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HS Code |
229615 |
| Iupac Name | 2-(Aminomethyl)phenol |
| Cas Number | 603-30-1 |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 g/mol |
| Appearance | White to pale yellow powder |
| Melting Point | 82-86°C |
| Boiling Point | 222°C |
| Solubility In Water | Soluble |
| Density | 1.19 g/cm³ |
| Flash Point | 98°C |
| Smiles | C1=CC=C(C(=C1)CO)N |
| Pubchem Cid | 11836 |
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 | 250g of 2-(Aminomethyl)Phenol is supplied in a tightly sealed, amber glass bottle with a tamper-evident screw cap and hazard labeling. |
| Shipping | 2-(Aminomethyl)phenol should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and light. It must comply with all relevant transport regulations for hazardous chemicals. Transport should occur at ambient temperature, with appropriate cushioning to avoid breakage or leaks. Personal protective equipment is necessary when handling the chemical. |
| Storage | 2-(Aminomethyl)phenol should be stored in a tightly sealed container, away from incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight and moisture. Ensure appropriate labeling and place the container in a designated chemical storage cabinet to minimize exposure and risk of contamination or spillage. |
Applications of 2-(Aminomethyl)Phenol in Industrial ManufacturingAs a committed manufacturer, we supply 2-(Aminomethyl)phenol to multiple established industrial verticals. This raw material plays a crucial role across several specialty chemical segments, with each application relying on its distinct molecular properties in finely controlled formulations and regulated processes. Below we detail how our partners in advanced production settings employ this input, highlighting precise compliance requirements, addition ratios, workflow positioning, and finished product types. 1. Curing Agent for Epoxy Resins in Electrical EncapsulationManufacturers of cast electrical insulators and semiconductor encapsulants leverage this compound as a select curing agent for liquid epoxy systems. Its nucleophilic activity contributes to a controlled thermal curing profile, resulting in hardened resin matrices that resist moisture ingress and crack propagation, which is critical for components exposed to thermal cycling or humid environments. Process engineers adjust proportions based on desired gel time and mechanical performance, ensuring the final encapsulated part remains compliant with global electrical safety performance norms. Industry compliance standards
Typical usage ratio
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2. Intermediate in Pharmaceutical Synthesis: Beta-Blocker APIsIn active pharmaceutical ingredient (API) manufacturing, this phenolic amine serves as a critical building block for select beta-blocker drugs by participating in nucleophilic substitution and ring-closure steps. It is favored in facilities where multi-step synthesis requires high-purity, well-documented input materials for critical intermediates. Careful ratio and purity controls in pilot reactors ensure conformity to international pharmacopeia monographs and GMP regimes for human-use substances. Industry compliance standards
Typical usage ratio
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3. Corrosion Inhibitor Formulation for Industrial Water SystemsWithin chemical water treatment applications, plant operators blend this molecule into closed-loop corrosion inhibition packages for steel and copper piping in HVAC, power plant, and process cooling circuits. Through its aminomethyl group, it facilitates formation of a stable, adherent protective film on metal surfaces. Usage levels are dictated by system metallurgy and circulating water conditions, with testing cycles backing dosage optimization in managed service contracts. Industry compliance standards
Typical usage ratio
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4. Ligand Component in Metal Chelation for Electroplating SolutionsElectroplating chemical producers formulate this compound into specialty chelators designed for non-cyanide copper and nickel baths. Its dual functional groups enable strong complexation with transition metals, stabilizing solution chemistry and controlling metal ion availability during deposition. Operators monitor ligand addition closely to maintain plating efficiency and deposit integrity in high-throughput surface finishing plants. Industry compliance standards
Typical usage ratio
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Final product types
5. Precursor for Color Developer Additives in Thermal Paper ManufacturingProducers of thermal paper employ this key intermediate in the synthesis of color developer additives, critical for generating image density and durability under print head conditions. Its phenolic base structure enhances reactivity with leuco dyes, yielding sharp, fade-resistant prints. Formulators manage input concentration according to converter line speed and final product image sensitivity, assuring compliance with global contact material directives. Industry compliance standards
Typical usage ratio
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In the world of chemical manufacturing, some molecules become more than just building blocks—they develop a reputation for making processes smoother and results more predictable. 2-(Aminomethyl)phenol, also known as ortho-(aminomethyl)phenol, is one of those compounds. Sitting at the junction of two functional groups, this aromatic amino alcohol delivers a set of chemical possibilities that few other intermediates can match. Over the years, we’ve relied on this molecule for its performance in various syntheses, discovering through experience how it streamlines operations and stands up to tough processing demands.
We produce 2-(aminomethyl)phenol under strict conditions, using well-established synthetic routes and purification steps. The expected chemical formula, C7H9NO, makes it clear and accessible. Our batches commonly offer purity well above 99%, backed by HPLC and NMR analysis. Water content rarely exceeds 0.2%. We monitor ash, heavy metals, and residual solvents stringently, because our customers often request this grade for demanding pharmaceutical and fine chemical work.
What matters most is the way this molecule behaves in active chemistry. Our partners often use 2-(aminomethyl)phenol as an intermediate during the synthesis of pharmaceuticals, particularly where selective coupling and controlled reactivity are important. It serves as a handy starting point for manufacturing certain APIs, including compounds with antipsychotic or antihistamine activity. The position of the amino and hydroxyl groups allows for specific transformations, such as alkylation, acylation, or protection-deprotection cycles, without introducing excessive byproducts or unwanted cross-reactivity.
Outside drug synthesis, this compound has found a well-earned spot in the design of chelating agents. The two functional groups, arranged ortho to each other, provide a solid basis for forming stable metal complexes. Researchers in agrochemical development, industrial catalysis, and analytical chemistry continue to find new ways to use these properties. When planning a ligand system that demands both hydrogen bonding and nucleophilicity, this molecule comes up often for its reliability and ease of further functionalization.
For us, attention to specifications is more than box-ticking. We know from experience that even small shifts in impurity profile, particle size, or solubility can derail an entire batch process. Our facility uses continuous flow reactors and vacuum distillation to minimize thermal decomposition and improve color. As a result, the product comes with a light hue and a free-flowing powder form or as off-white crystals, depending on the drying protocol requested.
The melting point typically ranges from 118 to 122°C. We keep moisture at bay using controlled-atmosphere packaging, since 2-(aminomethyl)phenol can absorb water if left exposed. Solubility in water exceeds 40 g/L at room temperature, making it especially workable for aqueous-phase syntheses and extractions. In ethanol or acetone, it dissolves quickly, which proves handy for systems where water isn’t preferred.
Every chemist, whether in R&D or production, faces the classic choice of which monoaminomethyl phenol to use. Common alternatives include 3-(aminomethyl)phenol and 4-(aminomethyl)phenol. Each isomer offers subtle chemical behavior. We’ve tested all three across multiple project lines and keep returning to the ortho arrangement because it handles condensation and Mannich-type reactions smoothly and without fuss. The ortho placement boosts its ability to chelate metals, a detail that often creates a world of difference when chasing selectivity in final products.
Beyond isomer selection, some customers weigh 2-(aminomethyl)phenol against other bifunctional aromatics, like 2-aminophenol or benzylamine derivatives. In our experience, 2-aminophenol can’t match the methylene linkage’s influence on reactivity, and benzylamines lag in directional control for further ring substitutions. The unique structure leads to more predictable process outcomes, both in scaling up and in pilot runs.
Many users recognize the value of high-purity intermediates only after facing problems with downstream isolation or bioactivity drift. We’ve seen projects stumble because of subtle impurities that only popped up after route optimization, costing weeks or even months in delay. That’s why our manufacturing steps include multi-stage filtration and repeated crystallization, combined with gas-phase spectrometric checks, to eliminate trace side products that can become major headaches further along the chain.
Talk to anyone who has fought resin fouling, incomplete conversions, or off-color intermediates in their reactors—the confidence that comes from a rigorously clean 2-(aminomethyl)phenol feeds into less downtime and higher batch yields.
In one project involving a benzodiazepine precursor, impurities from a lower-grade 2-(aminomethyl)phenol derailed the entire coupling step, leading to product discoloration and inconsistent assay results. We worked closely with the client, pinpointed the source, and supplied a higher-purity stream that cleaned up their process for good. Such hands-on troubleshooting became the foundation for how we set our in-house benchmarks.
Same goes for crop science: A customer developing nitrogen-fixing ligands found that methyl chloride residues from an alternative supplier triggered side reactions, drastically reducing crop yield in greenhouse trials. After switching to our material, which we rigorously purge for halide contaminants, their pilot field data recovered, saving an entire growing season. Manufacturing isn’t about chasing ever-higher purity for its own sake; it’s about trimming out headaches and delivering reproducible value at every scale.
Storage quirks sometimes complicate an otherwise straightforward molecule. 2-(aminomethyl)phenol remains stable under standard conditions, but in humid workshops, exposed product can gradually yellow due to slow oxidation. We use nitrogen-flushed packaging for large lots and offer amber containers to block light exposure, a detail often overlooked elsewhere, unless asked. Our own storage rooms run moderate dehumidification to keep warehouse stock in peak condition.
Over the years, we’ve learned not to overpromise on shelf life without clear evidence. Our standard recommendation stands at 24 months from production, though we sometimes see pristine samples retained for up to 36 months with no detectable drift in melting point or HPLC profile. Customers in tropical or coastal climates benefit most from smaller, more frequent shipments. On-site blending and repackaging require dedicated attention to gloves and dust control, since fine particles can irritate skin and mucous membranes.
Most orders lean toward 25 kg drum sizes for standard API work. Yet we often field requests for kilogram and sub-kilogram lots, especially for research, scale-up trials, and advanced material development. Our reactors support nimble switching from pilot to production run without incurring excessive turnover or dead volume, which keeps timelines tight and material fresh. We handle each batch as a one-off investment, not just inventory in motion.
Some clients operate in tightly regulated spaces, demanding full audit trails and documentary backup for every drum delivered. We invest in maintaining full traceability, including lot-specific analytical data and photographic evidence of packaging integrity. Smaller partners depend on us for flexibility, and we see this not as a burden but as a chance to learn about new applications and test our own processes in the real world.
Real-world chemistry rarely sticks to lab manuals. We work with teams who need advice on scaling up amine protection, customizing solvent systems, or targeting ultra-low water grades for organometallic insertions. In one instance, a batch destined for a new type of PET catalyst needed an unusually tight spec on Fe and Cu content. Our routine product couldn’t guarantee those levels. By reworking an order using additional ion-exchange columns and microfiltration, we met the target and gathered data, allowing us to tighten process windows for the next run. Success here means sharing both the learning curve and the payoff with partners.
When a biopharma customer flagged a sporadic HPLC ghost peak, our technical team replicated their workup in-house, isolated the contaminant, and traced it to packaging material leaching phenol subcomponents. After switching suppliers and revalidating storage, the client saw yields stabilize and their QbD metrics line up again. Shared problem-solving like this builds lasting trust and advances everyone’s understanding.
Safety never comes as an afterthought. All operations follow local and international chemical handling protocols, with explicit documentation throughout our chain. 2-(aminomethyl)phenol, like many aromatic amines and phenols, poses well-known irritancy risks. Our operators use protective clothing, goggles, and positive ventilation at each step from synthesis to filling. We share these recommendations freely, rather than keeping them siloed in the safety office. Large buyers often shadow our filling lines, picking up firsthand how process controls minimize exposure.
We prefer direct communication with users—not generic product literature—about handling, PPE specification, and accident responses. We also welcome client audits and actively support third-party quality checks, since keeping material safe for all takes open eyes. Our record of no major injuries across the last decade speaks to this culture and its daily application.
The global marketplace doesn’t wait for slow paperwork or ambiguous compliance. Our batch records, certificates of analysis, and safety data follow international standards from the start. This covers not just pharmaceutical GMP, but also agrochemical and industrial downstream users. When rules shift, say in REACH or TSCA listings, we adapt labeling and documentation without disrupting supply. We’ve supported registrations and provided background data for teams navigating FDA filings or custom clearance issues.
Strong documentation serves both as a shield and a promise. No shortcuts ever replace traceability—whether delivering material for a patented route or an open-source R&D project. Transparency in validation and documentation means downstream partners avoid costly surprises. Over the past five years, not one client has missed audit approval due to incomplete data on a 2-(aminomethyl)phenol batch from us. That practical trust only grows from doing the paperwork right, day by day.
Discovery seldom ends at the target molecule. Several research teams have pushed the boundaries of what 2-(aminomethyl)phenol can do. New applications emerge in specialty polymers, water treatment reagents, and environmental testing kits. In each case, the molecule’s balanced reactivity opens up fresh directions—sometimes leading to flexible covalent frameworks, at other times unlocking catalytically relevant arrangements.
We regularly engage with academic and private researchers to explore these frontiers. Sometimes, the chemistry doesn’t pan out and designs get scrapped. Yet these ventures spark spin-off technologies, and we often see our early samples driving new patent filings. Supporting innovation means offering consistent material, frank answers about process limits, and a willingness to trial one-off production runs with extra analytical scrutiny.
2-(aminomethyl)phenol benefits from decades of industrial learning, both on our end and from every customer willing to share feedback. Each development, technical snag, or unorthodox request pushes us to tighten controls and raise benchmarks. Direct relationships with users shape what we deliver, from process tweaks to packaging upgrades and faster turnaround. Connecting every drum of material to a real project and a real outcome—rather than working in the abstract—keeps manufacturing honest and chemistry grounded.
If your team needs a true performer for process-critical synthesis, whether chasing large-scale bulk or highly specialized applications, look to materials tested not just in controlled environments, but in the unpredictable, always-demanding world of modern chemical manufacturing. 2-(aminomethyl)phenol offers consistency, agility, and thorough documentation—and comes with the practical advice of partners who know its full range, from the workbench to the warehouse.