|
HS Code |
481634 |
| Iupac Name | 4-[(2S)-2-Amino-3-Hydroxypropyl]phenol |
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.21 g/mol |
| Cas Number | 51-67-2 |
| Synonyms | Norepinephrine, Noradrenaline, 4-(2-Amino-1-hydroxyethyl)phenol |
| Appearance | White to off-white solid |
| Melting Point | 248-250 °C (decomposes) |
| Solubility In Water | Freely soluble |
| Smiles | C1=CC(=CC=C1C[C@@H](CO)N)O |
| Inchi | InChI=1S/C9H13NO2/c10-7(5-11)6-8-1-3-9(12)4-2-8/h1-4,7,11-12H,5-6,10H2/t7-/m0/s1 |
| Chirality | Contains one stereocenter at the 2-position (S-configuration) |
| Pka | 8.6 (phenol group) |
| Storage Temperature | Store at 2-8°C, protected from light |
| Ec Number | 200-204-7 |
As an accredited 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25 g amber glass bottle with tamper-evident seal, labeled "4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol, ≥98% purity, store cool, dry." |
| Shipping | The chemical 4-[(2S)-2-Amino-3-hydroxypropyl]phenol is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Handling follows standard safety procedures for organic compounds, including labeling and documentation in compliance with local and international regulations. Expedite shipping methods may be used for sensitive or perishable research-grade materials. |
| Storage | 4-[(2S)-2-Amino-3-hydroxypropyl]phenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Store at room temperature and ensure proper labeling. Avoid sources of ignition and excess heat. Follow all relevant safety guidelines and local regulations during storage. |
Competitive 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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As manufacturers with decades invested in research, synthesis, and scale-up, we view 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol as more than a raw material on a catalog page. It’s been a subject of careful process optimization, driven by the needs of our pharmaceutical and fine chemical partners. From our earliest days, the challenge has always centered on delivering reliable chemistry, and this compound’s pathway provided an ideal testbed for quality improvements and real risk reduction.
The unique character of 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol lies in its chirality and the interaction of its functional groups. We learned early that even small variations in the (S)-enantiomer’s proportion impact final product profile in downstream synthesis, especially for customers pushing the boundaries in drug discovery or specialty polymer modification. We built our manufacturing to consistently deliver a high (S)-isomer ratio, minimizing the ambiguous results that can slow research or create drift in batch records.
Over time, our analytical group worked shoulder-to-shoulder with production. The techniques they deployed — chiral HPLC, NMR and polarimetry — became routine, not academic. With each production run, we reinforce the integrity of every shipment. Customers have come to rely on that fingerprint of ours, knowing their processes won’t falter due to subtle inconsistencies that traders and resellers might miss.
Our process doesn’t scale up by simply multiplying batch size. Each new reactor volume invited a learning curve; ramping up from hundreds of grams in glassware to tens of kilograms. Those scale jumps highlight impurities and color metrics you might not see at smaller volume. This compound in particular put our purification design through its paces, forcing us to rethink filtration materials and crystallization conditions.
Some of our most successful collaborations started with a customer sample request for a model batch. We never viewed these as an inconvenience. Each batch, no matter the volume, undergoes the same technical scrutiny. Documenting each parameter — from water content to residual solvents, from melting behavior to enantiomeric excess — became expected. Years of customer feedback hammered home which specifications truly matter, pushing our median assay above 99%, ensuring moisture falls below 0.3%, and keeping oxidized by-products below trace detection. For our partners, those numbers aren’t empty targets. They mean fewer rejections, tighter process yields, and steadier output downstream.
In recent years, 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol has gained traction in both pharmaceutical intermediates and certain medical research fields. Scientists exploring neuroactive compounds or novel functional materials have relied on its high reactivity and its particular pattern of amine and phenolic groups. Unlike basic derivatives or unsubstituted phenols, this compound offers a specific three-point attachment for synthetic elaboration, often providing a springboard for exploratory medicinal chemistry.
We often listen to researchers complain about the tedious protection and deprotection steps customary with less advanced building blocks. Our product short-circuits some of that difficulty. The specific 3-hydroxypropyl side chain, along with the (S)-configured amino group, lets chemists build into complex side chains without sacrificing stereochemical purity. That’s an advantage not just in medicinal chemistry but also in the design of imaging agents, where chiral resolution post-synthesis can drain time and resources.
Producing 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol at significant scale has taught us humility. Early pilot campaigns revealed the instability of certain intermediates. We lost more than one batch to air oxidation and learned to adapt the workup to exclude oxygen, rather than hoping for the best. Our technical staff realized that controlling temperature deviations by just a few degrees influenced the minute impurity profile, and that color retention depended on the careful stepwise adjustment of pH.
No one outside the plant often sees the process pipeline — but customers benefit. We drive home the storage best practices, because our material remains less prone to color drift or loss of activity long term. Our decades of cumulative process knowledge get built into every drum or bottle leaving the site, so that quality doesn’t drop off after just a few months, particularly under varying climatic conditions.
We understand purity goes further than a single assay result. Our commitment means rigorous scrutiny during every stage. We look for low water content, monitor for process-derived by-products, and insist that no batch leave without verifying both chiral and chemical purity. In practical terms, that gives chemists at the next step confidence to trust the material’s behavior, reducing the likelihood of repeated screening or modified protocols during scale-up. For teams on a tight project timeline or grant funding, that reliability can make the difference between a successful or stalled research campaign.
Compared to other building blocks we've made, such as simple p-aminophenols or related hydroxyalkylphenols, this molecule occupies a more specialized space. Its simultaneous possession of both an amino group in the (S)-configuration and a hydroxypropyl moiety makes it attractively versatile, especially where selective reactions and advanced coupling methods are needed. It acts as an enabler for certain reactions, letting downstream chemists skip steps, cut costs, and minimize error-prone handling with chiral selectivity that's hard to retrofit.
Our more standard phenolic products tend to cater to bulk applications, dyes, or resins, where enantiopurity plays a secondary role. But this compound finds its natural home in critical pharmaceutical intermediates — places where each atom matters, and assays track more than just a main peak. We’ve supplied it for projects involving CNS-active molecules as well as for conjugates used in high-value diagnostics.
We know well that a promise on paper is meaningless without the muscle to back it up. Our deep vertical integration has minimized reliance on outside vendors for key raw materials, which over the years shielded many of our partners from supply shocks and price volatility. By owning our process from raw selection through final QC release, we've kept the timelines short and offered dependable planning for ongoing campaigns. Customers who’ve experienced delays or batch variations with traders and brokers recognize this as a differentiator.
Fluctuation in global logistics over the past years has taught us to build safety stock and to use robust packaging, not just chasing short-term gains but sustaining reputation. For a high-value item like 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol, avoiding cross-contamination and controlling temperature fluctuations have been non-negotiable, and we’ve invested heavily in upgraded facilities as a result.
One truth emerged after years spent fielding urgent phone calls and emails from labs in a bind: real troubleshooting doesn’t happen in isolation. Our technical team routinely consults on handling and use, taking calls directly from chemists at the bench, not just procurement offices. We share protocols proven to maintain optical purity or minimize side reactions, saving precious time downstream. Where a project faces a design-of-experiments bottleneck, we provide candid data from our archives, guiding partners over hurdles we know too well.
Not every supplier invests in this give-and-take. We have found it pays dividends in trust. Repeat collaborations with academic labs and industrial R&D centers have yielded both better chemistry and long-term partnerships. Over time, we’ve adapted our batch documents, safety records, and even packaging, based on real laboratory feedback, all to ensure smoother adoption and fewer surprises.
Responsibility means more than meeting a checklist. It sits at the root of our decision to limit residual solvents and transition away from certain hazardous catalysts, despite the challenges to cost and throughput. We invested in improved waste recovery, both for solvents and for phenolic mother liquors, not just to comply but to reassure both our clients and regulatory agencies.
Clients with tightening sustainability requirements appreciate these choices. Minimizing discharge, documenting compliance, and offering transparent batches not only improves trust, but meets the growing regulatory and reputational needs in pharma, biotech, and advanced manufacturing. We believe tomorrow’s chemistry must combine high quality with respect for both the bench and the broader environment.
Working directly with us, end users don’t just buy a bottle off a shelf — they access proven chemistry shaped by experience and by continual listening to the people who actually use the product. We remain ready to customize parameters where possible, or to dig into the root of a technical obstacle, because that’s where we’ve built our reputation. Most of our long-term partners stay for more than just consistent results — they value our ability to adapt processes and specifications as new challenges emerge.
Researchers drawing up a new synthetic route or an alternative analog design aren’t left in the dark. We routinely provide technical data and can run small pilot lots to help de-risk a scale-up. By prioritizing open communication, we’ve helped teams avoid the hidden expense of trial-and-error purification, reducing lost time and wasted material. Through every interaction, our goal remains to make the journey from raw material to finished molecule as predictable and safe as possible.
Many enter the market with closely related phenolic intermediates, yet miss the mark of what advanced research and production actually require. We’ve analyzed rival products from distributors and know from customer testimonials that subtle compositional drifts often go unnoticed — until a reaction stalls or a downstream test fails. Residual metal content, off-ratio enantiomers, or hidden hydrate levels — we’ve seen how small inconsistencies cause major headaches. Our direct control and in-house analytics give our customers transparency and assurance, batch after batch.
Off-the-shelf alternatives can't always match the tightly controlled (S)-enantiomeric content or the minimal by-product signature we routinely uphold. Where less controlled suppliers may face frequent product recalls or requalifications, our track record shows a system of prevention, driven by real-world demands rather than just regulatory minimums. This focus sets our product apart in settings where consistency, safety, and reliability matter most.
No plant, process, or team is ever finished learning. Our ongoing investments in equipment, staff training, and analytics stem from concrete customer challenges, not from abstract managers’ plans. By continuously seeking feedback and tracking the field’s evolving trends, we sharpen our offering year after year. For 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol, this approach means better materials show up in customer labs, on time, and ready for the tasks that push modern chemistry forward.
We take pride in seeing our product make an impact. Whether a new treatment platform, a diagnostic innovation, or simply a smoother full-scale process, each success for our partners reaffirms the quiet effort, deep technical care, and ongoing attention that our team brings to work every day.
As the needs of science and manufacturing evolve, we welcome every challenge as the next opportunity to advance our craft. Our hope is that every bottle of 4-[(2S)-2-Amino-3-Hydroxypropyl]Phenol we produce earns its place in your research and production, delivering the confidence and results you deserve.