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4-Methoxy-3-Nitrobenzoic Acid

    • Product Name 4-Methoxy-3-Nitrobenzoic Acid
    • Alias p-Anisic acid, 3-nitro-
    • Einecs 219-984-0
    • 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

    904371

    Chemical Name 4-Methoxy-3-Nitrobenzoic Acid
    Cas Number 619-17-0
    Molecular Formula C8H7NO5
    Molecular Weight 197.15 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 188-190 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.49 g/cm³
    Purity Typically ≥98%
    Synonyms p-Anisic acid, 3-nitro-; 3-Nitro-4-methoxybenzoic acid
    Smiles COC1=CC(=CC(=C1)C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C8H7NO5/c1-14-7-3-5(9(12)13)2-4-6(7)8(10)11/h2-4H,1H3,(H,10,11)
    Storage Temperature Room temperature, protected from light
    Ec Number 210-601-4

    As an accredited 4-Methoxy-3-Nitrobenzoic 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 with a screw cap, labeled "4-Methoxy-3-Nitrobenzoic Acid, 25g," includes hazard symbols and handling instructions.
    Shipping 4-Methoxy-3-Nitrobenzoic Acid is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Packages are clearly labeled according to regulatory standards and handled as a potentially hazardous chemical. Shipping complies with relevant safety regulations and includes appropriate documentation for safe transport and delivery.
    Storage 4-Methoxy-3-nitrobenzoic acid should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers and bases. Ensure appropriate labeling and avoid exposure to heat, sparks, or open flames. Store at room temperature unless otherwise specified by the manufacturer or safety data sheet.
    Application of 4-Methoxy-3-Nitrobenzoic Acid

    Applications of 4-Methoxy-3-Nitrobenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 4-Methoxy-3-Nitrobenzoic Acid, we support clients across advanced chemical sectors. Our material plays a significant role in the synthesis of specialty chemicals, pharmaceuticals, and electronic chemicals. Each industry application below details integration points, regulated benchmarks, recommended usage strategies, and representative finished products.

    1. Pharmaceutical Intermediate for Sartan-Class APIs

    Pharmaceutical manufacturers use this acid as a key intermediate in the synthesis of several angiotensin II receptor blockers (ARBs), including Irbesartan and Candesartan. Our product’s purity and controlled particle size contribute to high-yield reactions during the coupling and condensation stages. Buyers require strict documentation for residual solvents and trace-level impurities throughout multistep synthesis. We support validated production streams meeting major pharmacopeial standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monographs for finished API quality
    • FDA 21 CFR Part 210/211 for drug substance processes
    • REACH registration for non-EU supply chains

    Typical usage ratio

    • Ranges from 0.25 to 0.40 molar equivalents relative to core ARB scaffold
    • Adjustment based on reaction scale, specific API, and stepwise conversion yield

    Downstream process integration

    • Used in the N-alkylation or esterification stage of ARB synthesis
    • Introduced after initial functional group protection and amidation

    Final product types

    • Irbesartan active pharmaceutical ingredient (API)
    • Candesartan cilexetil API
    • Validated sartan derivatives for generic and proprietary formulations

    2. Precursor in Liquid Crystal Material Synthesis

    Electronic chemical producers rely on this acid as an essential precursor for the synthesis of mesogenic esters and other intermediates involved in liquid crystal displays (LCD). Controlled purity levels mitigate ionic contaminants, safeguarding the electro-optic performance of LCD mixtures. Material integration occurs during the formation of arylbenzoate or biphenyl-based liquid crystals. Batch validation includes full traceability and conformance to electronic-grade purity norms.

    Industry compliance standards

    • IEC 61249-2-43 for halogen-free compositions in display technology
    • RoHS Directive (EU) 2011/65/EU controls
    • ISO 9001:2015 for quality management in specialty electronic materials
    • China GB/T 2423 test standards for electronic chemicals

    Typical usage ratio

    • 0.05–0.10 kg of intermediate per kilogram of final mesogenic mixture
    • Ratio adjusted for single- or multi-component LCD types

    Downstream process integration

    • Condensation with phenolic or biphenyl intermediates to form target mesogens
    • Incorporated at early-stage esterification before column purification

    Final product types

    • Twisted nematic (TN) LC fluid blends
    • Vertical alignment (VA) LC mixtures
    • Hard-coated LCD filter substrates

    3. Synthesis of UV-Absorbing Benzophenone Derivatives

    The fine chemicals sector uses this compound as a starting acid for preparing substituted benzophenone UV absorbers. The methoxy and nitro functionalities facilitate controlled coupling and substitution reactions for subsequent hydroxylation or methoxylation. Regulatory compliance with European and North American chemical control bodies governs both the synthesis and downstream use within protective coatings and specialty polymers.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006, REACH Annex XVII
    • Toxic Substances Control Act (TSCA) Inventory for U.S. import
    • ISO 14001 for environmental control in specialty chemicals
    • OEM-specific restricted substance lists for polymers

    Typical usage ratio

    • Typically 0.18–0.22 mole ratio for coupling reactions with diphenyl ketones
    • Loadings can shift based on target absorbance profiles and by-product optimization

    Downstream process integration

    • Inserted during aromatic acylation or halogenation reaction steps
    • Purified before integration into benzophenone-based UV additive systems

    Final product types

    • UV-327, UV-328 type light stabilizers
    • UV-blocking masterbatch for polyolefins
    • Solar-resistant industrial coatings

    4. Raw Material for Colorant and Dye Intermediate Production

    Textile and ink chemical specialists select our material for its suitability as a nitroaromatic building block in the synthesis of azo and anthraquinone dyes. The compound supports highly selective diazotization and coupling reactions, enabling precise chromophore modification and shade tuning. Compliance requirements target both process safety and restriction of hazardous amines in downstream pigment or dye use, especially for consumer textile applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 bans for certain amines in finished textiles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) for formulated dyes
    • ISO 9001:2015 for production and supply chain traceability
    • EU REACH Annex XVII restrictions for azo colorants

    Typical usage ratio

    • Used at 0.08–0.15 molar equivalents in diazo-coupling for pigment intermediates
    • Ratio adjusted for chroma intensity and shade depth requirements

    Downstream process integration

    • Initiates the nitro reduction and subsequent diazotization process
    • Dye or pigment precursor integrated before final coupling or sulfonation

    Final product types

    • Azo and anthraquinone-based textile dyes
    • Disperse colorants for polyester fibers
    • Pigment dispersions for inkjet inks and printing pastes

    5. Intermediate for Agrochemical Synthesis (Herbicide/Pesticide)

    Agrochemical formulators employ this acid as an intermediate for select nitrobenzoic and benzanilide-based herbicides. The molecule’s substitution pattern facilitates targeted chlorination or amide formation, essential in the development of active ingredients with controlled release and uptake profiles. Manufacturing partners adhere to regional environmental safety schemes and maintain strict documentation for crop protection applications.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • China ICAMA registration for agricultural inputs
    • ISO 17025 for analytical method validation
    • European Union Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • Generally 0.12–0.17 mole feedstock per mole target active ingredient
    • May vary with desired herbicidal spectrum and downstream formulation dilution

    Downstream process integration

    • Participates in primary amide/ester bond formation or selective halogenation
    • Incorporated after initial nitration and hydrolysis steps

    Final product types

    • Benzanilide and nitroaromatic herbicide actives
    • Pre-emergent and early post-emergent crop protection agents
    • Custom-blend pesticide technical concentrates
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    Certification & Compliance
    More Introduction

    4-Methoxy-3-Nitrobenzoic Acid: A Reliable Tool for Organic Synthesis

    Product Introduction and Manufacturing Experience

    From our facilities, 4-Methoxy-3-Nitrobenzoic Acid stands out as a quietly powerful chemical building block, appreciated by laboratories and manufacturers who value consistency and reliability. Over years of hands-on work, our team has learned that the real benchmark in specialty chemicals starts long before the product lands in a drum or bottle. Rigorous sourcing, hydrophobic process management, and close monitoring during every step pay off in the final purity and yield, especially when producing delicate nitroaromatics. Our 4-Methoxy-3-Nitrobenzoic Acid typically crystallizes as a faint yellow solid, and its melt point, solubility, and spectral features reflect the care taken during manufacture and purification.

    For those unfamiliar, the molecule features a methoxy group in the para position, and a nitro group in the meta position on the benzoic acid ring. This configuration influences reactivity in a way that synthetic chemists favor: the methoxy group increases electron density, changing how the ring reacts during further transformations, while the nitro group’s strong electron withdrawal enables selective activation. It’s this interplay that creates value in multi-step synthesis, including pharmaceuticals, advanced materials, and custom dyes.

    Specification Insights and Quality Focus

    The typical specifications most users expect—appearance, purity, melting range, and loss on drying—sound simple at first, yet the market never forgets how small variances can lead to major downstream headaches. We conduct high-performance liquid chromatography and gas chromatography-mass spectrometry assays to look for isomeric contaminants or unreacted starting material. Ultra-precise melting point checks root out hidden impurities. Our batches usually show purity over 99%, with a narrow melting range. We also make a point of maintaining consistent particle size and moisture content, since we’ve learned sensitive chemical transformations often respond poorly to batch-to-batch differences.

    The product carries a molecular formula of C8H7NO5, with a molar mass of 197.15 g/mol. After several years in scale-up production, we saw firsthand that keeping byproducts and trace residual solvents under strict control improves both reaction performance at the customer end and shelf life for inventory. This attention to detail helped forge long-term relationships with research labs, pharmaceutical makers, and suppliers to electronics industries—all dealing with projects where trace contaminants can undermine value.

    Application Experience and Advantages Over Similar Compounds

    Having supplied 4-Methoxy-3-Nitrobenzoic Acid into a wide range of research and industrial projects, we’ve mapped out the sorts of results that make this compound compelling. It acts as an intermediate in the synthesis of more complex carboxylic acids, and finds niches in pharmaceutical development, particularly for nonsteroidal anti-inflammatory drug research, and in pigment work where color fastness and brightness require reliable molecular scaffolding. Our experience shows the methoxy substituent, versus analogues like plain nitrobenzoic acids, imparts differing reactivity—making it easier to introduce further substituents or serve as a platform for new high-value molecules.

    Some clients once used 3-Nitrobenzoic Acid or 2-Methoxybenzoic Acid for similar applications, only to switch after discovering improved selectivity or reaction yields with the 4-methoxy, 3-nitro configuration. We attribute these differences to the way electron-donating and -withdrawing groups interact on the aromatic ring, a nuance sometimes missed in casual syntheses but proved out at scale. Feedback from formulation teams reinforced the benefit: more predictable outcomes in coupling reactions, cleaner conversion profiles, and easier purification at later stages, all thanks to those subtle electronic effects.

    Manufacturing Process and Commitment to Consistency

    Our own production line for 4-Methoxy-3-Nitrobenzoic Acid reflects years of tuning and investment. We source high-grade anisole or related precursors, use controlled nitration steps, and conduct hydrolysis with careful temperature and pH monitoring to prevent over-nitration or ring degradation. Solvent selection and phase-separation techniques were refined over repeated pilot runs; a single missed parameter could threaten yield or introduce chromatographic ghosts that show up much later in downstream processing. Our purification work includes multiple recrystallization steps and careful drying in inert environments, all aimed at beating industry benchmarks for clarity and shelf stability.

    The process evolved as we responded to customer complaints about batch variability and unwanted odors found in some grades from other suppliers. We used real-world analytical feedback, from both in-process monitoring and post-shipment testing at customer sites, to adjust nearly every step. Today, every batch draws on a core process, yet remains flexible enough to accommodate special customer requests on particle form, drying level, or even custom purity grades suited for regulated industries.

    Meet Challenges Beyond the Lab Bench

    In our experience, chemical manufacturing rarely stops at chemistry alone. Logistics, regulatory paperwork, and packaging also play a critical role in keeping customers productive and safe. 4-Methoxy-3-Nitrobenzoic Acid ships in sealed, moisture-resistant packaging to prevent hydrolysis and caking during long transport or storage. We keep careful documentation on batch traceability, and respond to customer audits with open manufacturing records and third-party analysis certificates. As regulatory frameworks increase, especially for pharmaceutical and food-adjacent applications, our long-term documentation includes risk assessments and impurity profiling—supporting customers in audits and new product submissions.

    Our technical team keeps close contact with clients in specialized fields such as API synthesis or dye manufacturing, where minor contamination or drift in specification could cause regulatory headaches. Whether the concern is levels of dichloromethane, possible nitrosamine precursors, or unwanted byproducts from side reactions, we never ignore such points. Many customers have moved projects to us out of frustration with third-party brokers or loosely tracked overseas producers unable to prove product lineage.

    Feedback from university labs and global pharmaceutical pilots has shaped how we verify our own storage and shipping protocols. More than once, a project hit a last-minute snag because a trace moisture pickup altered reaction kinetics. As a result, we now run atmospheric testing inside our packaging area and use desiccant indicators for shipments sent through high-humidity routes.

    Safety, Handling, and Real-World Use Cases

    For all the sophistication of this compound’s chemistry, real-world handling experience matters just as much. We train our team in the correct use of dust control, ventilation, and spill procedures. The nitro and carboxylic acid groups carry both health and reactivity signals, so experienced users watch for skin contact risk, inhalation risk, and heat sources during storage. Our safety team keeps updated with the wider literature on chemical incident reporting, adjusting our SOPs as improved practices emerge. A few years ago, a client flagged photodecomposition risk from direct sunlight through package windows; since then, we added an opaque secondary wrap for all inventory.

    In manufacturing environments that demand high-throughput dosing—such as pigment blending or pilot pharmaceutical synthesis—our customers often ask for bulk formats or specific container types to fit into their automation lines. Based on ongoing feedback, we diversified our available volumes, enabled easier lot segregation in shipment, and designed compatibility with standard feeding systems, which cuts down on bridging and clumping during dispensing.

    Over time, we’ve seen a growing interest from custom polymer manufacturers and electronic materials formulators, drawn by the controllable electronic features of the compound. One project from a specialty resin developer needed narrow distribution of fine particle size for dispersion into polyamide backbones; we supported it with specialty micronization on demand. This responsive approach creates the backbone of a real partnership, matching technical know-how to unpredictable real-world challenges.

    Competitive Advantages and Distinctions in a Crowded Market

    After years supplying 4-Methoxy-3-Nitrobenzoic Acid to global and regional markets, we’ve come to appreciate how its story differs from more commonly available benzoic acid derivatives. While standard nitrobenzoic acids often arrive with cost appeal, our own data and feedback from production environments show that seemingly minor impurities—sometimes 0.1% or less—can cause false negatives in analytical testing or trigger color shifts in dye processing that spoil entire runs.

    The methoxy component doesn’t just affect chemistry inside a flask; some of our electronics-sector customers exploit its reactivity to build more complex aryl ether architectures, giving rise to new performance materials with high dielectric strength or unusual thermal properties. The nitro group, in meta position, often creates a cleaner reduction path or allows better selectivity during catalytic hydrogenation, compared to ortho- or para-nitro isomers. These layers of practical difference add up, especially when working toward new molecular scaffolds for high-value final products.

    Unlike many commodity-level offerings, our batch tracking, shipment support, and live technical backup make a difference for companies scaling from lab to pilot to full production. Our practical, customer-driven adaptations—such as producing custom dried grades, adjusting mesh size, or preparing documentation for specific regulatory filings—reflect the hands-on relationship that seasoned personnel value. These distinctions aren’t just theoretical; they’re the difference between smooth scale-up and repeated troubleshooting.

    Responding to Industry Change and Future Trends

    The chemical industry never sits still. Our operations have had to keep pace with shifting demands from innovators in pharmaceuticals, electronics, and color sciences. Ten years ago, bulk shipments of 4-Methoxy-3-Nitrobenzoic Acid centered on large bottles bound for academic labs and pigment plants. More recently, as new therapies and specialty polymers have come into focus, the requests for documentation, batch reanalysis, and impurity breakdowns have multiplied. Our response grew from lessons learned the hard way—missed analytical details leading to project failures force improvement like nothing else.

    Today, a growing share of projects request gradematched lots, reduced residue solvents, and documentation stretching back to raw materials procurement. Sharp spikes in environmental regulation have required changes in waste management; we invested in closed-loop solvent recovery and improved filtration steps to minimize process output, both for compliance and to support sustainability mandates from large partners. Our team keeps close watch on changes to REACH protocols, new listings on restriction annexes, and advances in green chemistry.

    Supply chain stress taught us to maintain close supplier relations and in-house reserves, especially for key precursors. COVID-era disruption created a hard lesson in risk buffering; we now maintain more robust inventory management and staged production runs to cushion clients against unforeseen delays. Our transparency about batch readiness and lead times gives customers confidence as their own schedules tighten.

    Practical Case Studies and Lessons from the Field

    Several projects on both small and large scales have used our 4-Methoxy-3-Nitrobenzoic Acid as a pivotal intermediate. In one case, a pharmaceutical research group used our product in a late-stage functionalization for an experimental anti-inflammatory candidate. They reported strong batch-to-batch reliability, reducing lab downtime caused by requalification steps. Post-project discussions showed that more standard 3-Nitrobenzoic Acid, purchased from less rigorous producers, brought along enough isomeric impurity to slow their development timeline.

    A specialty dye manufacturer, aiming for high-brightness yellow pigments, used our material to build a chromatographically sharp intermediate. Their feedback underlined how tight control of both residual methoxy byproducts and trace organic acids made their process yield higher than previous lots of mixed-origin material. Feedback cycles like this aren’t just paperwork exercises; each time, new process tweaks helped us reduce subtle contamination risks or solve recurring bottlenecks.

    One electronics company leveraged the reactivity of our 4-Methoxy-3-Nitrobenzoic Acid to construct novel dielectric polymers. Here, the difference between success and an entire line shut-down came down to residual water content: a packing change and tighter storage protocol kept them in spec through several production shifts. As clients share their frustrations and wins, we adapt—often at the raw material procurement level—to keep performance consistently high.

    Continuous Improvement and Knowledge Sharing

    After operating in this specialty niche for more than a decade, our approach grows steadily out of shared learning and persistent experimentation. Mistakes—whether a poorly preserved batch or a lapse in trace impurity documentation—have always seeded better protocols. We now involve all production staff in suggestions for trial process tweaks; every operator holds practical insight gained on the shop floor. At the same time, close discussions with university research groups and scale-up engineers feed back into our analytical monitoring, risk management, and customer support protocols.

    Chemistry, at its best, is collaborative. Rather than setting specifications based solely on internal measures, we use field data and outside audits to review particle sizing, purity distributions, and thermal stability. Findings from one project—such as minimizing a trace byproduct formed during hydrolysis—often develop into updated procedures for the next cycle. This sharing process helped us outpace market averages for both batch reliability and customer satisfaction.

    Long-term trust grows from these careful, documented improvements. When new clients approach us with demanding project needs—say, for pharmaceutical registrations, high-performance dye applications, or advanced material development—they find the upshot of hundreds of small, practical upgrades. As hands-on users ourselves, we never take for granted the cost and safety implications of even minor slips in chemical supply. Our methods—rooted in real experience and daily problem-solving—keep those risks as low as humanly possible.

    The Path Forward for 4-Methoxy-3-Nitrobenzoic Acid

    We know the future will bring new challenges for this chemical. Whether it’s about meeting stricter regulatory criteria, finding safer and more sustainable manufacturing methods, or keeping up with surging demand for custom synthesis, our direction tracks these changes closely. Connecting our real-world insights, customer relationships, and technical expertise, we believe that high-quality 4-Methoxy-3-Nitrobenzoic Acid will keep opening doors in pharmaceutical innovation, advanced materials, and specialty synthesis.

    Working directly—from initial inquiry and order through full-scale integration at customer sites—deepens our understanding of what real users need from this specialty acid. The value comes not from a catalog description or a specification sheet, but from day-to-day, challenge-by-challenge, result-backed learning that endures across projects, people, and industries.