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(+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride

(+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride


    • Product Name (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride
    • Alias Salbutamol
    • Einecs 259-372-4
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    434933

    Chemical Name (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride
    Molecular Formula C17H23NO3·HCl
    Molecular Weight 325.83 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water
    Melting Point 150-155°C (dec.)
    Cas Number 32981-86-5
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms Salbutamol Hydrochloride, Albuterol Hydrochloride
    Ph pH of 1% solution is 4.5-5.5
    Usage Pharmaceutical intermediate, bronchodilator
    Purity Typically ≥98%
    Stability Stable under recommended storage conditions
    Inchi Key QAOWNCIDQFYFNM-UHFFFAOYSA-N
    Ec Number 251-038-7

    As an accredited (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed amber glass bottle containing 25 grams, labeled with the full chemical name and safety warnings.
    Shipping This chemical, (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride, is shipped in secure, airtight containers to prevent moisture absorption, degradation, or contamination. It is typically transported at controlled room temperature with appropriate labeling and documentation per chemical safety and regulatory guidelines. Handle with gloves and follow all safety instructions during receipt.
    Storage Store (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-methylpropyl]amino]-1-hydroxyethyl]phenol hydrochloride in a tightly sealed container at 2–8°C (refrigerator temperature), protected from light and moisture. Keep away from incompatible materials such as strong oxidizing agents. Ensure the storage area is well-ventilated, and clearly labeled. Follow institutional and regulatory guidelines for chemical storage and handling to maintain safety.
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    Competitive (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    Introducing (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride: Experience from the Manufacturer’s Line

    What Sets Our Production Apart

    People who seek out pharmaceutical intermediates or research compounds often focus on quality and technical details but sometimes overlook the lessons learned on the production floor. Every batch of (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride we produce reflects experience built from countless process runs, raw material selection, and fine-tuning during scale-up. Consistency starts long before the product reaches a laboratory shelf.

    By handling synthesis in-house, we control the journey of every gram of material, from the sourcing of raw phenols and amines to the precise formation of the hydrochloride salt. We pay close attention to reaction temperatures and times, solvent choices, pH adjustments—details that chemists appreciate once they start their own formulations or testing. These choices affect not just yield but the side profile and the ease of subsequent purification steps.

    Specifications Built on Practice

    Each lot is evaluated with attention to analytical reproducibility. HPLC purity levels reach above 98 percent, as steady as the instrumentation can detect. Water content and residual solvents fall within pharmaceutical expectations—tight control here keeps unexpected results out of research data later on. Consistent particle size has come up during feedback from partners who run solid dose formulation trials. Even the flow and appearance of the hydrochloride powder can influence material handling down the line, especially for scaled work.

    Our batch records reflect more than regulatory requirements. They include lessons learned from night-shift adjustments, seasonal shifts in humidity, or small tweaks to filtration media. Our team keeps logbooks with notes on color or odor deviations, findings that do not always show up on a standard spec sheet but can matter in sensitive applications. The remarks from our own operators often spark improvements in drying schedules or even changes in reaction quenching rates—every tweak leads to a more dependable product.

    Usage Rooted in Real Practice

    Most focus gravitates toward the role of this phenol derivative in the pharmaceutical pipeline, particularly as an intermediate in the synthesis of key active ingredients for certain therapies. Our partners, especially those in preclinical work, value the reliability of material supplied batch after batch. Teams working on process development have reached out to share how minor variances in crystal habit from other suppliers complicated their filtration or crystallization. Feedback guided improvements on our end, tightening the range of acceptable physical parameters.

    We have learned that material destined for solid formulation work fares better with a defined particle size range. Customers working in analytical method development need a consistent reference compound for calibration and validation. Sometimes the needs go beyond simple chemical specification sheets. We have supported quality control labs by helping them trace an unexpected impurity spike back to raw material changes, not contamination. Experience in the nuts and bolts of synthesis helps resolve such issues quickly.

    Some research partners rely on the material for in vitro activity profiling. They need a compound free from excess salts or colored residues, since even the faintest contaminants may obscure light-based readouts. Years on the manufacturing side prompt us to monitor not only for conventional purity but also for UV-active impurities. From our perspective, the best test of readiness for sensitive bioassays is a track record—real researchers running our material through their panels and coming back for more.

    Real-World Differences from Similar Products

    From experience, the hydrochloride salt form of this molecule offers much better stability for storage and transport compared to the free base. We have seen requests for the base form, but shipping under humid conditions prompts rapid degradation. Hydrochloride versions minimize that risk, preserving both purity and analytical consistency even over months in unrefrigerated environments.

    Compared to closely related analogs, the placement of the hydroxyphenyl group and protection of the secondary amine leads to changes in solubility and reactivity. Over time, customers have favored this specific structure because it brings a certain degree of aqueous solubility—a trait that streamlines analytical and formulation work. Where alternative intermediates from other manufacturers showed fluctuating solubility or batch inconsistencies, our process delivers precisely what formulation chemists have requested.

    During method troubleshooting, partners have flagged differences as small as trace residual solvents or shifts in melting point. For us, small deviations often signal a deeper issue in the process rather than an isolated occurrence. That’s why our team tracks both batch trends and one-off anomalies—not just passing or failing material against a spec, but understanding every inflection in the data. With so many steps in the synthesis, each possible impurity has an origin, whether from raw materials or handling, and we work to address those sources directly.

    Particular attention goes to the stereochemistry. Our process generates the racemate, not the single enantiomer, as this generally fits most early-phase research needs. Some labs target single-enantiomer synthesis further downstream, but the racemic material offers greater accessibility for screening studies. Over the years, we’ve guided customers who were unsure which isomer to use through the reasoning for choosing one over the other for initial R&D assays. Keeping both flexibility and clarity saves everyone time and avoids costly reformulation efforts later.

    Challenges and Solutions from the Manufacturing Front

    Producing this compound, especially at scale, doesn’t follow a simple recipe. Each year presents its own set of hurdles. For example, minor fluctuations in raw material quality can lead to subtle shifts in impurity profiles—something that would escape notice in gram-scale work, but sticks out as soon as a batch tips into kilogram territory. Our team spends significant time prequalifying suppliers for phenols, amines, and acid reagents. Even once a seemingly identical substitute at the chemical level hits the plant, it might carry micro-impurities that standard COAs won’t list. Regular supplier audits and deep-dive analytical comparisons keep consistency high.

    Handling the hydrochloride salt presents its own operational quirks. In our climate, ambient humidity varies with the seasons, making efficient drying a moving target. Operators swap notes on which drying schedules yield the ideal fine powder, rather than a cake that resists grinding. Every small change here ripples downstream, affecting how well the material dispenses and how readily it dissolves at the user’s end. Such insights rarely get much attention but make all the difference during scale-up or automated processing.

    Safety never stays static. As incident reports have taught us, static electricity and dusting in the drying and milling stages add an extra layer of risk—especially with phenol derivatives. Our plant grounds all equipment religiously, uses enclosed transfer systems, and monitors for airborne particulates. The protocols reflect more than compliance; they stem from real incidents on the floor. When an operator caught a small dust cloud during a filter bag change years ago, it led to a full review of our dust collection strategy. Operational history shapes safety as much as any written manual.

    Continuous Feedback Loop with End Users

    Direct communication with researchers and formulation teams shapes our product as much as any internal SOP. With so many projects underway, we make time to listen to every new request—be it for a tweaked particle size, alternative packaging, a tailored stabilization protocol, or a shift in documentation details. What seems like a minor request from an R&D chemist can trigger months of testing and process adjustment inside our plant. The result most often pays off in smoother downstream workflows for everyone.

    We have worked with firms who sought transition from lab-scale synthesis to commercial production for the compound. Many learned the hard way that scaling up a reaction on paper doesn’t always match reality: stir rates, heat transfer, impurity cleanup, and isolation all require iterative tweaks. Our process team works alongside the customer’s technical group, sometimes bringing in teams from both sides to walk through every step together. Face-to-face troubleshooting reveals solutions quickly—sometimes as simple as adjusting solvent ratios, sometimes as advanced as overhauling equipment.

    Every long-term user becomes a partner in improvement. Some have identified new impurity peaks at incredibly low detection thresholds—alerts that prompt us to expand analytical panels for future batches. We share findings for the benefit of all partners. Once, an issue flagged by a European lab led to us discovering a low-level photo-oxidation pathway, and we changed our storage recommendations for everyone thereafter.

    Sustainability and Responsibility in Production

    Contemporary expectations for chemical manufacturing go beyond just quality and cost. These days, regulatory pressures, customer values, and our own principles converge on the goal of safer, less wasteful production. Over the last several years, we have reduced solvent waste by recycling streams where possible and improved our reaction yields by running frequent in-process analyses. Doing so helps shrink both costs and environmental footprint.

    Wastewater from phenol and amine syntheses carries regulatory scrutiny, especially in jurisdictions with tight environmental limits. Investing in more advanced treatment systems paid measurable dividends—not only meeting compliance but also reassuring customers who share environmental concerns. Our plant’s regular investment in worker training, equipment updates, and greener alternatives comes from a belief that safety and stewardship never finish evolving.

    Packaging protocols also matter, especially for sensitive hydrochloride salts. We use lined, sealed drums designed to minimize exposure and absorb any trace moisture before it can permeate the product. Experienced warehouse staff handle everything from repacking to custom labeling, which limits the risk of cross-contamination with other compounds—a recurring pain point among customers who have received subpar material from less careful suppliers in the past. Cleanliness and documentation go hand-in-hand, and our team reviews all procedures regularly.

    Transparency, Traceability, and Trust

    Experience has shown us that trust builds in layers. Every lot sent from our facility carries not only standard certificates of analysis but also a process summary available for every regular customer who requests it. Researchers move faster with full insight into each lot’s process lineage and quality control data. Sometimes this means sharing chromatograms and spectra, other times it involves a conference call to walk through how a specific lot was handled from reaction to packaging. The feedback has shaped how we document our own production runs, improving the clarity and usability of provided information.

    From the start, our team recognized that gaps in documentation or unexplained deviations can stall projects and erode confidence. Track record counts. We keep deep historical records, so if a deviation or question arises, we can pinpoint a root cause quickly. Customers have flagged small discrepancies in molecular weight or melting point before—a sign of alert partners who keep us sharp. Every such exchange informs not only the next batch but also how we communicate outwards.

    Years of transparent interactions have led repeat users to rely more heavily on our recommendations, even when switching to new applications or considering alternative batch sizes. Clear communication about what our process can and cannot deliver keeps expectations realistic and reduces mismatches later on. Every lot, every discussion, every shipment: all are part of a larger commitment to reliability and openness.

    The Value of In-House, Experience-Driven Manufacturing

    Supplying (+/-)-4-[2-[[3-(4-Hydroxyphenyl)-1-Methylpropyl]Amino]-1-Hydroxyethyl]Phenol Hydrochloride isn’t just about following a synthetic route by rote. Our engineers, operators, and analysts stand behind every specification, every sample. They have reviewed near-misses and process improvements, riding the ups and downs of market demand and regulatory change. They know that questions from end users often reflect real, operational concerns that deserve more than a generic reply.

    Our roots in chemical manufacturing shape how we respond to each challenge. Whether it’s a big project preparing a custom kilo-scale lot or troubleshooting a novel analytical finding for a client, years on the production floor make all the difference. Our team knows from experience where bottlenecks hide, which parameters drive purity or stability, why a drying change matters to a downstream analyst or formulation scientist—and where to keep looking for the smallest improvements. We don’t just make molecules; we forge partnerships in the details and deliver everyday reliability in every bag or drum.

    Final Thoughts from the Plant Floor

    Every batch of this compound rolling off our lines carries more than just chemical value. Behind those bags, vials, or drums stands a tight-knit crew who have learned from each cycle, responded to changing needs, and invested in every incremental process upgrade that keeps our product ahead of demand. As a manufacturer, we see firsthand how the right tweak in the synthesis bottleneck, or a shift in drying and packaging, helps researchers do their best work. We look forward to new collaborations, new technical challenges, and more hard-earned lessons—each one feeding back into a compound that serves not just industry standards but the real-world needs of today’s scientists and technologists.