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Fasudil Hydrochloride

    • Product Name Fasudil Hydrochloride
    • Alias HA-1077
    • Einecs 685-002-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    739763

    Productname Fasudil Hydrochloride
    Casnumber 103745-39-7
    Molecularformula C14H17N3O2S·HCl
    Molecularweight 327.83 g/mol
    Synonyms HA-1077; AT 877
    Appearance White to off-white crystalline powder
    Solubility Soluble in water, DMSO, methanol
    Purity Typically ≥98%
    Storage Store at -20°C, protected from light
    Mechanismofaction Rho-kinase (ROCK) inhibitor
    Therapeuticuses Cerebral vasospasm, stroke, cardiovascular diseases
    Routeofadministration Intravenous
    Stability Stable under recommended storage conditions
    Iupacname 5-(1,4-Diazepan-1-ylsulfonyl)isoquinoline hydrochloride
    Ph 3.0–5.0 (1% solution in water)
    Target Rho-associated protein kinase (ROCK)

    As an accredited Fasudil Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Fasudil Hydrochloride, 10g, supplied in a sealed amber glass vial with tamper-evident cap, labeled with product details and safety information.
    Shipping Fasudil Hydrochloride is shipped in tightly sealed containers, protected from light and moisture. It is typically dispatched at ambient temperature unless otherwise specified. All packaging complies with regulations for safe transport of chemicals, including clear labeling and documentation. Hazard precautions are observed to ensure secure handling during shipping and delivery.
    Storage Fasudil Hydrochloride should be stored in a tightly sealed container, protected from light, and kept at 2–8°C (refrigerated conditions). Avoid exposure to moisture and air to maintain its stability and efficacy. Ensure the storage area is well ventilated and designated for chemicals, away from incompatible substances. Always follow manufacturer or laboratory safety guidelines for proper chemical storage.
    Application of Fasudil Hydrochloride

    Applications of Fasudil Hydrochloride in Industrial Manufacturing

    Fasudil Hydrochloride serves as a critical intermediate and active compound for advanced pharmaceutical synthesis and scientific research. Our production adheres to precise specification standards, supporting strict regulatory compliance and integration into multiple downstream biotechnological and pharmaceutical sectors. As a direct manufacturer, we enable reliable bulk supply for leading industry application tracks.

    1. Cardiovascular API Production

    Large-scale pharmaceutical processors use Fasudil Hydrochloride as an essential raw material for manufacturing targeted vasodilatory cardiovascular active pharmaceutical ingredients. Facilities deploy this compound in batch reactors with multi-step synthesis, guided by process analytical technology for purity assurance. Adjustments in synthetic protocol focus on reducing impurity profiles in final injectable and oral drug products for use in vascular disease management. In-process controls monitor impurity content and stability, ensuring reproducible lot-to-lot quality before further downstream formulation and packaging under GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Guidelines Part II
    • Chinese Pharmacopoeia (2020 Edition, Monograph for Fasudil Hydrochloride)
    • FDA 21 CFR Part 211

    Typical usage ratio

    • 70–85% Fasudil Hydrochloride per synthetic batch, variation depending on target API yield and by-product recapture protocols.

    Downstream process integration

    • Introduced after initial salt formation steps; purified via crystallization and solvent washing prior to micronization and formulation into dosage forms.

    Final product types

    • Injectable preparations for cerebral vasospasm
    • Film-coated oral tablets
    • Pre-measured intravenous vials

    2. Preclinical Research-Grade Compound Synthesis

    Innovative drug discovery and molecular biology institutes use Fasudil Hydrochloride as a core molecular probe for in vitro testing and cell signaling pathway research. The compound is processed in small- and mid-scale batches with sterility controls and is qualified for use in preclinical animal model studies after batch-specific certificate of analysis validation. Researchers incorporate it into test formulations in buffer solutions or as lyophilized powder blends, supporting diverse research pipelines focused on Rho-kinase inhibition.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Registration Requirements (for EU research supply)

    Typical usage ratio

    • 0.01–2% w/v in formulated research buffers, scaled by end-user protocol and required pharmacodynamics in test systems.

    Downstream process integration

    • Dissolved directly into sterile buffer solutions and loaded into assay plates or formulated into injection vials for animal studies.

    Final product types

    • Research reagent kits
    • Biological activity screening compounds
    • Preclinical study solutions

    3. Biotechnology Cell Culture Supplementation

    Bioprocessing companies add Fasudil Hydrochloride to cell culture media used for evaluation of intracellular signaling and cellular contractility in primary human endothelial and smooth muscle cell models. Specialists tune concentration profiles to minimize cytotoxicity while optimizing pathway inhibition, supported by stringent in-house validation and regular sterility monitoring. Quality control teams perform stability testing over extended storage and cell culture incubation periods, and compliance teams document all process modifications for traceability in regulated bio-lab environments.

    Industry compliance standards

    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • ISO 13485:2016 Medical Device Quality Management
    • CFR Title 21 Part 1271 (US Human Cells, Tissues, and Cellular and Tissue-Based Products Regulations)

    Typical usage ratio

    • Range: 5–30 μM concentration in defined cell culture systems, based on cell line sensitivity and experimental design.

    Downstream process integration

    • Prepared as a sterile stock solution; added to culture media immediately before cell seeding for pathway characterization assays.

    Final product types

    • Assay-ready cell culture media
    • Specialized cell-based assay kits
    • Experimental cellular model reagents

    4. Injectable Formulation Compounding

    Sterile drug manufacturers utilize Fasudil Hydrochloride in the preparation of bulk injectable solutions indicated for acute cerebrovascular management. The API undergoes final compounding in classified cleanroom environments, supported by validated aseptic technique and comprehensive filtration. Compounding staff maintain meticulous pH adjustment and isotonicity by managing excipient blend ratios and conduct strict microbial limits testing prior to final sterile filtration and filling into ampoules or vials. Release protocols follow product-specific monographs and real-time batch stability guidelines.

    Industry compliance standards

    • USP <797> Pharmaceutical Compounding—Sterile Preparations
    • Ph. Eur. Monograph 01/2018:2334 (Fasudil Hydrochloride for Injection)
    • Japanese Pharmacopoeia (JP17.31 Fasudil Injection standards)
    • WHO Good Manufacturing Practices for Sterile Pharmaceutical Products

    Typical usage ratio

    • 2–15 mg/mL API concentrations in finished injectable product, adjusted for regional prescriptive protocols and vial fill volume.

    Downstream process integration

    • Bulk raw delivered into Class 100 cleanrooms; dissolved in WFI, filtered, aseptically filled and terminally sterilized under batch certificate release.

    Final product types

    • Single-dose injectable vials
    • Ready-to-use ampoules
    • Pre-mixed infusion bags

    5. Analytical Reference Material Supply

    Analytical measurement laboratories and pharmacological QC departments require high-purity Fasudil Hydrochloride as a reference material for calibration and validation of chromatographic analysis methods. We supply batch-specific, traceable, and fully characterized standards, supporting downstream HPLC, LC-MS, and UV-Vis system setups. Testing teams develop independent validation protocols using our supplied reference material aligned with regulatory batch release specifications.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • EP 2.2.46 Chromatographic Separation Techniques
    • USP <621> Chromatography
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation

    Typical usage ratio

    • 100–1000 μg/mL stock solutions prepared for standard curve generation and limit testing in analytical assays.

    Downstream process integration

    • Accurately weighed and dissolved reference standard aliquoted into autosampler vials; introduced into system suitability assessments and routine batch testing for identification and quantification.

    Final product types

    • Certified reference standard kits
    • Quality control system calibration samples
    • Analytically qualified reference libraries
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    Certification & Compliance
    More Introduction

    Fasudil Hydrochloride: A Closer Look from a Manufacturer’s Lens

    What We Make and Why It Matters

    Day in and day out, our team dedicates itself to the production of Fasudil Hydrochloride, a potent Rho kinase inhibitor valued by research scientists and pharmaceutical developers worldwide. Among the diverse small-molecule toolkits circulating in laboratories, Fasudil Hydrochloride continues to gather attention because its applications stretch from neurological studies to cardiovascular therapy research.

    Our plant’s process borrows nothing from guesswork. Sourcing high-quality raw materials, controlling moisture at every step, and avoiding unnecessary residuals have never been afterthoughts. The material we ship leaves the reactor in a fine, snow-white crystalline form. This signals both physical purity and a properly conducted synthesis. You can recognize our batches by their sharp melting points and high solubility in water – two benchmarks no customer wants to compromise.

    Product Model and Specifications

    We offer Fasudil Hydrochloride primarily in its monohydrate form. Bulk customers request several particle size ranges, but typical demand centers around a firm, easily handled powder. Our most widely shipped model sits comfortably above 99% HPLC purity, established by batch-specific chromatography certificates. You’ll find lower impurity profiles when compared to most generic or overseas alternatives. That doesn’t happen by chance. Teams in quality control rely on state-of-the-art HPLC and NMR analysis. Our standard packaging absorbs little humidity and resists cross-contamination, preventing wastage and risk during transfer.

    It isn’t just about hitting an assay number on a certificate. Stability counts for more in real-world supply. Each lot runs stability tests at multiple temperature and humidity conditions. Samples are periodically tracked over several months, and we won’t green-light batches that show unacceptable degradation. This discipline defines a manufacturer’s promise – one we keep batch after batch.

    Practical Usage and Research Relevance

    Researchers recognize Fasudil Hydrochloride as a reversible, selective inhibitor of Rho-associated protein kinase (ROCK). In laboratory studies, this compound alters the phosphorylation of myosin light chains, with downstream effects on cell shape, motility, and vascular tone. Laboratories using our Fasudil Hydrochloride analyze its ability to blunt vasoconstriction in experimental models. Neuroscience projects leverage its protective effects after cerebral ischemia or spinal cord injury. Cellular biologists test its impact on smooth muscle, endothelium, and blood-brain barrier permeability.

    Supply chain issues can derail promising studies. Unlike distributors or brokers chasing market whims, we plan our output based on actual data, not last-minute forecasts. This consistency keeps prices rational and volume steady. We see returning clients opting to lock in supply with annual contracts. Their feedback shapes our production cycles.

    What Sets Fasudil Hydrochloride Apart from Others

    Comparing Fausdil Hydrochloride against similar Rho kinase inhibitors such as Y-27632 or ripasudil sheds light on unique differences. Our molecule, unlike Y-27632, brings a more potent and selective activity for both ROCK1 and ROCK2 isoforms. Pharmacologically, its clinical trajectory differs as well: Fasudil Hydrochloride moved beyond the academic sphere decades ago and saw human clinical use, especially in Japan, to manage cerebral vasospasm after subarachnoid hemorrhage.

    Clients often ask about equivalency. While several inhibitors show crossover applications, Fasudil Hydrochloride presents a known pharmacokinetic and toxicity profile thanks to extensive animal and clinical data amassed over decades. Its water solubility stands out, facilitating both in vivo dosing and in vitro system formulation. The hydrohalide structure offers stability during storage and minimizes loss during preparation. Our product avoids sticky or hygroscopic residues, which can wreck precise dosing and introduce uncontrolled variables in a sensitive experiment.

    Anyone involved in preclinical research will notice subtle differences between sources. Some products carry off-flavors: faint discoloration, unexpected clumping, or delayed dissolving in solution. We trace those issues to lapses in synthesis steps, washing, or drying. Instead of glossing over these problems, we keep our specifications honest and tight. Regular, open dialogue between production, QC, and our institutional clients tunes our process with every batch.

    Supporting Reliable Research Outcomes

    Years of feedback have shown us that even small deviations in material consistency push results off course. During pilot studies or when running animal models, lost time means lost grant funding and wasted effort. We remember one neurology research center relaying how a delayed shipment of an inferior product forced them to repeat weeks of surgeries. Since then, we have tightened our communication lines, putting realistic delivery windows ahead of marketing fluff.

    We keep client feedback central to improvements. Requests for finer particle sizes or alternate hydration levels get serious consideration, not quick brush-offs. Batch-level traceability means our partners know exactly what has gone into their study. The reports we supply highlight more than purity; they offer a full impurity profile and retention samples, ready for review if any questions arise years after purchase.

    Meeting the Challenges in an Expanding Field

    Demand for Fasudil Hydrochloride has grown as more biologists look to modulate the Rho/ROCK pathway across a range of models. Cancer labs evaluate its effects on tumor migration. Ophthalmology developers delve into its use for intraocular pressure regulation and fibrosis. Chronic inflammation studies, vascular researchers, and regenerative medicine projects reach for Fasudil Hydrochloride thanks to its predictable action and abundant supporting literature.

    As a manufacturer, we face challenges head-on that others may overlook. Sourcing precursor chemicals to meet every country’s regulatory requirements takes experience. Not every market allows the same solvent residues, and purity standards in Europe or North America can surpass those of other regions. Our regulatory and analytical staff follow evolving country-level expectations. Each export batch includes full documentation for customs and inspection purposes. Analytical data is never recycled or generic.

    We stay aware that price pressure sometimes tempts newcomers to sidestep difficult processing steps. Such shortcuts produce material with unacceptable impurity batches. We’ve taken the opposite route, investing in purification and high-throughput analytical screening so customers never face issues of off-target effects or flawed data. The real value in research chemicals comes not in the invoice but in the reliability that supports precise, reproducible data.

    What Experience Has Taught Us

    If twenty years of synthesis work have taught us anything, it’s that shortcuts today turn into headaches tomorrow. The research customers who stick with us often mention their desire for predictability – knowing each gram behaves exactly like the last. Our clients run everything from routine cell culture to highly regulated clinical studies. They rely on that predictability.

    Tight collaboration with scientists uncovers hidden bottlenecks. For clients scaling from milligrams to hundreds of grams, solubility and handling become vital. Variability in the bulk physical form can throw off dosing in animal models or lead to inconsistent results in cell-based assays. Consistency in both chemical and physical measurements sets trusted suppliers apart.

    Technicians and R&D specialists in our facility take pride in spotting early signals of trouble: haze in solution, inconsistent crystalline form, loss of white color, or sudden changes in melting behavior. Proactive inspection at each step lets us intervene before the product ever lands in a packaging drum.

    Building Trust, Batch by Batch

    Trust between the producer and the end user never happens overnight. Every year, we invest in process validation, cross-train staff, and replace outdated analytical hardware. In-house and third-party audits keep our hygiene, documentation, and batch control processes sharp.

    We know many buyers have spent years working with inconsistent quality, ambiguous labeling, or delayed paperwork. Each lot ships with full batch records, including all critical intermediates, so clients know exactly what backs up their COA. In academic partnerships, we’ve supplied reference lots to facilitate broader collaborations between labs. This model removes doubts about batch variability and supports reproducible science, an increasingly high bar in many funding agencies’ eyes.

    Over the years, several clients returned, telling us how a consistent Fasudil Hydrochloride supply opened new doors for them. A major cardiovascular research group credited our dependable material with the progress of their long-term animal studies. A regenerative medicine startup could move faster on IND-enabling work since they never faced interruptions from backorders or inconsistent batches.

    Limiting Risk and Maximizing Outcomes

    From our vantage point, the greatest risk to both researchers and manufacturers remains complacency. Unquestioned reliance on generic versions often leads to vague or irreproducible outcomes, which erodes the scientific process. Molecular studies using impure or poorly characterized compounds face additional variables, sometimes causing entire projects to stall or funding to be wasted. Clear presentation of analytical results, complete chain of documentation, and rapid response to customer inquiries cut down on such risks.

    There’s no simple formula for perfect chemical manufacturing. Each batch teaches something new. Our plant’s continuous feedback loops — production, analytics, logistics, and customer support — press against complacency every day. High standards come from curiosity: how does this impurity form, what drying technique yields the cleanest powder, which storage conditions protect long-term stability best? Attentive work pays off both in safety and in the scientific robustness of downstream research.

    Future Directions and Product Development

    Many of our customers move into ever more complex studies, involving combinatorial therapies and advanced in vivo models. As requirements shift, our R&D team seeks ways to refine not just purity but also function — for instance, ensuring the material remains stable combined with solvents or even in microencapsulated forms.

    We monitor literature and client requests for alternative forms or derivatives of Fasudil Hydrochloride that may offer new biological activity or better selectivity. Sometimes institutions request cGMP-grade material for clinical transitions. While our product lines primarily serve research, we track these broader requirements, validating our methods and documentation against evolving regulatory standards whenever possible.

    Continuous improvement in manufacturing processes means delivering not only on today’s metrics, such as purity and particle size, but also supporting tomorrow’s innovations. Maintaining open lines with active customers accelerates new development – feedback often drives decisions in scale-up, packaging upgrades, or documentation needs for tighter regulatory oversight.

    The Difference a Manufacturer Makes

    Buyers working directly with a producer notice real differences: shorter lead times, clear answers about process changes or technical questions, and greater accountability if issues arise. Unlike those who simply pass on a purchased product, we accept feedback as part of an ongoing relationship. That direct dialogue often brings new insight into practical challenges, from storage to novel application areas.

    Researchers aiming for consistent experimental results find little tolerance for uncertain supply chains or widely varying batches. Shortcuts, such as acquiring from generic brokers with little oversight, can save only pennies at best. The savings mean little when biological interpretation and project timelines hang in the balance. Stability, clarity, and responsiveness differentiate trusted suppliers from the rest.

    It also pays to remember that material traceability — from origin of synthesis to packaged powder — is a growing concern in both academia and industry. Our facility tracks lot history precisely, and retains samples long after shipment. Clients find this crucial not only in the event of follow-up analysis, but as regulatory scrutiny mounts in the research supply world.

    Supporting Science Beyond the Transaction

    Beyond delivering Fasudil Hydrochloride itself, our role extends into actively supporting the global research community. We assist in developing research protocols, share technical input on solubility and dosing, and troubleshoot unusual analytical results whenever needed. Our technical staff, with hands-on bench experience, respond quickly and in detail.

    This involvement fosters relationships extending beyond routine sales. Several collaborative projects have originated from troubleshooting together, whether that involves optimizing buffer conditions or identifying unforeseen interactions with other experimental components. For us, the product is just the start of a longer scientific journey shared with each customer.

    Conclusion

    Producing Fasudil Hydrochloride is more than synthesizing a compound and packing it for shipment. Each partnership, each conversation with a research scientist or pharmaceutical developer, points toward a larger goal: ensuring that this cornerstone molecule reaches investigations reliably and consistently. Years of process refinement, chemistry experience, and a hands-on approach to customer needs separate a manufacturer’s supply from any third-party alternative.

    As this essential molecule continues to power discoveries in neuroscience, vascular biology, oncology, and regenerative medicine, its quality and reliability will matter even more. We remain committed to staying out front — not just keeping pace with demand but anticipating the next set of scientific challenges. This dedication, batch after batch, keeps trusted research moving forward, made possible only by a focus grounded in experience, dialogue, and earned trust.