Name: China Source Factory Supply High Quality Levofloxacin Hydrochloride CAS 177325-13-2
Brand: Wuhan Fortuna Chemical Co., Ltd.

Specifications of Levofloxacin Hydrochloride CAS 177325-13-2

Items	Specifications	Results
Appearance	Off-white or light yellow needle crystalline powder	Light yellow needle crystalline
Specific rotation	-47°~-52°	-50°
Opticalisomer	≤1.0%	0.32%
pH value	3.5~5.0	3.9
Related substances	≤0.50%	0.07%
Loss on drying	≤5.0%	2.7%
Residue on ignition	≤0.2%	0.03%
Heavy metals	≤20ppm	＜20ppm
Assay	≥89.5%	90.4%

Parameters of Levofloxacin Hydrochloride CAS 177325-13-2

Product parameters
Cas number:	177325-13-2
Appearance:	Off-white or light yellow needle crystalline powder
Purity:	89.5%min
Package details:	25kg/drum
Brand:	Fortunachem

Levofloxacin Hydrochloride is the hydrochloride salt form of Levofloxacin, which is a broad-spectrum, synthetic antibiotic belonging to the fluoroquinolone class. It is the active, pure left-handed (L-) isomer of its parent compound, ofloxacin, and is significantly more potent. It is used to treat a wide variety of bacterial infections.

1. Chemical Identity

IUPAC Name: (2S)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.2.0⁵,¹⁶]hexadeca-5(16),6,8,11,13,15-hexaene-11-carboxylic acid; hydrochloride
Molecular Formula: C18H20FN3O4 · HCl
CAS Number: 138199-71-0

2. Chemical Structure and Key Features

Levofloxacin's structure is complex and defines its class and function:

Fluoroquinolone Core: It is based on a bicyclic core structure, which is a combination of a quinolone (a fused pyridine-pyrimidine ring) and a piperazine ring.
Key Functional Groups:

Fluorine Atom at C-6: This is the "fluoro-" in fluoroquinolone. It dramatically enhances the drug's ability to penetrate bacterial cells and increases its potency against a key bacterial enzyme.
Carboxylic Acid Group (-COOH): This group is essential for binding to the bacterial enzyme targets (DNA gyrase and topoisomerase IV). In the hydrochloride salt form, this exists as a carboxylate (-COO⁻).
Methylpiperazine Ring at C-7: This ring structure is crucial for broadening the spectrum of activity, particularly against Gram-positive bacteria, and improving pharmacokinetics.

Chirality (The "Levo-" Part):

Levofloxacin has a chiral center at the C-3 position of the oxazine ring.
It is the pure, active L-isomer (or S-isomer) of ofloxacin, which was a 50/50 mixture (racemate) of the L- and D-isomers.
The "Levo-" prefix means "left," referring to its levorotatory property (it rotates plane-polarized light to the left).
This specific 3D configuration is critical for its superior antibacterial activity compared to the D-isomer or the racemic mixture.

The "Hydrochloride" Part:

This indicates that the basic nitrogen atom in the piperazine ring has been protonated and forms a salt with a chloride ion (Cl⁻).
Purpose: Converting Levofloxacin into its hydrochloride salt significantly improves its water solubility, which is vital for formulating oral tablets and, especially, intravenous (IV) solutions.

3. Chemical Properties

Appearance: A light-yellowish-white to yellow-white crystalline powder.
Solubility: Freely soluble in water and glacial acetic acid. Sparingly soluble in methanol. The high water solubility is a direct result of the salt formation.
pKa: It is amphoteric, meaning it has both acidic (carboxylic acid, pKa ~5.7) and basic (piperazinyl nitrogen, pKa ~8.3) groups.

4. Mechanism of Action (How it Works in the Body)

Levofloxacin is a bactericidal antibiotic, meaning it kills bacteria directly. Its primary mechanism involves inhibiting two essential bacterial enzymes:

DNA Gyrase: A topoisomerase II enzyme critical for introducing negative supercoils into DNA, which is necessary for DNA replication and transcription in Gram-negative bacteria.
Topoisomerase IV: An enzyme that separates interlinked (catenated) daughter DNA chromosomes after DNA replication in Gram-positive bacteria.

Net Effect: By binding to and inhibiting these enzymes, Levofloxacin causes double-strand breaks in the bacterial DNA. The cell's attempts to repair this damage lead to fatal errors, rapid bacterial cell death, and destruction.

5. Spectrum of Activity and Medical Uses

Levofloxacin is a broad-spectrum antibiotic used to treat a wide range of bacterial infections, including:

Respiratory Tract Infections: Community-acquired pneumonia, acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis.
Skin and Skin Structure Infections
Urinary Tract Infections (UTIs): Including complicated and uncomplicated infections.
Prostatitis (bacterial)
Anthrax (Inhalational): As a post-exposure prophylaxis.

6. Important Considerations and Warnings

Due to its potent mechanism of action, Levofloxacin (and all fluoroquinolones) carries serious safety warnings ("Black Box Warnings" in the US):

Tendonitis and Tendon Rupture: Risk is higher in older adults and those using corticosteroids.
Peripheral Neuropathy: Nerve damage that can cause pain, burning, tingling, or weakness.
Central Nervous System Effects: Including seizures, dizziness, and confusion.
Exacerbation of Myasthenia Gravis: Can cause severe muscle weakness and respiratory failure.
Other Risks: Aortic aneurysm, QT prolongation, and blood sugar disturbances.

Because of these risks, its use is typically reserved for infections that do not have safer alternative treatment options.

In conclusion, Levofloxacin Hydrochloride is the water-soluble salt form of a potent, chiral, synthetic antibiotic. Its specific chemical structure allows it to inhibit critical bacterial enzymes, leading to cell death. While highly effective against a broad range of bacteria, its use is tempered by the potential for serious, disabling side effects.