|
HS Code |
137880 |
| Iupac Name | 2-(Hydroxymethyl)-4-(1-hydroxy-2-{[6-(4-phenylbutoxy)hexyl]amino}ethyl)phenol |
| Molecular Formula | C25H37NO4 |
| Molecular Weight | 415.57 g/mol |
| Cas Number | 115293-23-3 |
| Appearance | White to off-white solid |
| Solubility | Soluble in DMSO; low solubility in water |
| Storage Temperature | Store at -20°C |
| Purity | Typically ≥98% (HPLC) |
| Synonyms | 4'-Hydroxypropranolol derivative |
| Functional Groups | Phenol, alcohol, amine, ether |
| Chemical Category | Phenol derivative |
| Smiles | c1ccc(cc1)CCCCOCCCCCCNCC(O)c2ccc(CO)cc2O |
As an accredited 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 500 mg of 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)hexyl]amino}ethyl)phenol with tamper-evident cap. |
| Shipping | This chemical, 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol, is shipped in tightly sealed containers, protected from light and moisture. It is packed according to industry standards for hazardous chemicals, with labeling for safe handling and storage. Transportation follows all relevant regulatory guidelines to ensure safety and product integrity. |
| Storage | Store **2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)hexyl]amino}ethyl)phenol** in a tightly sealed container, protected from light and moisture. Keep at 2-8°C in a well-ventilated, dry area away from incompatible substances such as strong oxidizing agents. Handle under an inert atmosphere if possible, and use appropriate personal protective equipment to avoid direct contact or inhalation. |
Competitive 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol stands as one of those compounds that catches a chemist's eye for both structural uniqueness and application range. From development in our plant’s R&D benches straight to drums that leave our doors, every batch tells a story about synthetic consistency meeting unexpected real-world needs. This molecule’s backbone, an aromatic ring capped by a hydroxymethyl and phenolic group, with extended hydroxy-alkyl and phenylbutoxy side chains, opens uncommon routes in formulation work across several industries.
Unlike some simple phenolic resins or basic aminophenols on the market, this compound leverages its hybrid structure to build bridges between solubility, reactivity, and compatibility needs. The aromatic base gives thermal and chemical stability, while the hydroxy side groups support interactive hydrogen bonding. The bulky side chain, featuring the phenylbutoxy-hexylamino extension, stands as more than a structural feature — it directly impacts how users see wetting, emulsification, and solubility in both water-based and organic systems.
Producing this molecule has always challenged our synthesis team. Maintaining step-to-step control, from the initial ring substitution reactions to the final purification, demands deep process understanding. Small temperature swings during alkylation and hydroxy modification bring visible differences in yield, so we stick to constant in-line monitoring and frequent hands-on verification. Over time, our process chemists streamlined routes to keep down byproducts while optimizing throughput, and regular feedback from end users keeps us tuned in to performance gaps and possible improvements.
On the usage front, formulators reach for 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol mainly for two reasons: targeted reactivity and performance under practical conditions. In coatings and specialty polymer sectors, it often acts as a functional modifier, lending flexibility or improved adhesive properties. Comparative tests in polymer chains show how the combination of hydrophilic and hydrophobic zones in this molecule can control compatibility not just with the main resin but also with the various plasticizers, pigments, and cross-linkers. Besides that, the pharmaceutical and fine chemical sectors have explored it as an intermediate, especially when dealing with compounds requiring both aromatic stability and functional group diversity.
In our own practice, we've noticed end users often care less about abstract purity numbers and more about how the material behaves batch-to-batch. We supply this chemical under our standard production code with a purity above 98.5 percent by HPLC, limiting moisture and volatiles as much as our plant can handle in routine runs. Granular consistency, free-flowing powder, or even slightly sticky off-white solid — the exact form shifts with ambient humidity and storage, so we advise customers to store it dry and sealed. Some users with strict solubility or reactivity requirements ask for narrower impurity profiles, and we typically take up special campaigns for such requests, adjusting workup steps and solvent washes as needed.
One point often overlooked in wider industry write-ups: trace catalyst residues and process-derived ions can matter a lot, depending on end-use. Through our years refining the process, we've gradually cut those down, using extra ion-exchange steps when process feedback warrants. In the end, the real quality difference often shows up further down a customer’s process, and direct feedback from their own QC labs feeds back into our plant’s adjustments.
From a long-term manufacturing view, 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol does not exist alone in its class. Buyers can often choose among simpler aminophenols, or much bulkier specialty resin intermediates, depending on the job. What sets this molecule apart in everyday shop-floor terms is its dual solubility character and the way it can modify interfacial behavior in multi-phase systems. Unlike short-chain phenol derivatives that dissolve quickly but lack anchoring power, or unwieldy polymers that struggle with processability, this product hits a middle ground. It disperses well in a wide range of solvents, and its structure can bridge oils and water-loving components.
During pilot trials at one polymer additives customer, our product outperformed several older aminophenols in binder flexibility and pigment stabilization — the molecule’s hydrophobic chain seemed to keep pigment particles suspended longer than shorter analogues. Colleagues from industrial coatings noted increased resistance to yellowing under accelerated aging. Those kinds of differences matter more than spec sheet numbers, and repeat users come back for both the performance and our willingness to troubleshoot at the process level.
Within our own labs and customer sites, formulation staff regularly wrestle with balancing reactivity and stability, especially in multi-component systems. This chemical gives them a handle for both. If you’re dealing with polyester-urethane systems, for example, the hydroxy side groups allow for controlled crosslinking, but without the runaway gelling seen with low-molecular-weight triols or diols. The bulky side chain helps keep blends stable during processing, even under heat.
Medicinal chemists sometimes use the molecule as a starting point for advanced intermediates because the chain flexibility supports functionalization at several positions. Here, selectivity in reaction steps matters, and our process improvement teams continually refine purification to offer reliable input with consistent impurity profile. We keep in close touch with client process teams since even small variant impurities can shift downstream synthesis yields.
Cosmetic and detergent formulators show interest due to both the phenolic antioxidant aspect and the way that the phenylbutoxy tail offers mild surfactant properties. They often seek a balance between performance and regulatory compliance (such as low residual metals or allergen potential), so our process documentation focuses on traceability from raw materials all the way to finished goods.
In today’s market, more buyers look beyond classical specs and dig into sustainability, safety, and transparency across the whole production chain. We’ve fielded increasing requests for lifecycle data and environmental impact details. While the molecule itself is not inherently classified as dangerous under most current regulatory schemes, the routes to make it sometimes employ substances monitored for workplace safety. From our experience, every improvement in purification not only tightens specs but can help us minimize secondary process wastes — less need for neutralization steps, less solid residue, less off-gassing.
We often get involved in customer audits and supply chain documentation reviews. Our internal controls now track solvent recovery and catalyst re-use rates as a matter of course, since many clients want to see how our process avoids unnecessary waste or VOC releases. By investing incrementally in closed-process steps and pre-purification of starting materials, we cut down risk of persistent impurities that can travel with the product or appear in downstream waste streams.
For users needing compliance with specific regulatory standards, such as REACH, GHS, or even regional green certification, open dialogue helps both sides. We share processing documentation, help set up dedicated production windows for custom grades, and keep up with shifting compliance documents and labeling rules. It's a two-way street: users need our expertise in molecule handling, we get customer feedback on desired documentation or data transparency.
The chemical world knows cycles of tight supply. Sudden shifts in raw material prices or logistics disruptions can affect even the best-planned production campaigns. In years past, we've seen demand for this product spike in response to regulatory changes for alternative additives, or dips when new processes phased it out. There’s no substitute for having deep bench stock, clear supplier relationships for key precursors, and a workforce familiar with adapting batch sizes up or down.
Direct manufacturing experience teaches that buyers care less about “theoretical” plant capacity than about sustained, predictable delivery. We stagger production runs to maintain rolling inventory and give ourselves a buffer against supply shocks. Our logistics staff watch not only chemical markets, but also weather, ports, and regulatory news, since any of these can cause sudden delays. Repeat customers trust our flexibility — we’ve expedited shipments, split orders, and found creative options for short-term warehousing on client request. Physical product integrity remains a focus, too; double-bagged drums, lined containers, and clear labeling help minimize confusion when a load reaches a busy loading dock far from our own plant.
We do not approach synthesis or quality control as static challenges. Our QC lab works directly with feedback loops from customer results, not just in-house assay sheets. A client running high-throughput polymerizations reported unexpected gelling at a lower temperature range; our team took that back to our process engineers, who re-examined trace side product levels in drying and adjusted vacuum settings accordingly. Another client’s batch blending had issues with haze; collaborative investigation tracked it down to minor iron pickup from old process lines, which we replaced on our own dime.
This sort of iterative work changes the actual product as experienced on shop floors, in pilot plants, and eventually in market-ready goods. Most spec sheets never capture this level of process nuance, but as a manufacturer, we see it in the daily choices for feedstock source, operator training, and analytical method updates. This compound’s end users benefit when the manufacturer stays agile and technically responsive. Our own profit margin, capacity utilization, and technical reputation follow directly from that attitude.
Years of supplying to different sectors gives us a blend of detailed feedback and fresh challenges. Some formulation chemists want higher flowability for fast-dosing lines, so we've worked on particle size control in our drying and milling steps. Others need better performance in water-based systems, which has led us to investigate small tweaks in molecular architecture — sometimes even running custom pilot lots for R&D partners willing to co-invest in the improvement.
Customers working in electronics coatings tend toward high purity and ultra-trace metal control. That meant building new cleaning and filtration regimens in our plant, with special analytical runs on ICP-MS. Bulk commodity users, on the other hand, often want steady delivery and consistent reactivity in blends — here, process optimization for throughput without sacrificing spec remains our main focus.
We find that regular in-person or virtual meetings with technical end users turn up new ideas on both sides, whether it’s a better packaging format, split lot documentation, or faster response windows during supply chain crunches. The product may remain chemically defined, but the way it serves end users keeps evolving. We measure our success by repeat demand and technical troubleshooting solved, not by abstract specifications.
Most customers recognize the balance between the molecule’s reactivity and stability, but issues can still arise in scale-up or formulation. In cold weather, we’ve seen crystallization slow down dissolution, so we started offering technical notes on in-process warm-up steps and anti-static handling. For those working in high-shear mixing regimes, we've studied dusting risk and static pickup, adjusting our drying and screening steps to address it.
Some users working in sensitive downstream reactions had runs affected by sub-percent impurity fluctuations, typically from trivial changes in our own purification media. It’s in these troubleshooting moments that the difference between a generic supplier and a hands-on manufacturer becomes obvious. We keep all lab batch records tied to each bulk shipment and have sent field technical staff to customer plants on several occasions to help nail down issues that might at first seem trivial.
We also attend regulatory or technical conferences not just to market our goods, but to sit in on technical case studies where users have applied or formulated with our product. Direct, even sometimes blunt, Q&A with real users drives practical adjustments in the plant. A new client in the adhesives sector needed improved shelf-life consistency, so we modified our routine moisture checks.
Looking ahead, there is always pressure to squeeze out waste, boost batch throughput, and respond to shifting market demands. Market shifts may open up fresh uses — especially as environmental and synthetic chemistry priorities move toward greener, more selective, and traceable inputs. We have ongoing projects to refine the synthetic route to this molecule, including using more recyclable solvents, lower-pressure catalytic steps, and continuous flow reactors for some tricky transformations.
While some competitors talk a good game on “innovation,” our process improvement always starts with specifics: what’s not working in a client’s blender or reactor, and how can plant chemistry adapt? We invest in tooling, not just analytic paperwork. Everything from improved PPE for our operators to next-gen LIMS for end-to-end batch traceability flows into continuous quality upgrades. No chemical product subsists on initial process alone; the winners emerge from day-in, day-out troubleshooting and real-world learning.
As the applications for 2-(Hydroxymethyl)-4-(1-Hydroxy-2-{[6-(4-Phenylbutoxy)Hexyl]Amino}Ethyl)Phenol continue to evolve, both with regulatory frameworks and the practical demands of its users, our adaptation follows their lead. Whether for high-spec intermediates, specialty polymer blends, or new emerging uses, the experience at the plant level defines both the offering and the ongoing refinement, setting the compound apart not simply by a catalog description but by its record of successful integration in demanding industrial contexts.