Levofloxacin

Levofloxacin

Paramètre Spécifications
Nom du produit Levofloxacin
Numéro CAS 100986-85-4
Formule moléculaire C18H20FN3O4
Poids moléculaire 361.37 g/mol
Apparence Poudre cristalline blanche à blanc cassé
Essai (HPLC) 98.5% – 101.0% (on dried basis)
Solubilité Slightly soluble in water; soluble in acetic acid; practically insoluble in ethanol
Colis Fût en fibre de 25 kg avec double revêtement en polyéthylène

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Levofloxacin Structure

Synonymes : Levofloxacin, Levaquin, Cravit, Tavanic, Quixin, Ofloxacin S-(-)-isomer

Levofloxacin has become a staple in the global API market, driven by its broad-spectrum efficacy and favorable safety profile. As a third-generation fluoroquinolone, it is widely used in both oral and intravenous formulations for respiratory, urinary, and skin infections. Demand remains strong, particularly in Asia and Latin America, where generic penetration is high and healthcare access is expanding.

Chemically, levofloxacin is the levo-isomer of ofloxacin, belonging to the fluoroquinolone class. It works by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication. This mechanism gives it bactericidal activity against a wide range of Gram-negative and Gram-positive pathogens.

Our levofloxacin is manufactured under strict GMP conditions and is available in high purity, meeting pharmacopeial standards including USP, EP, and BP. It is supplied as a white to off-white crystalline powder, suitable for tablet, capsule, and sterile injectable production.

Function & Mechanism

  • DNA gyrase inhibition: Blocks bacterial DNA replication, leading to cell death.
  • Topoisomerase IV inhibition: Disrupts chromosome partitioning during cell division.
  • Broad-spectrum activity: Effective against Gram-negative and Gram-positive bacteria, including atypical pathogens.
  • Concentration-dependent killing: Exhibits rapid bactericidal effect at higher concentrations.

Source et normalisation

  • Source: Synthetic fluoroquinolone
  • Manufacturing: Multi-step chemical synthesis, followed by purification and crystallization
  • Normalisation: Complies with USP/EP/BP monographs
  • Formulaires: Crystalline powder
  • Applications: Oral solid dosage forms, sterile injectables, ophthalmic solutions

Quality Specifications (QC Tests)

Test Item Spécifications
Identification IR, HPLC retention time matches standard
Perte au séchage ≤ 0,5%
Résidu au feu ≤ 0,11 TP3T
Métaux lourds ≤ 20 ppm
Organic Impurities Meets USP/EP requirements
Limites microbiologiques Total aerobic count ≤ 1000 CFU/g; absence of specified pathogens

Bulk Supply & Documentation

  • Emballage: 25 kg fiber drum with double polyethylene liner
  • Quantité minimale de commande: 1 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

Foire aux questions

What is the minimum order quantity (MOQ)?

Our MOQ is 1 kg for stock items.

What is the delivery time?

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

Do you provide COA and samples?

Yes, we provide COA, MSDS, and TDS. Samples are available upon request.

How is the product packaged?

It is packed in 25 kg fiber drums with double polyethylene liners.

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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Room,5-0203, Unit 5, Beiyuanmen Street,Xi'an,Shaanxi,China

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