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2-Amino-5-Cyanobenzotrifluoride

    • Product Name 2-Amino-5-Cyanobenzotrifluoride
    • Alias 2-Amino-5-(trifluoromethyl)benzonitrile
    • Einecs 231-427-5
    • 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
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    Specifications

    HS Code

    728241

    Product Name 2-Amino-5-Cyanobenzotrifluoride
    Cas Number 327-74-2
    Molecular Formula C8H4F3N2
    Molecular Weight 184.13
    Appearance Off-white to light brown solid
    Melting Point 52-54°C
    Density 1.43 g/cm³ (estimated)
    Purity Typically ≥98%
    Solubility Slightly soluble in water
    Synonyms 2-Amino-5-cyano-1-(trifluoromethyl)benzene
    Structure Benzene ring with amino, cyano, and trifluoromethyl substituents
    Smiles NC1=CC(C#N)=CC=C1C(F)(F)F
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited 2-Amino-5-Cyanobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Amino-5-Cyanobenzotrifluoride is packaged in a 25-gram amber glass bottle with a secure, chemical-resistant screw cap.
    Shipping 2-Amino-5-Cyanobenzotrifluoride is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is typically classified as a hazardous material, requiring appropriate labeling and documentation. Shipping complies with regulations for chemical transport, including UN/NA classification and MSDS documentation. Handle with care, avoiding physical damage and accidental release during transit.
    Storage 2-Amino-5-Cyanobenzotrifluoride should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances, such as strong oxidizing agents. Protect from light and moisture. Ensure proper chemical labeling and restrict access to trained personnel. Follow all applicable safety and regulatory guidelines for storage of hazardous chemicals.
    Application of 2-Amino-5-Cyanobenzotrifluoride

    Applications of 2-Amino-5-Cyanobenzotrifluoride in Industrial Manufacturing

    2-Amino-5-Cyanobenzotrifluoride serves as a specialized intermediate in several advanced chemical manufacturing sectors. Each downstream field utilizes this material at optimized dosages and integration points within tightly regulated environments to support the synthesis of high-value end products. Below, we detail core application scenarios, specifying compliance standards, common formulation ratios, process roles, and resulting finished goods.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use this compound primarily as a building block for antihypertensive and antipsychotic drug APIs, particularly within triazine- and pyrimidine-based molecule pathways. Its trifluoromethyl and cyano functionalities promote targeted reactivity in multi-step syntheses, contributing to the structural frameworks required by various regulated small molecule medications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Pharmacopeial Standards
    • EDQM CEP Certificates (where APIs target the EU market)
    • Relevant FDA or EMA regulatory documentation for process intermediates

    Typical usage ratio

    • 0.5% – 5% w/w in targeted synthesis steps, adjusted by desired yield and pathway complexity. Actual proportion determined by the stoichiometry of heterocycle construction and substitution reactions.

    Downstream process integration

    • Integration occurs following initial condensation or coupling with protected amines, with the material introduced as a nucleophilic aromatic component in key carbon–nitrogen bond-forming reactions. Used in batch or flow reactors, typically following solvent preconditioning and analytical QC confirmation.

    Final product types

    • Antipsychotic drug intermediates
    • Antihypertensive compound precursors
    • Pyrimidine-based API candidates
    • Custom-developed specialty pharmaceuticals for R&D

    2. Agrochemical Synthesis (Herbicide & Fungicide Intermediates)

    Major agrochemical producers incorporate this material as a core aromatic nucleus in selective herbicide and fungicide molecule assembly. The electron-withdrawing trifluoromethyl coordinates stability during subsequent chlorination and methylation steps, supporting high-yield output in production of crop protection chemicals.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems in chemical process operations
    • REACH Registration (EU) for precursor import and handling
    • China National Standard GB/T 1601 for pesticide intermediates (where applicable)

    Typical usage ratio

    • 1% – 8% w/w depending on specific target molecule, modulated per downstream ring closure or nitrile-group transformation requirements.

    Downstream process integration

    • Raw material feeds directly into chlorination or amination stages of herbicide active ingredient synthesis, often in high-throughput stirred tank reactors. Process engineers introduce the compound after solvent charging and catalyst addition under inert atmosphere controls to prevent side reactions.

    Final product types

    • Triazine herbicide intermediates
    • Aromatic amine fungicide precursors
    • Pre-formulation bulk pesticide actives
    • Specialty crop protection synthesis stock

    3. Dyestuff and Pigment Intermediate Production

    Dye manufacturers utilize this compound as a key substrate in the preparation of specialty azo and anthraquinone dyes, where its fluorinated aromatic ring enhances dye brightness and resistance to photodegradation. The nitrile and amino groups streamline diazotization and coupling steps essential to high-performance pigment synthesis.

    Industry compliance standards

    • REACH Compliance for dye and pigment intermediates
    • OEKO-TEX® Standard 100 restricted substances list (textile dyestuffs)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 Process Documentation for specialty colorants

    Typical usage ratio

    • 2% – 12% w/w in pigment formulation batches; precise loading determined by color intensity, fastness targets, and coupling reactivity.

    Downstream process integration

    • Material enters the process after initial sulfonation or halogenation, feeding as the prime amine or cyano source in diazotization reactions. Plant technicians add the material in controlled temperature reactors to manage exotherms and maximize conversion yield before downstream purification.

    Final product types

    • Azo dye intermediates (for textiles and paper)
    • Special effect pigments (for plastics and coatings)
    • Acid dye synthesis blocks
    • Lightfast pigment concentrates

    4. Advanced Material Monomer and Polymer Additives

    Polymer and specialty material companies integrate this intermediate in the development of specialty fluorinated polymers and coatings, targeting applications requiring extreme chemical resistance and low surface energy. Its functional groups offer valuable points for incorporating rigidity and thermal stability in the resulting polymer backbones.

    Industry compliance standards

    • UL 94 Flammability Standards (for polymer components)
    • RoHS Directive (for electrical application polymers)
    • ASTM D638 and D790 (mechanical & thermal testing of plastics)
    • ISO 14001 Environmental Management (sustainable production environments)

    Typical usage ratio

    • 0.1% – 4% w/w in co-polymerization formulations; proportion adjusted according to required monomer reactivity and targeted end-use property enhancements.

    Downstream process integration

    • Introduced as co-monomer during bulk or emulsion polymerization, typically following initiator addition in nitrogen-purged kettles. Quality control monitors monomer purity and conversion efficiency at this point to prevent issues in polymer chain propagation.

    Final product types

    • High-durability fluorinated polymer films
    • Anti-stain and anti-graffiti coating additives
    • Electronic device encapsulants
    • Specialty engineering resin blends

    5. Specialty Chemical Synthesis for Electronic Materials

    Manufacturers supplying the electronics industry employ this compound to synthesize photoresist resins, liquid crystal intermediates, and other functional materials where high purity and reproducible electronic properties are critical. Its electron-withdrawing characteristics and steric profile promote precise substitution in aromatic systems required by modern display and microfabrication processes.

    Industry compliance standards

    • IPC-4101 Laminates and Prepregs Standard (for electronic substrates)
    • ISO 9001:2015 Quality Management
    • RoHS Compliance and SVHC Declarations for electronics
    • SEMI S2 Semiconductor Equipment Safety Guidelines

    Typical usage ratio

    • 0.2% – 3% w/w in advanced material resin formulations or photoinitiator precursor synthesis, regulated by performance test criteria such as dielectric constant and UV crosslinking behavior.

    Downstream process integration

    • Introduced after initial halogenation or methylation stages; used as a structural modulator in the synthesis of aromatic monomers for subsequent polycondensation or UV-curable photoresist blending. Compliance testing ensures electronic grade purity throughout the process.

    Final product types

    • Photoresist resin photoinitiator intermediates
    • Liquid crystal material blocks (for display panels)
    • High-frequency PCB laminate additives
    • Dielectric film precursors
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    Certification & Compliance
    More Introduction

    2-Amino-5-Cyanobenzotrifluoride: An Insider’s Look at Our Practical Chemistry

    What Sets 2-Amino-5-Cyanobenzotrifluoride Apart in Fine Chemical Production

    Making 2-Amino-5-Cyanobenzotrifluoride isn’t just about hitting a formula and sending material into drums. As a manufacturer, every campaign teaches something new about this subtle intermediate. Its chemical backbone—broadly referred to by its CAS number 444-16-6 in technical circles—combines a stable trifluoromethyl group with functional cyanide and amine moieties. The result is a raw material that serves chemists in sophisticated syntheses, especially when projects demand tight purity and a dependable supply chain.

    Our engineers and operators handle this compound in glass-lined reactors under precise temperature profiles. We have learned the hard way that shortcuts in pH control or solvent selection invite problems later in the pipeline. Even at small scales, careless exotherms or incomplete quenches ruin batches, wasting weeks of effort and frustrating partners downstream who depend on reliable imports. Our facility avoids these headaches by keeping a tight grip on every batch, applying GC and HPLC at each step so nothing slips through unnoticed.

    Unlike lower-value fluorinated aromatics, 2-Amino-5-Cyanobenzotrifluoride resists hydrolysis and survives the rigors of multi-step R&D. Organic chemists favor it because the combination of a nucleophilic amine and an electron-deficient cyano in the presence of trifluoromethyl allows for cross-coupling, condensation, and other cornerstone reactions. Others might opt for similar molecules, but without the same balance they run into issues with side product formation, environmental handling, or poor compatibility with downstream catalysts.

    Direct Input from the Production Line

    We’ve watched the industry shift from bulk commodity manufacturing toward specialty and pharma intermediates. End users want the confidence that comes from knowing exactly how we prepare these chemicals. For 2-Amino-5-Cyanobenzotrifluoride, our process draws from refined halogen exchange chemistry and controlled amination protocols. It’s tempting to speed up steps to chase yield, but consistent results come from patience at every stage, especially purification. Unchecked by-products, invisible to the naked eye, trigger headaches for downstream API teams. By investing in real analytical feedback—quick TLC, LC-MS in the pilot lab, and then validating at scale—we’ve earned trust, batch after batch.

    We understand that even minor adjustments in solvent ratios or pressure profiles cause significant differences in particle size, filtration performance, and even odor. Our QA team demands regular retraining, and we run regular root cause investigations if a shipment scores outside our custom purity benchmarks, by focusing on real-world outcomes rather than just ticking procedural boxes. This is how our material produces low background interference and performs reliably in final transformations. Every run we make gets full batch documentation and a thorough impurity fingerprint, not just a casual “meets spec” guarantee.

    Users and Applications: The Real Demand Behind the Molecule

    Innovation in the pharmaceutical and agrochemical industries has increased the need for versatile aryl building blocks. 2-Amino-5-Cyanobenzotrifluoride fits these demand spikes because it plugs straight into high-value synthetic routes. Most of our partners working in pharma or crop protection focus on speed and reproducibility. They expect a material that withstands the rigors of Suzuki-Miyaura and Buchwald-Hartwig couplings, nucleophilic substitutions, or even Grignard additions. They have learned—often the tough way—not to risk key steps on variable intermediates or questionable supply chains.

    Working alongside research chemists, we have tracked the main commercial applications. One group uses this molecule as the origin for pyrimidines and fused heterocycles, advancing pipeline drug candidates for oncology. Agrochemical teams transform it during the synthesis of functionalized benzonitrile herbicides and fungicidal cores. Some fine chemical firms rely on its resistant aromatic scaffold to derive electronic materials that tolerate harsh conditions. Each sector has specific priorities, but all trust our material to handle tough later-stage modifications when high throughput and minimal impurity bleed matter.

    Everything relies on the integrity of the starting material. Our collective experience as a manufacturing team has taught us to anticipate the pain points already familiar to our customers. Inconsistent melting point, poor solubility, or colored impurities in other grades have tanked entire research projects and driven teams to shop around for a true chemical manufacturer, not a broker with access to rejects or repacked stocks. That trust barrier motivates our crew every day at the plant.

    Specifications and Handling Built on Real-World Use

    Our regular lots for 2-Amino-5-Cyanobenzotrifluoride maintain a purity of over 99 percent by HPLC, with strict control over hydrolyzable impurities and trace metals. Over the years, several labs have brought us grading requests—tightened to accommodate more sensitive catalytic cycles or specialty formulation requirements. We welcome such direct feedback and bake it into our batch control protocols. Our operations group inspects moisture content, sieve residue, and bulk density on all outgoing shipments, reporting real values, not best guesses.

    Few things frustrate a chemist more than a parcel arriving with visible clumps or mysterious discoloration. We work with moisture-protected packaging and monitor warehouse conditions so that the product does not draw water and degrade in transit. Our QC team maintains retention samples and tracks long-term stability—even for custom micronized or slurry formats ordered by formulation partners dealing with mixing headaches or dust exposure in automated lines.

    The typical solid appears as a pale yellow crystalline powder. If a customer requires smaller particle fractions, we run post-processing in controlled mills. The workforce takes pride in visual and instrumental inspection, flagging issues before any drum is released. Each label contains clear manufacture and retest dates. Storing the product in sealed containers away from direct sunlight avoids surprises.

    Real Differences That Define This Material

    It’s easy to group 2-Amino-5-Cyanobenzotrifluoride alongside other trifluoromethyl-substituted benzonitriles, but experience confirms the unique balance of reactivity and stability inherent to this position isomer. For example, moving the amine or cyano group to an opposing ring position can compromise downstream yields or create unfriendly by-products during cyclization. Substituting a methyl for the trifluoromethyl can change the entire electronic profile, reducing shelf life and compatibility with sensitive synthesis.

    Our process avoids the “dirty” by-products left by less selective routes, like over-bromination or incomplete reduction seen in older benchtop syntheses. Rarely do we encounter requests for high impurity grades, but we have learned from forensic analysis that even trace organic or inorganic residues can derail high-value steps further along. For every new customer, we provide a tailored technical briefing, sharing both best practice and war stories from past challenges.

    Shipping practices define long-term relationships in this field, too. Improper storage of less stable analogs could lead to off-odors, tank leaks, or environmental concerns that force sudden shutdowns. We have made substantial investments in material compatibility studies. Over the years, we tracked packaging failures caused by inferior liners or untested closures, then adjusted our standard containers based on field feedback from partners worldwide.

    Manufacturing Insights: Where Chemistry Meets the Real World

    Scaling up the production of 2-Amino-5-Cyanobenzotrifluoride from lab glassware to high-throughput reactors brought surprises across the years. Expecting laboratory procedures to transfer “as is” always falls short. Issues like vapor load, fouling, or thermal runaway become more pronounced in big reactors. Our technical crew maintains a direct line to our process engineering group, iterating reactor loads, stirring speeds, and even jacket temperature gradients until output meets expectations. We keep a hazard map for each campaign, updating as new insights surface.

    Capacity planning means more than just keeping tanks full. Each campaign gets matched to real demand forecasts from our partners, reducing overstock and waste. We own our quality assurance program from start to finish, so all records get logged in-house, allowing us to trace any deviation within hours. During questions from customers—about trace solvents, rare outlier analyses, or even obscure analytical peaks—someone from our plant always takes responsibility for resolving the root issue, not just sending a lab report or shifting blame.

    Efforts to reduce environmental footprint form part of our daily operations. Controlling trace ammonia, recycling solvents, and capturing by-products enables us to reliably meet environmental regulations in multiple regions. Our efforts to minimize off-gassing during amination and reduce chemical usage in purification keep our operations sustainable, meeting not just compliance requirements but also internal goals for resource conservation and reduced waste.

    Trust Grown through Experience

    Long-term reliability comes from an understanding that the true customer is the project engineer or line chemist, not a distant procurement team. They've explained to us the pressures faced during late nights, trouble-shooting stalled synthetic sequences, or receiving raw material with inconsistent properties. Our commitment to fast technical support and clear documentation stems from a shared stake: if a batch causes someone trouble, our whole team digs in to solve it, learning and improving for the next run.

    Our team places special emphasis on continuous improvement. Any time new instrumentation becomes available, we assess its relevance for our QA group. Rather than blanket testing, we select and validate new methods, often drawing on direct feedback from partners who have encountered stubborn impurities or challenging analytical gaps. Our aspiration remains delivering a product that exceeds, not merely meets, project requirements.

    The Broader Role of 2-Amino-5-Cyanobenzotrifluoride in Advanced Chemistry

    The materials landscape grows more competitive with each new patent and regulatory requirement. We have spent years building a technically resilient offering for 2-Amino-5-Cyanobenzotrifluoride. Its reliable electron distribution and robust structure ensure performance in specialized drug synthesis and crop science applications. Most competing intermediates either lack the purity, come from unclear sources, or miss the attention to analytical detail that advanced users demand. Our value grows from not just making molecules, but supporting the transformative work our partners are pushing forward in their industries.

    Many of the older supply chains for similar compounds relied on batch brokers or distributorships with no real process accountability. Lab notebooks disappear, and unanswered deviations frustrate busy labs. Our experience as manufacturers—handling surprises, resynthesizing rare batches for under-pressure researchers, and constantly adjusting to evolving technical specifications—has made us flexible and responsive. This allows our partners to focus on creative chemistry without sweating over the reliability of each drum.

    Feedback and Responsible Growth

    We welcome direct communication from users. Whenever someone notices a minor deviation or has special requirements—such as requests for higher chiral purity, tighter filtration, or moisture-resistant handling—we mobilize our specialists to deliver those adjustments. Listening to the field teaches us more than formal audits ever could. We recognize the stakes for each downstream application—when a batch underperforms, the potential cost isn’t just in lost work, but in missed innovations and delayed product launches.

    Societal and regulatory shifts prompt us to constantly reassess every part of our manufacturing. Our team regularly reviews REACH, TSCA, GHS, EPA, and country-specific rules. We adjust documentation and labeling accordingly, keeping customers up to date and out of trouble with audits. Commitment to traceability extends beyond just our plant; it reaches our raw material supply chain. We scrutinize every supplier to avoid unexpected contamination, unreliable lead times, or shifting impurity profiles.

    Wherever our product gets used—whether as a staple in medicinal chemistry or a functional additive in specialized materials—the same discipline in manufacturing and transparency ensures our customers receive what they expect with every order. Our team treats every run as an opportunity to strengthen the line of trust and support innovation across the chemical industry. Behind every drum stands a crew experienced in both the art and science of fine chemical manufacturing, ready to tackle new challenges today and welcome more tomorrow.