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Cefotaxime: Chemical Properties, Uses, and Safety

What is Cefotaxime?

Cefotaxime comes from the cephalosporin class of antibiotics, recognized for its strong action against a wide selection of bacteria. It plays a major role in hospital treatment, tackling everything from pneumonia to septicemia. With the urge for antibiotics rising, enough people have either experienced its effects directly or known someone treated with it. My own experience working in pharmacy showed me the demand for this drug. Healthcare providers reach for cefotaxime when quick, reliable intervention is needed. The way it interferes with bacterial cell wall formation leads to cell death—a straightforward, trusted approach that’s kept patients alive in high-stakes scenarios.

General Product Overview

Cefotaxime arrives as a white to slightly yellowish powder or crystalline solid. Its texture ranges from fine powder to more flaky or granular states. When kept dry and in a sealed container, stability holds steady for proper use. The compound dissolves in water, giving a clear, colorless solution used for intravenous or intramuscular injection. Unlike some older antibiotics, cefotaxime remains largely odorless, which helps with preparation and reduces complaints from sensitive users in medical settings. Its shelf life, when stored as directed, matches other sterile pharmaceutical raw materials, minimizing product loss and keeping warehouses organized and efficient.

Chemical Structure and Specifications

Cefotaxime’s chemical formula is C16H17N5O7S2, and its molecular weight lands at 455.47 g/mol. A β-lactam ring is central to its structure, typical for cephalosporins, responsible for antibacterial action. The compound features an oxyimino side chain, making it stronger against β-lactamase-producing bacteria. Examining its solid state, cefotaxime often appears as fine crystals under the microscope, with a density slightly above 1 g/cm³, typical for pharmaceutical-grade powders. The melting point hovers above 150°C, meaning it stays stable at room and refrigerated temperatures. Anyone involved in material quality control will know the importance of this, as consistent melting point readings point to high purity.

Physical Forms: Powder, Crystal, Solution

Pharmaceutical-grade cefotaxime usually comes as a sterile powder for reconstitution, sealed in glass vials. Once reconstituted with sterile solvent, the solution clears quickly without visible particles, ready for precise dosing. The powder, sometimes described as “pearls” when loosely compacted, avoids caking during transportation. Flakes appear when the compound recrystallizes due to shifts in storage temperature. On large scales, the material’s morphology affects packaging choices; flaky or grainy product might slow down automated filling equipment, a headache for manufacturing specialists. As a solid, bulk cefotaxime ships safer and with fewer regulatory headaches than liquid preparations, lowering transport costs.

HS Code and Regulatory Information

For international trade, cefotaxime typically falls under HS code 29419090, a category for antibiotics not elsewhere specified or included. Customs officers look for this code on import documentation, speeding up clearance and reducing unexpected fees. Regulatory bodies like the FDA or EMA require certificates of analysis showing compliance with pharmacopoeial standards—parameters include assay results, microbial contamination limits, and residual solvent levels. With governments cracking down on counterfeit medicine, detailed paperwork protects both shippers and buyers. Having worked with import teams, I can say that one missed document can block lifesaving drugs at the border. Good recordkeeping on cefotaxime batches smooths out distribution, especially during outbreaks.

Density, Solubility, and Other Physical Properties

The density of cefotaxime powder hovers around 1.7 g/cm³. Its solubility in water exceeds 80 mg/mL at room temperature, making it ideal for injection. This dissolving profile proves crucial when hospitals require quick preparation of high-concentration doses for acute infection management. The solution remains stable for a limited period at room temperature and degrades under strong light, prompting the use of amber vials and prompt administration. Some users underestimate the importance of simple parameters like solubility. Poorly soluble drugs clog needles and waste time, but cefotaxime’s reliability here makes it a favorite in emergency settings. Its compatibility with sodium chloride and glucose solutions streamlines mixing at the bedside.

Raw Material Sourcing

Most cefotaxime production starts with the fermentation of raw materials to create 7-aminocephalosporanic acid, the core nucleus. Chemical groups are then added in tightly-controlled batches to yield cefotaxime. The process demands pure solvents and certified intermediates—the wrong supplier can introduce impurities that ruin the antibiotic’s action or trigger allergic reactions. Rigorous QC testing in the lab screens for such problems. Global supply chains introduce pressures, like spikes in cost or delays in raw material shipment. Having faced procurement issues firsthand, I appreciate reliable vendor relationships and certified material sources; missed deadlines directly impact clinic shelves and patient outcomes.

Hazards, Safety, and Waste

Cefotaxime must be handled with care by all workers. Powdered form can be an irritant if inhaled or if dust contacts the skin. Laboratory staff need gloves, dust masks, and well-tuned fume hoods to work safely. Containers display hazard pictograms warning against accidental ingestion or eye contact. Waste disposal calls for dedicated pharmaceutical incineration—flushing cefotaxime down laboratory drains risks developing resistant bacterial strains in the environment. Hospitals and manufacturers collect unused stocks and expired material for secure destruction. Harm to aquatic life from cephalosporin contamination has been reported, driving stricter controls on disposal and urging manufacturers to develop greener synthesis technologies.

Molecular Property, Formula, and Application

Chemically, cefotaxime’s formula C16H17N5O7S2 captures a robust structure, rich in nitrogen and sulfur. The molecule features a six-membered dihydrothiazine ring fused to a four-membered β-lactam, a classic cephalosporin feature. Each piece of the molecule plays a role in docking at bacterial enzymes, blocking cell wall synthesis and clearing infection. Having dispensed this drug to many who needed swift recovery, I value its place on the frontline of severe infection treatments. In many medical crises, cefotaxime kept at the right temperature and correctly reconstituted matters as much as any new diagnostic tool.