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

2,6-Dihydroxy-3-Nitrobenzonitrile

    • Product Name 2,6-Dihydroxy-3-Nitrobenzonitrile
    • Alias 2,6-Dihydroxy-3-nitrobenzenecarbonitrile
    • Einecs 629-081-4
    • 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

    428783

    Iupac Name 2,6-Dihydroxy-3-nitrobenzonitrile
    Cas Number 59544-18-4
    Molecular Formula C7H4N2O4
    Molar Mass 180.12 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 225-228 °C
    Solubility In Water Slightly soluble
    Smiles C1=CC(=C(C(=C1O)C#N)[N+](=O)[O-])O
    Inchi InChI=1S/C7H4N2O4/c8-3-4-1-2-5(11)7(13)6(4)9(12)10/h1-2,11,13H
    Storage Conditions Store at room temperature, keep container tightly closed
    Hazard Statements May cause respiratory and eye irritation

    As an accredited 2,6-Dihydroxy-3-Nitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package is a sealed amber glass bottle with a white label stating "2,6-Dihydroxy-3-Nitrobenzonitrile, 100g, for laboratory use."
    Shipping 2,6-Dihydroxy-3-Nitrobenzonitrile is shipped in tightly sealed chemical containers, protected from moisture and direct sunlight. It should be handled according to relevant hazardous material transport regulations. Temperature control is recommended to avoid decomposition, and containers must be labeled with chemical identification and hazard warnings to ensure safe handling during transit.
    Storage 2,6-Dihydroxy-3-Nitrobenzonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Protect the chemical from light and moisture. Use secondary containment and properly label the storage container. Always follow standard laboratory safety procedures when handling and storing this compound.
    Application of 2,6-Dihydroxy-3-Nitrobenzonitrile

    Applications of 2,6-Dihydroxy-3-Nitrobenzonitrile in Industrial Manufacturing

    As a direct producer of 2,6-Dihydroxy-3-Nitrobenzonitrile, we supply this specialty intermediate to a select range of downstream industries where precise formulation control, regulatory compliance, and dedicated process parameters define its role in the creation of advanced materials and high-value products. Below, we present real-world application scenarios, each backed by practical formulation experience and established manufacturing requirements.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient Synthesis

    Sterically-substituted benzonitriles bearing hydroxyl and nitro groups form critical intermediates in the multi-stage synthesis of small-molecule APIs, especially in selective kinase inhibitors and antimicrobial agents. Pharmaceutical manufacturers rely on this material to introduce nitro functionalities into core scaffolds under tightly regulated cGMP environments. Reaction control and impurity profiling remain central during API synthesis using this intermediate.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Directive 2018/0118(COD)
    • United States Pharmacopeia (USP) for relevant APIs
    • EDQM Certificates of Suitability (CEP) reference

    Typical usage ratio

    • Added at 8–15% molar ratio versus core starting structure, with precise ratio based on desired yield and downstream side reaction control

    Downstream process integration

    • Introduced during the electrophilic substitution or nucleophilic aromatic substitution stage in stepwise API synthesis
    • Integrated in closed-system reactors under inert conditions to minimize by-product formation

    Final product types

    • Small molecule kinase inhibitors (e.g., ortho-nitroaryl scaffold APIs)
    • Antimicrobial actives with substituted benzonitrile cores

    2. Agrochemical Active Ingredient Manufacturing

    Producers of selective herbicides and fungicides utilize this compound as a precursor in the formation of substituted aromatic ring systems offering bioactivity. Its unique substitution pattern serves as a backbone for triazole and benzonitrile-type actives that require controlled nitro group introduction for optimal field performance, primarily in broadleaf weed treatments.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 for active substance approval
    • ISO 9001:2015 certified QC processes for agrochemical intermediates

    Typical usage ratio

    • 6–12 wt% relative to total batch mass for pre-finished herbicide synthesis, adjusted for conversion efficiency and batch scaling

    Downstream process integration

    • Dosed during the condensation and cyclization stage in technical active synthesis
    • Blended with chlorinating or triazole-forming agents in jacketed pressure reactors

    Final product types

    • Triazole class herbicides (e.g., those with dihydroxy-nitrobenzonitrile backbones)
    • Pre-formulated fungicides for seed treatment applications

    3. Advanced Pigment and Dye Intermediate Sector

    High-performance pigment and dye manufacturers incorporate this intermediate in the synthesis of azo and anthraquinone colorants. Its electron-withdrawing nitro and nitrile groups enhance shade depth and fastness properties in finished products. Stringent purity must be maintained to prevent tint inconsistency in automotive coatings, plastics, and textile dyes.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for coloration materials
    • ISO 18314-1 for Analytical Colorimetry in pigment QC
    • GMP for intermediate preparation in regulated pigments (e.g., for toy safety)

    Typical usage ratio

    • 1.5–4.5 wt% relative to complete dye or pigment charge, adjusted in laboratory development based on shade intensity requirements

    Downstream process integration

    • Kick-off material for diazotization or coupling reactions leading to target chromophores
    • Added directly to reaction batches during intermediate pigment synthesis under controlled temperature and pH

    Final product types

    • Azo pigments for plastics (e.g., hues for automotive interiors)
    • Reactive dyes for cellulose-based textiles
    • Anthraquinone dye intermediates for industrial coatings

    4. Electronic Materials: Hole Transport Layer Precursors

    Manufacturers fabricating advanced organic semiconductors leverage this nitrile-containing aromatic intermediate to construct molecules with modifiable electronic properties. It participates in syntheses of hole transport materials (HTMs) used in OLED displays and photovoltaic devices, where tailored nitro and hydroxyl substitution supports targeted energy levels and high device stability.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance limitations
    • IEC 62899 series for printed electronics performance standards
    • ISO 9001:2015 quality management system for functional chemicals

    Typical usage ratio

    • Between 0.7–2.3 mol% in multi-step synthesis of molecular HTMs, with the exact percentage optimized for layer thickness and charge transport efficiency

    Downstream process integration

    • Enter the coupling reaction as a primary raw material during HTM core synthesis
    • Integrated within vacuum or inert atmosphere labs to preserve material integrity

    Final product types

    • Hole transport materials for OLED and QLED displays
    • Molecularly engineered layers for organic solar cells

    5. Specialty Resin and Polymer Modifier Synthesis

    Producers of specialty resins exploit this benzonitrile intermediate to introduce polarity and modify glass transition temperatures in engineering plastics and thermosetting resins. The aromatic structure imparts rigidity as well as tailored surface properties for advanced composites deployed in automotive and electronics.

    Industry compliance standards

    • UL 94 flammability standards for plastic materials
    • ASTM D638 for tensile properties of plastics
    • ISO 14001:2015 for environmental management in polymer synthesis

    Typical usage ratio

    • Incorporated at 2–7 wt% in resin polymerization batches; proportion set by required mechanical and thermal attributes of the targeted resin system

    Downstream process integration

    • Charged to prepolymer resin mixtures during initial polymerization
    • Postblended in finishing operations for custom copolymer solutions

    Final product types

    • Rigid thermosetting plastics for automotive components
    • Modified engineering resins for printed circuit boards and connectors
    • Specialty adhesives with engineered aromatic content
    Free Quote

    Competitive 2,6-Dihydroxy-3-Nitrobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    2,6-Dihydroxy-3-Nitrobenzonitrile: Proven Value in Chemical Synthesis

    Understanding 2,6-Dihydroxy-3-Nitrobenzonitrile from the Manufacturer’s Bench

    In the world of chemical manufacturing, we often get asked why certain molecules matter so much and how they actually behave outside theory. Take 2,6-Dihydroxy-3-Nitrobenzonitrile — also known by its reference of DHNB. Those working day in and day out with nitriles recognize the significance of this particular molecule. Its unique blend of functional groups (a nitro, two hydroxyls, and a nitrile) creates points of reactivity you don’t find by chance. We’ve run it across pilot plants, lab-scale vessels, and full manufacturing lines, checking consistency, yield, and behavior under variable moisture or pressure conditions.

    In our shop, DHNB most often goes out as a high-purity crystalline powder, consistent with research and commercial-scale syntheses. We monitor specification tightly; the active content exceeds 98% by HPLC, matched well to the needs of pharmaceutical intermediates, specialty pigments, and advanced material building blocks. Moisture content stays low — generally less than 0.5% because even a slight shift there can complicate downstream handling. Our experience proves the difference between a reliable batch and an unpredictable one almost always comes down to these subtle details.

    How Our Process Shapes This Molecule’s Reproducibility

    Production involves a controlled sequence of nitration and hydrolysis that avoids harsh temperature swings. Over the years, we’ve invested time and headspace into refining yield without sacrificing product purity. Reaction quench rates and filtration pH seemed minor topics at the outset, but our operators learned quickly that these stages determine particle morphology and capacity for long-term storage. We keep analytical checks at every step; UV-Vis, FT-IR, and proton NMR spectra show tight peaks, and this data has guided improvements from lab scale through scale-up.

    Take shelf-life: Some nitrated benzonitrile analogs start to degrade above ambient humidity or after long-term exposure to light. We store DHNB in amber drums, lined with moisture barriers. Our packaging has gone through dozens of real-world shipping scenarios (sea, air, land) to hold up over weeks. Feedback from reaction engineers using the material months after delivery prompted our packaging upgrades years ago, and these incremental steps reflect the deeper collaboration we foster with end-users. We’ve seen less than 0.2% return rate due to quality concerns since adopting these standards — a real-world measure that technical datasheets rarely touch.

    Why Not Use a Simpler Nitrobenzonitrile Derivative?

    Anyone with experience in aromatic chemistry knows the difference between theory and scale reality. Simple mono- or di-hydroxy nitrobenzonitrile derivatives draw broad interest for fine chemicals, but process chemists demand more than just availability; they pursue reliability, purity, and predictable reactivity. The ortho-hydroxyl groups on DHNB allow for directed hydrogen bonding in functional group transformations. In catalysis and cross-coupling, this molecule proves less prone to byproduct formation—chemical pathways sometimes blocked or slowed by less substituted analogs.

    Compare with 3-nitrobenzonitrile or 2,6-dihydroxybenzonitrile: DHNB introduces a steric environment that lets organic chemists achieve selective conversions with fewer purification headaches. Sometimes these advantages seem small when penciled into a workflow, but any operator who tunes a column or validates an assay against unknown side-products understands the practical edge a well-characterized intermediate like DHNB brings to the table. Over dozens of campaigns, we’ve saved hours of troubleshooting by leaning on predictable purity and well-defined melting points.

    Our Experience Supporting Diverse Applications

    We’ve seen DHNB show up in everything from pharmaceutical intermediate syntheses to polymer modification projects. Medicinal chemistry teams rely on the clean reactivity profile—often as a synthon for more complex heterocycles or as an intermediate in kinase inhibitor or anti-infective routes. The nitrile group serves as a valuable anchor for further modifications, while the ortho-dihydroxy motif lends itself to easy protection or etherification. In pigments, color bodies derived from this template exhibit higher fastness and stability in comparison with parent hydroxybenzonitrile derivatives.

    Partners in high-performance material manufacturing use DHNB when tight control over substitution pattern translates into better electronic or optical behavior in the finished article. The molecule’s stability and reactivity window line up well with steps such as Suzuki coupling, nucleophilic displacement, or even multi-step condensation. Our technical service team spends time collaborating on such projects — working through solubility and compatibility assessments or scaling solvent recovery as operators move up from research scale to demonstration or commercial runs.

    Risk, Control, and the Realities of Sustainable Production

    Modern supply chains have their share of hurdles, from raw material unpredictability to evolving health and environmental regulations. Looking back ten years, we drew much of our starting nitrobenzene feedstock from domestic producers, but rising demand and volatility forced us to retool our sourcing and logistics. As a manufacturer, we made conscious investment in traceability; our batches come with full synthesis records, including all in-process controls. Our engineers shaved down solvent and water loads, cut unwanted byproducts, and developed energy recovery loops in the reactor train. The changes didn’t just check regulatory boxes — they cut costs on waste treatment and improved worker safety.

    Hazard management is not showy work, but real handling experience exposes the friction points. Sulfonation and nitration steps need fine-tuned monitoring, with continuous on-site air quality curve records rather than just annual spot-checks. We introduced continuous monitoring and targeted extraction air at the nuisance sources, rather than relying on broad general ventilation. These process changes kept our emissions profile in compliance and allowed for easier audit trails, benefiting both partners and our own regulatory workload.

    Protecting Product Integrity

    Lab and plant operators know that dehydration and exposure to contaminants undermine the stability of sensitive reactants like DHNB. Each batch ships in certified moisture-barrier packaging, and batches are retested after storage periods to confirm stability. Over the course of product launches for new applications, we fielded questions on long-term oxidation or rearrangement of aromatic nitro compounds. Our in-house storage studies provided real numbers: minimal assay loss over 18 months at standard warehouse conditions, even prior to opening. This offered reassurance to partners needing bulk but gradual drawdown in process campaigns.

    Shipping logistics always introduces risk. Run-of-the-mill flatbed hauling doesn’t meet our criteria. We spent time discussing transport practices with carriers handling hazardous chemicals. It’s not just about tariff codes—everytime a batch left our dock and hit a steamy port in late summer, we tracked proof of humidity and temperature control. Our return statistics stand as proof-of-principle for how a direct manufacturing presence can tune supply performance for demanding downstream chemistries.

    Cost Control and Value-Added Support

    Some buyers ask why our process costs what it does, especially with rising energy and labor prices. The answer lies in a production workflow centered on well-maintained reactors, precise environmental control, and operator experience. Automating every step isn’t always the answer—human judgment still plays a key role in checking endpoint reactions and separation quality. Our facility invests in training and cross-checks batch records, ensuring the people making DHNB understand how and why every parameter matters.

    Beyond product shipment, our technical team provides application feedback. Over the years, partners switched from trial-scale syntheses to full campaign volumes. We fielded questions about solvent compatibility and waste treatment, and helped develop methods to optimize both. This boots-on-the-ground interaction often helps us catch potential bottlenecks for scale-up and suggest tweaks that save hours in campaigns or analytics. Being a manufacturer, we know that feedback from the floor matters more than spreadsheets—they show where margins are real and where downtime can creep in.

    How Our Process Differs From Non-Manufacturing Channels

    There’s a clear difference between buying DHNB from those who make it and those who warehouse or resell. Direct manufacturing means full batch records, access to technical operators, and real-time response to out-of-spec events. Our blending, filtration, and drying procedures are tuned specifically for this product. As new inquiries come in or as more demanding use cases appear, we move directly from bench to pilot to plant, without dependency on a third-party toller. This speeds up improvements and gives partners real peace of mind about continuity.

    In practice, this upstream position means changing parameters as trends shift. We replaced older filtration solutions with inert, PTFE-lined units following discovery of trace contamination. Before scaling up a new batch size, our chemists run physical and analytical exercises on small lots to see how the target molecule survives each step. This degree of vigilance is possible only with hands-on knowledge—something our customers value in every project, as challenges rarely follow expectations.

    Broader Impact: Safety, Training, and Future Directions

    Operating a manufacturing process for aromatic nitro compounds comes with workplace safety and community stewardship responsibilities. We have in-house training modules drawn from actual incidents—these drive responses to deviations and foster an environment where reporting of near-misses is encouraged, not punished. Trends in chemical safety underscore the risks of static discharge, improper transfer techniques, and trace oxidant build-up. Our continuous improvement cycle adapts our procedures to new information, including data from global partners who manage similar chemistries under different climates or regulatory regimes.

    Our view of the future tracks broader chemical industry concerns: The need for green chemistry, responsible waste handling, and minimizing hazardous intermediates where possible. While DHNB synthesis is challenging to “green” completely, we research alternate feedstocks and lower-impact solvents every planning cycle. Customer feedback often steers us to find new approaches—perhaps with improved reaction catalysts, more selective purification, or even in-line process analytics that shave seconds and waste from washing cycles. This dialogue continues to shape our roadmap.

    Conclusion: Manufacturer’s Experience Makes the Difference

    Only by running real-world process lines, troubleshooting deviations, and seeking input from operating chemists do we understand what separates a specialty chemical like DHNB from generic analogs. Our team’s commitment to reliable synthesis, rigorous quality control, and direct communication with users ensures that material moving from our dock to your workspace meets the standards demanded by modern synthetic chemistry. We draw pride and purpose from decades of experience, not just formulas on a page.

    Building molecules like 2,6-Dihydroxy-3-Nitrobenzonitrile at industrial scale requires sweat, vigilance, and respect for the detail. Behind every shipment lies the hands-on effort of operators, chemists, and technicians who have spent years refining the process—not only in the name of efficiency, but in the belief that well-made chemicals power discovery and innovation across the industries we serve.