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5-Chloro-2-Hydroxybenzonitrile

    • Product Name 5-Chloro-2-Hydroxybenzonitrile
    • Alias 5-Chloro-2-cyanophenol
    • Einecs 256-815-3
    • 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

    745971

    Name 5-Chloro-2-Hydroxybenzonitrile
    Cas Number 32719-56-1
    Molecular Formula C7H4ClNO
    Molecular Weight 153.57 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 108-110°C
    Boiling Point 382.5°C at 760 mmHg
    Density 1.37 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1Cl)O)C#N
    Inchi InChI=1S/C7H4ClNO/c8-5-1-2-6(10)7(3-5)4-9
    Synonyms 5-Chlorosalicylonitrile, 5-Chloro-2-cyanophenol
    Storage Temperature Store at room temperature

    As an accredited 5-Chloro-2-Hydroxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Chloro-2-Hydroxybenzonitrile, 25g, is supplied in a sealed amber glass bottle with secure cap and hazard labeling.
    Shipping **Shipping Description:** 5-Chloro-2-Hydroxybenzonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical should be handled according to standard hazardous material protocols. Proper labeling and documentation are required, and transportation must comply with local and international chemical shipping regulations to ensure safety and regulatory compliance.
    Storage 5-Chloro-2-Hydroxybenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers. Protect from moisture and avoid prolonged exposure to air. Store at room temperature and ensure proper labeling. Use appropriate personal protective equipment when handling to avoid inhalation and contact with skin or eyes.
    Application of 5-Chloro-2-Hydroxybenzonitrile

    Applications of 5-Chloro-2-Hydroxybenzonitrile in Industrial Manufacturing

    As a specialist manufacturer, we deliver 5-Chloro-2-Hydroxybenzonitrile for advanced synthesis requirements across high-value chemical sectors. Our material remains consistently selected for critical reactions and performance-driven formulations, with strict control over trace impurities and batch repeatability. Below, we outline the main downstream industrial applications of this key intermediate, categorizing its differentiated contributions to each field.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers incorporate our product as a key intermediate in multi-step syntheses of selective antihypertensive and anti-inflammatory drugs. Its unique substitution pattern supports targeted nucleophilic substitution and coupling reactions in heterocycle formation processes, crucial where stringent impurity profiling and full reaction conversion are required to meet regulatory agency approval.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary) for residual solvent and impurity thresholds
    • European Pharmacopoeia (Ph. Eur.) for API precursor quality
    • US FDA cGMP (21 CFR Part 210/211) for process validation

    Typical usage ratio

    • 5-12% by weight in API intermediate reaction schemes; ratio adjusts based on target molecule and stepwise yield optimization

    Downstream process integration

    • Charges into heterocycle or amide bond-forming steps after pre-drying in jacketed reactors; reacts under controlled temperature with alkali or acid catalysts

    Final product types

    • Active pharmaceutical ingredients (APIs) for antihypertensive agents (e.g., specific angiotensin II antagonists)
    • Non-steroidal anti-inflammatory drug (NSAID) actives
    • Custom intermediates for generic drug synthesis

    2. Agrochemical Intermediate for Selective Herbicide and Fungicide Synthesis

    Agrochemical synthesis units select our material for constructing core aromatic scaffolds in classes of systemic herbicides and triazole fungicides. Its defined chloro and hydroxy substitution pattern provides structural requirements for chlorination and etherification reactions, serving as a building block for downstream active molecules without contributing to off-target byproducts.

    Industry compliance standards

    • FAO/WHO Technical Grade Active Ingredient Specifications (JMPS)
    • REACH Regulation (EC) No 1907/2006 for registration, evaluation, and traceability in the EU
    • US EPA 40 CFR Part 158 for pesticide chemical standards
    • ISO 9001:2015 for quality management in agrochemical manufacturing

    Typical usage ratio

    • 6-15% by weight of active ingredient precursor, with precise charge determined by the targeted synthesis pathway and molar equivalency to downstream reagents

    Downstream process integration

    • Added in the initial aryl halide activation or condensation stage under inert atmosphere; often involved before alkylation or sulfonation for class-specific crop protection agents

    Final product types

    • Selective herbicide technical concentrates (e.g., for grass and broadleaf weed control)
    • Triazole or strobilurin fungicide actives used in seed treatment and foliar applications
    • Post-patent pesticide intermediates for local market customization

    3. Dye and Pigment Intermediate in Performance Colorants

    Producers of specialty dyes and high-performance pigments use this material as a central aromatic intermediate. Its electron-donating hydroxy function and halogen atom enable color-tuning through azo-coupling or oxidative polymerization, creating chromophores with specific fastness and spectral properties demanded across textile, plastic, and coating sectors.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Chemical Safety)
    • EN 71-3:2019 (Safety of Toys—Migration of Certain Elements in pigments)
    • ISO 13320 for particle size determination in pigment dispersions
    • ECHA SVHC compliance for hazardous substance restrictions

    Typical usage ratio

    • 8-20% by weight of dye intermediate mass; formulation depends on desired color intensity and application substrate

    Downstream process integration

    • Blends into diazotization or coupling steps within dye manufacturing; may be pre-dissolved and metered in with pH control for pigment precipitation or resin encapsulation

    Final product types

    • Reactive and disperse dye powders for synthetic fiber coloration
    • Organic pigment dispersions for inks, plastics, and industrial coatings
    • Specialty dyes for electronics or medical diagnostic reagents

    4. Intermediate in Photographic Chemicals and Imaging Materials

    Manufacturers in the imaging sector use the compound as a precursor in the synthesis of light-sensitive compounds, such as cyanine dyes and organic photoactive coatings. Its structural profile suits selective nucleophilic substitution and condensation reactions, crucial in building functional groups for film and digital imaging applications.

    Industry compliance standards

    • ISO 18902:2013 for processed imaging materials storage and handling
    • RoHS Directive 2011/65/EU regarding hazardous substances in imaging electronics
    • EN 62321 for determination of restricted chemicals in imaging products
    • GMP guidelines for production of medical x-ray film chemicals

    Typical usage ratio

    • 3-10% by weight of the organic component in light-sensitive intermediate synthesis; proportion matched to molecular design and exposure performance requirements

    Downstream process integration

    • Introduced during initial condensation or etherification steps; undergoes further derivatization prior to grafting to resins or coating onto film base

    Final product types

    • Photographic color-couplers and image-forming dyes in film production
    • Organic coatings for printed circuit board imaging
    • Sensitizing agents for medical and industrial X-ray plates

    5. Building Block for Electronic Chemicals in Liquid Crystal and OLED Synthesis

    Producers of advanced electronic materials rely on the specific halogenated phenolic structure for the synthesis of high-purity monomers in liquid crystal displays and organic electroluminescent devices. Its controlled reactivity provides for clean coupling and functionalization steps, ensuring precise molecular architecture suitable for modern display technologies.

    Industry compliance standards

    • IPC-4101C for base materials in electronics assembly
    • IEC 62474 for material declaration in electronic components
    • TSCA (Toxic Substances Control Act) compliance for US manufacturing
    • RoHS (Restriction of Hazardous Substances) compliance

    Typical usage ratio

    • 4-10% based on the monomer batch size; quantity closely controlled by stoichiometry and molecular weight target

    Downstream process integration

    • Fed into Suzuki or Buchwald–Hartwig couplings following careful drying and purification; reacts in palladium-catalyzed systems under nitrogen atmosphere

    Final product types

    • Liquid crystal monomers and oligomers for display manufacturing
    • Blue- and green-emitting OLED intermediate materials
    • Specialty electronic polymers for touch panels and displays
    Free Quote

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    Certification & Compliance
    More Introduction

    5-Chloro-2-Hydroxybenzonitrile: Reliable Chemistry for Today’s Applications

    Real-World Product Introduction

    Every day at our facility, we handle thousands of kilograms of fine chemicals that support critical work in pharmaceuticals, materials, herbicides, and dyes. Among the compounds that have earned steady demand is 5-Chloro-2-Hydroxybenzonitrile (also referred to by its synonym 5-chlorosalicylonitrile). As a direct manufacturer, we keep our eyes on the details that matter—not just for purity, but also for real-life consistency, transparency, and adaptability.

    What Sets Our 5-Chloro-2-Hydroxybenzonitrile Apart

    We have seen clients struggle with off-spec materials—moisture fluctuations, inconsistent particle sizes, or troublesome side products. Poor batch repeatability in chemical manufacturing can result in failed reactions downstream. In our experience, few intermediates highlight the need for tight process control better than 5-Chloro-2-Hydroxybenzonitrile. This compound, C7H4ClNO with a molecular weight of about 153.6 g/mol, is not just a building block; it is part of the backbone for a range of both research and commercial synthetic pathways.

    Our chiral and aromatic chemistry programs have leveraged 5-Chloro-2-Hydroxybenzonitrile as a precursor, particularly when a reactive phenolic position is essential. This compound’s halogenated ring and nitrile functional group allow for versatile chemical modification. Nearly every batch leaving our plant holds a purity above 99 percent by HPLC, supporting pharmaceutical applications where residual contaminants might compromise therapeutic profiles.

    Specifications and Experience from the Source

    As chemists who manufacture, we learn every cycle from raw material handling, processing, and purification. This experience led us to fine-tune parameters like solvent choices, drying techniques, and packaging. Water content shifts can accelerate hydrolysis or cause unwanted dimerization over months of storage, so our final product routinely measures below 0.5 percent moisture by Karl Fischer titration.

    We avoid “batch-to-batch surprise” by returning COA data on heavy metals, residual solvents, and particle size distributions for each lot—data drawn from in-house QA as well as third-party confirmation at times, especially for regulated industries. Granular review of UV-Vis and NMR spectra gives transparent assurance: what our clients receive performs the same, whether ordered in a drum for pilot production or in a sealed bag for a specialty synthesis.

    Some users ask about the differences between 5-Chloro-2-Hydroxybenzonitrile and similar halogenated or hydroxybenzonitrile compounds. Over decades, we have found structural substitutions at the 4-position versus the 5-position on the arene ring matter greatly for reactivity. For example, the 5-chloro group brings a different electronic effect than a 4-chloro or a non-chlorinated analog, influencing rates of nucleophilic aromatic substitution or coupling reactions.

    5-Chloro-2-Hydroxybenzonitrile exists as a crystalline powder, off-white to light beige, with a melting range around 110-114°C. Compared to some lower purity options on the market, ours minimizes fine particulate that can cake during long-term storage or complicate handling under dry-room conditions. Bulk density and uniformity, although they sound minor, actually impact meter dosing in continuous flows—insight born of our routine bench-to-plant scale-ups.

    Applications: Value Beyond the Catalog

    Researchers and manufacturing chemists use 5-Chloro-2-Hydroxybenzonitrile for a spectrum of synthetic tasks. Our own teams have applied it as a precursor for pharmaceutical intermediates, chelating resins, and agricultural active ingredients. We frequently discuss with partners why the difference between a random catalog sample and a manufacturing-grade option matters: contaminants, trace isomers, and subtle impurities can severely disrupt downstream reactivity.

    Take, for instance, Suzuki-Miyaura or Buchwald-Hartwig coupling protocols. We have a client who depends on consistent aryl chloride content for ligand-controlled cross-coupling, where even minimal phase impurities can drop yields from 90 percent to below 70. With trusted supply, they cut troubleshooting time and reduced the need for repeat purifications, which benefits cost and sustainability metrics.

    In dye and pigment manufacturing, the hydroxy and nitrile combination gives robust options for introducing azo groups or for further halogenation and sulfonation. We don’t just talk lab results; clients from this sector showed us, through their own analytics, that impurities from poor crystallization routines impact both chroma and solubility in their final dispersions.

    Our own technical group has pushed the boundaries of chlorinated aromatic intermediates for biocidal agents. They teach us that neglecting the trace-level presence of ortho- or para-isomers generates headaches during regulatory filing—especially in Europe, where REACH dossiers require full impurity profiles down to the lowest ppm. It's not enough to simply reach an assay number; every material detail affects compliance and end-use reliability.

    Manufacturing: Details from the Production Floor

    Seeing the synthesis of 5-Chloro-2-Hydroxybenzonitrile up close clarifies what “quality” really means. Our routes typically begin with a monochlorinated benzonitrile, followed by hydrolysis under controlled acidic or basic conditions, then crystallization for purification.

    Failures in temperature ramp rates or inefficient solvent removal often show up as broad melting ranges and off-color batches. Over time, we’ve invested in automated in-process analytics, like real-time FT-IR, to avoid out-of-spec product before it even enters the dryers. We also keep close watch over washing filters and recycling mother liquor. Knowledge gained on our shopfloor translates directly to the confidence end users can place in our batches.

    One persistent challenge involves the safe management of hydrogen chloride evolution and caustic effluent during hydrolysis. Part of our routine includes running closed systems with careful vent scrubbing and effluent neutralization, not cutting corners to push out more product. That mindset springs from both regulatory compliance and the occupational safety culture that’s central to how we operate. Deviations in process water pH or byproduct salt content signal to our crews when upstream tweaks are needed, keeping the process both safe and robust for continued operation.

    Packing, Storage, and Handling Based on Practical Experience

    The journey from our reactors to your receiving dock doesn’t stop with bulk purity. Poorly chosen packaging or a missed moisture spec can create headaches in user labs, from caked blocks that resist dissolution to subtle color changes that suggest incipient degradation. From routine experience, we learned to use multi-layered, vapor-barrier bags, sealed under nitrogen, and then housed in fiber drums or HDPE containers. The color stability and free-flowing appearance of every shipment reflect these details, down to a tracked lot number.

    Our warehouse team maintains climate control, not just for headline products, but also for intermediates like 5-Chloro-2-Hydroxybenzonitrile. Tracking best-by dates, FIFO usage, and scheduled retention analyses underscores our commitment to predictable performance. From time to time, feedback from a customer facing sticky flow or altered appearance moves us to adjust settings, such as drum liners or even including small molecular sieves inside packs bound for humid climates. We find this “listen and adjust” rhythm does more for real-world reliability than theoretical expiry guidelines or standard shelf life projections.

    Comparison: How 5-Chloro-2-Hydroxybenzonitrile Stands Out from Its Analogs

    Market shelves feature a variety of hydroxybenzonitriles and their halogenated relatives. Over years of close work, both at the bench and in the reactor hall, we found that choices like para versus meta chlorine have pronounced downstream effects. In practical pyrimidine or biaryl syntheses, 5-Chloro-2-Hydroxybenzonitrile’s regiochemistry minimizes unwanted regioisomer byproducts and supports selectivity in subsequent reactions.

    Non-chlorinated 2-Hydroxybenzonitrile handles differently under standard nitration and diazotization—often giving lower conversions or less stable intermediates due to electron density on the ring. On the other hand, shifting the chloro group from the 5- to the 4- position changes both reactivity and solubility profiles, which our customers see reflected in color, crystallinity, and even the ease of further functionalization.

    Process chemists appreciate that the 5-chloro group offers better performance in nucleophilic aromatic substitution, particularly in the case of introducing bulkier amines or thioethers. This subtle difference supports cleaner reaction mixtures, less side product scavenging, and easier scale-up. Those working in pigment and dye synthesis echo similar findings: color depth and resistance to fading outperform in tests using our 5-chloro derivative compared with non-chlorinated or 4-chloro analogs.

    There is no substitute for hands-on feedback over decades, and it is this dialogue—with chemists, formulators, regulatory experts—which hones our interpretation of the analytical data. We recommend end users always profile reaction outcomes for each key starting material, especially when regulatory or patent-sensitive milestones are in play. Our labs remain open to collaborative troubleshooting, ranging from customized grind size to trace residual solvent removal, responding directly to each unique synthetic hurdle.

    Engagement with Industrial and Research Partners

    Our company ethos centers more on supporting practical outcomes than simply shifting containers. This means fielding questions on scale-up stability, working closely with analytical labs to confirm impurity fingerprints, and even providing reference spectra for batch comparison. Many larger manufacturers focus only on throughput, but our approach takes feedback from actual applications seriously—whether from multinational pharma or startup material developers.

    University labs and small-scale startups have different needs compared to industrial plants buying by the ton. They often require flexibility in packaging, verification of batch consistency at the kilo scale, or rapid response to technical queries. Having built our technical team from practicing chemists, our responses begin with chemistry, not stock answers. We've witnessed, on several occasions, how custom recrystallization runs or real-time consultation have saved research projects from stalling midstream.

    Large industrial clients may face cost structures dictated by process losses, regulatory filings, or security of supply. Over decades, we have kept back-up capacity and alternate raw supply validated and on-standby, minimizing disruptions. Our quality department keeps proactive compliance documentation for 5-Chloro-2-Hydroxybenzonitrile, matched to evolving standards for pharmaceutical, agriculture, and specialty chemicals. Whenever standards update, we push notification out early rather than catching clients unaware.

    Navigating Market Fluctuations and Supply Challenges

    Raw material volatility and changing regulations challenge even well-run supply chains. We have weathered fluctuations in key building block supplies, chlorinating agents, and solvent availability that can catch traders or smaller operators off guard. As the actual producer of 5-Chloro-2-Hydroxybenzonitrile, we keep transparent communication lines open, flagging potential delays or pricing shifts as early as possible.

    During periods when certain chlorinated intermediates moved to allocation due to environmental audits, we invested early in alternative synthesis routes and additional QA checkpoints. This commitment to redundancy has allowed us to maintain uninterrupted shipments, avoiding the “just in time” bottlenecks that can ripple through complex downstream manufacturing.

    We also lean on long-standing supplier partnerships, so backup and counterparty audits stay central to our operation. Many in our industry focus narrowly on margin or sales velocity, missing how these upstream details impact batch quality and regulatory traceability for customers. All it takes is one recall or complaint to underscore the immediate value in robust supply oversight. Lessons learned through tight spots—the value of a strong vendor, the risk of a borderline material—remain embedded in how we manage our production priorities today.

    Real-World Quality Control: Going Beyond the Basic Specs

    Running a chemical manufacturing plant means you encounter every possible batch hiccup, from unexpected particulate to off-odor issues. We see, in practice, that quality assurance must go further than just “meets spec.” A carefully monitored synthesis and isolation program has allowed us to weed out sources of inconsistent batches — ensuring trace metal content stays low, off-purity isn’t masking side isomers, and color stability holds true batch after batch.

    Our QA protocol routinely checks against not just the usual HPLC and GC-FID runs, but also broader spectroscopic and physical characterization. Melting point analysis, ash content, moisture loss on drying, and microscale titrations reveal earlier if a batch will fail in a customer’s next synthetic step. Opening dialogues with users means learning directly when a feature—like particle flow property or color on standing—is impacting their productivity.

    Continuous improvement arises from owning the entire process chain. We push changes from plant to warehouse within a single quality management system, so feedback about a late-dissolving batch or slight visual shift gets logged and addressed more promptly. Our involvement does not end at the dock: we pursue project-specific questions to ensure each application, be it in complex pharmaceutical syntheses or as a fine chemical for diverse industrial needs, runs smoothly.

    Conclusion: Trust Built Through Real-World Experience

    After years spent in chemical production, our respect for details has only grown. The chemistry behind 5-Chloro-2-Hydroxybenzonitrile stays as relevant as ever, but the success for our customers comes down to reliability, transparency, and continual engagement. Consistent purity, responsive packaging, supply chain depth, and hands-on problem-solving reflect our approach.

    There’s no substitute for the accumulated knowledge found on a working plant floor: understanding how an extra percent of moisture can ruin a reaction, how trace isomers challenge analytical traceability, or why clients need more than just a paragraph of specs. Our product stands for more than a sum of its assay or cert points. It is a result of decades of deliberate production choices—guided by the lessons our customers and teams have lived, not just read about.

    Choosing a manufacturer for key intermediates is about more than transaction—it is about real-world resilience and having a partner that understands both the theory and practice of chemical supply. That’s the experience we bring to every shipment of 5-Chloro-2-Hydroxybenzonitrile, and it’s what continues to drive our industry forward.