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4-Hydroxy-3-Nitrobenzoic Acid

    • Product Name 4-Hydroxy-3-Nitrobenzoic Acid
    • Alias 4-Hydroxy-3-nitrobenzenecarboxylic acid
    • Einecs 223-009-4
    • 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

    780502

    Product Name 4-Hydroxy-3-Nitrobenzoic Acid
    Cas Number 619-73-8
    Molecular Formula C7H5NO5
    Molecular Weight 183.12 g/mol
    Appearance Yellow crystalline powder
    Melting Point 225-228°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 3-Nitro-4-hydroxybenzoic acid
    Inchi Key JNLCTOVKBFHAQW-UHFFFAOYSA-N
    Smiles C1=CC(=C(C=C1C(=O)O)[N+](=O)[O-])O
    Density 1.71 g/cm³
    Hazard Statements May cause skin and respiratory irritation

    As an accredited 4-Hydroxy-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 labeled "4-Hydroxy-3-Nitrobenzoic Acid, 25g" with hazard symbols, safety information, and lot number displayed.
    Shipping 4-Hydroxy-3-Nitrobenzoic Acid is shipped in tightly sealed containers, protected from light, moisture, and sources of ignition. It must be packed following local, national, and international regulations for hazardous chemicals, typically under UN number 3077 (environmentally hazardous substance, solid). Appropriate hazard labeling and documentation accompany the shipment to ensure safe handling.
    Storage 4-Hydroxy-3-nitrobenzoic acid should be stored in a tightly closed, clearly labeled container in a cool, dry, and well-ventilated area, away from light and incompatible substances such as strong oxidizing or reducing agents. Protect from moisture and sources of ignition. Handle with appropriate personal protective equipment and follow all relevant safety guidelines to prevent exposure or contamination.
    Application of 4-Hydroxy-3-Nitrobenzoic Acid

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

    As a core chemical intermediate, 4-Hydroxy-3-Nitrobenzoic Acid supports high-value synthesis for colorant, pharmaceutical, agrochemical, and electronics manufacturing. Our production adheres to internationally recognized benchmarks required by advanced downstream formulators and converters.

    1. Synthesis of Specialty Azo Dyes for Textile Applications

    4-Hydroxy-3-Nitrobenzoic Acid functions as an essential coupling agent in the preparation of high-grade azo dyes. Its electron-withdrawing nitro and hydroxyl groups facilitate chromophore development, increasing shade intensity and fastness on cellulose fibers. Leading textile dyehouses adopt this intermediate to achieve brighter hues, improved color strength, and compliance with restricted substance protocols. The acid integrates in diazotization and coupling stages, yielding stable dye intermediates for cotton and rayon printing lines. Stringent bath monitoring and product purification enhance downstream reproducibility and minimize unreacted starting materials.

    Industry compliance standards

    • ZDHC MRSL V3.1
    • OEKO-TEX Standard 100 Annex 6
    • REACH Regulation (EC) No 1907/2006 – Appendices XVII and XIV
    • BfR XXXVI Recommendation

    Typical usage ratio

    • 5–15% w/w of formulated dye paste depending on required shade depth
    • Ratio adjusted by fiber type, dyeing method, and targeted chromaticity

    Downstream process integration

    • Serves as a key substrate during dye intermediate coupling
    • Introduced after diazotization step in batch reactors
    • pH- and temperature-controlled conditions to maximize conversion yield
    • Purity verified by HPLC before packaging into dye pre-mixes

    Final product types

    • Reactive and direct azo dyes
    • Textile printing pastes
    • Disperse dye powders for synthetic fibers
    • Fiber-specific high-purity dye solutions

    2. Active Pharmaceutical Intermediate for Analgesics

    4-Hydroxy-3-Nitrobenzoic Acid constitutes a core structural element for drug manufacturers producing select analgesic APIs. In these synthetic routes, the acid group and ring substituents enable stepwise construction of more complex benzoate derivatives. GMP manufacturers utilize this intermediate under validated protocols to minimize impurity profiles and satisfy traceability from raw material to tablet production. Process engineers must optimize hydrolysis, esterification, and reduction steps to ensure purity before further API derivatization or crystallization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 211 (FDA US cGMP Regulations)
    • European Pharmacopoeia Monographs
    • USP-NF General Chapter 1079

    Typical usage ratio

    • Varies depending on specific API synthesis—typically 1.0–1.5 molar equivalent per batch step
    • Scaled relative to desired output and reaction stoichiometry

    Downstream process integration

    • Introduced during multistep benzoic acid functionalization
    • Serves as a starting point for nitration and acylation chemistry
    • Material tracked under lot-controlled logistics from intake through finishing
    • QC release performed after each purification stage

    Final product types

    • Benzoic acid-based analgesic APIs
    • Intermediate building blocks for anti-inflammatory compounds
    • Pharmaceutical excipients (in select cases)
    • Finished tablet formulations

    3. Agrochemical Synthesis: Herbicide Formulation Intermediates

    Major agrochemical companies employ 4-Hydroxy-3-Nitrobenzoic Acid as a critical intermediate to synthesize benzoate-class herbicides. The molecule’s functionality allows the introduction of side chains specific to weed control agents, with emphasis on selectivity and environmental persistence. Reactor charging protocols and phase separation schemes ensure controlled processing, meeting regulatory thresholds on residuals. Final herbicide actives undergo stringently monitored finishing to ensure stability and safe handling.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (2016 revision)
    • ISO 9001:2015 quality systems
    • EPA 40 CFR Part 180 (US pesticide residue regulation)
    • China GB 2763 Maximum Residue Limits for Pesticide

    Typical usage ratio

    • 0.2–0.7 mole per mole of target herbicide for intermediate formation
    • Level adjusted per process kinetics and end-use selectivity profile

    Downstream process integration

    • Feeds into nucleophilic substitution and esterification steps onsite
    • Employed in closed-reactor systems for safe handling of nitrobenzoic chemistry
    • Sampled post-reaction for residual QC and process validation
    • Intermediate output stored under inert atmosphere before final formulation

    Final product types

    • Selective post-emergent herbicide actives
    • Herbicide technical concentrates
    • Granular pre-mix herbicide formulations
    • Water-dispersible granules for broadleaf weed control

    4. Monomer Precursor in High-Performance Electronic Resins

    In specialty electronics, manufacturers utilize 4-Hydroxy-3-Nitrobenzoic Acid as a monomer precursor for advanced polyester and polyarylate resin systems. Its aromatic framework introduces rigidity and thermal stability into finished materials used for printed circuit boards and optoelectronics. Polymerization protocols require precise charge ratios, catalyst selection, and impurity control to prevent defects in downstream laminates. Due diligence on monomer incoming quality, moisture control, and batch-to-batch traceability underpin its successful industrial use.

    Industry compliance standards

    • IEC 61249-2-7 Base materials for PCBs
    • IPC-4101D Laminate and Prepreg Material Specification
    • RoHS Directive 2011/65/EU
    • UL 94 Flammability Standard

    Typical usage ratio

    • 15–30% molar in aromatic polyester formulations
    • Level varies by required resin modulus and thermal target

    Downstream process integration

    • Fed into melt polycondensation and solution polymerization reactors
    • Monomer purity and moisture content controlled at <0.1% water
    • Directly affects dielectric and mechanical performance of end-resin
    • Upstream batch documentation tied to each production lot

    Final product types

    • PCB-grade polyarylate and polyester resins
    • High-performance electrical laminates
    • LED encapsulation coatings
    • Optoelectronic polymer films

    5. Photographic Chemical Manufacturing

    Producers in the imaging sector use 4-Hydroxy-3-Nitrobenzoic Acid as an intermediate in the synthesis of reduction-resistant photographic developers. Its presence in the formulation ensures precise redox potential stabilization for black and white film and X-ray plate processing. Batch operations optimize dosing, temperature, and pH to maximize development efficiency and limit fog. Strict environmental and workplace standards apply when handling chemicals for photographic use, especially in medical or industrial radiography supply chains.

    Industry compliance standards

    • ISO 18917 for photographic processing
    • ANSI/NAPM IT9.11 for imaging chemicals
    • EU Directive 98/24/EC (chemical agents workplace risk)
    • OSHA 29 CFR 1910.1200 (Hazard Communication Standard)

    Typical usage ratio

    • 2–6% by weight in developer concentrate blends
    • Adjusted for developer dilution factor and film sensitivity requirements

    Downstream process integration

    • Integrated at blending stage of photographic developer concentrate manufacture
    • Monitored for purity with UV-Vis or TLC prior to bottling
    • Downstream storage in light-protected and climate-controlled conditions
    • Strict batch referencing for traceability in medical imaging chains

    Final product types

    • Photographic developer concentrates
    • X-ray plate chemicals
    • Ready-to-use black and white film developers
    • Specialty imaging kit solutions
    Free Quote

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    Certification & Compliance
    More Introduction

    4-Hydroxy-3-Nitrobenzoic Acid: A Practical Introduction From the Manufacturing Floor

    A Glimpse Into Our Daily Production Experience

    Our team has handled the synthesis and purification of 4-Hydroxy-3-Nitrobenzoic Acid for more than a decade. This molecule—formula C7H5NO5, often called by its CAS number 619-73-8—shows up across industries, known for its role in both research and industrial development. We’ve seen it ask for careful attention during every process stage, starting with raw material screening right through to inbound and outbound quality checks.

    In our reactors, each batch follows a strict timeline, hitting temperature targets and stirring speeds we've dialed in over years of hands-on work. The right nitrobenzoic acid derivatives are not just about purity on paper. Actual consistency in bulk shipments comes from troubleshooting hundreds of small challenges, like adjusting for reaction exotherms that shift with ambient weather, or tuning crystallization rates to manage particle size. Examining product under real plant lighting, checking for hue and granule morphology, counts as much as HPLC data. Employees who have spent years by the filter press or drying line notice the differences regularity brings.

    Breaking Down Specifications That Actually Matter

    We manufacture this compound with a minimum purity of 99%. This specific cutoff always comes up in customer audits. In the lab, purity gets confirmed by HPLC, checked against both in-house reference material and international standards. Moisture content typically tests below 0.5%, and residual solvents remain under detection. Melting point, measured in each batch, runs in the narrow range expected—ensuring no surprises in downstream processing.

    Particle size and bulk density don’t always get the front-row attention in academic papers, but in large-scale drum fills or automatic feeders, variances cause flow issues and waste. During grinding and sieving, our crews document the outcome with every batch. Even the color tone—light yellow, with an obvious intensity compared to non-nitrated analogs—tells us about batch stability.

    How Customers Use It—Real-World Applications and Our Experience

    We have shipped 4-Hydroxy-3-Nitrobenzoic Acid to institutions and downstream manufacturers who use it in specialty chemical syntheses, especially as an intermediate to more complex molecular targets. Some use this acid in the creation of dyes, thanks to the distinct electron-withdrawing effect of the nitro group. Others request our product for pharmaceutical research. The precision of its functional groups—both nitro and hydroxy—makes it a smart building block for further chemical transformations, including amide coupling and esterification.

    Veteran development chemists care about reactivity and purity, but production supervisors often call us with practical questions. Issues such as dustiness, tendency to cake, or reactivity with storage liners can matter as much as melting point data. Our plant has responded by offering the product in specialty packaging: lined drums for large orders, inner-lined bags for lab-scale work. Each change led to measurable improvements. Customer feedback keeps us honest; when a batch once arrived with clumping in the tropics, revised drying procedures solved the recurrence.

    Understanding Where It Fits Among Similar Compounds

    Anyone who has handled both 4-Hydroxy-3-Nitrobenzoic Acid and its isomers—like 2-Hydroxy-3-Nitrobenzoic Acid—knows they look almost identical out of the dryer. But side by side, subtle differences in solubility, reactivity, and even smell emerge. Our acid dominates as a synthetic intermediate because the hydroxy group sits in the para position relative to the carboxylic acid, giving a different reaction profile from the ortho derivatives.

    Comparing with non-nitrated hydroxy benzoic acids, the presence of the nitro group reduces electron density, shifting reactivity toward conjugation reactions or nucleophilic substitution. This changes performance in dye manufacture and influences coupling rates in pharmaceutical targets. Process engineers who have switched from other benzoic acid derivatives have reported improved yields in certain condensation reactions.

    Our 4-Hydroxy-3-Nitrobenzoic Acid has shown a more consistent dissolution rate compared with some substituted analogs. This helps especially in automated chemical reactors, where mechanical agitation can only do so much to compensate for slower-breaking or clumping crystals. We know through repeated flow and solubility tests, some of which helped customers avoid settling and clogging in their feed systems.

    Pitfalls and Lessons Learned Over Years Of Manufacture

    Nitro aromatics receive scrutiny for their impact on personal and environmental safety. On our floor, years of production drove home the need for isolated air movement, and specialized filtration in both venting and wastewater. Handling nitration introduces risks some other chemical processes avoid. Safety protocols evolved over time through real trial and error, influenced just as much by operator input as safety audits.

    We learned that scaling up synthesis invites surprises. On paper, doubling reactor size seems easy. In practice, heat transfer and mixing rates behave differently, sometimes creating local hotspots. Our product’s consistency only arrived after months of iterative adjustment. Staff operating crystallizers began mapping routines for colder months—slightly extended chill-down phases helped secure expected yield and purity.

    Waste treatment methods also adjusted over time. The typical nitro group requires more robust handling than hydroxy acids do. Instead of just using standard neutralization, we set up a flocculation step that captures trace nitro compounds, protecting our local waterway standards.

    Supporting Customer Research and Production

    Many research sites regularly connect with us for sample runs as they trial a new reaction route. Drug discovery teams pursue bioactive heterocyclic compounds starting from our product, and paint or pigment formulators use it as a template material for new shades. Downstream success depends on reliable, reproducible raw materials. Our involvement sometimes stretches into pilot-scale feedback, with customers noting which features—such as lack of residual chlorides or predictability in particle behavior—contribute to successful scale-up.

    Our staff pay attention to differences caused by shipping overland versus by sea. Even sealed containers experience vibration, and powder handling after long journeys demanded we re-seal or double-line bags. International temperature changes affect caking and flowability. That is why our team adjusted moisture control, especially for customers shipping to humid climates.

    Working With Downstream Partners

    Collaboration between our technical staff and customer process engineers creates actual results—not just theoretical improvements. Some started with basic technical inquiries, such as optimizing solution pH for their next step or identifying which impurities would interfere with their catalysts. By sharing batch chromatograms and processing insights over years of partnership, we've watched companies dial in chemical efficiency and cut production time.

    Typical questions revolve around how fast and completely our product dissolves under different conditions, how to avoid dust formation in auto-feeders, and whether residual nitrate content stays below threshold limits. We review these metrics regularly. Input from repeat users often leads us to tweak our own procedures.

    What Sets Our Product Apart In Real Practice

    Labs and plants both value reliability. Out of hundreds of batches, the percentage meeting all QC targets climbed as we developed fine-tuning in drying, filtration, and impurity removal. No two synthesis runs are exactly alike, but tracking deviations and recording exact material profiles gave us the level of consistency customers now expect.

    Packaging upgrades—suggested by industrial users dealing with spillage or dust—resulted in shorter cleaning times and less material loss at customer sites. Real feedback showing which container types work best for liquid addition or solid feed applications comes from users who process multiple drums every month.

    In terms of performance, the specific para arrangement of hydroxy and nitro groups opens more reaction routes than many isomeric competitors. This isn’t just an academic point. Process teams who have tested both tell us they see cleaner product isolation and better compatibility with various solvents. Technicians handling our acid for dye work or pharmaceutical studies report faster, more predictable results than with positional isomers, especially when scaling their syntheses.

    Challenges We See in Industry-Wide Production

    Global demand for reliable specialty intermediates—especially with environmental and cost pressures—never slows. New regulations hit nitro chemicals almost every year, particularly with regard to waste handling. We’ve navigated evolving demands, from local agencies and international partners, revising both process analytics and reporting to keep shipments uninterrupted.

    Batch traceability grew from a regulatory convenience into a fundamental practice. For 4-Hydroxy-3-Nitrobenzoic Acid, we trace raw materials down to source batches, track every transformation step, and record atmospheric conditions in every major process phase. This hands-on tracking allowed us to resolve a past issue where trace impurities traced back to a single raw material supplier, and changes in environmental control helped stabilize finished product quality.

    Supply chain hiccups—especially during global events—force planning far upstream. Our plant expanded raw material storage and now sources from at least two vendors per precursor chemical. Each change ripples through final product stability.

    Continuous Improvement Grounded in Experience

    Manufacturing knowledge isn’t static. Every process change, customer issue, or regulatory adjustment prompts new trials, staff training, and lab validation. A batch that once failed to meet a pharmaceutical partner’s colorimetric test led to our team revising carbon filtration steps. Another time, recurring packaging tears drew quick prototype testing of stronger liners.

    Digital batch records lessen error rates, while new sensor data give granular feedback on reactor and filter conditions. Operators bring up practical points about air quality, powder handling, and ergonomics, fine-tuning procedures every month. Improvements in our drying and sieving routines, shaped by years of feedback and minor setbacks, now pay off more clearly.

    Partnering with customers stirs ongoing procedural adjustments. A pigment manufacturer pushing for a narrower particle size band led our milling team to test different screens. Pharmaceutical raw materials needed ever-tighter purity that conventional checks didn’t catch, prompting investment in more sensitive analytics and higher frequency of spot checks. All these inputs filter into daily practice.

    What We See for the Future of 4-Hydroxy-3-Nitrobenzoic Acid

    The uses for this compound continue to grow. We see inquiries from electronics and advanced materials teams looking to leverage nitrohydroxybenzoic acids in new functional coatings or as templates for new catalysts. As regulatory bodies raise standards, and as end-users push for technical refinements, the payoff from process discipline and technical know-how grows.

    Staff on the production floor stay sharp, knowing that each order isn’t just a shipment, but a foundation for a lab’s next breakthrough or a manufacturer’s next product line. The reliability of our 4-Hydroxy-3-Nitrobenzoic Acid reflects every improvement, lesson, and case study drawn directly from daily work. This hands-on experience, combined with an open channel for technical feedback, makes sure we are not only manufacturers, but problem-solvers shaping both our process and our partners’ successes.