers to maintain stability.
  • Zastosowania: Widely used in pharmaceutical formulations, including tablets, capsules, and oral solutions, as well as in analytical method development.

Dokumentacja i zaopatrzenie

  • Dokumentacja: certyfikat pochodzenia (COA), karta charakterystyki substancji niebezpiecznej (MSDS), karta techniczna produktu (TDS)
  • Czas realizacji: In stock for immediate dispatch; bulk orders typically ship within 5-7 working days.
  • Opakowanie: Available in 25g, 100g, 500g, and 1kg containers; custom packaging available upon request.

Zapytanie ofertowe

  • Nasz adres: 280 Main Street, Xi’an, Shaanxi, Chiny
  • LyvBio Sp. z o.o. — E-mail: info@lyvbio.com

BĄDŹ W KONTAKCIE

Zapytanie ofertowe

Nasz adres

Room,5-0203, Courtyard 205, Lianhu District,Xi'an,Shaanxi,China

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