|
HS Code |
458943 |
| Chemicalname | 2-(Aminomethyl)phenol |
| Casnumber | 603-34-9 |
| Molecularformula | C7H9NO |
| Molecularweight | 123.15 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 74-77°C |
| Boilingpoint | 275°C |
| Solubilityinwater | Moderate |
| Density | 1.18 g/cm³ |
| Pka | 9.36 (phenol), 9.62 (amino group) |
| Smiles | C1=CC=C(C(=C1)CN)O |
| Inchi | InChI=1S/C7H9NO/c8-5-6-3-1-2-4-7(6)9/h1-4,9H,5,8H2 |
As an accredited 2-(Aminomethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical 2-(Aminomethyl)phenol is supplied in a 100-gram amber glass bottle with a secure, tamper-evident screw cap. |
| Shipping | **2-(Aminomethyl)phenol** should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Ensure packaging complies with local and international regulations for chemicals. Label as hazardous, and handle with care to avoid spillage. Transport via approved carriers and provide safety data sheets with the shipment. |
| Storage | **2-(Aminomethyl)phenol** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use only non-sparking tools, and avoid dust formation. Proper labeling and secure shelving is essential to prevent spills or accidental mixing with other chemicals. |
Competitive 2-(Aminomethyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Working in chemical manufacturing brings a close perspective on how each molecule finds a place and purpose in the industrial world. Among our product offerings, 2-(Aminomethyl)Phenol often finds itself requested by research teams who need real reliability and purity. In the plant, we’ve seen this product go from a mystery on the batch list to a standard name in the workflow of specialty chemical synthesis, especially for custom intermediates and active building blocks.
We produce 2-(Aminomethyl)Phenol by direct routes that tighten each process stage, making sure that raw materials undergo vigilant monitoring and stepwise checks. Years on the production line taught us not just the technical recipe, but the importance of handling exothermic amination and unique phenolic ring substitutions with careful attention. Each run begins with nothing more than stainless reactors, clean solvents, and skilled technicians who track every shift in color, viscosity, and pH.
Production scale varies, but whether the order lands at a few kilograms for pilot projects or moves up to commercial lots, the material gets the same diligence at the filtration stage as at the charging of starting aromatics. A hands-on approach and batch-to-batch evaluation allow us to build up consistent lots that our partners recognize by smell, shine, and compliance data. The final product often appears as a crystalline solid, white to off-white, and moves through our final dryer with full attention to air flow, temperature, and possible residual solvent—a lesson learned early in production scale-up.
Chemists choose 2-(Aminomethyl)Phenol because they want a compound blending reactivity with tangible stability. With both amine and phenol functional groups, this molecule offers two reactive handles, which open up a spectrum of downstream options. We watch our product headed for projects in pharmaceuticals, from initial research through to pilot medicines, especially in the early rounds of synthetic route scouting. The double-reactive positions make forming new carbon-nitrogen bonds much more direct, and the phenolic hydroxyl works wonders as a point of further derivatization or for chelation in metal-complex formation.
As a team that’s produced this compound, we’ve had many conversations with formulators frustrated by less-active, over-protected aromatic building blocks. The accessible amine gives an edge for reductive amination schemes, and the hydroxy placement offers entry into etherification and esterification cycles you won’t see with plain aminophenols. It’s simple to see why project teams like this molecule for constructing more advanced intermediates that feed straight into active pharmaceutical ingredient work, agrochemical development, and advanced material science research.
Achieving high-purity 2-(Aminomethyl)Phenol never feels routine. We’ve built specifications starting with core purity, usually not below 98 percent by HPLC assay, because many customers run synthesis in sensitive settings where contaminants can stall an entire campaign. Over years of feedback and troubleshooting, we maintain strict residual solvent levels, as outlined in modern pharmacopeia, and emphasize minimal heavy-metal content. In the QC lab, analysts run a consistent program, comparing retention times, spectral fingerprints, and getting spectral confirmation by IR and NMR.
We often get special requests: some teams want a powder for easy weighing, others choose a granular form to reduce dust and loss. Our packaging line responds by modifying fill lines and delivery weights. Each run ends with clear labeling of lot code and packaging date, because traceability matters more than any abstract guarantee. More than once, product managers have called us looking to backtrack a batch origin, and our traceability logs have rescued collaborations headed for regulatory submission.
Many buyers arrive at this material after trying various aminophenols or benzylamines. We’ve compared lots of isomers and close relatives. The key is in the ortho-relationship: the amine sits right next to the phenolic group. This orientation brings remarkable differences in reactivity compared to para- or meta- relatives. Synthetic chemists see sharper nucleophilicity, and the position effect means certain couplings, like Schiff base formation, run much more cleanly.
Some companies source para-aminomethyl or meta variants, which shift the balance of their synthetic route, often needing higher catalyst loads or forcing agents for steps that run smoothly with ortho position. Our product’s structure makes condensation and cyclization reactions more feasible, saving precious time and reducing scale-up headaches.
In process development, that difference moves out of textbooks and into real savings. A customer once described how moving from an aliphatic amine to our 2-(Aminomethyl)Phenol trimmed two steps out of their synthetic sequence. They’ve since adjusted their plans for kilo-scale work. That type of application story happens often, especially when the compound lets downstream chemistry run under milder conditions.
We’ve seen many approaches to product drying and particle sizing. Customers sometimes express concern about phenolic sticking or solid caking during storage. By adjusting dryer temperature ramps and managing vacuum levels, we keep the free-flowing character intact. Inevitably, questions arise on moisture content. Regular Karl Fischer titration, carried out as a routine here, drops batch moisture well below one percent—an expectation we take seriously after years of managing moisture-sensitive downstream routes.
Stability remains a priority. 2-(Aminomethyl)Phenol stores best in amber glass or HDPE, out of direct sunlight, because prolonged UV exposure can promote discoloration or slow polymerization at the exposed functional groups. In our warehouse, palletized drums stay away from the traffic lane and forklifts; dust and exterior contamination bring issues no one wants. Chemical producers learn quickly that packaging and storage matter as much as any upstream process tweak.
Shipment arrangements keep the product in shape. Whether leaving packed in drums, bottles, or bags, we review logistic partners for their record with chemical shipments. Insulation against cold snaps or heat waves goes beyond a checklist, especially with valuable, high-purity lots.
Downstream, uses range widely. Researchers in pharmaceutical synthesis use this molecule as a starting point for β-blocker frameworks, anti-inflammatory agent construction, or as spacer units in advanced peptide modification. In the plant, we’ve seen it shipped off for macrocycle formation in new antibiotics. It’s also valuable as a precursor for ligands in metal-organic framework research, where the chelating power of neighboring amine and hydroxyl matters for stability and target uptake.
Industrial resin makers sometimes query us on phenol-amine condensation, searching for higher-performance resins or tailored cross-link density in specialty applications. We’ve seen formulators in specialty coatings order samples, testing for improved reactivity and film formation, using our several-kilogram lots in pilot coatings.
Agricultural chemistry sometimes calls for precise amine substitution patterns. Our ortho arrangement goes head-to-head with other aminophenols, often winning repeat orders where downstream reactions stalled using traditional alternatives. One story stands out—an agrochemical startup shared data showing faster field degradation profiles in test runs, thanks to easier, predictable downstream derivatization starting from our material.
Handling 2-(Aminomethyl)Phenol, especially in larger quantities, reminds us that chemical manufacturing is an active, tactile experience. Our plant workers wear well-fitted gloves and eye protection, since skin contact often brings redness due to phenolic functional groups. Over time, our safety program reinforced open ventilation and fume extraction at each weigh and charge station, especially during manual additions.
We maintain MSDS libraries for each lot, but it’s the daily operational check-ins and feedback from seasoned operators that prevent minor exposure events from escalating. That culture of vigilance means less downtime and a stronger record for both our team and downstream formulation labs.
Today, buyers and end-users expect trace documentation. That demand finds us investing in batch analytics and increasingly digital records. We log every incoming raw material source, batch mixing, reaction time, and post-processing parameter. Environmental, health, and safety checks shape these workflow steps, especially where new regulatory limits appear in key markets.
On the sustainability front, many in our team ask about energy load during production and about waste minimization. We’ve spent cycles testing alternative solvents and recycling lines, reducing overall VOC emissions during both reaction and cleaning steps. Steam traps and modern condensers recycle heat load, saving energy and lowering both cost and footprint.
Regulatory groups sometimes ask for deeper impurity analysis or for certification against listed substance registries. Our QC and compliance teams work with customers to pre-qualify lots and prepare information for global filings, especially for pharmaceutical and agricultural customers navigating evolving registration processes.
Every few months, a customer brings us a request for a new derivative or custom purification, often starting with 2-(Aminomethyl)Phenol as a core intermediate. Years of partnering with innovation teams taught us that dialogue beats assumption. We hold technical sessions and run trials together, scaling adjustments as synthesis shifts from flask to kilo tank. Customers appreciate real-world feedback, not marketing speak—practical insight on thermal ramp, expected yield profile, and cleaning techniques.
That communication extends through every handoff, from sales support to logistics planners, who detail pack-out times and all handling idiosyncrasies. We adjust production schedules to match project rollouts, understanding delays cause real cost hits in time-critical campaigns. Feedback comes full circle; chemists share data from their optimization, letting us refine drying, screening, or packaging for the next season’s run.
Several trends shape our product strategy. Demand from pharmaceutical and research firms moves in cycles, traced to drug discovery initiatives and regulatory shifts. We’ve monitored surges where 2-(Aminomethyl)Phenol plays a starring role in promising new molecules. Those times, output ramps and raw material stocks pivot quickly.
Materials science represents a slower but sustained market, where our customers investigate molecular electronics, specialty polymers, or rare catalysis paths requiring this aminomethylphenol core. Feedback from those sectors tends to focus on purity and unusual combination of functional groups for structural innovation.
With raw material markets becoming less predictable, we’ve prioritized securing multiple streams for aromatic feedstocks and take safety stock levels seriously. Tight relationships with raw suppliers, built over years, allow us to ride out hiccups rather than pausing production in the face of market swings.
With each batch run and customer request, our experience with 2-(Aminomethyl)Phenol has grown. Continuous direct feedback—whether it’s from a process engineer struggling with clogged transfer lines or a researcher chasing a higher-yield coupling—shapes how we refine, handle and respond.
Chemical manufacturing feels real and immediate, not theoretical. Our team’s familiarity with the nuances of 2-(Aminomethyl)Phenol translates to a material that meets performance expectations project after project. By addressing challenges in every aspect—from operational safety to reagent sensitivity, from material sourcing to storage optimization—we ensure our customers receive material that is ready, reliable, and suited for their next steps.
We believe depth comes from getting our hands dirty, listening to granular feedback, and tracking shifting market and regulatory demands. 2-(Aminomethyl)Phenol stands as a prime example of how fine chemical manufacturers can offer not just a product, but added value through partnership, technical integrity, and practicality gained from every batch produced.