Levofloxacin

Levofloxacin

パラメータ 仕様
製品名 Levofloxacin
CAS番号 100986-85-4
分子式 C18H20FN3O4
分子量 361.37 g/mol
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) 98.5% – 101.0% (on dried basis)
溶解度 Slightly soluble in water; soluble in acetic acid; practically insoluble in ethanol
パッケージ 25 kg fiber drum with double polyethylene liner

Levofloxacin Structure

同義語: 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 & Standardization

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

Quality Specifications (QC Tests)

Test Item 仕様
識別 IR, HPLC retention time matches standard
乾燥減量 ≤ 0.5%
焼失残渣 ≤ 0.1%
重金属 ≤ 20 ppm
Organic Impurities Meets USP/EP requirements
Microbial Limits Total aerobic count ≤ 1000 CFU/g; absence of specified pathogens

Bulk Supply & Documentation

  • パッケージ: 25 kg fiber drum with double polyethylene liner
  • 最小注文数量(MOQ): 1 kg
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS available upon request

よくある質問

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

send us your specification for a quotation.

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

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