|
HS Code |
380408 |
| Generic Name | Hydroxocobalamin Hydrochloride |
| Chemical Formula | C62H89CoN13O15·HCl |
| Molecular Weight | 1382.38 g/mol |
| Dosage Form | Injection |
| Therapeutic Class | Vitamin B12 analog |
| Color | Red crystalline powder |
| Route Of Administration | Intramuscular or intravenous |
| Indications | Treatment of vitamin B12 deficiency, cyanide poisoning |
| Storage Conditions | Store below 25°C, protect from light |
| Solubility | Soluble in water |
| Atc Code | B03BA03 |
| Stability | Stable under recommended conditions |
| Appearance | Hygroscopic powder |
| Cas Number | 13422-51-0 |
| Ph Range | 3.5 - 6.0 (when dissolved in water) |
As an accredited Hydroxocobalamin Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial with 10g Hydroxocobalamin Hydrochloride, sealed with a rubber stopper and aluminum cap, labeled with product details. |
| Shipping | Hydroxocobalamin Hydrochloride is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. It is labeled according to hazardous material regulations if required and packaged to prevent contamination or degradation during transport. Standard shipping generally includes secondary containment and temperature control, depending on stability data and specific recipient requirements. |
| Storage | Hydroxocobalamin Hydrochloride should be stored in a tightly closed, light-resistant container at a controlled room temperature, typically between 15°C and 25°C (59°F and 77°F). Protect from moisture and excessive heat. Avoid freezing and keep away from incompatible substances. Ensure the storage area is well-ventilated and access is restricted to authorized personnel to maintain safety and stability. |
Competitive Hydroxocobalamin Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
We will respond to you as soon as possible.
Tel: +8615365186327
Email: sales3@ascent-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Hydroxocobalamin Hydrochloride stands out for its vital role in clinical medicine, research, and diagnostics. Over many years, our manufacturing experience has shown that reliability in vitamin B12 analogs often makes the greatest difference in downstream applications. Our teams have encountered wide-ranging needs—ranging from bulk pharmaceutical compounding to specialized injectable formulations used in cyanide poisoning treatment. This diversity of demand calls for a flexible approach to grade, size, and lot control, which only a direct producer can manage at scale.
Our batches of Hydroxocobalamin Hydrochloride follow a strict process flow, monitored using robust analytical methods such as HPLC and spectrometry. Frequent feedback from end-users (from formulation chemists to pharmacologists) reminds us that trace impurities or non-reproducible potency lead to lost time in clinical and research settings. Unlike more common substances, even organic impurities in this coenzyme analog impact both safety and performance at minuscule thresholds. We routinely exceed compendial requirements—meeting criteria such as the European Pharmacopeia or USP monographs—to support customers who operate under regulatory inspections or require consistent results over many months.
Our most popular material comes as a crimson-red loose powder, with a moisture content well below accepted pharmacopoeial limits. Typical particle size distribution remains stable over long-term storage, because variable flow properties have created issues for labs focusing on automated dosing or sterile filling in the past. Documentation shows that even within accepted specifications, batch-to-batch differences can alter outcomes in lyophilized formulations. With our own in-house granulation and micronization lines, we keep control over physical characteristics, adapting sieve parameters when needed for specific delivery forms.
We maintain distinct production lines for pharmaceutical (injection-grade) quality and for analytical or food-grade lots. Customers in pharma request our injectable grade Hydroxocobalamin Hydrochloride for emergency antidote kits and clinical nutrition, which means keeping particulate loads low, confirming bacterial endotoxins are below 0.5 IU/mg, and delivering material in tamper-evident packaging. For analytical users in public health labs, we provide options that emphasize stability and colorimetry accuracy, supporting use in cyanide test kits or reference standards.
Much gets said about vitamin B12, but users often discover practical differences between Hydroxocobalamin Hydrochloride and other analogs like cyanocobalamin or methylcobalamin only once they start formulating. As a primary manufacturer, we continually compare chromatographic purity and manufacturing economics between B12 derivatives. Hydroxocobalamin Hydrochloride shows superior stability to light and oxidation than reduced forms like methylcobalamin or adenosylcobalamin. In our production environment—where open handling of solution intermediates sometimes exposes material to bright lighting—only Hydroxocobalamin regularly maintains its color and potency during purification and drying.
Medical protocols recommend Hydroxocobalamin over cyanocobalamin for cyanide poisoning due to its rapid complexation with cyanide ions and safer conversion in vivo. In tests run by our compliance team, we see practically no off-target reactivity, ensuring safety in environments where staff prepare antidote kits on tight timelines and cannot risk technical surprises. Its aqueous solubility and compatibility with injections make it easier to formulate stable, concentrated solutions than lipophilic forms—a factor that speeds up both R&D and production cycles.
Spec sheets only capture part of the story behind Hydroxocobalamin Hydrochloride quality. Customers in research or clinical diagnostic sectors share concerns with us about batch uniformity, especially during large runs. Many users fail to spot the connection between visually minor color changes and actual loss of chromophoric activity. Years ago, we learned this lesson when a series of batches—each within spec by HPLC—showed reduced color yield for a customer’s colorimetric reagent set, traced back to handling during intermediate filtration.
To avoid this recurring problem, our process minimizes heat exposure and uses inert atmospheres during sensitive stages. Such changes required investment in automated environmental controls and specialized filtration housings—choices traders and small-scale repackers tend to overlook in favor of quick-throughput handling. As a result, our lots offer reliable reactivity in kits that detect or scavenge cyanide at low part-per-billion levels, benefiting both hospital labs and environmental safety agencies.
Running a direct synthesis and finishing plant gives our team control over not just the product, but also supply continuity. Over the last decade, we have watched the global ingredient sector go through waves of disruption, especially for fermentation-based vitamins. Synthetic intermediates and raw cobalamin sources can vary batch-to-batch when they come from fragmented supply chains. Our practice is to secure raw material contracts at least a year out, and we maintain dual-source stock for critical reagents. When geopolitical or logistics problems surface (such as sudden port closures or border holdups), our forward inventory planning ensures delivery timelines for hospitals and bulk buyers.
Documentation doesn’t stop at batch COAs or TSE/BSE certifications. Regulatory agencies conducting site inspections often audit our process logs, cleaning records, and deviation reports. Over the years, we’ve learned that only direct manufacturers can quickly address documentation gaps or compliance queries—allowing R&D partners in the pharmaceutical sector to save time during regulatory fillings. Customers frequently point out that gaps from repackers or traders slow their own projects due to missing data on process aids or supply chain maps.
Hydroxocobalamin Hydrochloride appears in a surprising spread of end-products. Pharmacists rely on its solubility and rapid bioavailability in injectable forms for acute care settings, especially in emergency rooms dealing with smoke inhalation victims. Nutritionists and food scientists have used the molecule for fortification in animal feeds and health drinks—partly due to the superior absorption profile in humans and animals. For most manufacturers, the challenge isn’t just sourcing the right substance, but making it fit their particular process. We keep direct feedback channels open with partner companies, offering technical input about hydration, blending, and storage in different climates.
Our longer supply contracts show the effect of tailored technical support. One partner in the point-of-care diagnostics space saw their QC nonconformance rate drop by over 70% after optimizing their reagent prep with our guidance. Even small tweaks in buffer selection or hydration speed improved test shelf lives. Where others see just a raw material, the people in our teams see complicated process-chemical relationships that determine whether research or clinical projects succeed on time.
Producing consistent Hydroxocobalamin Hydrochloride takes more than technical compliance. Lessons learned over years include unexpected seasonal variation in raw cobalamin fermentation yields, which can shift impurity profiles. Our chemists recalibrate pre-treatment routines each season after trending data shows emerging solvent traces or unwanted mineral content, which can throw off HPLC peaks or optical density. Direct, hands-on manufacturing gives our teams the flexibility to run real-time adjustments.
Packaging, too, challenges any producer working with sensitive vitamins like Hydroxocobalamin Hydrochloride. Some of our biggest headaches have come from the tendency of red crystalline powder to adsorb moisture or oxygen. Early on, we responded to repeated customer complaints by investing in high-barrier packaging options and custom desiccant combinations. Lab testing, run both internally and at outside reference sites, demonstrated these changes more than doubled on-shelf potency retention during long-haul export situations.
Documenting these incremental gains—and the occasional failures—has built organizational expertise that downstream partners trust. Leadership in the company has encouraged sharing near-misses and regulatory audit challenges during our regular quality meetings, which has created a culture where technical staff and production teams work closely together.
During market turbulence, traders often treat commodities like vitamins as generic stock, blurring important distinctions between product grades. From our seat as a manufacturer, the picture looks different: each run of Hydroxocobalamin Hydrochloride represents hundreds of process variables tracked and logged. Oversupply a few years ago triggered a race to the bottom in pricing, bringing low-grade material into markets where stability and purity matter most. We doubled-down on transparency, opening up lot-level data releases, and explained the practical downside of sub-par vitamins. A major clinical customer pointed out that insufficiently pure Hydroxocobalamin led to failures during pyrogen and sterility testing, delaying batch approvals for hospital use.
Direct feedback from the field continually shapes our in-process testing. In one example, we initiated continuous in-line monitoring for residual solvents after several consignments detected off-putting odors during pilot formulation. This didn’t appear in routine spec sheets, but our intervention prevented recalls and allowed our partners to keep their clinical trial timelines—something bulk distributors couldn’t match. Our experience matches that of other established producers: relationships built on direct support and accountability produce more stable business and technical outcomes for all sides.
Hydroxocobalamin Hydrochloride manufacturing relies on complex chemical synthesis and significant energy inputs, so sustainability matters. We’ve made a conscious effort to recover solvents, cut water use, and switch to photovoltaic power for much of our site. A measurable drop in chemical effluent and electricity cost shows in our operating reports. Several years ago, we introduced a closed loop system for solvent capture, eliminating much of the off-gassing hazard and reducing regulatory burden in our region. Clients in Europe and North America notice the difference, since end-users must now demonstrate responsible sourcing under tightening GxP and green chemistry standards.
Occasional setbacks in safety or process reliability—such as pump failures, unexpected product spills, or filter ruptures—happen even in the best-run facilities. We’ve learned from operational incidents and now run regular emergency drills, maintaining a near-perfect site safety record over the last five years. Full traceability for byproduct and waste streams allows us to partner with regional waste handlers to minimize landfill exposure. Rather than merely describe these precautions, we demonstrate them to regulatory visitors, auditors, and supply chain partners.
No manufacturing process reaches perfection. Technical teams attend frequent formulation troubleshooting sessions with external R&D partners struggling with poor blending, off-spec colors, or solubility headaches. Our documentation library of over a thousand tracked inquiries contains repeated references to matters like pH variation, salt content adjustment, and unwanted color shifts in diagnostic strip manufacturing. Partners using our direct hotline often get practical advice on adjustment strategies that prevent loss of production lots.
In ongoing collaboration with formulation partners, we dig into problems like unexpected variation in color intensity or poor shelf stability in end-user packaging. Field reports on real-world failures feed into tweaks in our synthesis, drying, and packaging routines. Only by working directly with formulation and QC personnel do we learn what actually limits performance or causes material wastage.
Supporting these projects generates mutual trust, letting our partners book long-term contracts—giving both sides budget and production predictability. Our technical and commercial managers maintain regular touchpoints, offering access to analytical data, spec change logs, and tailored advice. From experience, direct manufacturer backing makes a clear difference to partners juggling production deadlines, audit pressures, and regulatory change.
Taking a hands-on role in every aspect of Hydroxocobalamin Hydrochloride production—fermentation, chemical synthesis, purification, drying, and final packaging—propels knowledge transfer throughout our company. Each setback or improvement, from adapting to new regulatory demands to troubleshooting a client’s colorimetric kit, shows the value of direct production knowledge. Beyond simple compliance, this enables a cycle of rapid feedback, problem-solving, and continuous improvement, giving our partners peace of mind in quality-sensitive applications.
Hydroxocobalamin Hydrochloride, in our experience, shouldn’t be viewed as a generic chemical commodity. Each kilo delivered confirms the link between rigorous process control, technical support, transparent documentation, and real-world results for the people and industries relying on these molecules—whether that’s a hospital pharmacy, a food scientist, or a field diagnostics lab. We remain committed to advancing both our product and our process, helping our customers reach safer, faster, and more reliable outcomes, batch after batch.