Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Amino-4-(Trifluoromethyl)Benzoic Acid

    • Product Name 2-Amino-4-(Trifluoromethyl)Benzoic Acid
    • Alias 2-Amino-4-(trifluoromethyl)benzoic acid
    • Einecs 223-043-4
    • 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

    648089

    Product Name 2-Amino-4-(Trifluoromethyl)Benzoic Acid
    Cas Number 74609-33-1
    Molecular Formula C8H6F3NO2
    Molecular Weight 205.13 g/mol
    Appearance Off-white to beige solid
    Melting Point 165-168°C
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 2-Amino-4-trifluoromethylbenzoic acid
    Storage Temperature 2-8°C
    Smiles NC1=CC(C(F)(F)F)=CC=C1C(=O)O
    Inchi InChI=1S/C8H6F3NO2/c9-8(10,11)5-2-1-4(12)6(3-5)7(13)14/h1-3H,12H2,(H,13,14)

    As an accredited 2-Amino-4-(Trifluoromethyl)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams net, sealed with a screw cap and labeled with chemical name, formula, hazard warnings, and supplier logo.
    Shipping 2-Amino-4-(Trifluoromethyl)benzoic acid is shipped in tightly sealed containers to prevent moisture ingress and contamination. It should be stored at room temperature and kept away from strong oxidizing agents. Transportation complies with chemical safety regulations, ensuring proper labeling and documentation for safe, regulated delivery. Handle with appropriate protective equipment during transit.
    Storage Store 2-Amino-4-(Trifluoromethyl)benzoic acid in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from light and moisture. Clearly label the container, and follow standard laboratory safety practices, including the use of appropriate personal protective equipment when handling the compound. Store at room temperature unless otherwise specified.
    Application of 2-Amino-4-(Trifluoromethyl)Benzoic Acid

    Applications of 2-Amino-4-(Trifluoromethyl)Benzoic Acid in Industrial Manufacturing

    2-Amino-4-(Trifluoromethyl)Benzoic Acid serves as a precision intermediate in advanced industrial sectors. Our facility supports demanding OEM and system integrator specifications through consistent process control and traceable quality documentation. Below, we detail real-world manufacturing pathways and integrations for this raw material in downstream business operations.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers employ our product to construct key tricyclic and heterocyclic scaffolds, necessary for active pharmaceutical ingredients targeting CNS, anti-inflammatory, and antimicrobial indications. Typical usage involves multi-step coupling or condensation reactions in GMP batch or continuous lines, under validated procedures. Production teams control reactant ratios based on mole-to-mole conversions, adjusting for yield and impurity profile optimization. Final APIs move directly into finished dosage production after comprehensive release testing.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • EU EudraLex Volume 4 Part II
    • US FDA cGMP 21 CFR Part 210/211
    • ChP/USP/Ph. Eur. reference monographs for related APIs

    Typical usage ratio

    • Varies from 0.5 to 1.3 molar equivalents per batch, depending on API structure and yield; process engineer determines precise ratio.

    Downstream process integration

    • Charged as a core intermediate within amidation, reductive amination, or Suzuki-Miyaura coupling steps of API synthesis.

    Final product types

    • Medical active pharmaceutical ingredient (API) isolates
    • Branded or generic CNS agents
    • Bulk drugs for oral solid and parenteral formulations

    2. Advanced Agrochemical Intermediate

    Agrochemical formulators use the material to build fluorinated aromatic backbones found in new generation selective herbicides and fungicides. Synthesis lines incorporate the molecule at key Grignard, acylation, or cyclization stages, with strict monitoring of trace metal and halogen content to ensure crop safety and environment regulation compliance. Final actives undergo downstream formulation to EC, SC, or WG product types.

    Industry compliance standards

    • ISO 9001:2015 certified quality management
    • FAO/WHO pesticide specification standards
    • REACH Regulation (EC) No 1907/2006
    • OECD Good Laboratory Practice (GLP) principles

    Typical usage ratio

    • Typically dosed at 1.02–1.10 molar equivalents relative to the primary starting aryl unit, adjusted for target yield and process losses.

    Downstream process integration

    • Introduced during intermediate synthesis before formulation blending and microencapsulation of active ingredients.

    Final product types

    • Selective herbicide active ingredients
    • Triazole-based fungicide actives
    • Agrochemical bulk intermediates for direct formulation

    3. Fluorinated Dye Synthesis for Specialty Pigments

    Dye manufacturers integrate the compound when synthesizing metal complex dyes and specialty organic pigments for textile and fiber applications. Operators employ direct coupling or condensation protocols, optimizing yields and purity via HPLC and GC controls. Traceability of each production lot supports regulatory documents required for export and supply-chain auditing. The raw material’s substitution pattern ensures high-performance dye fastness and shade reproducibility.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textiles)
    • EU REACH Annex XVII restricted substances
    • ISO 105 Series for color fastness
    • ZDHC MRSL manufacturing-restricted list

    Typical usage ratio

    • Ranged from 5–15% w/w of total dye batch, tailored for target hue and desired performance specifications.

    Downstream process integration

    • Added in coupling stage of pigment or dye synthesis before precipitation, filtration, and drying.

    Final product types

    • Metal complex dye powders and concentrates
    • Water- and solvent-based printing inks
    • High-durability textile colorants

    4. Building Block for Electronic Chemicals

    Electronics chemical manufacturers utilize this building block to produce specialty photoresist and fluorinated polyimide resins for semiconductor patterning and flexible substrate manufacturing. Batch chemists introduce the compound during precursor monomer synthesis, ensuring rigorous control of fluoride and amine residuals. Structured documentation and lot tracking meet major fab customer audit requirements.

    Industry compliance standards

    • SEMI Standard M1 for electronic chemicals
    • IATF 16949 (applicable for automotive electronics supply)
    • RoHS Directive (EU) 2015/863
    • ISO 14001 for environmental management

    Typical usage ratio

    • 0.8–1.1 molar equivalents based on stoichiometry with comonomers; fine-tuned by R&D chemists for film thickness and dielectric properties.

    Downstream process integration

    • Feeds into monomer synthesis, then polymerization, filtering, and solvent casting into films or resists.

    Final product types

    • Photoresist chemicals for lithography
    • Fluorinated polyimide films
    • Electronic-grade polymers for flexible circuits

    5. Intermediate for Fine Chemical Synthesis in Fragrance Ingredient Production

    Fine chemical companies incorporate the intermediate in the formation of aroma compounds used in regulated fragrance applications. Processing involves selective amidation or esterification, typically under CFR Title 21-compliant documentation systems. Specialists monitor for unreacted amines and verify analytical traceability to meet IFRA submission files.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • US FDA 21 CFR Part 182 (GRAS substances)
    • EU Regulation (EC) No 1223/2009 (cosmetic products)
    • ISO 22716:2007 (GMP for cosmetics)

    Typical usage ratio

    • Typically 2–8% by weight in synthesis of target aroma intermediates; exact concentration set by targeted olfactory profile.

    Downstream process integration

    • Enters as a primary aromatic acid input for further chemical conversion before downstream blending into formulated fragrances.

    Final product types

    • Synthetic musk and aldehyde fragrance intermediates
    • Specialty aroma building blocks for perfumery
    • Traceable GRAS-listed raw materials for flavor and fragrance finishers
    Free Quote

    Competitive 2-Amino-4-(Trifluoromethyl)Benzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    2-Amino-4-(Trifluoromethyl)Benzoic Acid: Direct From Chemical Manufacturer

    Here at our facility, we develop and manufacture specialty chemicals for pharmaceutical, agrochemical, and materials science industries. Among our advanced intermediates, 2-Amino-4-(trifluoromethyl)benzoic acid delivers consistent demand for both research and commercial-scale synthesis. Through years of production, our team has come to value the capabilities and versatility this compound brings to multiple sectors.

    Model and Specifications

    Our current batch of 2-Amino-4-(trifluoromethyl)benzoic acid maintains a white to pale yellow crystalline form through careful control of synthesis and purification. Our process achieves a chemical purity that typically exceeds 98 percent by HPLC, while melting point remains in the 178-182°C range. Moisture and volatile content are tightly monitored, ensuring reliable performance across reaction schemes. We craft material for both gram-scale and industrial multi-kilo requirements, with revalidation at every step to assure reproducibility. Analytical validation includes NMR, LC-MS, and IR as routine, with sample comparison checked for batch consistency. Packing adapts to your process needs, whether sealed HDPE drums for bulk or smaller amber glass for bench chemistry, always in inert atmosphere to prevent degradation.

    We have spent years refining production to minimize byproduct formation and allow straightforward downstream processing. Early runs often suffered from trace halide or aminobenzoic acid isomers, but more robust methods now produce highly selective output, cutting waste and easing final product purification. We maintain real-time access to stoichiometry adjustments and solvent handling, so our operators can address unexpected issues without long downtime or excessive waste. Feedback from long-term pharmaceutical partners led us to tighten limits on residual solvents, especially DMF and DCM traces. Getting below 0.05 percent took numerous trials and a close partnership with our analytical team, but purer output improved not only environmental performance but downstream yield and color in customer syntheses.

    Usage and Real-World Application

    2-Amino-4-(trifluoromethyl)benzoic acid serves primarily as a synthon for specialty heterocycles and substituted aromatic systems, many of which contribute to high-value drug molecules or advanced materials. Chemists appreciate its electron-withdrawing trifluoromethyl group coupled with the amino donor at the ortho position, which opens access to regioselective substitutions and cyclizations that are otherwise tough to achieve. We see regular usage in Suzuki or Buchwald-Hartwig couplings, often as a building block for fluorinated benzanilides and polyfluorinated pharmacophores.

    In pharmaceutical work, this product often leads to fluorinated prostaglandin analogs, kinase inhibitors, and even radiolabeled PET tracers. Nearly every month, a customer approaches us asking for feedback on a new route or scale-up—sometimes focused on batch robustness, sometimes pushing for higher initial purity to save cost and time in downstream chromatography. For custom research clients, the acid group provides a clean handle for amide coupling, esterification, or urea formation, while the electron-deficient ring encourages selectivity in halogenation or nitrosation. Our technical support partners work with medicinal chemists to troubleshoot purity or batch records, so intellectual property filings never run into ambiguous impurities or undocumented synthetic routes.

    On the agrochemical front, experience shows that fluorinated aromatic intermediates deliver improved stability, plant uptake, and in some cases, higher bioactivity against specific pathogens. We have received requests for custom cuts—gram to kilo range—to support development of patent-protected crop protection agents. For material science, the unique fluorinated group alters polymer backbone flexibility and surface energy, leading to more robust films or specialty coatings. Our supply to university and government labs often supports research into these novel properties, with researchers supplying in-depth feedback on batch quality and analytical results.

    Process Advantages Compared to Related Compounds

    In daily operations, we work with a spectrum of substituted aminobenzoic acids, each with its own quirks. The trifluoromethyl group in 2-Amino-4-(trifluoromethyl)benzoic acid means it displays higher acid resistance and lower nucleophilicity on the ring compared to plain 2-aminobenzoic acid. This lets process chemists perform selectivity-demanding reactions with less risk of undesired side-products. Our customers notice improved overall yield, particularly in routes that use strong base or demanding coupling conditions.

    Other isomers, such as 3-amino-4-(trifluoromethyl)benzoic acid, demonstrate different reactivity. Strecker or Sandmeyer-type transformations may proceed poorly or deliver alternate products, so researchers with tight patent windows come to us for help designing more selective routes starting with 2-amino. We constantly cross-check analytical data to confirm ring substitution patterns, using 19F-NMR or two-dimensional NMR methods, and share those results with partners focused on scale-up. Only a few other manufacturers offer these capabilities at this scale, especially in regions where environmental and regulatory oversight place a premium on clean processing.

    Practicality counts at every stage. Some competitive suppliers may only offer ‘technical grade’ or less rigorous post-synthesis purification due to costs; our lineup focuses on giving the option of high-purity material for those who demand full transparency for clinical, regulatory, or safety profiles. We have improved our process to avoid persistent trace residues, which commonly appear if starting from poorly characterized halide or trifluoromethyl sources. Each new production lot benefits from feedback taken during scale-up and continuous integration of in-line analytical improvements.

    Handling, Packaging, and Environmental Responsibility

    Over decades of shipping experience, we have learned the importance of both robust packaging and clear documentation. This compound remains stable for extended periods when kept away from moisture and direct light—less so for poorly capped containers or high-humidity regions during storage. For research laboratories, 25g units in amber glass minimize the risk of UV exposure and degradation, while multi-kilo volumes move in nitrogen-purged HDPE drums with tamper-resistant seals. Clients with specialty storage requirements, such as low-oxygen atmosphere or minus 20 degrees Celsius, receive tailored packing to reduce caking or hydrolysis during transport.

    Sustainability and compliance guide our operation throughout production and logistics. Waste reductions achieved in the last five years cut byproduct generation by nearly 30 percent, mainly via solvent recovery and sharper reaction stoichiometry. Effluent from fluorinated process streams meets all current discharge limits before reaching external treatment facilities. On request, we provide batch-specific life-cycle data to European and North American customers fulfilling REACH or TSCA reporting requirements. This traceability proves crucial to partners in regulated industries and gives research scientists an added layer of confidence in their sourcing.

    We have faced and overcome real-world supply chain shock, including raw material interruption or abrupt changes in upstream halide sourcing. Rigorous vendor qualification and close coordination with logistic partners allow us to honor both short lead times and just-in-time requests for kilo-scale delivery. Quality and compliance teams document all raw materials, operators, and process conditions, ensuring accountability—a factor especially important for pharma customers undergoing audits or clinical trial initiation.

    User Experiences and Ongoing Partnerships

    Our routine day-to-day includes direct engagement with customers scaling a candidate compound from bench to preclinical, or updating a regulatory filing for a long-standing API. The research teams at universities and contract labs frequently approach us for technical validation of synthetic intermediates—this includes data support for grant applications, patent filings, or peer-reviewed publication. Industrial users often provide ‘post-mortem’ analysis after pilot plant runs or failed scale-up attempts, seeking modified particle size, specific surface area, or even custom labeling to streamline their downstream chemistry.

    Feedback cycles have shaped not only technical aspects but also supply chain support. Five years ago, repeated feedback from one major pharmaceutical group highlighted issues with batch-to-batch variability and shipment documentation from global sources. In response, we implemented real-time online COA access with full batch data and chain-of-custody reporting for every shipment. Customers needed little persuasion to trust a source willing to stand behind every lot with quality, purity, and analytical detail.

    Through every engagement, we build relationships that hold up over time. For a crop protection firm, successful formulation trial runs using our material led to a multi-year supply partnership with defined supply schedules and shared intellectual property milestones. Academic collaborators report higher citation rates for their new molecule syntheses when they can cite reliable sourcing and detailed material validation instead of bulk catalog chemicals. We continue to refine not only synthetic process but every layer of support, including technical application workshops, collaborative troubleshooting, and joint process development for new transformations not yet published in literature.

    Comparisons With Other Market Offerings

    Chemists who work with multiple suppliers often describe frustrating differences in trace impurity profiles, flowability, or the need for additional purification. Our batches are known for their clarity in NMR, IR, and other chromatographic methods right out of the drum. We invest extra time in sample retention and analysis for every output, tracking each anomaly, no matter how small, for audit and troubleshooting. This approach often means more sample testing and internal review, but it reduces out-of-spec incidents and unscheduled downtime in our partners’ pilot or production facilities.

    Having vertical integration in raw material sourcing means our process stability far exceeds that of resellers working from secondary intermediates. With every shift and every batch, our production team enters variables into a live system, flagging unusual results in real time before a batch progresses to final purification. Users who come to us after equipment fouling or color changes find the transparency refreshing, especially after unsuccessful attempts with lesser grades.

    As analytical method development becomes more sophisticated, customers place greater importance on reproducibility for reference standards and impurity tracking. By holding the same validation protocols and raw material sources across batch runs, we provide a degree of confidence needed for both established and emerging regulatory frameworks. In one case, a customer was unable to pass a new lot release due to unexpected NMR peaks; after switching to our product, not only did the issue clear, but the client also reported a measurable uptick in yield at milligram and gram scale for each step of their synthesis.

    We encourage prospective partners—whether scaling a breakthrough fluorinated drug or refining new agrochemicals—to discuss specific process needs or analytical hurdles with our development team. Our experience shows that thorough communication and rigorous validation yield not just compliant product, but also supply reliability and better research outcomes. No matter the scale or complexity, we remain committed to direct dialogue and continuous improvement, built on decades of hands-on manufacturing and customer feedback.

    Innovations and Future Developments

    Over time, both regulatory landscapes and discovery research place new demands on synthetics. Increasingly stringent limits on metal and halide residues, or even stricter documentation on origin and process contaminants, drive us to continually revise not just manufacturing but post-purification handling. Our R&D group investigates greener solvent alternatives and real-time analytics, chasing the goal of reducing environmental load and improving operator safety without sacrificing chemical performance.

    We work closely with equipment suppliers to design reactors and purification systems that meet new legislative and industrial guidelines. Recent upgrades allow for in-situ monitoring of reaction progress and impurity formation, cutting cycle times up to 15 percent and sharply reducing energy consumption. Our long-term PI partners in government and industry supply detailed case studies showing how these improvements contribute to carbon reduction targets and waste minimization.

    Looking forward, we anticipate a new set of challenges. Synthetic routes to heavily fluorinated aromatics continue to grow more complex as biology and materials research reach for sharper selectivity or new electronic properties. Advanced analytics, from multi-dimensional NMR to high-resolution mass spec, push us to keep up with identification and minimization of side-products, even at trace levels. Through these developments, our corporate and research partners rely on us to share practical knowledge, ensuring that each ton or kilo delivered fits evolving research and regulatory needs.

    Commitment to E-E-A-T: Real-World Expertise

    Our company doesn’t just sell chemicals, we operate as a full-spectrum manufacturer with decades of hands-on experience in specialty intermediates. Our team includes process chemists, analytical specialists, and supply chain coordinators who all participate directly in production runs, quality control, and problem-solving. Most of our senior staff hold advanced degrees and have experience running their own synthesis projects before joining us. Internally, data from every batch is shared across process and QC—a practice that helps identify trends, uncover process improvements, and inform future technical support.

    Education also matters. We regularly hold supplier-customer workshops and technical webinars to keep partners updated on both production advances and potential pitfalls. For new users, we work out full traceability pathways, supply case studies, and share technical bulletins detailing synthetic challenges or opportunities with 2-Amino-4-(trifluoromethyl)benzoic acid. This approach aligns with our long-running goal—to advance chemistry not as isolated transactions, but through knowledge-sharing and close partnership with the scientific community.

    Real-world problems don’t get solved in a vacuum. Every cycle of production, shipment, and customer feedback makes us better at what we do. Each technical detail, from higher purity to robust analytical support, responds to the real needs of pharmaceutical, agrochemical, and materials researchers. Our product exists not as an off-the-shelf commodity, but as a joint result of manufacturing, rigorous validation, and partnership.

    Closing Perspective: Value Through Direct Manufacturing

    As one of the few direct manufacturers of 2-Amino-4-(trifluoromethyl)benzoic acid, we deliver a product shaped by continuous improvement and customer collaboration. The confidence that comes from knowing exactly how, where, and by whom a chemical is made matters now more than ever. Pharmaceutical, crop protection, and advanced materials companies rely on us not just for molecules, but for seamless scale-up, comprehensive analytical transparency, and partnerships rooted in mutual trust. With every batch, we uphold those commitments and stay ready to help research groups and industrial clients transform new ideas into real results.