Duloxetine hydrochloride

Duloxetine hydrochloride

Nom du produit Duloxetine hydrochloride
Numéro CAS 136434-34-9
Formule moléculaire C18H19NOS·HCl
Poids moléculaire 333.88 g/mol
Apparence Poudre cristalline blanche à blanc cassé
Essai (HPLC) ≥99%
Perte au séchage ≤0.5%
Résidu au feu ≤0.1%
Métaux lourds ≤20 ppm
Point de fusion 168-172°C
Rotation spécifique +120° to +130° (C=1, Methanol)
Spécifications 99% HPLC

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Duloxetine hydrochloride Structure

Synonymes

(S)-N-Methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine hydrochloride, Duloxetine HCl, LY-248686 hydrochloride, (S)-Duloxetine hydrochloride

Duloxetine hydrochloride is a high-purity, pharmaceutical-grade active pharmaceutical ingredient (API) widely recognized for its efficacy in treating major depressive disorder, generalized anxiety disorder, and neuropathic pain. As a potent serotonin-norepinephrine reuptake inhibitor (SNRI), it plays a critical role in modern therapeutic regimens. Our product, with a purity of ≥99% (HPLC), is meticulously manufactured to meet the rigorous demands of pharmaceutical formulation and research applications.

We supply Duloxetine hydrochloride in bulk quantities with competitive pricing, ensuring fast delivery worldwide. Each batch is accompanied by a Certificate of Analysis (COA) to guarantee consistency and quality. Whether you are scaling up from R&D or require a reliable source for commercial production, our team is ready to support your needs with professional service and technical expertise.

Fonction

  • Antidepressant API: Acts as a dual serotonin and norepinephrine reuptake inhibitor, providing effective relief for depression and anxiety disorders.
  • Pain Management: Clinically proven to manage chronic musculoskeletal pain and diabetic peripheral neuropathy, offering a broad therapeutic window.
  • Research Compound: Ideal for preclinical studies and formulation development, thanks to its high purity and consistent batch-to-batch quality.

Origine et pureté

  • Source: Synthesized through advanced chemical processes, ensuring high enantiomeric purity and consistent quality.
  • Normalisation: Each batch is rigorously tested using HPLC to guarantee ≥99% purity, meeting international pharmaceutical standards.
  • Formulaires: Available as a white crystalline powder, easily handled and formulated into various dosage forms.
  • Applications: Suitable for oral solid dosage forms, including tablets and capsules, as well as for research and development purposes.

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 shipped within 5-7 working days.
  • Emballage: Custom packaging available, from 1kg to 25kg drums, with tamper-evident seals and moisture-proof liners.

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

Notre adresse

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

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