Products

2-Methoxy-5-(trifluoromethyl)aniline

    • Product Name: 2-Methoxy-5-(trifluoromethyl)aniline
    • Chemical Name (IUPAC): 2-methoxy-5-(trifluoromethyl)benzenamine
    • CAS No.: 328-84-7
    • Chemical Formula: C8H8F3NO
    • Form/Physical State: Liquid
    • Factroy Site: Nanbao Development Zone, Tangshan City, Hebei Province
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Tangshan Sanyou Group Co., Ltd
    • CONTACT NOW
    Specifications

    HS Code

    292373

    Chemical Name 2-Methoxy-5-(trifluoromethyl)aniline
    Cas Number 886762-23-0
    Molecular Formula C8H8F3NO
    Molecular Weight 191.15
    Appearance Light yellow to brown liquid
    Boiling Point 114-116°C at 18 mmHg
    Density 1.282 g/cm3
    Purity Typically ≥97%
    Solubility Soluble in organic solvents, insoluble in water

    As an accredited 2-Methoxy-5-(trifluoromethyl)aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, labeled "2-Methoxy-5-(trifluoromethyl)aniline," hazard symbols, and manufacturer details printed clearly.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 160 drums (200 kg/drum) of 2-Methoxy-5-(trifluoromethyl)aniline, total net weight 32,000 kg.
    Shipping 2-Methoxy-5-(trifluoromethyl)aniline is typically shipped in secure, sealed containers to prevent leakage. The packaging complies with applicable chemical safety regulations and may include cushioning to prevent breakage. Shipping is restricted to trained personnel, with appropriate labeling and documentation, and precautions are taken to avoid extreme temperatures and exposure to incompatible substances.
    Storage **2-Methoxy-5-(trifluoromethyl)aniline** 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. Ensure the storage area is equipped with appropriate spill containment and safety equipment. Label the container clearly and follow all relevant safety and regulatory guidelines.
    Shelf Life 2-Methoxy-5-(trifluoromethyl)aniline is stable under recommended storage conditions; typically, its shelf life exceeds two years when unopened.
    Application of 2-Methoxy-5-(trifluoromethyl)aniline

    Purity 98%: 2-Methoxy-5-(trifluoromethyl)aniline with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and consistent product quality.

    Melting Point 49°C: 2-Methoxy-5-(trifluoromethyl)aniline with a melting point of 49°C is used in agrochemical formulation processes, where it facilitates precise compound integration.

    Molecular Weight 191.15 g/mol: 2-Methoxy-5-(trifluoromethyl)aniline with a molecular weight of 191.15 g/mol is used in fine chemical research applications, where it allows for accurate stoichiometric calculations.

    Stability Temperature 120°C: 2-Methoxy-5-(trifluoromethyl)aniline with a stability temperature of 120°C is used in high-temperature organic synthesis, where it maintains structural integrity during reactions.

    Low Water Content (<0.5%): 2-Methoxy-5-(trifluoromethyl)aniline with low water content (<0.5%) is used in polymer modification, where it prevents unwanted side reactions and enhances material properties.

    Free Quote

    Competitive 2-Methoxy-5-(trifluoromethyl)aniline prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    Get Free Quote of Tangshan Sanyou Group Co., Ltd

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Methoxy-5-(trifluoromethyl)aniline: Reliable Sourcing from a Dedicated Chemical Manufacturer

    Understanding this Specialty Aniline

    Making specialty aniline derivatives like 2-Methoxy-5-(trifluoromethyl)aniline takes focus, commitment to safety, and an appreciation for the fine details of chemical production. As a manufacturer who handles this molecule at scale, we can share what matters most with this product and why it stands out for research development and industrial users who require consistent purity and performance.

    Our Approach to Consistency and Quality

    Every batch of 2-Methoxy-5-(trifluoromethyl)aniline leaving our plant goes through a closely monitored process. Years of manufacturing fine chemicals have taught us that customers remember the outcome of one mistake far longer than a dozen batches supplied on time. For this reason, we prioritize clear labeling, verified raw materials, and repeatable downstream processing. This compound's purity, usually maintained at 98% or higher by GC and HPLC, plays a large role in meeting client project requirements—whether customers are engaged in pharmaceutical, agrochemical, or material science research.

    We source starting materials directly, avoiding substitutions that might introduce trace contaminants or cause shifts in reaction output. The dehydration steps, solvents, and temperature controls in production aren’t just add-ons; they anchor the batch-to-batch reproducibility our downstream partners expect. This approach keeps our 2-Methoxy-5-(trifluoromethyl)aniline within tight color and solubility specifications, helping eliminate surprises in process validation or later scale-up.

    Why Customers Use This Compound

    Research and development labs reach for this particular aniline for syntheses that require the combined influence of a methoxy and a trifluoromethyl group on the same aromatic ring. These substituents tune the electron density, shape physical properties, and alter reactivity. Chemists aiming at new APIs or crop protection actives might be exploring SAR (structure-activity relationships), and they count on reproducible inputs. For those targeting fluorinated aromatic amines in drug design, the trifluoromethyl group offers metabolic stability and increases lipophilicity. The ortho relationship between the amino function and the trifluoromethyl group isn't common in most widely-available anilines. The presence of a methoxy group at the meta position can adjust reactivity, NMR signatures, and even the product’s odor—useful cues for analysts and practitioners.

    In material science, the fluorinated and methoxylated structure brings unique dielectric and solubility properties. Customers developing polymers, resins, or specialty dyes frequently examine the influence of both methoxy and trifluoromethyl groups on surface energy and optical properties. It's not simply a question of bulk substitutions; downstream effects in terms of final product durability and finish play directly into chemical selection. The compound also sees use as a privileged building block for more elaborate functional molecules, such as ligands in catalytic chemistry, where geometric and electronic influences from these substituents direct complex formation and selectivity.

    What Sets This Chemical Apart?

    Plenty of aromatic amines show up in supplier inventories, but 2-Methoxy-5-(trifluoromethyl)aniline delivers a rare combination of properties. Unlike the standard unsubstituted aniline or even its simple fluorinated derivatives, this compound provides a significant shift in electron density due to the trifluoromethyl group, which sits opposite the amino function. Working with this molecule, we've seen how the electron-withdrawing effect from the CF3 dampens nucleophilic attack, while the methoxy adds subtle stabilization and alters the ring's electronic profile. This dual influence proves challenging to replicate with simple blends or substitutions, so synthetic chemists frequently seek this exact substitution pattern.

    From a practical manufacturing standpoint, handling the trifluoromethyl group means paying careful attention to both environmental controls and final product purity. This isn’t the same as handling, for example, 4-methoxyaniline, which lacks the fluorinated group and can be more forgiving both in handling and downstream reactivity. Stringent controls over by-products, waste capture, and emissions govern operations here. Over the years, our process engineers have fine-tuned how we incorporate these highly electronegative groups safely, reducing unnecessary exposure, boosting yields, and reducing waste.

    Customers ask about isomerism: both substitution order and pattern can mean the difference between a successful reaction and weeks lost to troubleshooting. We routinely confirm position and purity using detailed NMR, mass spectrometry, and chromatographic analyses, not simply relying on listed CAS numbers or label claims.

    Physical Characteristics and Handling Wisdom

    Our experience shows that handling 2-Methoxy-5-(trifluoromethyl)aniline brings particular challenges in storage and transfer. Moisture control matters, since amines and their derivatives may absorb water, shifting solubility or crystallinity in unplanned ways. We pack this compound under nitrogen, in HDPE or glass, preventing exposure to air and light that can trigger subtle decomposition or color change. In our early years, we experimented with open transfers and found even a day at ambient humidity changed the product enough to complicate downstream reactions.

    As a noted low-melting-point solid or viscous oil (depending on storage and purity), each lot receives careful attention during grinding, filling, and sealing. Our plant staff watch out for crystal aggregation that might cause dosing errors. Little details like these make an outsized difference at kilo scale, where process mishaps can mean delays or yield loss.

    Many aromatic amines are known for either their strong odor or for volatility that can irritate. The methoxy and trifluoromethyl pattern here produces a less irritating, but still distinct, scent—a minor but relevant detail for colleagues who work at the bench. Attention to personal protective equipment and reputable exhaust capture is routine, not because regulations say so, but because experience has taught that trace exposures add up over time.

    Critical Purity Considerations

    There’s little room for shortcuts in high-spec applications. Every kilogram that leaves our facility comes with a certificate of analysis, not as a marketing tool but as a transparent record of quality. We see variation between suppliers who use mixed or impure starting materials, resulting in off-colors, odors, and trace isomers. Customers working with sensitive catalytic systems notice these edges—they appear later as poor reproducibility or unexpected side products. Over the years, analysis techniques like quantitative GC, HPLC, and advanced NMR profiling have caught more than one off-spec lot before it could reach clients. For scale-up users, these differences can shift entire reaction pathways, so we’ve made ongoing investment in in-house analytical capability.

    Impurity profiling extends beyond the main compound. Customers developing pharmaceuticals often ask for details on trace halides, unreacted aniline, or solvent residues. Our close integration between lab and production teams has allowed us to lower these traces to below most reporting thresholds, reducing the risk of downstream contamination. In contrast, producers who skip this step often see unexpected chromatographic peaks or fluorescing impurities in final products—something we take pride in avoiding by tackling contaminants at their source.

    Process Safety and Environmental Insight

    Few tasks in fine chemical manufacturing demand more vigilance than the safe scaling of aromatic amines with fluorinated side chains. Several decades ago, the industry managed fluorine introduction with hazardous intermediates, leading to difficult waste management and exposure issues. Our modern process employs closed systems and scrubbing to manage emissions. We invested in multi-stage filtration and solvent recycling, further reducing environmental impact while meeting regulatory thresholds.

    Applied experience has shown that proper thermal management, careful feeding, and robust equipment delivers both safety and improved yield. The trifluoromethyl group brings stability to the product, but it can raise exotherm risk if introduced improperly during synthesis. Through dozens of scale-ups and small molecule campaigns, we’ve tuned our controls to detect the earliest signs of unwanted reactivity, stopping problems before they affect the finished product or surrounding environment.

    Scale-Up and Customization: Serving Diverse Industries

    Research institutions may seek gram-scale quantities for screening, while process chemists from multinationals often order at multi-kilo scale to support larger campaigns. Our plant’s infrastructure supports both. We learned—through more than a few rushed early deliveries—that stockpiling inventory or relying on third-party intermediaries can invite trouble. Instead, steady in-house production aligned to actual customer requests keeps quality under our control and speeds delivery.

    Some users require additional purification or particular polymorphs tailored to proprietary processes. Working directly from a manufacturer's perspective, we offer process notes and adjustment options to clients with special needs, sharing best practices on how to handle the product for their setting. The feedback loop from users helps us improve recipes and avoid pitfalls seen in earlier runs.

    Customers often ask what sets our approach apart from traders who simply relay drums or bottles from a stockpile. We’ve seen firsthand how skipping process discussion or background checks leads to avoidable problems—a shift in melting point, unexpected color, or yields that never quite add up. Regular dialogue with users keeps our feedback loop fresh and our batches more consistent.

    Comparing to Similar Aromatic Amines

    The majority of aromatic amine products in catalogues are based on simple substitutions—methyl, methoxy, or halogenated rings. Very few vendors deliver reliable lots of this exact combination at meaningful scale. Clients moving from standard methoxyanilines to the 2-Methoxy-5-(trifluoromethyl) variant comment on the improved chemical resistance, altered solubility, and unique reactivity brought on by the CF3 and methoxy effects.

    Switching from para- or ortho-methoxyanilines to this compound means gaining precise control over both electronics and sterics. Typical unsubstituted aniline or para-trifluoromethylaniline lacks the intermediate electronic profile or resistance to metabolism researchers may seek. Specialty synthesis or late-stage diversification routes often succeed only when exact isomers and purity thresholds are available. Over the years, we have seen R&D managers come back for this product because alternative substitutions failed to deliver needed pharmacokinetic or process metrics.

    Supporting Pharmaceutical Innovation

    Pharma innovators prize this compound for more than its novelty. The pairing of a methoxy at position 2 and a trifluoromethyl at position 5 shapes both synthetic access and downstream metabolism in lead molecules. Medicinal chemists report that this pattern boosts both in vitro and in vivo performance, often by delaying metabolism or shifting partition coefficients in favor of tissue targeting. Reproducibility counts, and every slip in isomer ratio or process contamination can knock a candidate drug from late-stage studies. For these reasons, we subject pharmaceutical-destined lots to greater scrutiny—retaining retain samples, archived spectra, and trending data so that no surprises arise during regulatory filing or patent defense.

    Only small changes in impurity content, residual solvents, or ring isomerism can spell disaster in regulatory contexts. Our production lab, informed by cycles of feedback from both bench chemists and documentation experts, keeps analytical methods current with evolving pharmacopoeia requirements.

    Integrating with Custom Chemistry and Scale-up R&D

    Collaborating with contract manufacturers and startups developing new manufacturing methodologies has exposed us to many creative routes for using 2-Methoxy-5-(trifluoromethyl)aniline. Partners have used it in Suzuki, Buchwald, and Ullmann couplings, developing cross-coupled targets by leveraging both fluorine and methoxy's directing effects. Offering technical support to optimize reaction setups, solvent choices, and purification strategies demonstrates the practical support a dedicated manufacturer can provide, compared to off-the-shelf catalog companies.

    Practical process improvements have emerged from these collaborations. A recent client, developing an advanced coating, found that preheating the compound in a dry nitrogen environment reduced batch inconsistencies dramatically. A pharmaceutical partner gained a significant purity boost by switching from direct distillation to vacuum crystallization, guided by our empirical feedback and samples from the line. These steps add value to research and make a case for ongoing cooperation between producer and consumer, rather than episodic buying from anonymous traders.

    Continual Improvement and Customer Focus

    It’s tempting to treat chemical manufacturing as a solved challenge, fixed forever after initial setup. Our experience tells a different story. New uses, regulatory changes, and technology shifts require an ongoing investment in new ideas and flexibility. We learn from each new request or application: transitioning from glass to stainless steel, tweaking crystallization times, or deciding on better packing for improved shelf life. What customers try and discover often becomes part of our standard playbook.

    Latest environmental standards push us to innovate in solvent recycling and emissions controls. Waste management isn’t only about staying legal, but about maintaining relationships with customers who care about impact and ingredient stewardship. Many partners value knowing their raw materials come from firms who do more than the minimum.

    Over the years, we have migrated from isolated batch records into an integrated digital platform, letting quality, analysis, and tracking teams view a single data set for each batch. This integrated oversight ensures traceability, improves response time, and supports transparency—qualities many clients cite as reasons to choose direct sourcing over anonymous, third-party intermediaries.

    Final Thoughts

    Producing and supplying 2-Methoxy-5-(trifluoromethyl)aniline is neither a casual sideline nor a simple commodities business. It demands technical attention, investment in people and equipment, and a focus on the details that quietly shape customer outcomes. The compound’s unique substitution pattern translates into advantages for pharmaceutical, agrochemical, and material science applications that generic amines can't provide. We’ve learned—through scores of delivered lots and conversations with neighboring plants and distant labs—that true value in chemical manufacturing stems from consistency, conversation, and a willingness to improve. This approach builds trust batch by batch, for clients and their own customers, across sectors pushing for better science and more reliable results.