|
HS Code |
843103 |
| Generic Name | Dexrazoxane Hydrochloride |
| Chemical Formula | C11H16N4O4·HCl |
| Molecular Weight | 292.27 g/mol (base); 328.73 g/mol (hydrochloride) |
| Synonyms | ICRF-187, Zinecard, Totect |
| Drug Class | Cardioprotective agent |
| Route Of Administration | Intravenous |
| Mechanism Of Action | Chelates iron and reduces free radical formation |
| Indication | Prevention of anthracycline-induced cardiotoxicity |
| Appearance | White to off-white crystalline powder |
| Storage Conditions | Store at 20° to 25°C (68° to 77°F); protect from light |
| Solubility | Soluble in water |
| Cas Number | 24584-09-6 |
As an accredited Dexrazoxane Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dexrazoxane Hydrochloride packaging: 500 mg sterile powder per vial, sealed in a labeled box, typically containing 10 single-use vials. |
| Shipping | Dexrazoxane Hydrochloride is shipped as a hazardous material, following all relevant regulations for pharmaceuticals and chemicals. It is typically packed in secure, leak-proof containers, protected from moisture and light. Shipping includes appropriate labeling, documentation, and temperature controls as required, ensuring compliance with safety and transport guidelines during transit. |
| Storage | Dexrazoxane Hydrochloride should be stored at controlled room temperature, typically between 20°C to 25°C (68°F to 77°F), and protected from light and moisture. It should be kept in tightly closed, original containers and away from incompatible substances. Proper storage ensures the chemical remains stable and maintains its efficacy throughout its shelf life. |
|
Purity 99%: Dexrazoxane Hydrochloride with purity 99% is used in chemotherapy protocols, where it ensures maximum cardioprotection against anthracycline-induced toxicity. Molecular weight 297.72 g/mol: Dexrazoxane Hydrochloride with molecular weight 297.72 g/mol is used in intravenous infusion formulations, where it provides reliable pharmacokinetic profiles for consistent therapeutic outcomes. Stability at 25°C: Dexrazoxane Hydrochloride stable at 25°C is used in hospital storage environments, where it maintains chemical integrity and extended shelf-life. Solubility in water 50 mg/mL: Dexrazoxane Hydrochloride with solubility in water 50 mg/mL is used in reconstitution of injectable solutions, where it allows rapid and complete dissolution for immediate clinical use. pH 3.0–4.0 (1% solution): Dexrazoxane Hydrochloride at pH 3.0–4.0 in a 1% solution is used in sensitive infusion preparations, where it minimizes the risk of local tissue irritation. Endotoxin level <0.5 EU/mg: Dexrazoxane Hydrochloride with an endotoxin level below 0.5 EU/mg is used for parenteral administration, where it reduces the risk of adverse immunological reactions. Particle size <50 μm: Dexrazoxane Hydrochloride with particle size less than 50 μm is used in sterile injectable formulations, where it ensures homogenous suspension and prevents clogging of infusion equipment. Residual solvent <0.1%: Dexrazoxane Hydrochloride with residual solvent content less than 0.1% is used in pharmaceutical manufacturing, where it assures compliance with regulatory safety standards. Melting point 196–198°C: Dexrazoxane Hydrochloride with melting point range 196–198°C is used in thermal processing steps, where it ensures solid phase stability during formulation development. Heavy metals <10 ppm: Dexrazoxane Hydrochloride with heavy metals content below 10 ppm is used in advanced oncology applications, where it guarantees patient safety and high product purity. |
Competitive Dexrazoxane Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Cancer can be an ugly word, and chemotherapy looms as one of its ugliest necessary evils. Everyone who has sat in the chair at a cancer clinic knows more than they ever wanted about tradeoffs: attack the tumor with everything modern medicine can offer, but brace for the damage those same tools can cause. Among the nastiest risks is heart damage, especially for people treated with anthracycline drugs like doxorubicin. Suddenly, you’re not only fighting cancer—you’re fighting for your heart, too.
Dexrazoxane Hydrochloride quietly took up this job a while back. It’s not one of those big-name drugs advertised on glossy pages or TV screens, but for people who know, it’s a game changer. The molecule itself isn’t new; doctors in hospitals across the world have leaned on it for decades now. Dexrazoxane’s main trick is straightforward but vital: it shields the heart from the toxic effects of certain chemotherapy drugs, especially anthracyclines.
Most oncology drugs look for cancer cells to ruin them, but anthracyclines do this job in a way that produces free radicals—tiny, hyperactive molecules that, when piled up, put healthy heart cells in peril. Dexrazoxane walks into this scenario with a single clear goal. It bends the laws of chemistry to grab hold of iron molecules, yanking them away before they can fuel those free radicals. By slashing the free radical fireworks, dexrazoxane gives the heart a fighting chance to weather the chemical storm that chemotherapy brings.
You won’t find dexrazoxane being given to every patient who gets doxorubicin. Oncology teams select it for those at higher risk or who are about to receive a cumulative dose of anthracyclines that moves into risky territory. Plenty of patients get by without it—usually younger people or those who won’t need repeated chemotherapy cycles. Yet, for children, for adults with longer journeys ahead, or for anyone who’s taken doxorubicin before, dexrazoxane can be the quiet difference between surviving cancer and thriving once treatment ends.
From a prescribing standpoint, dexrazoxane comes as a sterile powder for reconstitution, often in single-use vials. The doctor or nurse mixes it right before it’s given, then runs it as an infusion in the vein, usually just ahead of the chemotherapy pump starting up. The familiarity of this choreography—draw, mix, walk it to the chair, start the drip—means dexrazoxane slips easily into the rhythm of daily cancer care.
It isn’t always obvious that “dexrazoxane” refers to a whole class of products, not just a single bottle. In practice, plenty of small differences matter: available strengths, purity levels, and handling cautions can vary depending on the manufacturer. Standard vials typically appear in 250 mg or 500 mg volumes, formulated as hydrochloride for stability and consistent dosing. Each batch should meet strict criteria: pharmaceutical-grade purity, sterile presentation, no extraneous fillers that might complicate delivery into a vulnerable patient.
The patient never asks about the spec sheet—they shouldn’t have to. Still, there’s reassurance knowing that pharmaceutical teams and pharmacists hold these details tightly. Each lot faces scrutiny before it ever touches a patient line. In my own work watching oncology pharmacy techs, I’ve seen the extra caution given to agents like dexrazoxane. No one wants an error in a product meant to spare a heart working overtime to keep up with cancer and chemo. The vials usually require storage at room temperature, but handling and reconstitution demand training and steady hands.
A cynic might look at a box of dexrazoxane next to a full suite of chemo drugs and see just another add-on, another line on the pharmacy bill. That’s missing the point. Dexrazoxane flips an ugly truth about chemotherapy on its head. For years, we accepted that cancer treatment would “often” leave a patient with a battered heart. Take the cure, hope for the best, live with the scars. Now, with dexrazoxane, there's room for hope beyond that rushed compromise.
Randomized clinical trials have underpinned its value, especially for children, whose young hearts could face a lifetime of fallout from intensive anthracycline exposure. In practices I’ve witnessed, families granted extra peace of mind with each round of chemotherapy learn that safeguarding life isn’t always about the dose or dramatic intervention—a small infusion like dexrazoxane sometimes guards a child’s future every bit as fiercely as the “main” drug being pumped.
Other drugs hope to limit side effects, but few move with such a clear and measurable target as dexrazoxane does. Long-term studies highlight reductions in both detectable cardiac damage and real-world cases of heart failure. Sure, there are always tradeoffs—some studies debate about whether dexrazoxane could affect the overall effectiveness of chemotherapy, but by now, decades of follow-up tip the balance toward its benefit in groups most at risk.
Many interventions in cancer care try to shield healthy tissue: anti-nausea drugs, growth factors, pain medication. Dexrazoxane stands a bit apart because its action is target-specific. You’ll hear talk about alternatives like careful dose adjustments of anthracyclines, schedule changes, or cardiac monitoring. None of these actively blocks the chemical chain reaction that triggers heart cell damage. They focus on early detection or volume management. Dexrazoxane, instead, acts before catastrophe happens.
Unlike general protectors or modified dosing, dexrazoxane requires a clear justification. Its use is recommended only after a certain cumulative dose threshold of anthracyclines or in patients flagged as higher risk for heart injury. The evidence doesn’t support scattering it everywhere; it saves its best work for cases where the balance of risk and reward is sharpest.
Other “cardioprotective” agents in the oncology arsenal don’t operate quite like dexrazoxane. Beta-blockers and ACE inhibitors play roles in treating or preventing heart failure once warning signs appear. Their use sometimes grows out of necessity, patched on after the horse’s out of the barn, so to speak. Dexrazoxane offers preemptive action—a way to keep the barn doors shut in the first place.
There are differences between brands, too, which can make a difference depending on access and insurance coverage. Not all manufacturers produce the same presentations, and variation in product availability can cause headaches for clinics, especially in lower-resource settings. Some institutions favor long-standing brands; generic versions have grown more widespread and reliable over the past ten years. As with all critical medications, confidence comes from transparency around clinical data, manufacturing practices, and ongoing pharmacovigilance.
From a patient’s seat in the chemo bay, choices about side-effect prevention rarely stand out above the anxiety of the main event. People focus on beating cancer—the heart, the nerves, the everyday costs all blur behind the bigger danger. Having a drug like dexrazoxane on the table shifts that dynamic, even if it only gets mentioned briefly before an infusion. Physicians often have tough conversations balancing hope against risk, and dexrazoxane’s arrival in that conversation signals that someone is thinking beyond survival to the life that continues afterward.
I’ve watched nurses and pharmacists explain the role of dexrazoxane with a kind of relief—they’re not only managing today’s emergency, but also planning against tomorrow’s crisis. For parents watching a child go through multiple rounds of doxorubicin, or for adults already handling other heart issues, that support carries real weight. Not all drugs deserve celebration; this one, even with its silence, has earned it.
No medication comes without its shadows. For all its promise, dexrazoxane did hit roadblocks in the early days, particularly in pediatric oncology circles, where worries arose that it could dampen chemotherapy’s cancer-killing effect. Subsequent research in children and adults built more confidence, showing there’s little if any compromise in long-term outcomes for most tumor types.
Some regulatory bodies were slow to endorse it for the youngest cancer patients, and in certain regions the indication remains less broad than adults. There are also concerns about cost and equitable access. Insurance and national health systems track the use closely; no one wants overspending on a drug meant for a specific group. Sometimes that means paperwork and debates, perhaps even delays, before a patient actually receives it once the threshold is reached.
The side effect profile also counts. Dexrazoxane can lower blood counts, and add its own burden of fatigue, risk of infection, or even interfere with kidney and liver function. These effects are familiar enough in any cancer patient, but the hope is always that the benefit—preserved heart function—tips the scale firmly toward its use when the balance requires it. Everything in oncology is measured, debated, reconsidered at every round. Dexrazoxane isn’t exempt from that constant scrutiny.
The landscape for survival in cancer keeps shifting. More people than ever live longer after diagnosis, thanks to new drugs, personalized regimens, and greater awareness. Protecting quality of life during and after treatment should ride along with survival as a top priority. Dexrazoxane embodies this more thoughtful approach—the medicine oncologists reach for to guard their patient’s future, not just their present fight.
This sort of care, thinking ahead instead of only reacting, pushes oncology beyond its old boundaries. In my experience talking with survivors, the relief at keeping their hearts strong often matches—or even outpaces—the memory of their cancer ordeal. Survivors who dodge heart failure or years of cardiac drugs realize that every part of their body counts, not just the visible scars.
Some may argue the long-term cost of widespread dexrazoxane use, but the bill for treating chemotherapy-induced heart disease stacks higher. Rehospitalizations, surgical interventions, and years of medication all add up. Prevention, when applied judiciously, can mean not just sparing money but saving real joy and function for people who’ve already paid a high enough price.
Delivering better results isn’t only about a new chemical discovery. Doctors and nurses need the authority—and trust from policymakers—to prescribe dexrazoxane where the evidence is strongest. Timely, clear protocols help ensure that access stays open to those who benefit the most. Educating patients empowers them to join in these decisions, learning why protecting the heart matters as much as any tumor scan.
Healthcare systems need to smooth the journey from prescription to administration. Enough supply, flexible insurance options, and training make a difference. Pharmaceutical companies, for their part, can shoulder responsibilities for transparent studies and regular updates. As new formulations or generics reach the market, every improvement in purity, safety, or cost counts for clinics that sometimes balance access on a razor's edge.
Cancer treatment, for better or worse, often feels like a moving target. New innovations, therapies, and genetic insights create reasons for hope while unveiling fresh dangers. No miracle solution exists, but every addition like dexrazoxane changes what’s possible. It shows that the best medical care never stops at “good enough”— there’s always a way to press further, to secure more years, less pain, better lives.
For all its technical talk and stuffy scientific language, dexrazoxane ends up reflecting a deeper value, too: the respect for people who put everything on the line in their cancer battle. It arose from decades of listening to survivors and families say that living with a weak heart is not much of a victory. Oncology teams owe their patients more, and drugs like dexrazoxane help make that promise real.
The hope moving forward sits not just in getting the science right, but in making sure no one needing this safeguard is left behind. As understanding deepens and access grows, dexrazoxane’s silent guard over the human heart should become as familiar—and as trusted in the years to come—as the therapies it helps to support.