sertraline hydrochloride

sertraline hydrochloride

Nom du produit Sertraline Hydrochloride
Numéro CAS 79559-97-0
Formule moléculaire C17H17Cl2N
Poids moléculaire 342.69 g/mol
Apparence Poudre cristalline blanche à blanc cassé
Essai (HPLC) ≥99%
Perte au séchage ≤0.5%
Résidu au feu ≤0.1%
Métaux lourds ≤ 10 ppm
Point de fusion 243-245°C
Rotation spécifique [α]D20 = +30° to +34° (c=1, methanol)
Spécifications 99%HPLC

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sertraline hydrochloride Structure

  • Synonymes
  • 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.

Fonction

  • 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.

Origine et pureté

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

Documentation et approvisionnement

  • Documentation: certificat d'analyse (COA), fiche de données de sécurité (FDS), fiche technique (TDS)
  • Délai de livraison: In stock for immediate dispatch; bulk orders typically ship within 5-7 working days.
  • Emballage: Available in 25g, 100g, 500g, and 1kg containers; custom packaging available upon request.

Demande de devis

  • Notre adresse: 280, rue Main, Xi'an, Shaanxi, Chine
  • LyvBio Co. — E-mail : info@lyvbio.com

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Demande de devis

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