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HS Code |
299443 |
| Name | 2-Methylphenethylamine |
| Iupac Name | 2-(2-Methylphenyl)ethan-1-amine |
| Cas Number | 3855-98-5 |
| Molecular Formula | C9H13N |
| Molar Mass | 135.21 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 223-225 °C |
| Melting Point | -7 °C |
| Density | 0.956 g/cm³ |
| Solubility In Water | Slightly soluble |
| Pka | 9.38 (for the amine group) |
| Smiles | CC1=CC=CC=C1CCN |
| Inchi | InChI=1S/C9H13N/c1-8-4-2-3-5-9(8)6-7-10/h2-5H,6-7,10H2,1H3 |
As an accredited 2-Methylphenethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, sealed with a screw cap; labeled “2-Methylphenethylamine, C9H13N, for laboratory use, handle with care.” |
| Shipping | 2-Methylphenethylamine is shipped in tightly sealed containers, typically made of amber glass or high-density polyethylene, to prevent contamination and light exposure. Packaging complies with chemical safety regulations, labeled with hazard and handling information. Transport follows UN guidelines for hazardous materials, ensuring safe delivery under controlled temperature and secure conditions. |
| Storage | 2-Methylphenethylamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers or acids. Keep the container protected from light and moisture. Proper labeling and secure storage are essential to prevent accidental contact or release. Store according to local chemical safety regulations. |
Applications of 2-Methylphenethylamine in Industrial Manufacturing2-Methylphenethylamine is widely used across multiple industrial sectors owing to its unique amine structure, which enables selective reactivity in advanced synthesis environments. Below, we detail the specific downstream scenarios where this intermediate plays an essential role in formulation, processing, and finished product development, accompanied by industry compliance benchmarks and technical integration details from a manufacturing perspective. 1. Pharmaceutical Intermediate SynthesisIn pharmaceutical manufacturing, 2-Methylphenethylamine functions as a crucial building block in the controlled synthesis of central nervous system (CNS) active compounds and certain antihypertensive agents. Process engineers introduce this raw material during the initial amination or condensation steps, as its methyl substitution pattern provides the necessary reactivity for constructing complex arylethylamine derivatives while maintaining rigorous control over chirality and side-product profiles demanded by regulated markets. Batch traceability and residual solvent management are strictly maintained during upstream and downstream purification. Industry compliance standards
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2. Agrochemical Active Ingredient Synthesis2-Methylphenethylamine serves as an intermediate in manufacturing selective herbicides and growth regulators used for high-value specialty crops. Chemical engineers use this amine to introduce tailored side chains onto heteroaromatic rings, which impart selectivity and improved environmental stability to the active molecule. Purity assurance and batch reproducibility are critical for agrochemical downstream processors facing strict maximum residue level (MRL) controls across export markets. Industry compliance standards
Typical usage ratio
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3. Dye and Pigment Precursor ManufacturingThis amine compound enables the synthesis of specialty azo and anthraquinone dyes required by textile, plastics, and inkjet formulation industries. Process specialists exploit its nucleophilicity and methyl-side group for efficient amine coupling, resulting in colorants with enhanced thermal and light stability. Material inputs must comply with both end-user safety assessments and regional banned amine lists, driving rigorous input documentation and batch-level verification at every stage of the pigment supply chain. Industry compliance standards
Typical usage ratio
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4. Epoxy Curing Agent AdditiveChemists in polymer resin production leverage 2-Methylphenethylamine as a reactive modifier in advanced epoxy formulations, where its controlled nucleophilicity allows precise adjustment of pot life and cross-link density. This additive, while not a primary hardener, improves flexibility and anti-yellowing properties in specialty coatings and structural adhesives, subjected to full validation under customer-specific mechanical and weathering test criteria. Industry compliance standards
Typical usage ratio
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5. Custom Fragrance Intermediate for Fine ChemicalsFine aroma chemical producers employ 2-Methylphenethylamine in proprietary syntheses of specialty amine side chains present in high-value fragrance molecules targeting luxury perfumery markets. Quality controllers oversee ultra-low impurity specifications and residual amine endotoxin levels, particularly in processes where downstream hydrogenation and acylation follow initial amination chemistry. Finished bases must pass not only regional allergen declarations but also internal olfactory performance benchmarks set by multinational branding customers. Industry compliance standards
Typical usage ratio
Downstream process integration
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On a typical production run, the hum of reactors and the pulse of progress fill our facility. Among the compounds we craft, 2-Methylphenethylamine stands out: a clear, oily liquid with a sharp aromatic profile that regular chemists recognize before it even loads into a sample vial. For those who work with complex synthesis, this molecule—CAS 636-55-9—delivers an unmistakable backbone for building more intricate structures in pharma, fine chemicals, and biochemical research. Customers working in laboratories, process development, and small-scale manufacturing often order our product with a purity above 99 percent, supported by chromatograms and spectral data we personally verify with our instruments.
A closer look shows how this amine differs from the crowded field of substituted phenethylamines. By placing a methyl group on the benzene ring’s 2-position, you see small shifts in reactivity that matter for downstream chemistry. Our team noticed early on that this subtle change impacts coupling reactions and offers unique routes for preparing intermediates in specialty building blocks.
Chemists sometimes ask about its solubility and stability under harsh conditions. Our batches handle exposure to a range of common solvents and tolerate atmospheric handling for short workups. Instead of broad claims, we stand by specific processing advantages: the viscous liquid form draws straightforward pipetting, the aromatic methyl substitution creates less steric challenge than bulkier analogs, and our QA team runs GC-MS checks for residual solvents to meet exacting purity standards.
Every shipment leaves with a COA referencing lot-specific analytical results. This comes from years of answering technical questions for customers preparing reference materials, optically active amines, or new candidates for preclinical assays. People say, “Does this batch degrade if left open for hours during extractions?” Based on thousands of liters and dozens of pilot runs, this molecule resists oxidation during normal use. Of course, all amines need careful storage, but compared to aliphatic analogs, ours sits stable through typical synthetic cycles.
Chemical manufacturers like us learn how a slight tweak in a molecule’s structure changes its entire behavior. 2-Methylphenethylamine is formally listed as 2-(2-Methylphenyl)ethanamine, and its structure—an ethylamine chain linked to a methylated benzene ring—invites analog comparison to chemicals like phenethylamine or 3-methylphenethylamine. But in our reactors, you spot differences by smell, viscosity, volatility, and how fast it travels down a GC column. In the hands of experienced operators, these physical properties influence purification steps, recovery yields, and overall cost.
The extra methyl group on the ortho position does more than shift UV spectra. It modifies hydrogen bonding and changes the outcome of certain reductive aminations and acylations. We ran side-by-side tests with both methylated and non-methylated phenethylamines, noting that ortho substitution occasionally leads to higher selectivity in electrophilic aromatic substitutions. This matters most for medicinal chemists racing the clock to optimize bioactives, but even in standard research labs, it shapes which auxiliary strategies succeed.
Our experience tells us—slight impurities sneak past generic testing and can throw off scaleups or reactions sensitive to trace metals or residual solvents. We invest in closed-loop solvent recovery and always dedicate separate reactors for amine products. That way, carryover from previous productions never compromises later batches. Extensive washing, high-vacuum distillation, and custom filtration form our daily work, not marketing jargon.
End users report stronger reproducibility in pharmaceutical and intermediate synthesis when source material meets true analytical standards. Sometimes newcomers ignore the importance of authentic purity data, learning only after a failed reaction or misinterpreted result. Our process engineers and QC staff pick up the phone, work through chromatograms, and point out what might have gone wrong—a step traders and brokers simply skip.
Not all chemical suppliers watch for subtle batch differences that might throw off a GC trace or push a process outside regulatory windows. We built in-line QC sampling into every production run, relying on HPLC checks to catch deviations in aromatic content or trace by-products. Technicians spend hours training under seasoned chemists who teach that a single missed impurity or miscalibrated column can undermine weeks of lab work for a customer.
Consistency stems from more than automation. It means recalibrating equipment seasonally, auditing internal SOPs, and running cross-lab comparisons with reference standards. Some years, raw material markets create pressure to cut corners. We kept toamed a while maintaining old-fashioned control over each process variable—temperature ramps, agitation rates, and hold times—because we produce chemicals named on the bottle, not anonymous intermediates.
Most requests for 2-Methylphenethylamine come from synthesis staff at pharmaceutical starts-ups and established process development groups. Biotech researchers synthesizing custom ligands rely on our product to build out molecular libraries with minimal cross-contamination. The purity and batch reproducibility matter most for those designing small molecule candidate drugs or exploring SAR on aromatic amines. Other buyers run pilot-scale transformations, chase new agrochemical leads, or prepare analytical standards for environmental monitoring—fields where trustworthy raw materials spell the difference between clear results and clouded failure.
We track these requests not out of curiosity but to align our synthesis scale, optimize delivery timing, and create a real-world feedback loop. When the chemical structure itself could preclude reactivity or form an unwanted side product, customers share solvent preference, handling quirks, and isolation anecdotes that shape how we engineer future product lines. For 2-Methylphenethylamine, we settled on a standard packing in amber glass and high-density polyethylene containers, shipping fresh-distilled material under nitrogen for sensitive applications after requests from specific sectors.
Questions about “difference” arise in nearly every technical conversation. Some users seek direct comparison between 2-Methylphenethylamine and other ortho-methylated aromatic amines. Others benchmark it against structural analogs like 3-methylphenethylamine, noting performance shifts in Friedel-Crafts acylation or Mannich-type condensation. We encourage clients to share their routes and challenges; teams running similar syntheses may see higher conversions or better selectivity using the ortho-substituted form.
Unlike longer-chain aromatic amines, our 2-Methylphenethylamine condenses cleanly at atmospheric pressure and maintains stability through most routine operations. The slightly increased boiling point over unsubstituted phenethylamine offers more fate control in distillation and purification—a relevant fact for those with limited vacuum capacity or looking to avoid product loss. From our decades in production, the ortho methyl group reduces basic nitrogen atom exposure to oxidizing environments, so less color forms during extended storage and fewer impurity peaks emerge in high-sensitivity HPLC assays.
Users in medicinal chemistry often cite lower off-target reactivity with 2-methyl substitution, especially for SAR libraries involving alkylated rings. Scaleup technicians noticed less fouling in glassware and improved throughput on recovery compared to para- and meta-methylated amines. Pure speculation never satisfies researchers, so we process actual samples from clients and run them through our own NMR and purity assessment before sharing insights. Over years of inquiry, no two applications finish exactly the same, but trends emerge: ortho-substituted amines like ours often deliver improved selectivity for certain condensation reactions, minimize non-specific binding as reagents, and offer a tangible performance edge where batch reliability counts.
Shortages of key precursors show up from time to time across our sector. Manufacturing 2-Methylphenethylamine reliably takes careful supplier vetting, documentation, and raw material testing pre-synthesis. Over the years, manufacturers learned to lock in backup sources for methylated benzene ring starting materials, manage logistics bottlenecks, and monitor evolving regulations for shipped amines worldwide. A sudden run on aromatic amines rarely disrupts us because we maintain stocks based on hard-won experience.
Our own process improvements—deployment of automated distillation systems, investment in local environmental controls, and relentless attention to solvent recycling—let us avoid both downtime and erratic product quality. When transportation delays slowed international suppliers, feedback from our production partners in the field supported just-in-time adjustments, while documentation disciplined to QA best practices soothed concerns in regulatory filings. Colleagues from procurement to quality assurance understand: stable supply chains are not a luxury in advanced chemical synthesis, especially with specialty compounds like 2-Methylphenethylamine.
Scientists, R&D directors, and technical buyers need assurance beyond sales claims. Decades of direct manufacturer experience taught us to document every batch, share real-life outcomes of downstream processing, and remain open about methods—filed under best practices upheld by international certifications and audits. Many projects start with a request for data. We supply full characterization, including NMR and elemental analysis, on every lot. Residual solvent and water data go out with each shipment; our QC chemists take calls from customers wrestling with challenging extractions or protecting amines from air and moisture during multistep reactions.
Real transparency grows from decades of hands-on manufacturing, not middleman trading. Whether customers run tiny benchtop experiments or scale up to hundreds of kilograms, we document our inputs, show our data, and invite technical discussion. Our chemists—seasoned in troubleshooting and process optimization—provide practical advice: safeguarding product from light, keeping service containers dry, and how to minimize loss during vacuum transfer. This on-the-ground knowledge reflects years of running actual production units, not just trading paperwork.
One of the most common technical hurdles researchers face is maintaining purity post-delivery. Overexposure to air, light, or moisture can degrade similar amines or add byproduct peaks that baffle spectrum analysis. That experience guides how we recommend users store and handle 2-Methylphenethylamine—cool, dry, sealed, and if possible, under inert gas for long-term work. Our own labs learned these lessons by testing products under stress conditions. Storage at room temperature, shielded from excessive humidity and light, preserves analytical quality for months, even years.
Handling and transferring neat amine requires care because it stains, emits a characteristic odor, and can engage with environmental acids if containment slips. Our staff instructs clients on best-use dispensing techniques and tracks the origin of every packaging component back to source, avoiding cross-contamination from plastics, leaching, or external residues. Even small differences in container liner material can impact purity outcomes, a detail uncovered by years of investigating returned samples or troubleshooting unexpected failures with our most demanding customers.
The demand for ortho-substituted aromatic amines grows as research moves toward ever more complex and site-directed synthesis. 2-Methylphenethylamine plays a supporting role in many new amide, imine, and chiral intermediate preparations, particularly those where slight modification makes a difference in biological or catalytic studies. As a direct manufacturer, we listen to customer input about reaction conditions, choose solvents and process controls that echo real-world lab preferences, and update equipment to reduce unwanted waste streams.
Client-led innovation drives our scale-out plans, from pre-packed cartridges for microreactors to custom labeling for traceability in regulatory filings. A chemist’s insight about handling quirks or isolation problems leads us to trial new closure types, amber bottles, or altered shipping logistics. In one example, high-throughput labs requested sample packs with multiple cap styles; we built that customization into our workflow, reflecting a collaborative relationship with the research world.
Our business sits at the intersection of technical know-how and regulatory demands. Academic researchers preparing fine-scale transformations rely on clear labeling, complete documentation, and ethical sourcing. Each order includes full details on storage recommendations, impurity profiles, and guidance on downstream handling, shaped by life in the lab—not marketing assumptions. Ongoing updates to internal compliance protocols, regular external audits, and active engagement with changing global regulations keep us ready for inspections and transparent with information.
Internally, staff training focuses on safe handling practices and effective communication with clients. We don’t wall off our technical knowledge behind generic advice—our technical support team shares workplace-tested tips on extraction, evaporation, and container closure. Partnerships with academic and industrial collaborators ensure continual improvement. Maintaining trust means telling users what works, what does not, and what we’ve learned through decades of manufacturing and supply.
No two days in the facility follow the same script. Someone might need 500 mL for targeted synthesis, another calls for 100 kg bulk runs. Each request passes through eyes and hands trained to recognize minute impurities, color shifts, or strange scents familiar to anyone working in a synthesis lab. Through years spent making, testing, and refining amine products, our team shapes the outcome of research efforts in ways that simple purity numbers never tell.
The story of 2-Methylphenethylamine reflects the real world of chemical manufacturing: precise but never routine, deeply technical yet shaped by collaboration with end users who work at the edge of what’s possible. Regular dialogue, constant improvement, and an unwavering focus on batch quality keep our product in research protocols and on production lines year after year.