Favipiravir

Favipiravir

Paramètre Spécifications
Nom du produit Favipiravir
Numéro CAS 259793-96-9
Formule moléculaire C5H4FN3O2
Poids moléculaire 157.10 g/mol
Apparence Poudre cristalline blanche à blanc cassé
Essai (HPLC) ≥99,01 TP3T
Solubilité Slightly soluble in water, soluble in DMSO, methanol
Colis 25 kg net weight in fiber drums, double polyethylene bags inside

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Favipiravir Structure

Synonymes : Favipiravir, T-705, 6-fluoro-3-hydroxy-2-pyrazinecarboxamide, Avigan, Toyama Chemical

Favipiravir is a broad-spectrum antiviral agent developed by Toyama Chemical (now Fujifilm) in Japan. It is a pyrazinecarboxamide derivative that selectively inhibits the RNA-dependent RNA polymerase (RdRp) of many RNA viruses, including influenza, Ebola, and SARS-CoV-2. Since its approval in Japan in 2014 for pandemic influenza, it has drawn global attention as a potential treatment for emerging viral infections.

Chemically, favipiravir is a synthetic small molecule with a molecular weight of 157.10 g/mol. Its active form, favipiravir-RTP, acts as a purine analog that competes with GTP for incorporation into viral RNA, effectively terminating viral replication. Unlike neuraminidase inhibitors, it targets a broad range of RNA viruses, making it a versatile candidate for antiviral research.

LyvBio supplies high-purity favipiravir (≥99.0% by HPLC) that meets stringent pharmacopeial standards. Our product is manufactured under GMP conditions and is suitable for pharmaceutical manufacturing, clinical research, and antiviral drug development. With reliable supply and comprehensive documentation, we support partners in bringing antiviral therapies to market efficiently.

Function & Mechanism

  • Broad-spectrum antiviral activity: Inhibits replication of influenza A, B, and C viruses, as well as other RNA viruses.
  • RdRp inhibition: Competes with GTP for incorporation into viral RNA, causing chain termination.
  • Activity against emerging viruses: Demonstrates in vitro efficacy against Ebola, Lassa, and SARS-CoV-2.
  • Synergistic potential: May enhance the effects of other antivirals like oseltamivir.
  • Favorable safety profile: Well-tolerated in clinical studies with manageable side effects.

Source et normalisation

  • Source: Synthetic chemical synthesis
  • Manufacturing: GMP-compliant process
  • Normalisation: ≥99.0% purity by HPLC
  • Formulaires: White to off-white crystalline powder
  • Applications: Pharmaceutical manufacturing, clinical research, antiviral drug development

Quality Specifications (QC Tests)

Test Item Spécifications
Identification IR and HPLC retention time match reference standard
Perte au séchage ≤ 0,51 TP3T
Résidu au feu ≤ 0,11 TP3T
Métaux lourds ≤ 20 ppm
Limites microbiologiques Total aerobic count ≤1000 CFU/g; Yeast & Mold ≤100 CFU/g
Organic Impurities Any individual impurity ≤0.1%, total impurities ≤0.5%
Solvants résiduels Meets ICH Q3C requirements

Bulk Supply & Documentation

  • Capacité mensuelle: 500 kg
  • Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
  • Documentation: Certificat d'analyse (COA), fiche de données de sécurité (FDS) et fiche technique (TDS) disponibles sur demande
  • Emballage: 25 kg fiber drums with double polyethylene liners

Foire aux questions

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

Our standard MOQ is 1 kg, but we can accommodate smaller quantities for research purposes. Please contact us for specific requirements.

What is the delivery time?

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

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

Yes, we provide a COA for each batch and can supply samples for evaluation. Sample delivery takes 1-2 days after 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

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