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3-Amino-4-(4-Morpholino)Benzotrifluoride

    • Product Name 3-Amino-4-(4-Morpholino)Benzotrifluoride
    • Alias 3-Amino-4-(4-morpholinyl)benzotrifluoride
    • Einecs 433-940-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    363736

    Chemical Name 3-Amino-4-(4-Morpholino)Benzotrifluoride
    Molecular Formula C11H13F3N2O
    Molecular Weight 246.23
    Cas Number 1032211-73-6
    Appearance Off-white to pale yellow solid
    Solubility Soluble in DMSO, methanol
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 3-Amino-4-(4-Morpholino)Benzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, labeled "3-Amino-4-(4-Morpholino)Benzotrifluoride," with hazard warnings and handling instructions.
    Shipping **Shipping Description:** 3-Amino-4-(4-Morpholino)Benzotrifluoride is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported as a non-hazardous chemical under ambient conditions, following standard chemical handling protocols. Packaging complies with regulations to prevent leaks or contamination during transit. Handle with appropriate personal protective equipment (PPE).
    Storage Store **3-Amino-4-(4-morpholino)benzotrifluoride** in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, incompatible substances (such as strong oxidizers and acids), and ignition sources. Keep the storage area clearly labeled and restrict access to trained personnel. Use appropriate secondary containment to prevent leaks or spills. Always follow local regulations and institutional safety guidelines.
    Application of 3-Amino-4-(4-Morpholino)Benzotrifluoride

    Applications of 3-Amino-4-(4-Morpholino)Benzotrifluoride in Industrial Manufacturing

    3-Amino-4-(4-Morpholino)Benzotrifluoride serves key roles in specialized downstream sectors. Our production partners depend on its precisely controlled quality attributes for high-performing, regulation-compliant finished goods. Below, we outline its established industrial applications across select niche segments.

    1. Pharmaceutical Intermediate for Kinase Inhibitor Synthesis

    Innovator and generic pharma manufacturers use this compound as a premium intermediate in targeted small-molecule kinase inhibitor development. Its unique structure, with the morpholino and trifluoromethyl substituents, enables efficient synthesis of complex pharmaceutical APIs, underpinning rigorous compound purity and traceability required for new molecule launches and scale-up projects.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.)
    • US FDA 21 CFR Part 211
    • China GMP for APIs (2010 edition and later)

    Typical usage ratio

    • Usually 0.8–1.2 molar equivalents per target intermediate; adjusted based on reaction pathway stoichiometry and scale.

    Downstream process integration

    • Introduced at the heterocyclic condensation or amination stage in multi-step synthesis of pharmaceutical actives, followed by further functionalization and purification.

    Final product types

    • Targeted kinase inhibitor APIs (oncology and rare diseases)
    • Advanced pharmaceutical intermediates (drug precursors)
    • Regulatory submission batches (clinical stage and commercialization)

    2. Agrochemical Building Block for Herbicide Manufacturing

    Leading crop protection formulators apply this molecule as a specialized ring-structure source within syntheses of proprietary triazine-based and pyridine-based herbicides. Its electron-withdrawing trifluoromethyl group improves bioavailability and activity spectrum in finished actives, strictly within the parameters of modern sustainability and operator exposure guidelines.

    Industry compliance standards

    • FAO/WHO JMPR guidelines for pesticide technical materials
    • ISO 9001:2015 for production quality assurance
    • REACH (EC 1907/2006) for registration, evaluation, and authorization
    • EPA 40 CFR Part 174 (US tolerance and MRLs for agrochemicals)

    Typical usage ratio

    • Routinely 3–5% w/w in total reactant charge for core structure elaboration, optimal ratio determined by desired substitution pattern and yield targets.

    Downstream process integration

    • Added during nucleophilic aromatic substitution or cyclization in the main synthetic stage, followed by formulation of technical concentrate and field-ready mixtures.

    Final product types

    • Selective post-emergence herbicide actives
    • Water-dispersible granule and suspension concentrate herbicide formulations

    3. Advanced Intermediate for Specialty Dyes and Pigments

    Industrial dye and pigment producers incorporate this compound to create high-performance chromophores for electronic and fiber applications. Its stable aromatic backbone and electron-donating amine support production of dyes with enhanced lightfastness, solvent resistance, and color intensity for technical textiles and specialty inks.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemicals)
    • EN 71-3:2019 (toxic elements for colorants in toys)
    • ISO 13320:2020 (particle size distribution analysis)
    • REACH Annex XVII (restricted substances in colorants)

    Typical usage ratio

    • 1–4% molar content relative to core diazo precursor; varied for targeted hue intensity and application substrate.

    Downstream process integration

    • Employed in diazo coupling or aromatic substitution during pigment/dye core synthesis; followed by filtration, purification, and dispersion formulation for downstream markets.

    Final product types

    • Electronics-grade colorants
    • Fiber- and polymer-compatible pigments
    • UV-resistant specialty inks

    4. Intermediate for High-Performance Polymer Additives

    Materials manufacturers leverage this molecule to develop chain-extending or functionalized side groups for advanced polyimide, polyamide, and fluoropolymer additives. Its integration increases thermal stability and chemical resistance of high-end performance plastics used in semiconductor, aerospace, and specialty cable applications, all within stringent production documentation and downstream trace-resin requirements.

    Industry compliance standards

    • UL 94 (flammability standards for plastics)
    • RoHS Directive (2011/65/EU) for hazardous material restriction
    • IPC-4101D/126 (laminate and prepreg base materials)
    • ISO 14001 for environmental management of chemical processing

    Typical usage ratio

    • 0.5–2.5% by weight in additive masterbatch; flexibly set depending on resin type, target decomposition temperature, and extrusion conditions.

    Downstream process integration

    • Fed into monomer blending prior to main condensation or polymerization; post-polymer functionalization or granulation steps to ensure additive dispersion in engineered plastics.

    Final product types

    • Thermally stable polyimide films and powders
    • High-voltage cable insulation masterbatches
    • Low-outgassing electronic device resins
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    Certification & Compliance
    More Introduction

    3-Amino-4-(4-Morpholino)Benzotrifluoride: Experience at Scale

    Direct from the Manufacturer: What 3-Amino-4-(4-Morpholino)Benzotrifluoride Means for Today’s Research

    At our chemical production site, every new batch of 3-Amino-4-(4-Morpholino)Benzotrifluoride carries the lessons learned from years working with complex fluorinated molecules. We have seen this compound, often referred to by its CAS number 112762-28-2, steadily gain the attention of pharmaceutical innovators and specialty chemical developers. From the earliest small-batch orders to regular shipments now leaving our reactors in metric ton volumes, our relationship with this molecule happens on the floor, alongside the technicians who keep operations safe and the chemists who insist on rigorous purity every single time.

    Consistency, Reactivity, and Real-World Utility

    The interest in 3-Amino-4-(4-Morpholino)Benzotrifluoride springs from both its unique structure and functional versatility. Around our plant, the standout feature is its trifluoromethyl ring, linked to an aminated aromatic core, which is further modified by a morpholino moiety. This combination gives rise to characteristics not found in simpler aromatic amines or other basic trifluoromethylated compounds.

    Traditional aromatic amines, such as aniline derivatives, do not bring the same electron-withdrawing backbone or steric freedom. Substituting the ring with a trifluoromethyl group stabilizes potential intermediates for cross-coupling reactions. The morpholine ring further boosts solubility in polar and mixed organic systems, reducing the headaches of phase issues that slow down multi-step syntheses. Colleagues working up pilot campaigns appreciate how the morpholino group can minimize fouling and improve flow rates during industrial chromatography or crystallization. Compare this with options such as unsubstituted aminobenzotrifluorides: these blend less easily in some reaction setups, and they can fall short during salt formation experiments where tight pKa control is essential.

    Meeting the Demand: Batch Quality Control and Real-World Challenges

    Production chemists get a front-row seat to the quirks of each batch. Purity doesn’t just come from buying the best raw materials or having a clean reactor — it arrives through attention every step of the way. Our team found that side reactions, such as N-oxidation of the morpholine, crop up in certain preps if the pH shifts or oxygenation drifts. We confront these challenges by dialing in the right reaction atmospheres and implementing intermediate sampling schedules, always benchmarking GC-MS and NMR spectra at each stage.

    The resulting product consistently exceeds 99 percent by HPLC, passing through a multi-solvent recrystallization that strips out trace amine and ether impurities. Each drum or kilo pack receives full lot documentation and spectral printouts before release, keeping every batch accountable to the standards we’d want in our own downstream labs.

    Real-World Applications and the Benefits over Other Aromatic Amines

    3-Amino-4-(4-Morpholino)Benzotrifluoride rarely ends up on the warehouse shelf for long. Pharmaceutical manufacturers gravitate toward this intermediate to build scaffolds for kinase inhibitors, antivirals, and agrochemical leads. The morpholino substituent lays groundwork for easy hydrogen bonding and salt formation, favored during fragment-based drug discovery and preclinical investigation.

    Process chemists have commented that this product stands out when compared to 3-aminobenzotrifluoride or 4-aminobenzotrifluoride, both of which lack the morpholino ring’s handling advantages. Morpholine-lacking versions can pose issues during suspension prepping, and they may require more frequent pH adjustments. One major difference becomes obvious when you run scale-ups intended for heterocyclization: yields drop, and isolations turn messy without the morpholine moiety to steer product formation and bolster purification.

    At our plant, we occasionally field questions about using more generic aminotrifluorotoluenes as drop-in substitutes. From firsthand experience, the transition rarely works out; downstream yields and impurity profiles simply don’t compare in the hands of skilled process teams. With 3-Amino-4-(4-Morpholino)Benzotrifluoride, reaction streams clarify quickly, and both crystallizability and assay outcomes stabilize batch to batch. This allows drug makers more certainty as projects move from the bench to pilot scale and on toward commercialization.

    Specifications Informed by Industry Demands

    Every major customer group brings different cutoffs for trace residuals, water content, and solid handling. Over time, we’ve adjusted our specifications based on hard-won feedback. The target purity sits above 99 percent by HPLC, water content remains strictly below 0.5 percent, and we set strict controls for chloride, sulfate, and low-mass ketones, which can slip through if the morpholine comes from lower-grade sources.

    Particle sizing gains importance for formulations aimed at solid dosage or granule formation. We process with an eye for uniform, free-flowing solids, keeping bulk density in a narrow band to ease transfer through feeders and reactors. Each batch undergoes Karl Fischer titration and full spectroscopic confirmation in-house, supported by archives of MS and NMR spectra for ongoing reference.

    Safer Handling and Shelf Stability

    Operators notice quickly how the morpholine ring moderates odor and volatility, making handling safer and less irritating compared with more volatile aminobenzotrifluorides. The powder form resists clumping, allowing for longer open transfer windows and improved air quality inside drum-filling areas. Downstream users say the easy weighing and dosing save both time and labor during pilot and full-scale synthesis.

    Our warehouse crews prefer this product for its resistance to hydrolysis and its long shelf life; it survives variable shipping conditions and still meets full analytical specification after months in storage. Unlike simpler aromatic amines, which may degrade or lose mass under ambient temperatures, our product maintains both color and purity in sealed drums.

    Addressing Supply Chain Pressures

    The specialty amines market swings between feast and famine as pharmaceutical cycles ebb and flow. Predictable supplies don’t happen by accident. A good example unfolded two years ago: upstream fluorinated ring intermediates began facing production bottlenecks at global suppliers. Instead of shifting blame or stretching out lead times indefinitely, we added new purification trains and streamlined solvent recovery, increasing yield from every run. No small feat given the sensitivities involved with morpholine groups.

    Our output expanded, and deliveries continued on schedule at the height of demand. We prefer transparency with buyers instead of vague promises. Commercial teams actively share real-time inventory updates instead of smoothing over delays. Over multiple cycles of raw material scarcity, firms who keep lines of communication open with their manufacturing partners secure a steadier flow of chemicals — not just for our flagship products, but for the experimental candidates that pave the way for future discoveries.

    Working with Partners on Scale-up and Innovation

    Process innovation rarely happens in isolation. We learned this firsthand during a recent project with a medicinal chemistry group pushing to scale from multi-gram to multi-kilogram production. Their reaction scheme demanded a custom purity grade, omitting certain halide residuals below 50 ppm. To meet their spec — and compress lead time — our technical teams revised workup procedures, added column chromatography steps, and ran parallel batches to fine-tune particle morphology.

    The result: a dedicated supply chain ready to roll as the client advanced through milestone studies. The approach provided both sides with insight — our formulation chemists gained experience running high-throughput crystallizations with unconventional solvents, while the partner group shaved weeks off their project schedule.

    Environmental Health and Safety Realities

    Worker safety and downstream environmental impact drive every review we conduct. With 3-Amino-4-(4-Morpholino)Benzotrifluoride, the built-in stability of its molecular framework means it generates lower levels of hazardous off-gassing during processing and blending. Solid residues and waste streams undergo rigorous collection and neutralization before leaving our plant. Auditors have pointed out the reduced VOC footprint during drum filling versus other aminobenzotrifluorides, a direct benefit to both local staff and surrounding areas.

    On the regulatory side, we keep up-to-date records on occupational handling — from dust exposure assessments to emergency protocol drills. Major customers, especially pharmaceutical end users, review this data before approving new suppliers, so exhaustive documentation stays ready for inspection. It matters for our downstream reputation to account for every kilogram and guarantee that packaging meets reinforced environmental standards.

    Customers pursuing greener processes notice that the morpholine ring in this compound enables milder dilution protocols and reduces the need for strong acid or base during workup. Fewer harsh wash steps mean lower corrosion on equipment and less hazardous effluent.

    Looking Ahead: Where 3-Amino-4-(4-Morpholino)Benzotrifluoride Is Headed

    Continued growth in custom fluorinated intermediates depends on reliability — and adaptability. Manufacturing experience informs every decision we make, from adjusting batch sizes to forecasting the demands of our drug developer partners. Over the past three years, we have observed a steady uptick in demand for higher-purity, morpholine-functionalized building blocks. Research groups keep pushing toward greater complexity. The versatility offered by the amino-morpholino-trifluoromethyl architecture helps meet these new targets, both for classic API development and for emergent needs in advanced materials or crop science.

    One area that excites our technical team involves expanding post-synthetic modifications, such as linking the core fragment to sulfonamide, urea, or pyrimidine motifs. These campaigns require access to kilogram-scale, ultra-pure intermediates with robust supply. Having a production base able to quickly ramp up or tweak reaction conditions leaves our partners less exposed to changing requirements or surprise technical glitches during process scale-up.

    Why Experience Matters in Real Chemistry

    Sophisticated molecules offer few second chances when it comes to commercial scale-up. Minor shortcuts in purity or process control cost both time and money if rework or troubleshooting becomes necessary. Direct experience with the quirks and needs of 3-Amino-4-(4-Morpholino)Benzotrifluoride forms the backbone of our delivery. Production staff recognize that the science extends beyond glassware and theoretical yields, involving everything from plant scheduling to environmental compliance.

    Research and process teams deserve more than a generic spec sheet. They rely on documented, repeatable processes and personal support to hit demanding timelines safely. Our own story with this compound illustrates the difference: every drum shipped contains the work of people who know the chemistry, care about the outcome, and pay attention not only to numbers, but to how users will implement the product at the bench and in the reactor.

    Choosing 3-Amino-4-(4-Morpholino)Benzotrifluoride with us means tapping into years of firsthand knowledge. We focus exclusively on manufacturing and providing the critical building blocks chemists use to innovate and improve lives. As new challenges and discoveries continue to surface, our company stands ready to deliver not just materials, but solutions built on experience, science, and trust.