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4-Hydroxy-3-Nitrobenzaldehyde

    • Product Name 4-Hydroxy-3-Nitrobenzaldehyde
    • Alias 4-hydroxy-3-nitrobenzenecarbaldehyde
    • Einecs 221-528-0
    • 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

    697099

    Cas Number 619-95-4
    Molecular Formula C7H5NO4
    Molar Mass 167.12 g/mol
    Appearance Yellow solid
    Melting Point 162-166 °C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Density 1.54 g/cm³
    Synonyms 4-Hydroxy-3-nitrobenzaldehyde; 3-Nitro-4-hydroxybenzaldehyde
    Smiles C1=CC(=C(C=C1C=O)[N+](=O)[O-])O
    Inchi InChI=1S/C7H5NO4/c9-4-5-1-2-6(8(11)12)7(10)3-5/h1-4,10H

    As an accredited 4-Hydroxy-3-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 4-Hydroxy-3-Nitrobenzaldehyde comes in an amber glass container with a tightly sealed screw cap and hazard labeling.
    Shipping 4-Hydroxy-3-Nitrobenzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It is typically packaged in amber glass bottles or chemical-resistant containers, cushioned to avoid breakage. The shipment complies with local and international regulations, including labeling for hazardous materials, and is accompanied by a safety data sheet (SDS) for safe handling.
    Storage 4-Hydroxy-3-nitrobenzaldehyde should be stored in a tightly sealed container, away from light, heat, and moisture. Store it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Keep away from incompatible substances such as strong oxidizing agents and bases. Ensure proper labeling and follow all relevant safety guidelines for hazardous chemicals.
    Application of 4-Hydroxy-3-Nitrobenzaldehyde

    Applications of 4-Hydroxy-3-Nitrobenzaldehyde in Industrial Manufacturing

    As a dedicated producer specializing in fine chemical intermediates, we supply 4-Hydroxy-3-Nitrobenzaldehyde to advanced manufacturing sectors. This compound supports the synthesis of complex molecules, enabling various chemical transformations in pharmaceuticals, dyes, and agrochemicals. Below, we detail major downstream applications with process, compliance, formulation, and product information for industrial partnerships.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical synthesis uses this material as a key building block for specific molecules, especially benzaldehyde-based API segments. It participates in route-specific condensation or reduction reactions for anti-inflammatory, antimicrobial, and cardiovascular drug candidates. Manufacturers control impurity profiles in high-purity grades to meet stringent regulations. Formulation chemists adjust concentration based on desired API characteristics, and ensure strict traceability during batch-wise production.

    Industry compliance standards

    • ICH Q7 GMP Guide for API Manufacturing
    • European Pharmacopoeia Monograph 01/2020:1651
    • US FDA cGMP 21 CFR Parts 210 and 211
    • CFDA Drug Registration Management Measures (China)

    Typical usage ratio

    • Used within 5-15% w/w in multi-step synthesis stages, depending on final molecular requirements; adjusted per route efficiency and impurity load.

    Downstream process integration

    • Direct incorporation in condensation or cyclization as early to mid-stage intermediate; followed by purification and further derivatization to API core structure.

    Final product types

    • Anti-inflammatory API intermediates
    • Antimicrobial drug candidates
    • Cardiovascular agent scaffolds
    • Custom contract synthesis molecules for branded pharmaceuticals

    2. Colorant Precursor in Azo and Disperse Dye Manufacturing

    Dye manufacturing sectors use 4-Hydroxy-3-Nitrobenzaldehyde for synthesizing specialized pigments and azo dyes. Chemists activate the aldehyde or nitro group to introduce chromophores in aryl coupling or diazotization reactions. Accurate dosing is necessary to control hue, shade stability, and eco-toxicological limits. Production plants adhere closely to environmental regulations and quality checks, monitoring for prohibited aromatic amines and waste streams.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical management
    • OEKO-TEX Standard 100 (Appendix 6) for restricted substances in dyes
    • ZDHC (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 for production quality control

    Typical usage ratio

    • 1-8% by weight of dye batch, adjusted to chromogenic specificity and color depth targets; exact ratios set during pilot-scale matching.

    Downstream process integration

    • Condensed with anilines or phenols in situ after pH adjustment and introduction of solvents/catalysts; intermediates isolated then further processed for final dye crude.

    Final product types

    • Disperse dyes for polyester and acetate fabrics
    • Azo pigments for plastics and ink formulations
    • Reactive dye intermediates for cellulosic fibers
    • Custom colorants for high-performance coatings

    3. Agrochemical Intermediate for Herbicide and Fungicide Synthesis

    The crop protection sector relies on this chemical as a precursor for select herbicides and fungicide actives. It enables formation of substituted aromatic systems through controlled nitration or reduction steps. Factories manage handling, containment, and storage under chemical hazard codes to ensure worker and environmental safety. Application engineers tailor input concentration during upscaling, keeping within technical grade purity requirements and downstream compatibility specifications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical processes
    • Globally Harmonized System (GHS) for classification and labelling
    • China ICAMA Product Registration for pesticides

    Typical usage ratio

    • Concentrations of 3-10% relative to total active synthesis mass; optimized for reaction yield and reduced unreacted starting material.

    Downstream process integration

    • Enters main synthesis route after initial charge materials in controlled reactor environments; proceeds through isolation and formulation to technical concentrate or EC products.

    Final product types

    • Phenolic herbicide bases
    • Nitroaromatic fungicide actives
    • Custom pesticide intermediates for contract manufacture
    • Precursor molecules for safeners and additive blends

    4. Monomer and Cross-Linker in High-Performance Polymer Synthesis

    Leading material science companies integrate this aromatic aldehyde as a functional monomer or cross-linkable building block in specialty polymer and resin systems. Its presence introduces unique mechanical or electrical properties in thermosetting matrices. Technicians follow precise handling guidelines for stability and compatibility during batch-reactor charging. Process engineers calculate dosage with attention to desired molecular weight and end-group functionality across automotive, electronics, or industrial coatings applications.

    Industry compliance standards

    • RoHS 2011/65/EU Directive for electronics applications
    • UL 94 Flammability Standard for polymers
    • ASTM D638 for tensile strength evaluation
    • ISO 14001 for environmentally responsible production

    Typical usage ratio

    • Employed at 1-5% against total polymer weight for cross-linking or copolymerization; ratio tuned for molecular architecture and performance metrics.

    Downstream process integration

    • Introduced during oligomer synthesis or post-polymerization step; batch timing and temperature profiles optimized for full conversion and stable network formation.

    Final product types

    • Advanced thermosetting resins
    • Specialty printed circuit board substrates
    • High-durability industrial coatings
    • Functional adhesives for electronics

    5. Chemical Intermediate in Flavors and Fragrances Manufacturing

    Certain regulated processing channels utilize this compound as a scaffold for niche aroma chemicals via selective reduction and condensation, primarily for high-value fine fragrance bases and functional additives rather than direct food application. Production observes strict controls under food safety and hazardous substance rules. Chemists optimize feed ratios to balance target odor group yield and downstream byproduct minimization, especially in high-purity, low-volume fragrance development laboratories.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Regulation (EC) No 1334/2008 on flavorings and food ingredients
    • Food Chemicals Codex (FCC) – ingredient and purity for aroma chemicals
    • ISO 22000 Food Safety Management, on production lines where risk applies

    Typical usage ratio

    • Applied at 0.5-3% in reaction mixture; concentration varies by aroma compound conversion efficiency and extraction yield.

    Downstream process integration

    • Charged to reactors under catalytic or reducing conditions; active aldehyde or nitro group forms base note or aroma precursor, followed by distillation and purification.

    Final product types

    • Fragrance intermediate bases for fine fragrances
    • Aroma ingredient precursors for flavor houses
    • Key note molecules used in fragrance accord formulation
    • Functional additives for limited non-food technical flavoring uses
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    Certification & Compliance
    More Introduction

    4-Hydroxy-3-Nitrobenzaldehyde: A Closer Look at Its Production and Utility

    Introduction to 4-Hydroxy-3-Nitrobenzaldehyde

    4-Hydroxy-3-nitrobenzaldehyde, known to chemists as a key building block in a range of specialty syntheses, represents more than just another aromatic compound from our catalog. Decades of experience in producing this molecule, recognized by its CAS number 619-45-4, have taught us the subtle balances and precise conditions that separate a high-purity batch from a mediocre one. Where some suppliers treat every benzaldehyde derivative as the same, consistent yields, impurity profiles, and handling can tell a different story. Every operation working with advanced intermediates faces the challenge of reliability and batch-to-batch consistency, so providing steady output takes careful control from the very beginning.

    The Manufacturing Process: Where Experience Sets Quality Apart

    Our understanding of 4-hydroxy-3-nitrobenzaldehyde starts on the plant floor. Synthesis typically involves the careful nitration of 4-hydroxybenzaldehyde, which demands not only accurate temperature management, but real-time monitoring of minor impurities throughout the process. Small deviations in temperature or excess oxidizing agent change impurity levels remarkably. Customers regularly share stories of failed downstream reactions when using material from sources that cut corners.

    To deliver reproducibility, our chemists run every reactor batch with inline checks, confirming that aldehyde and nitro group placements match precise specifications. Having encountered a wide set of customer needs over the last decade, our plant teams refined wash cycles, filtration media, and solvent treatments to reduce isomeric by-products and remove colored impurities. These details never appear on standard technical data sheets, but a glance at the crystalline color or the results of spectral scans makes differences quite visible for those who have handled low- and high-grade outputs.

    Physical and Chemical Features: Specifying for Real-World Utility

    The compound presents as a yellow solid with a distinctive pale to vibrant hue depending on the batch preparation, which often signals its relative purity. Odor and solubility also tell important stories. Only moisture-controlled environments and refined drying cycles deliver a final product with the sharp characteristic aldehyde scent that organic chemists recognize, rather than dusty off-notes that signal residual processing contaminants. The melting point, hovering close to 152-158°C, shows just one measure of integrity. Some competitors market products with a wider melting range, relying on residual solvents to fudge the numbers.

    High-purity 4-hydroxy-3-nitrobenzaldehyde dissolves consistently in polar solvents such as ethanol and DMSO, ensuring uninterrupted reagent transfer and reliable mixing in synthetic flows. The presence of water-sensitive nitro and aldehyde groups means that handling must avoid both moisture and prolonged light exposure. Over the years, we have developed tried-and-true packaging and storage practices, avoiding the yellowing or clumping that downgrade poorly handled stocks. Because each drum or multi-kilogram package could travel halfway around the world, only rigorous attention to sealing and desiccant use preserves usability upon arrival, even if shipping conditions fluctuate.

    Major Applications: More Than an Intermediate

    Users approach 4-hydroxy-3-nitrobenzaldehyde primarily as an intermediate for pharmaceuticals, pigment synthesis, and specialty polymers. The benzaldehyde core, modulated with both electron-rich hydroxy and electron-deficient nitro functionality, unlocks a range of later-stage transformations. Medicinal chemists value this scaffold because it accommodates both nitration and protection reactions, allowing for further manipulation in the construction of active pharmaceutical ingredients. Dyes and pigment manufacturers demand the highest purity grades, aware that even trace byproducts can discolor final batches and alter fastness properties.

    In our own pilot-scale work with dye producers, we have witnessed the impact of minor impurities firsthand — even a trace of unreacted starting hydroxybenzaldehyde can force a recall on thousands of liters of pigment paste. Applications in organic electronic materials also reveal subtle performance losses linked to inconsistent aromatic substitution patterns. Many manufacturers, motivated by cost, have tried replacing hydroxy or nitro aldehydes with lower-cost analogues, only to encounter reduced reactivity, lower color vibrance, or problematic side product formation.

    Why Specifications Matter: Lessons from Real Production

    Industry experience shows that nominal purity percentages often miss subtle factors important for scale-up. Analytical lab results may declare “99%+” purity, but these numbers can mask the presence of troublesome trace isomers or residual decomposition products — especially if brought in from a trader with no clear line of sight to manufacturing methods. Many customers have reported failed follow-up reactions when switching to cheaper sources, finding that single-digit impurity percentages spiral into double-digit product losses down the chain.

    Our approach focuses on thorough impurity profiling, not just the headline purity. Gas chromatography and HPLC methods, routinely calibrated and assessed, monitor side-product trends over hundreds of batches. This data provides a practical feedback loop: if even a small distribution shift shows up, we track it back to temperature, moisture load, or even minor supplier ingredient variances. Over the years, these controls let us offer a product tailored more for consistent results than for minimum specification box-ticking. Open dialogue with synthesis teams using our material further closes the loop—feedback from bench chemistry and industrial reactors guides our ongoing process tweaks.

    Comparisons: How 4-Hydroxy-3-Nitrobenzaldehyde Stands Out

    Over the years, many chemists let us know how frustrating it can be to deal with product “interchangeability” myths. While catalogs may show a line-up of aromatic aldehydes and nitrobenzene derivatives as almost generic, practical lab use reveals otherwise. This molecule’s dual substituent pattern — with a hydroxy at the para position and a nitro at the meta position relative to the aldehyde — drives unique reactivity. Neighboring group effects can determine if a synthetic route proceeds cleanly or fails, and this balance often explains why pushing another nitrobenzaldehyde into an established route brings disappointment.

    Some users try to cut costs by substituting with the 2-hydroxy-5-nitro- or 4-nitro-3-hydroxybenzaldehyde variants, only to find solubility drops off or desired condensation reactions give poor conversions. In dye and polymer chemistry, side chain placement influences not just reaction kinetics but also product hue and application stability. Our long-term relationships with downstream formulators show that seemingly minor changes at the aromatic ring swap can write off months of formulation work.

    Another frequent comparison centers on 3-nitro-4-methoxybenzaldehyde. While methoxy substitution provides some synthetic convenience in methylation or ether cleavage steps, the hydroxy group in 4-hydroxy-3-nitrobenzaldehyde opens direct, clean reactions with acylating and alkylating agents under mild conditions. The open pathway means a broader set of end products can be prepared, which matters for contract research and process development units aiming for a one-pot workflow.

    End-Use Quality: Building Trust with Reliable Output

    A chemical like 4-hydroxy-3-nitrobenzaldehyde faces a simple test: does it let your downstream chemistry work as planned? Many companies, especially those developing patented API intermediates or fast colorants, cannot afford surprises from their building blocks. Over the last decade, we’ve seen firsthand the issues that cut-rate material invites: reactor fouling, need for repeated crystallization, long filtration times, and contamination that’s costly to flush from equipment lines. Each of these problems ties back to how the intermediate behaved on the plant floor, from nitration selectivity to moisture management prior to packing.

    Over thousands of batches, teamwork between scale-up chemists and process engineers shaped our methods. Batch records, impurity logs, and electronic monitoring systems all contribute, but experience handling product on the packing line makes just as much difference. Identifying which storage drums are fit for transit to high-humidity or temperature-variable climates stems from seeing how product crystals shift or cake in different conditions. High reliability on arrival matters most to busy production plants, where re-testing or unexpected re-washing cut into timelines and budgets.

    Reliable color, consistent melting behavior, and a sharp TLC or HPLC profile define material that will drive your application forward, not hold it back. We know this from working alongside customers as they troubleshoot, iterate, and scale up their processes. The lessons gathered go well beyond textbook synthesis and trace their roots to attention paid at every production, packing, and storage step.

    Practical Handling and Safety

    4-Hydroxy-3-nitrobenzaldehyde should never be treated as just another powdered intermediate. The nitro aldehyde structure brings both reactivity and some hazard, especially in larger plant or R&D environments. Technicians dealing with volatile organic compounds and moderately toxic aromatics recognize the requirement for well-ventilated hoods and appropriate PPE. 

    Through years of incident-free operation, our facility protocols call for double-walled containment during packaging, dust-controls at all transfer points, and direct-to-container filling so product never sits exposed to humid air. Because aldehyde-containing intermediates can polymerize or degrade under poor storage, all shipping containers use welded liners and desiccant packs, which we hand-inspect before sealing. Action like this may seem minor, yet time and again it marks the difference between material that behaves as promised and product that causes unpredictable batch results or safety complaints in customer plants.

    Knowing this compound’s specific sensitivity to light, we choose dark bottles or drums and label all secondary containers for short-term staging. Over time, we learned that material exposed too long to strong UV sources not only darkens but can lose reactivity — another example of process insight not captured in standard supplier paperwork. Customers handling large volumes, especially when re-packing or scaling up, often receive storage best-practices learned through decades of first-hand experience. Sometimes it’s advice as simple as which tape seals best, which labels won’t fade, or even which loading-bay practices avoid moisture contamination.

    Challenges and Solutions: Staying Ahead in Specialty Chemical Supply

    Today’s specialty chemical market faces intense cost and quality pressures. Distributors and resellers often chase the lowest landed cost, but trading away control for price puts end-users at risk. We have seen market cycles where low-cost imports flood supply chains — until quality issues show up or users discover downstream product performance drops. Once a product like 4-hydroxy-3-nitrobenzaldehyde gets flagged for unreliability, rebuilding reputation takes years. As direct producers, we bear that responsibility every week.

    We commit resources not just to finished product checks, but to deep supplier vetting for starting materials and in-process controls. Early detection of out-of-spec batches — sometimes flagged by a single off-odor or color note — heads off risk before it leaves our site. In markets demanding ever-shorter turnaround times, long-term supply agreements and secure inventory planning let us avoid spot shortages that can push customers into poor buying choices. Our technical staff keeps open lines with users, trading advice on process, helping integrate product into new routes, and sharing lessons learned from setbacks as well as successes.

    Solutions to market uncertainty come from investment in technology and people. Continuous process monitoring, staff training, and supply chain coordination underpin the steady availability and reliable performance our customers trust. If a batch ever shows an outlier parameter, we track, segregate, and reprocess or rework the material. No “good enough” leaves our site onto a truck — because our partners downstream build their own business on the foundation of predictability that real manufacturers offer.

    Ongoing Innovation and Customer Partnership

    Developing high-quality 4-hydroxy-3-nitrobenzaldehyde means ongoing collaboration, not just one-off shipments. As new reaction methods, green chemistry initiatives, or advanced analytics become available, we adapt and refine our operations to support next-generation chemistry needs. Open sharing of impurity spectrum studies, method validation data, and practical application notes are part of our partnership approach. Adjusting processes to meet evolving pharmaceutical or electronic material standards has challenged us to revisit old assumptions and try new techniques, sometimes prompted directly by customer insight.

    Our chemists and engineers attend industry forums, contribute to process improvement studies, and keep labs open for joint trials or pilot batches. Many times, feedback from an advanced materials project helps us fine-tune not just this product, but larger segments of our aromatic intermediate range. Customers investing in new synthetic methodology get access to a team eager to solve problems, whether it's bench-level troubleshooting or plant-scale optimization.

    The story of every lot shipped ties back to honest, rigorous work carried out on the plant floor, tightened and improved by years of facing real-world demands. Anyone who has faced a failing reaction, a discolored pigment, or a delayed process knows how quickly minor changes upstream can grind progress to a halt downstream. High-quality 4-hydroxy-3-nitrobenzaldehyde, trusted for its consistency and integrity, enables smoother, faster, and less wasteful manufacturing of finished products.

    Conclusion

    Our journey with 4-hydroxy-3-nitrobenzaldehyde proves time and again that manufacturing skill, operational discipline, and a respect for the chemist’s craft separate reliable partners from the crowd. This compound, with its recognizable structure and complex reactivity, shows just how important careful production and honest communication remain — both for today’s industry demands and the innovations that will define the future. Years of experience and open customer dialogue guide our path in making sure every batch stands up to scrutiny, supports end-user creativity, and builds enduring trust in the quality of specialty chemicals.