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

3-Hydroxy-4-Nitrobenzaldehyde

    • Product Name 3-Hydroxy-4-Nitrobenzaldehyde
    • Alias 3-Hydroxy-4-nitrobenzenecarbaldehyde
    • Einecs 253-755-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    905164

    Product Name 3-Hydroxy-4-Nitrobenzaldehyde
    Chemical Formula C7H5NO4
    Molecular Weight 167.12 g/mol
    Cas Number 619-19-8
    Appearance Yellow to orange crystalline powder
    Melting Point 145-149°C
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically ≥98%
    Density 1.53 g/cm³ (approximate)
    Smiles C1=CC(=C(C=C1[N+](=O)[O-])O)C=O
    Inchi InChI=1S/C7H5NO4/c9-4-5-1-2-6(8(11)12)7(10)3-5/h1-4,10H

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Hydroxy-4-Nitrobenzaldehyde, tightly sealed with a screw cap and labeled with safety information.
    Shipping 3-Hydroxy-4-Nitrobenzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It should be packed in accordance with local, national, and international regulations for hazardous chemicals. The package includes safety labeling, handling instructions, and documentation. Avoid exposure to sunlight, heat, and incompatible substances during transit.
    Storage Store **3-Hydroxy-4-Nitrobenzaldehyde** in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and direct sunlight. Keep away from incompatible substances such as strong oxidizing agents and bases. Ensure the storage area is free from moisture and label containers clearly. Use appropriate secondary containment to prevent spills and leaks.
    Application of 3-Hydroxy-4-Nitrobenzaldehyde

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

    3-Hydroxy-4-Nitrobenzaldehyde serves as a highly selective raw material in fine chemical synthesis for pharmaceuticals, agrochemicals, dyes, and specialty polymers. The following industry scenarios represent the main downstream sectors in which this intermediate sees large-scale adoption, each requiring tailored manufacturing protocols.

    1. Synthesis of Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers employ this compound as a key intermediate for synthesizing API scaffolds bearing nitro-activated aromatic rings, including anti-inflammatory and anticancer compounds. It enters amidation and reduction sequences where purity, residual solvent control, and robust impurity profile documentation form essential compliance requirements. Manufacturers typically adjust the molar equivalents based on step yield and desired API structure to eliminate side-chain nitro reduction risks, which may affect final bioactivity. Chemical engineers integrate this input at the initial coupling reaction, downstream from prior raw aromatic aldehyde derivatization, ensuring controlled temperature and pH for the condensation and subsequent transformations. Finished products include substance master APIs and regulated final dosage forms, subject to batch release testing.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient manufacture
    • USP-NF and Ph. Eur. monographs for process chemicals
    • 21 CFR Part 210/211 (US FDA)
    • Chinese Pharmacopoeia raw material quality requirements

    Typical usage ratio

    • 0.8–1.2 equivalent per target API scaffold, calculated from stoichiometry and byproduct minimization requirements. Adjust for final yield and impurity carryover.

    Downstream process integration

    • Input for initial condensation or amide coupling in pharmaceutical synthesis lines.
    • Processed in jacketed reactors, integrated with in-process monitoring for residual nitro group content.

    Final product types

    • API intermediates (e.g. nitrobenzamide derivatives)
    • Finished solid dosage form medications
    • Active substances for new chemical entity (NCE) development

    2. Production of Azo and Anthraquinone Dyes

    Dye and pigment manufacturers select this intermediate for its electron-deficient aromatic structure, facilitating high-yield diazotization and coupling reactions in nitro-functionalized dye molecules. The material feeds into key condensation steps that enable controlled chromophore orientation and colorfastness in resulting textile-grade dyes. Formulators calibrate input at the color base synthesis phase, correlating material charge with dye intensity and complementary dye dispersants. Quality assurance necessitates monitoring trace metal levels and confirming batch-to-batch reactivity. End-use manufacturers employ the synthesized dyes for fiber, leather, and plastic coloration meeting commercial wash and lightfastness standards.

    Industry compliance standards

    • OEKO-TEX Standard 100 for dye chemical safety
    • EN 71-3 for toys and textiles dye applications (Germany/EU)
    • GB/T 7573 textile industry chemical quality requirements
    • ISO 9001 for colorant manufacturing process controls

    Typical usage ratio

    • 0.7–1.4 molar ratio to base amine or coupling component, precisely tuned for target chromophore formation.

    Downstream process integration

    • Introduced during key diazotization and coupling reaction stages in dye manufacturing reactors.
    • Monitored for complete consumption and residual aromatic contaminants.

    Final product types

    • Azo dyes for viscose and cotton textiles
    • Polyester-compatible anthraquinone dyes
    • Leather and plastic mass colorants

    3. Agrochemical Intermediate Synthesis

    Agrochemical producers use this benzaldehyde derivative as a precursor for synthesizing selective herbicide and pesticide actives containing nitro-aromatic pharmacophores. The compound undergoes step-controlled reductive amination or etherification to produce granulated actives with improved plant uptake and field stability. Material input strictly aligns with per-batch process safety documentation and local residual solvent regulations. Plant chemists insert this intermediate post-halogenation, ensuring real-time monitoring for nitro-to-amine conversions that affect active species formation. Downstream goods focus on crop protection, offering extensive residue studies and environmental persistence data for compliance.

    Industry compliance standards

    • FAO/WHO specification for technical grade active ingredients (AGP:CP/9)
    • US EPA 40 CFR Part 180 (tolerance requirements for pesticide chemicals)
    • China NY/T standards for agrochemical production
    • ISO 17025-accredited lab QC systems for impurity profiling

    Typical usage ratio

    • 0.6–1.0 equivalent per batch, dependent on pesticide active yield parameters and downstream synthesis efficiency.

    Downstream process integration

    • Input for reduction or O-alkylation in pesticide synthesis trains.
    • Handled in closed reactors with process-side venting and exothermic control protocols.

    Final product types

    • Herbicide pre-mixtures for cereals and legumes
    • Pesticide actives for formulation into EC, WP, or SC types
    • Seed coating agents for improved field persistence

    4. Specialty Polymer and Resin Modification

    Producers in the specialty polymer segment adopt 3-Hydroxy-4-Nitrobenzaldehyde to introduce nitro and hydroxy functionalities into aromatic polymer chains, targeting advanced thermal and UV-resistant resins for coatings and electronics. Formulation chemists calculate introduction ratios based on crosslinking requirements and segmental glass transition temperature targets. The material enters at the pre-polymerization monomer blend phase, requiring controlled mixing and monitored exotherm during batch polymerization. Consistency in molecular weight distribution and minimal nitro group decomposition are critical for downstream physical properties. Final products include high-performance laminates and specialty coatings.

    Industry compliance standards

    • RoHS Directive for restricted substances in electrical/electronic equipment
    • REACH Annex XVII for monomer precursors (EU)
    • UL 94 flame retardancy classification
    • ISO 9001:2015 for polymer and resin quality systems

    Typical usage ratio

    • 1–5% by weight within monomer blend, adjusted according to desired functional property enhancement and polymer backbone compatibility.

    Downstream process integration

    • Premix with core aromatic monomers in controlled environment mixers.
    • Integrated at pre-polymerization step for downstream thermal-cure or addition polymerization processes.

    Final product types

    • Heat-resistant coating resins
    • UV-stabilized polymer sheets
    • High-temperature printed circuit laminates
    Free Quote

    Competitive 3-Hydroxy-4-Nitrobenzaldehyde 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

    Exploring 3-Hydroxy-4-Nitrobenzaldehyde from the Manufacturer’s Perspective

    Introducing 3-Hydroxy-4-Nitrobenzaldehyde: Depth Beyond the Formula

    Direct experience in producing 3-Hydroxy-4-Nitrobenzaldehyde has revealed that each batch tells a story—right from the selection of raw materials to packaging. Chemists and engineers who work in manufacturing settings like ours remember long shifts on the synthesis line or the familiar tang of aromatic chemicals in the air. This is not a faceless commodity, but a specialized aldehyde built for reliability across R&D and industrial sectors.

    With a chemical structure defined as C7H5NO4 and a molecular weight just over 167 g/mol, 3-Hydroxy-4-Nitrobenzaldehyde stands out for its combination of functional groups. The presence of both hydroxy and nitro moieties on a benzaldehyde backbone brings reactivity and selectivity to the table. Over decades, we have refined yields, improved crystallization steps, and noticed trending applications emerge with new advances in material and medicinal chemistry. The underlying chemistry remains low-key, but the product’s impact has scaled.

    Practical Details: Model, Specifications, and Quality That Matters

    Lab and bulk users share one thing in common—they expect consistency. Thoughtful manufacturing brings this quality assurance to their doorstep. We offer 3-Hydroxy-4-Nitrobenzaldehyde with assay values routinely exceeding 98%. For most research functions, this meets or exceeds technical requirements. In cases where demand leans toward pharmaceutical or other downstream syntheses, even minor impurities can complicate isolation and reactivity. Experience tells us that careful control during each reaction, distillation, and crystallization step makes a difference not just in the certificates but in the hands-on usability of the finished material.

    Particles in our powder pass 40-mesh sieves, bringing flow and dispersibility that bench chemists appreciate. Packing under nitrogen, in amber-glass drums or lined fiber containers, preserves the stability and color of this golden yellow solid. We monitor for moisture levels below 0.5% and chloride traces well under typical thresholds for organic synthesis.

    What Experience Teaches About Real-World Usage

    Some colleagues insulate themselves behind technical data sheets, but chemical plants know the stories that come from talking with users. The main draw of 3-Hydroxy-4-Nitrobenzaldehyde stems from its pivotal place in heterocyclic synthesis. Especially in medicinal chemistry, this compound helps construct ligands, build Schiff bases, and form part of multi-component reactions for drug lead candidates. Universities and research labs order modest lots, either for fragment libraries or as key intermediates. On the pilot and production scale, users look for reproducibility over many batches, judging the consistency down to HPLC purity profiles.

    Other industrial users tap into the aromatic aldehyde functionality to develop specialty dyes or optical brighteners. Agrochemical researchers use it for building blocks in new bioactives or evaluating transformation patterns in plant protection molecules. Our in-house technical group often consults on optimizing working solutions, handling stability, and post-use waste management—long after the initial sale.

    Differences That Set This Product Apart

    Many customers ask, “What’s different here compared with generic or alternative aldehydes?” Based on our own quality control logs, conversations with downstream technical users, and side-by-side lab tests, a few things stand out.

    Hydroxy-substituted benzaldehydes often present challenges in crystallization. Our finished product does not clump or cake during normal storage intervals, and the crystal lattice reduces hydrolytic decomposition. Some competitors in the market struggle with darker, impure lots that signal residual iron or side-reaction products. GLC and NMR analysis on our batches shows clean integration profiles, with limited signal broadening—something discerning researchers quickly recognize.

    The nitro group in the para position increases electron withdrawal, which shifts the reactivity window in condensation steps or redox cycling, compared to more basic analogues like 4-nitrobenzaldehyde or 3-hydroxybenzaldehyde. Synthetic chemists mention in post-purchase discussions that this subtle shift lets them fine-tune yields or avoid some purification headaches.

    Not all materials labeled “3-Hydroxy-4-Nitrobenzaldehyde” deliver consistent melting points or moisture stability in humid environments. We have spent years tweaking drying cycles, monitoring storage rooms, and running accelerated aging studies to ensure this aldehyde keeps its integrity—right from day one through to late-stage project requirements.

    Supporting Claims With Daily Production Insights

    One overlooked reality in specialty chemical manufacturing concerns the variance between published literature purities and commercial-scale production. For us, a 98.5% minimum purity is not just a number on a report; it plays into extraction rates, mass transfer coefficients, and color stability during storage and shipping. Every week, our QC team runs retention samples from current production against reference lots synthesized months earlier. These side-by-side analyses have exposed shelf-life trends and slow shifts that can only come from experience. We revise process controls or introduce filtration tweaks so that each order remains within a narrow variance band.

    By tracking shipment stability, we’ve learned that temperature spikes in transit or high relative humidity in sea containers can turn a once-fine solid into an off-color, mildly sticky mass. We carry out real-world transit trials and pick packaging that minimizes these risks before customer complaints can arise. These are not theoretical details—they matter to scientists who unseal a drum expecting clean, free-flowing yellow crystals, not unknown byproducts.

    Insights on Improving Product and Reducing Waste

    Continuous manufacturing pushes us to look beyond simple purity and into broader environmental and operational impacts. Solvent recovery, raw material sourcing, and utility consumption are daily talking points in our plant meetings. We cycle solvents in closed loops to cut the waste load, and we’ve worked with catalyst manufacturers to select systems minimizing trace-metal carryover. For users who want to avoid solvent residues like DMF or chlorinated solvents, we custom-tailor runs and provide lot-specific solvent profiles on request.

    From process optimization teams, feedback highlighted short spins on vacuum dryers at too low a temperature could leave more residual moisture, decreasing the effective shelf life. Collaboration between our engineering and QC divisions led to new drying protocols using slightly elevated vacuums, monitored via in-line probes, to uniformly bring down water content. The feedback loop between customer labs and operator shifts keeps our process responsive and evidence-driven.

    Addressing Challenges in Synthesis and Application

    Not every synthetic route responds equally to standard conditions. With 3-Hydroxy-4-Nitrobenzaldehyde, slight variations in order-of-addition or temperature control during Grignard reactions or multi-component couplings can shift yields or select for side-products. Many academic groups report issues in reproducing literature results because of minor differences in commercial sample quality.

    To address this, our technical support team works directly with labs, offering advice on reaction setup or troubleshooting. We routinely supply preparation notes and sample chromatograms that guide researchers unfamiliar with this class of benzaldehydes. Many of our long-term customers appreciate having insight into our internal process flow—clarifying why certain batches might behave a little differently from one another and providing a transparent basis for their own experimental repeatability.

    Downstream users in scale-up differentiation appreciate being able to schedule regular QC updates or on-the-ground visits from our team. Long-term partnerships have grown around this open communication. This is not just about selling a reagent; it is about reducing cycle times, improving reliability during multi-step syntheses, and having confidence in source material consistency.

    Why Down-to-Earth Production Ethics Matter

    As a chemical manufacturer, we do not just ship powder. Each container we fill reminds us that every gram enters a research chain or process line where inefficiency or contamination can derail hours or weeks of work. We see the results of careful production in lower return rates, positive feedback from process engineers, and minimal technical support calls. Success here is not just technical range, but deep, day-in-day-out discipline.

    Regulatory compliance shapes significant aspects of our workflow. Batch traceability, occupational safety monitoring, and disposal practices all stand behind the as-sold material. We create and maintain internal documentation to chart every phase from acquisition to shipment. In recent years, our plant has invested in multi-stage dust collection and volatile containment to cut occupational exposure and surrounding environmental risks.

    Reflection on Industry Trends and Customer Demands

    Market trends for 3-Hydroxy-4-Nitrobenzaldehyde have shifted in the past decade. Original demand from dye and pigment companies gave way to pharmaceutical startups, contract research organizations, and new materials labs exploring custom sensors and electronic components. As synthetic biology opens up, our sales include more exploratory users trying out structural analogues in green chemistry and biotransformation experiments.

    Some sectors still operate on tight budgets, insisting on bulk orders at price points only achievable through scalable batch production. Others require just a few grams, requesting detailed spectral data, analysis certificates, or non-standard pack sizes. Every new request pushes the technical boundaries; we adapt by streamlining operations, retraining batch operators, and tuning inventory controls so niche orders do not delay bread-and-butter shipments.

    Our policy supports product customization—different particle sizes, solvent-specific washes, or value-added services like co-crystallization or integrated supply logistics. End-users benefit from this modularity, knowing their needs are not lost inside a faceless distribution pipeline.

    Real Solutions for Real-World Chemical Challenges

    No matter how elegant the chemistry, manufacturing brings the complexity of converting laboratory-scale favorite reactions into tonnage-capable, repeatable operations. The most reliable path lies in maintaining open channels with industrial partners, implementing real-time process analytics, and empowering operators to halt production when quality slips. Our own plant’s accident logs show that most issues trace back to simple preventable missteps—temperature overshoots on the main reactor, operator distraction during transfer, or aging of auxiliary materials like filter aid.

    We detect and correct these issues before they reach the customer, running extra quality checks and realigning training. Internal feedback loops ensure process improvements do not remain wishful thinking but become standard operating procedures. The focus remains steady: make better batches, meet evolving client standards, and stay engaged with the scientific details shaping each user’s success.

    One practical solution emerged from collaborating with end-users seeking new routes for synthesizing more functionalized benzaldehyde analogues. By jointly developing new catalytic reduction steps or upgrading our purification columns, both sides found cost savings and technical innovation in tandem. Regular technical exchanges help us avoid the blind spots that can come from working behind company gates.

    True Value Emerges From Collaboration and Experience

    For our team, 3-Hydroxy-4-Nitrobenzaldehyde forms part of a family of aromatic intermediates that link classic chemistry and new discovery. The value of this product does not just lie in its percent purity or mesh size, but in the layers of experience attached to each milestone in its manufacture. Every user request—whether for a kilogram shipment, a custom purity fraction, or a safety protocol—draws from a shared body of practice.

    Ongoing customer input, plant-floor troubleshooting, and technical innovation carry us forward. We improve safety by hardening process isolation or reducing waste through re-crystallized wash streams. As the regulatory landscape shifts and international compliance requirements grow more stringent, we continue updating internal protocols, ensuring materials like 3-Hydroxy-4-Nitrobenzaldehyde remain both reliable and responsible.

    A Manufacturer’s Commitment to Quality and Advancement

    There is no magic shortcut in fine chemical manufacturing. Decades of steady investment in analytical equipment, staff training, and process audits have given us the perspective to judge incremental improvement over reactive patchwork. We listen to feedback from researchers who flag minor inconsistencies, and we log the tough lessons learned from pilots and failed scale-ups.

    3-Hydroxy-4-Nitrobenzaldehyde may not carry the glamour of biopharmaceutical blockbusters, but its dependable reactivity and specificity keep it front and center in many ambitious syntheses. Our goal remains clear: supply more than just a reagent. We seek to offer a partnership grounded in reliability, technical transparency, and shared problem solving—drawing on daily manufacturing realities and a firm grasp of what works and what never quite does.

    This approach drives us. It fuels progress and lets both manufacturer and customer move forward, step by step, in a field where precision and trust shape results that always matter.