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HS Code |
673375 |
| name | Metrizamide |
| chemical_formula | C18H22I3N3O8 |
| molecular_weight | 789.101 g/mol |
| appearance | White to off-white powder |
| solubility | Freely soluble in water |
| CAS_number | 31110-74-6 |
| usage | Non-ionic, water-soluble contrast agent |
| route_of_administration | Intrathecal, intravascular |
| storage_conditions | Store at room temperature, away from light |
| ATC_code | V08AA03 |
As an accredited Metrizamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Metrizamide is supplied in a 10-gram amber glass vial, sealed with a rubber stopper and aluminum cap, with clear labeling. |
| Shipping | Metrizamide should be shipped in tightly sealed containers, protected from light and moisture. It must be handled as a non-hazardous material but with care to avoid exposure. Transport at controlled room temperature is recommended. Always comply with local and international regulations for chemical shipment, including proper labeling and documentation. |
| Storage | Metrizamide should be stored in a tightly closed container, protected from light, moisture, and excessive heat. Keep it at controlled room temperature (15–25°C/59–77°F). Avoid freezing and ensure the storage area is well-ventilated and secure, away from incompatible substances. Follow institutional and regulatory guidelines for handling and disposal to maintain chemical stability and safety. |
Applications of Metrizamide in Industrial ManufacturingAs an established manufacturer, we supply metrizamide for specialized industrial applications requiring high-purity radiopaque agents. The following sections outline verified downstream scenarios, precise usage practices, compliance expectations, and process integration in regulated industries. 1. Medical Imaging Contrast Media ProductionManufacturers use metrizamide as a core ingredient in the formulation of non-ionic, water-soluble X-ray contrast agents for intrathecal administration. Its low osmolality and high radiodensity make it ideal for spinal cord and brain imaging procedures, especially in CT myelography. Production demands stringent quality checks on purity, pyrogen levels, and sterility throughout compounding, filtration, and aseptic filling. Regulatory requirements drive rigorous batch validation, with tight control of API-to-excipient ratios and final product concentration. Customer formulations often adjust the metrizamide content for pediatric versus adult dosing, always adhering to approved injectable solution protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Radiology Research Kit FormulationAcademic and commercial research institutions utilize metrizamide for laboratory-scale development of novel radiopaque formulations. Its predictable solubility profile, stable iodine content, and low interaction with biological matrices support experimental imaging kits for animal model studies and in vitro radiological research. Labs typically formulate small batches under controlled variables, focusing on reproducibility, accurate contrast calibration, and easy dissolution. The research use necessitates precise documentation and often follows institutional quality protocols adapted from the relevant pharmacopoeial standards for diagnostic substances. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. In Vitro Diagnostic Device (IVD) Component SynthesisManufacturers of in vitro diagnostic devices incorporate metrizamide in specific density gradient media for the quantitative separation of cellular components in clinical laboratory applications. The defined molecular weight and high solubility in aqueous media preserve cellular viability and morphology, making it a preferred medium for leukocyte isolation and nucleic acid purification kits. Consistent lot-to-lot purity, absence of interfering ions, and controlled osmolality assure reproducibility in standardized blood separation protocols. Regulatory focus targets low endotoxin content and confirmed biocompatibility with medical laboratory systems. Industry compliance standards
Typical usage ratio
Downstream process integration
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4. Pharmaceutical Radiopaque Marker SynthesisSpecialized pharmaceutical manufacturers use metrizamide for the production of radiopaque markers incorporated into implantable medical devices such as temporary stents or catheters. Its controlled radiodensity and compatibility with biocompatible polymers enable clear X-ray visibility of devices during placement and monitoring. The integration process requires purification to minimize extractables and leachables, and compositions must meet both function-specific and patient safety specifications. Stringent manufacturing and inspection processes support traceability from technical grade input to finished medical device approval. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Years of experience in specialty chemicals have taught us that every substance has its unique character, and Metrizamide stands out as a workhorse in diagnostic radiology and neuroimaging. Unlike commodities traded around facelessly, this product requires careful stewardship from source material right through to the final drying and packaging.
As direct manufacturers, we witness the process of converting each gram of raw material into a medium that radiologists and neurologists across the world rely upon for high-stakes diagnostic procedures. Metrizamide is an iodinated, non-ionic, water-soluble contrast agent best known for its low osmolality and high contrast effect, particularly in myelography and cisternography. Our plant specializes in high-purity metrizamide, typically formulated at concentrations between 170 and 370 mg iodine per milliliter, with precise control over molecular weight distribution to meet the rigorous standards imposed by healthcare regulations.
A lot of people in the supply chain talk about quality, but once you get close to the production line, you see what it takes to maintain a consistent product every time. With Metrizamide, absolute purity isn’t just a marketing point—it’s an operational necessity. Our installations use a closed-loop process to control every variable under pharmaceutical GMP guidelines: temperature, pH, water content, and even the air quality in controlled environments. Testing uses high-performance liquid chromatography, and any batch outside tight tolerances doesn’t make it to the next phase of production.
Compare Metrizamide to older ionic contrast agents, and you see a very real difference in patient reaction and diagnostic clarity. Ionic compounds, such as diatrizoate, draw water into the spinal canal and can cause significant adverse reactions. We have shifted entirely to non-ionic production in response to demand from practitioners who need lower neurotoxicity risk, reduced pain during injection, and clearer radiological results. Our technicians see the chemistry play out first-hand on lab benches where every batch’s osmolality, viscosity, and iodine content are measured to the decimal.
Metrizamide comes in several standardized concentrations. Each batch runs through a demanding process that starts with carefully sourced iodine and ends with sterile, clear solution, free from particulates and pyrogens. The most demanded grade is 370 mgI/mL, but our facility also prepares 170 mgI/mL and 200 mgI/mL concentrations by request. Each is transparent, virtually odorless, and colorless—qualities we view as early indicators of a process run to completion. Specific gravity is checked against reference standards, and we regularly chart viscosity at 37°C, as this directly affects injection pressure and patient comfort.
Some markets ask about shelf life and storage. What matters in our plant is inert glass vials, batch-coded and sealed right after sterilization. Each run is stored in temperature- and humidity-controlled conditions, then transported to hospital customers with full traceability. We keep samples from every batch in our retained-sample archive, which allows us to run retrospective tests if ever needed. Over decades, this archive has supported both product improvements and post-market surveillance.
You cannot cut corners in this industry. The synthesis of Metrizamide demands high precision, as even trace levels of impurities can reduce contrast quality or introduce safety concerns. Our labs use advanced purification, including multiple steps of recrystallization and filtration, to achieve final products that routinely exceed pharmacopeia benchmarks for heavy metals, residual solvents, and bioburden.
We regularly invest in better analytical instrumentation so our in-house quality analysts can monitor for any batch-to-batch variations. Products are always tested for pH, particulate matter, osmolality, and low-level chemical contaminants. Besides, we take feedback directly from clinical partners regarding injection experience and image clarity, keeping our standards grounded in real-world data rather than just laboratory numbers.
Customers working in neurology and radiology trust Metrizamide for its reliable imaging properties. It remains one of the few contrast media approved and thoroughly validated for intrathecal use. Myelography, which exposes spinal pathologies including tumors, herniated discs, and spinal cord injuries, sees its greatest accuracy with non-ionic contrast like Metrizamide. The low risk of meningeal irritation and seizures compared to ionic agents like meglumine iothalamate means clinicians can work with more confidence.
The breadth of uses once extended into CT cisternography and even arteriography, before more modern, sometimes lower-risk agents entered the market. Even so, many specialized neuroimaging centers value the clarity that our Metrizamide provides, especially in complex spinal cord mapping or to confirm subtle leaks of cerebrospinal fluid.
Veterinary professionals have also approached us for Metrizamide suited for animal diagnostics, especially larger animals where diagnostic accuracy can be a challenge through non-invasive methods. We have worked with academic hospitals to adapt packaging sizes and concentrations, based on their detailed feedback about tissue compatibility and optimal contrast levels.
Having produced both ionic and non-ionic lines through our history, we’ve seen exactly where Metrizamide offers clinical and workflow improvements. Ionic agents, while less expensive, increase risk of neurological complications and often cannot pass institutional review for use in sensitive areas like the subarachnoid space. Operators notice reduced incidences of patient discomfort, lower frequency of delayed adverse events, and, not insignificantly, quicker post-procedure recovery.
Chemical stability stands out as another advantage. Many older agents degrade under heat or prolonged light exposure; Metrizamide, correctly produced and stored, resists breakdown, giving clinics a usable window that supports efficient operation and minimal wastage. While some newer non-ionic agents, like iohexol and iopamidol, have gained ground for their low toxicity, Metrizamide continues to be a mainstay for high-resolution work. Its molecular structure, based on the N-methylglucamine derivative of the tri-iodinated benzoic acid ring, offers high x-ray absorption and minimal interference with surrounding tissues. We've run comparative studies in-house, showing contrast-to-noise ratios that often surpass generic alternatives in spinal and neural imaging.
Metrizamide’s water solubility, another key factor, allows for gradual metabolic clearance primarily via the kidneys, reducing systemic toxicity and shortening the residual exposure period. This property, verified at our plant with daily chromatography runs, supports customer arguments for repeat or staged imaging. Even after decades, Metrizamide’s formulation provides an intersection of safety and effectiveness that older formulations and some newer analogs cannot always match.
Manufacturing high-grade Metrizamide isn’t without its obstacles. Consistent supply of pharmaceutical-grade iodine sometimes faces pressures from shifts in global mining and extraction. We source from long-term partners audited both on quality and their environmental, social, and governance records. Chemical intermediates require continuous monitoring; any inconsistencies show up quickly in purity tests.
Sterilization also poses operational challenges, especially at scale. Many years ago, the industry favored wet heat sterilization for such agents, but that left trace impurities and batch variability. We transitioned steadily to low-temperature sterile filtration methods verified with in-line monitoring—an investment that paid off with less product loss and tighter microbiological safety margins.
From our point of view, automation marks the frontier in next-generation manufacturing. Automated sampling and real-time analytics cut human error out of critical points, while still allowing for direct intervention if machine-readings stray from the ideal. We routinely work with equipment manufacturers to iterate on custom production lines: more reliable automated valves, smoother sensor integration, and data logging software that gives us a digital fingerprint for each batch ever produced.
On the regulatory front, new standards and pharmacopoeial updates are always on the horizon. We participate in industry consortia so we get advance notice about expected changes. Our technical team tracks every revision, sometimes fine-tuning our process mid-cycle to keep ahead of compliance requirements. This dialogue with regulators also informs our choices in excipients and secondary packaging, as we avoid substances flagged for long-term health or environmental impacts. Each change, from solvent switch to packaging redesign, runs through a full battery of toxicological, chemical, and mechanical testing before it ever reaches customers’ hands.
Engaging with customers, especially clinicians working under high-pressure conditions, filters out impractical suggestions and spots genuine opportunities for improvement. Years back, we overhauled our vial design after neuroimaging teams asked for easier needle access and reduced risk of breakage. That prompted investment in premium borosilicate glass and a thicker stopper, now standard in every batch.
Feedback on batch-to-batch clarity and ease of handling also led us to set stricter controls for turbidity and particulate count than what's written in official regulations. We have maintained these standards even in tight supply situations, judging the short-term inconvenience worthwhile by the long-term trust we build with our medical partners. In this business, a missed speck can mean a failed scan or a patient call-back—mistakes we never want to see.
Our technical team remains in frequent contact with research hospitals who run clinical studies using Metrizamide, not only for imaging but also for emerging therapeutic applications such as targeted drug delivery. These collaborations spark real innovation, prompting us to test variant formulations, develop new extension-set compatible caps, and even support hospitals in their requests for regulatory submissions.
As the original producers, we never lose sight of safety and environmental responsibility. Each kilogram of waste solvents, byproducts, or spent charcoal gets recycled or neutralized in our certified facilities. We monitor emissions and water usage with digitized, network-linked monitoring stations. All staff take part in ongoing training: understanding how small tweaks to the process reduce environmental footprint, recognizing early signs of process drift, or handling emergencies. Every batch has a traceable record that follows it from raw material all the way to delivery.
We believe transparency in ingredients matters. With every order, we supply full certificates of analysis detailing actual batch measurements—not just regulatory minimums. We often work directly with hospital procurement teams to answer questions about sourcing, stability, or clinical data, remembering that patient outcomes depend squarely on process reliability.
Science never stands still, and neither can any reputable manufacturer. Metrizamide has offered decades of proven performance, but the pipeline of new materials and hybrid agents is always growing. Inside our R&D suites, chemists work to adjust iodine payload, tweak viscosity, and lower clearance times even further. We are investigating new purification resins to tighten impurity profiles and exploring eco-friendly solvent systems that don’t compromise product safety. In parallel, we support academic collaborations looking at novel dosage forms such as scatter-resistant coatings or adjunct modifiers for MRI compatibility.
We remain dedicated to sharing data—good or bad—which in turn drives refinements not just at our facility but throughout the global manufacturing network. As regulations, best practices, and hospital procurement guidelines evolve, we stay proactive, ensuring Metrizamide keeps meeting both contemporary expectations and emerging clinical requirements.
Our tradition of openness, attention to real-world performance, and investment in process resilience means that customers who choose our Metrizamide line get more than a product—they get decades of expertise, constant innovation, and unmatched reliability straight from the manufacturer’s floor.