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5-Chloro-2-Hydroxy-3-Nitropyridine

    • Product Name 5-Chloro-2-Hydroxy-3-Nitropyridine
    • Alias 5-Chloro-3-nitro-2-pyridinol
    • Einecs 615-111-5
    • 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

    996628

    Chemical Name 5-Chloro-2-Hydroxy-3-Nitropyridine
    Cas Number 54745-70-5
    Molecular Formula C5H3ClN2O3
    Molecular Weight 174.54
    Appearance Yellow to light brown crystalline powder
    Melting Point 162-165°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.69 g/cm3 (approximate)
    Smiles C1=CC(=NC(=C1O)[N+](=O)[O-])Cl
    Inchi Key UENOBQKQYUUFPW-UHFFFAOYSA-N
    Storage Conditions Keep container tightly closed in a dry, cool place
    Purity Typically ≥98%
    Synonyms 5-Chloro-3-nitro-2-pyridinol

    As an accredited 5-Chloro-2-Hydroxy-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25-gram package contains 5-Chloro-2-Hydroxy-3-Nitropyridine in a sealed amber glass bottle with clear hazard labeling.
    Shipping 5-Chloro-2-Hydroxy-3-Nitropyridine is shipped in tightly sealed containers to prevent moisture and contamination, conforming to relevant transport regulations. The package is clearly labeled with hazard information, and shipping is typically carried out by certified couriers, using protective outer packaging to minimize risk during transit. Handle according to MSDS recommendations.
    Storage Store **5-Chloro-2-Hydroxy-3-Nitropyridine** in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and moisture. Keep away from incompatible substances such as strong oxidizers and reducing agents. Ensure proper chemical labeling and access control. Avoid contact with skin and eyes; use appropriate personal protective equipment when handling.
    Application of 5-Chloro-2-Hydroxy-3-Nitropyridine

    Applications of 5-Chloro-2-Hydroxy-3-Nitropyridine in Industrial Manufacturing

    As a direct manufacturer of 5-Chloro-2-Hydroxy-3-Nitropyridine, we supply fully controlled product grade designed for several advanced industrial applications. Major global companies adopt this material as a key intermediate in regulated, multi-step synthetic routes. Below, we detail four main downstream applications, with process and compliance specifics for each.

    1. Pharmaceutical Intermediate for Antimalarial APIs

    Advanced pharmaceutical companies use 5-Chloro-2-Hydroxy-3-Nitropyridine as an essential intermediate in the synthesis of certain antimalarial active pharmaceutical ingredients, including pyrazine and pyridine-based molecules. Our product integrates into the late-stage heterocycle assembly, where its unique substitution pattern drives selective transformation during API precursor synthesis. Downstream partners strictly monitor residuals and trace impurities through validated HPLC and GC protocols to meet international import standards for regulated APIs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for APIs
    • USP, EP, BP monographs as relevant for downstream drug substances
    • FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU Directive 2001/83/EC compliance for human medicinal products

    Typical usage ratio

    • Varies from 0.08–0.15 molar equivalents relative to final API batch size, adjusted based on route efficiency and validation protocols
    • Batch synthesis scale subject to in-house QP review and validation documentation

    Downstream process integration

    • Entered after initial ring formation and protection/deprotection steps
    • Engages as coupling partner or halide substrate in nucleophilic substitution, ring closure, and/or reduction stages
    • Purification via crystallization or preparative chromatography before proceeding to final API coupling or salt formation

    Final product types

    • Chloroquine analog intermediates
    • Specialized heterocyclic pharma APIs
    • Commercially registered tablet and injectable antimalarial drugs

    2. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers incorporate our product in the manufacture of selective herbicide and fungicide actives, particularly where pyridine or related ring systems impart target specificity. The material functions as a core scaffold in multi-step routes, enabling site-specific halogenation and nitro reduction under tightly monitored process safety and effluent control. Manufacturers require consistent lot traceability and full COA disclosure to comply with environmental and operator exposure limits.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • OECD Principles of Good Laboratory Practice
    • REACH Annex VII for downstream chemical safety reporting
    • ISO 9001:2015 for consistent quality management

    Typical usage ratio

    • 0.12–0.30 molar equivalents, dependent on the targeted mode of action and final molecule design
    • Adjusted for yield optimizations during scale-up and pilot production

    Downstream process integration

    • Initial conversion typically via nucleophilic aromatic substitution or nitro reduction in stainless steel reactors
    • Material enters the process before formulation of the final technical concentrate
    • Purification protocols include aqueous work-up and phase separation

    Final product types

    • Pyridine-based herbicide actives
    • Systemic fungicide technical concentrates
    • Commercially registered crop protection formulations (EC, SC, WG)

    3. Dye and Pigment Intermediate for Specialty Colorants

    Specialty dye manufacturers adopt our product as a crucial intermediate for complex azo and heterocyclic pigment synthesis, especially where intense, stable color strength is required in plastics, textiles, and ink applications. The material’s functional groups support stepwise condensation and coupling under pH-controlled conditions, where accurate dosing and minimal residual chlorides directly impact final pigment quality. Large-scale end-users demand batch-to-batch spectral reproducibility and conformance to amine impurity thresholds.

    Industry compliance standards

    • ISO 9001:2015 for pigment batch quality
    • EN 71-3:2019 restrictions for migration of certain elements (toys, textiles)
    • REACH Annex XVII for restricted amines in final dyes
    • OEKO-TEX® Standard 100 for human ecology product safety

    Typical usage ratio

    • 0.05–0.18 molar equivalents depending on pigment hue and end-use substrate
    • Dosing optimized during small-lot trialing and scaled per in-line colorimetric QC

    Downstream process integration

    • Introduced upstream during condensation or coupling runs with diazonium salts
    • Undergoes controlled reactions in glass-lined reactors
    • Pigment extract purified with Soxhlet or column techniques prior to drying and finishing

    Final product types

    • High-performance yellow and orange pigments for plastics/extrusion
    • Textile-reactive azo dyes
    • Special inkjet and offset ink dispersions

    4. Fine Chemical Synthesis for Electronic Materials

    Electronic chemical manufacturers use this material as a building block for high-purity, functionalized pyridines in the production of active organic semiconductors, OLED materials, and specialty ligands for display or photoresist manufacturing. Stringent QC demands require trace metal, halide, and amine monitoring with ICP-MS and HP-TLC for each lot, enabling integration into highly sensitive electronic-grade formulations. Downstream processes demand single-digit ppm impurity profiles and conformance to SEMI purity guidelines.

    Industry compliance standards

    • SEMI C93-0919: Guide for High Purity Chemicals for Electronics
    • ISO 14644 Cleanroom and Controlled Environment requirements
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • Customer-specific advanced specification sheets for display material vendors

    Typical usage ratio

    • 0.03–0.07 molar ratio of total organic material, with adjustment for purity demands and functionalization depth
    • Ratio set by target conductivity or emission property in final material

    Downstream process integration

    • Material enters after initial lithiation/halogen exchange in glovebox or dry-room environment
    • Functionalization under anhydrous conditions with in-process NMR confirmation
    • Integrated into multi-step syntheses for photoluminescent or conductive targets

    Final product types

    • Small-molecule OLED emitters
    • Specialty ligands for metal-organic frameworks
    • Electronic photoresists for IC manufacturing
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    Certification & Compliance
    More Introduction

    Introducing 5-Chloro-2-Hydroxy-3-Nitropyridine: A Chemist’s Perspective from the Factory Floor

    Meeting Market Demands with Real Results

    5-Chloro-2-Hydroxy-3-Nitropyridine is one of those compounds that stands out in a crowded field of niche pyridine derivatives. Having spent years developing and scaling up its production, I've seen how this molecule quietly shapes the backbone of several specialty segments. Whenever project teams scout for a functionalized pyridine, they’re looking for reliability, not just a chemical name on a list. Our job as manufacturers is not simply to fill barrels but to deliver a product that performs batch after batch, whether shipped across the city or halfway around the world. That relies on clear understanding of the chemistry and the process that gives this compound its value.

    What Sets 5-Chloro-2-Hydroxy-3-Nitropyridine Apart

    In the plant, chemists and engineers talk about this molecule using its shorthand, CHNP. Unlike other pyridine-based ingredients, CHNP carries a rare trio of groups positioned just right on the ring structure—a chloro, a hydroxy, and a nitro—each adding a specific character. The chloro group sits in the 5-position, stubbornly resisting some reactions, but offering excellent pathways for further derivatization. The hydroxy group at 2- makes it especially handy as an intermediate for more complex molecules, supporting reliable hydrogen bonding both in synthesis and when incorporated into finished products. The 3-nitro group opens doors to both electron-withdrawing effects and further reductive transformations.

    The precise arrangement of these groups means you’re not just swapping out one pyridine for another. Each substituent influences the molecule’s reactivity and application profile. Plenty of pyridine derivatives can function as pharmaceuticals intermediates or crop protection building blocks, but few handle these specialized transformations as predictably.

    Product Consistency from a Manufacturer’s Lens

    Delivering CHNP isn't just about running a synthesis and collecting the yield. Daily, our team checks that incoming raw materials stay within tight purity limits. We track every variable—solvent grade, reaction temperature, atmospheric pressure, and even the stirring speed. After several years at commercial scale, even small changes ripple through the process, sometimes bumping up unwanted byproducts or shifting the color. Consistency means dialing in after every maintenance cycle, recalibrating instruments, and not assuming past batches can predict the next.

    For this particular product, we have standardized a model that effectively isolates 5-Chloro-2-Hydroxy-3-Nitropyridine at purities commonly reaching 99%. That’s not marketing speak; it’s the number you need to prevent downstream crystallization headaches, and it’s measured in every batch. Achieving that, while controlling for trace metals, moisture, and residual solvents, matters whether you’re preparing for a medicinal chemistry run or planning a multi-ton crop protection launch.

    Real-World Properties Our Customers Rely On

    People in the lab often ask about its melting point, solubility, and color stability. We find the material keeps its yellow tint even when stored under ambient conditions, thanks to the robust nitro group. Apart from the standard lab solvents, CHNP dissolves with less fuss in polar aprotic liquids and recovers easily in typical crystallization workflows. These physical traits show their value only after you’ve tried to swap it for a similar molecule and hit unexpected snags—maybe the substitution reactivity drops, maybe side-products creep in, or perhaps the yield takes a dip without clear explanation.

    While some close analogs might share one or two functional groups, we rarely see them match this molecule’s balance between processability and reactivity in industrial-scale settings. Our plant engineers have run side-by-side trials with cousins like 5-Chloro-2-Methoxy-3-Nitropyridine and 2-Hydroxy-3-Nitropyridine, documenting significant differences in purity levels after crystallization and ease of downstream transformations. It isn’t just about the naming—subtle changes in molecular structure lead to real differences in handling, storage, and transformation.

    Current Use Cases Shaped by Reliable Sourcing

    The most common demand arrives from pharmaceutical research. Medicinal chemists structure-activity relationship (SAR) campaigns frequently probe derivatives of pyridine scaffolds, and CHNP acts as a flexible intermediate for these targeted explorations. Requests for scale-up often arrive with urgent timelines, and with regulatory submissions, gaps in impurity profiles just aren’t an option.

    Outside pharma, agrochemical development teams use CHNP as a starting point for synthesizing advanced crop protection agents. Chemical manufacturers, whether working in-house or for multinational conglomerates, appreciate the direct transformations available via nucleophilic aromatic substitution, or employing the nitro group for selective reduction. These options provide routes that can cut total process steps and simplify purification for new candidates.

    In our plant, we know which grades will work best for each application—whether a kilogram synthesis in an R&D pilot, or multi-ton supply for qualified development partners. The established specs allow us to have real conversations with our customers, reducing surprises and unnecessary back-and-forth.

    Why Quality Differences Matter

    In theory, sourcing CHNP should be straightforward. In practice, small departures in purity or form can turn a straightforward synthesis into a waste of time and money. Some materials arrive with excessive moisture or trace halides leftover from the chlorination step. These impurities don’t always emerge until a downstream reaction stalls, product color drifts into unacceptable ranges, or yield drops inexplicably.

    From firsthand experience, I’ve watched as a difference of 0.2% in an HPLC purity reading derails a medicinal chemistry project. The chemists at the bench notice it long before anyone in procurement spots the trend. It’s not enough to post a specification once and forget about it. We test every batch, not just because that’s what’s required under GMP, but because we face those phone calls when things aren’t working as planned.

    Over time, we have honed protocols that reduce the risk of cross-contamination, and our drying systems are set up to hit even the tightest moisture thresholds. Our customers in regulated sectors don’t want to repeat analytical checks—they want confidence that what they receive will perform exactly like the previous lot.

    Practical Handling and Storage Approaches

    5-Chloro-2-Hydroxy-3-Nitropyridine ships as a stable, non-hygroscopic crystalline solid. We pack it into fiber drums with protective liners or, for research quantities, into amber glass bottles that prevent photodegradation. End users typically transfer the material under nitrogen, but our product keeps well at room temperature, and bulk lots store safely for extended periods without significant changes in color or purity.

    From a manufacturer’s perspective, the true test isn’t the shelf life written on a data sheet, but how the chemical performs after six months in storage or after shipment across three climate zones. Field experience tells us this compound sticks to specifications, provided that containers remain tightly sealed and away from direct sunlight or extreme humidity.

    I’ve seen bulk samples recover their original crystal structure after recrystallization even after prolonged storage, confirming chemical stability. For customers rolling out new processes or running pilot-scale experiments, the confidence this provides makes a real difference.

    Comparisons with Related Pyridine Compounds

    Looking beyond the basics, chemists are always comparing similar pyridine derivatives. Some newer entrants on the market promise lower costs but often cut corners with respect to side product removal or heavy metal control. CHNP, as we make it, supplies a tight impurity profile, especially when supplied for the pharmaceutical sector.

    Its closest relatives either drop the chloro group or alter the nitro position, each change impacting the molecule’s suitability for further transformations. For example, 2-Hydroxy-5-Nitropyridine trades away the chloro group for a more open synthetic handle, but the lack of electron-withdrawing chlorine can destabilize certain intermediates. Customers chasing high yields in halogenated product lines quickly discover that not every starting material matches up, especially under scaled-up reaction conditions.

    From conversations with formulation chemists, I’ve heard plenty of frustration when swapping to cheaper analogs. Slower dissolving rates, unexpected darkening, and sluggish filtration can turn a minor substitution into a costly exercise. In this respect, we always recommend running a direct A/B trial—results tell their own story.

    How Upstream Processes Shape Downstream Success

    Manufacturing CHNP gives insight into the chain of decision-making that starts with how you chlorinate the pyridine ring and doesn’t end until tight quality checks are wrapped up. Our reactors run on batch recipes derived from years of iterative improvements. Changing a solvent or swapping a catalyst to push a little more yield often means addressing new classes of byproducts or slowing purification steps. We invest in regular analytics—not just during commercial production, but also upstream, tracking raw material purity and even the water quality used in reaction workups.

    Our engineers view upstream decisions as the front line in controlling color and physical form. A slightly elevated temperature, left unchecked, can bump impurity counts that cause problems days after the product leaves the plant. These small adjustments, repeated over hundreds of batches, form the foundation for predictable, high-purity lots.

    Over time, sharing process modifications with trusted customers prompts mutual improvement. Several clients pursuing continuous processing for crop protection pipelines have worked with us to match our process controls to their downstream equipment. The feedback loop here—between our manufacturing line and the customer’s bench—has led to tighter specs and lower wastage.

    Environmental, Health, and Safety Under Real Conditions

    Chlorinated and nitrated intermediates demand careful handling during production. We monitor airborne levels in the production area using real-time detectors, and our staff rotates regularly to limit exposure, even when concentrations remain within globally accepted standards. Beyond what regulations require, we offer practical guidance for customers scaling up processes, particularly around dust generation and containment.

    Waste streams from CHNP syntheses tend to include some halogenated solvents and traces of unreacted starting materials. We’ve invested in on-site treatment, capturing volatile organic compounds and neutralizing aqueous waste through dedicated systems. Working every day with the material, we know which steps offer genuine risk reduction, as well as which ones simply look good in documentation but don’t move the real hazard needle.

    From an upstream supplier’s point of view, ensuring safe and sustainable production builds trust. Repeat audits from multinational clients and regular certification updates keep us sharp, pushing us to be both transparent and responsive.

    Pricing, Scalability, and Global Supply Realities

    Many see specialty chemicals as commodity products, but the price of CHNP reflects more than the cost of raw materials. Energy use, skilled labor, ongoing process improvements, and compliance to GMP for pharmaceutical grades all factor in. Years ago, buyers might have sourced smaller lots from different continents interchangeably. Today’s climate priorities and supply chain realities demand a realistic appreciation of what it takes to reliably deliver kilo, multi-kilo, or even multi-ton lots within agreed timelines.

    We’ve increased reactor capacity, invested in solvent recovery, and built contingency stocks to buffer against shipping delays or raw material fluctuations. Still, the supply chain for precursor chemicals, especially those tied to halogenation or nitration, remains sensitive to regulation and trade logistics.

    As the original manufacturer, we stay close to changes in upstream material markets, quickly flagging any blips in both price and lead time to our customers. Years of experience show that keeping up open dialogue with downstream partners—not only when times are easy—lets everyone adapt to shifting regulatory or market environments.

    Supporting Research and Innovation

    Bench chemists—whether developing blockbuster drugs or new agricultural agents—depend on swift feedback and a flexible supply chain. Our team gets requests not only for standard powder lots, but also for custom particle sizes or material packaged specifically for high-throughput screening robots. We don’t see ourselves as just bulk handlers. Having worked with development chemists under time pressure, we know the difference a quick redesign or a small tweak in drying protocol can make.

    With partnerships in academic and industrial research, we share data on process impurities, stability under unusual storage conditions, and even results of new derivatization procedures. These exchanges fuel improvements both in our own plant and for end-users, turning a commodity into a solve-it-once problem for others.

    Future Opportunities for 5-Chloro-2-Hydroxy-3-Nitropyridine

    With ongoing shifts in green chemistry and demand for less hazardous reagents, process chemists continue searching for new roles for CHNP across pharmaceutical and agricultural portfolios. Our ongoing pilot plant runs have tested out catalytic transformations and more sustainable solvents. Every successful iteration not only trims down waste but also opens new application possibilities for clients expanding beyond current uses.

    We remain deeply invested in collaborative improvement, listening for feedback and fielding custom syntheses when needed. Our day-to-day experience confirms that the road toward reliable, high-purity CHNP is paved with careful decisions, relentless pursuit of process consistency, and a willingness to try new methods.

    If you work with pyridine derivatives, the differences between similar-seeming options might look small on paper, but in production or development, those details decide timelines, budgets, and ultimately, successful project launches. From our position inside the plant, we see 5-Chloro-2-Hydroxy-3-Nitropyridine as more than just another chemical—it’s the product of years of fine-tuning, thousands of quality checks, and close teamwork between factory and bench.