|
HS Code |
557020 |
| Iupac Name | 4-cyano-2-nitrophenolate |
| Molecular Formula | C7H3N2O3^- |
| Molecular Weight | 163.11 g/mol |
| Cas Number | 33400-36-9 |
| Appearance | Yellow to orange solid |
| Melting Point | Decomposes before melting |
| Solubility In Water | Soluble |
| Pka | Approximately 7.5 |
| Chemical Structure | OC1=CC=C(C#N)C=C1[N+](=O)[O-] |
| Synonyms | 2-hydroxy-5-cyano-1-nitrobenzene, 4-cyano-2-nitrophenol (deprotonated) |
| Smiles | C1=CC(=C(C=C1O)[N+](=O)[O-])C#N |
As an accredited 4-Cyano-2-Nitrophenolate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 4-Cyano-2-Nitrophenolate, securely sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 4-Cyano-2-Nitrophenolate is shipped in tightly sealed, chemical-resistant containers under dry conditions to prevent moisture absorption. Clearly labeled with hazard classifications, it is transported according to relevant regulations for hazardous chemicals. Adequate packaging ensures containment, and accompanying documents provide handling, storage, and emergency information for safe shipping. |
| Storage | 4-Cyano-2-nitrophenolate should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separated from incompatible substances such as acids and strong oxidizers. Proper chemical labeling and handling procedures should be followed, and access should be restricted to trained personnel wearing suitable protective equipment. |
Competitive 4-Cyano-2-Nitrophenolate prices that fit your budget—flexible terms and customized quotes for every order.
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As a company dedicated to producing specialty chemicals across multiple sectors, we find that 4-Cyano-2-Nitrophenolate draws regular attention from research chemists and formulators for good reason. With its unique combination of electronic properties and stable structure, this compound opens up pathways for advanced synthesis, analytical detection, and materials science projects, especially where reactivity and selectivity make or break an experiment. Over the years, direct conversations with our customers taught us which qualities matter most: reliability, purity, and consistency. The only way to meet those expectations is through rigorous in-house manufacturing—starting from raw material selection, every batch of 4-Cyano-2-Nitrophenolate gets run through our tailored process, fine-tuned over numerous production cycles.
We synthesize our product under strictly controlled conditions. This method yields the sodium salt form as a bright yellow powder or crystalline substance—free-flowing, low in moisture, and packed in inert atmosphere containers to help prevent oxidation or degradation. Our routine testing includes HPLC and NMR identification, purity assessment well above 99%, and checks for trace contaminants. These aspects cannot be left to chance; failure at any step risks introducing variables that quietly undermine a chemist’s work downstream. In our experience, customers who require this compound often pursue novel aromatic substitutions, fluorescent probes, or nitroaromatic conversions. Repeat users look for clear, reproducible melting points, batch certificates referencing both chemical structure and functional purity, and—if projects scale—reliable delivery across kilogram lots.
Few molecules in our lineup combine the dual reactivity of the nitrile and nitro groups with the phenolate backbone. This pairing supports synthetic transformation not only as a building block, but as a versatile reagent. The electron-withdrawing nature of both groups influences nucleophilic aromatic substitution and other downstream reactions—properties that help distinguish 4-Cyano-2-Nitrophenolate from more common phenolate salts that lack such activation. For research teams designing heterocyclic libraries, the positioning of the cyano and nitro substituents on the aromatic ring guides regioselective functionalization, aiding scaffold diversity. Many customers highlight this compound in their development of pharmacologically active intermediates; since subtle structural changes in a candidate series influence biological response, rigorous lot-to-lot consistency stays non-negotiable.
Outside medicinal chemistry, our regular customers count on 4-Cyano-2-Nitrophenolate for its optical and electrochemical characteristics. In the preparation of dyes, sensors, and advanced polymers, its role often shifts from core reactant to performance enhancer. The presence of the para-cyano group and ortho-nitro combination results in a distinct UV-visible absorption spectrum—an advantage researchers use for sensitive detection or monitoring of transformation. Several collaborations with academic labs have demonstrated that our product delivers clear, intense signals with low background interference, essential for accurate analysis in both small-scale and pilot settings. This optical signature also makes the compound appealing for photophysical studies, especially where precise calibration trumps cost or ease of use.
Demand for 4-Cyano-2-Nitrophenolate comes in waves. Our strengths as a manufacturer lie in scaling production without sacrificing quality, responding to shifts by holding buffer stock and working with our logistics team to ship on a tight schedule when new orders arise. In our early years, delayed feedback from users sometimes pointed to trace lot variability—something that taught us to tighten our recrystallization and drying processes. Chemical manufacturing invites inevitable problems: subtle shifts in temperature, humidity spikes, or an unexpected impurity in a raw material lot. Every time these unforeseen changes arose, we re-optimized that section of the process, drawing from both instrument data and chemical intuition built over decades.
Today, no part of the synthesis or workup goes unmonitored. We batch test every shipment for particle size distribution, solubility in common laboratory solvents, and active pH profile—practices based on direct requests from end users who share their analytical pain points. This granular tracking not only reduces the risk of cross-contamination but speeds up troubleshooting and strengthens trust. Unlike generic marketplaces, we take direct accountability for what bears our label. Laboratories in synthesis, materials engineering, and analytical development rarely have time for delays or the complications of inconsistent product. By managing our own supply chain, and investing in dedicated lines for sensitive phenolate derivatives, we align stock movement with real-world needs.
Several features make this compound distinct among our product range. Many customers ask how 4-Cyano-2-Nitrophenolate compares to standards like sodium phenolate or para-nitrophenolate—compounds that carry lower price tags but not always the right reactivity. The reason comes down to the heightened electron-withdrawing power of its substituents, which impart both increased acidity and unique resonance stabilization. This means our product dissolves in polar solvents at room temperature, forms stable salts with alkali metals, and lends itself to multistep sequences in both aqueous and organic media. By comparison, simpler phenolates require harsh conditions or additional activators to match its performance in certain coupling or condensation reactions.
We measure our compound’s performance through customer results rather than abstract descriptors. Over repeat cycles, we’ve learned that pharmaceutical and specialty chemical producers want more than theoretical suitability. They report on yields, color development in downstream reactions, ease of filtration, and the precision of analytical signatures in NMR or LC-MS characterization. The main difference between our 4-Cyano-2-Nitrophenolate and more common alternatives shows up in those demanding applications—particularly where background reactivity, trace water, or byproduct formation can jeopardize a project. Our process produces minimal inorganic residues, so finished material achieves high reproducibility in colorimetric assays and can be pushed to higher concentrations without precipitation issues.
Starting from concept-stage R&D to pilot plant trials, the demand for 4-Cyano-2-Nitrophenolate continues to grow. In-house trials and customer case reports show clear advantages in the assembly of nitroaromatic intermediates for crop protection agents and fluorescent labels. Researchers developing electroactive polymers note that our material’s solubility and clean decomposition pattern assist both in formulation and in testing. On the analytical chemistry front, the distinct UV-Vis absorption delivers cleaner baselines, which supports trace analysis and method calibration for QC labs.
Some of our more technical customers use it in custom sensor design, where performance metrics hinge on precise chemical identity. In those cases, any deviation in the salt content, moisture, or minor byproducts affects device reliability. Our process audits, conducted every quarter, ensure the product not only matches published specifications but remains predictable at gram, hundred-gram, and kilogram scales. Such attention to detail matters most for teams who cannot afford to repeat a three- or four-step sequence only to discover off-spec feedstocks.
We treat every inquiry about downstream customization seriously. In some instances, a customer needs the potassium or lithium salt instead of sodium; in other settings, additives or micronized particle sizes support more efficient blending in automated reactors. Since we run our own production, these technical adjustments can be reviewed, trialed, and delivered without unnecessary delays—cutting out guesswork or long supplier chains. Repeat customers have taught us to invest time in these conversations, because challenges in the field usually surface only after a few cycles and are often unique to the local process.
Our plant operates within nationally recognized safety and environmental regulations. Handling nitrophenolate compounds at scale brings certain risks, so our facilities integrate engineered controls, direct venting, and strict batch monitoring. Workers undergo updated safety training each year, and our materials handling, storage, and shipping policies meet both government and customer audit checks. Waste minimization strategies have evolved—recovery of process solvents, closed-system filtration, and responsible waste disposal anchor our daily routines.
For chemists interested in sustainability, the production route we follow generates lower volumes of hazardous side streams compared to legacy processes. Continuous improvement involves regular reviews by both our technical and ESG compliance teams. Product labeling for 4-Cyano-2-Nitrophenolate includes batch numbers, shelf-life validation, and traceability protocols, so laboratories can reference relevant data if questions ever arise during use or inspection. Our dedication to transparency comes directly from years of open dialogue with customers who value not just a quality product but also clear sourcing information.
Some of the most meaningful product advances stem from on-the-ground collaboration. We actively encourage customers to ask about alternate packaging, unusual solubility requirements, or documentation requests that may differ from standard expectations. By tracking feedback, including performance under non-standard reaction conditions, we refine not only the synthetic recipe but every layer of support around the product—technical data sheets, regulatory paperwork, and after-sale support that steps in quickly if troubleshooting becomes necessary. There is no substitute for the insight that comes from seeing outcomes in both successful and failed experiments.
We maintain an open line with contract researchers and manufacturing-scale users to adapt to changing regulations and technical demands. In recent years, advances in automation and reaction engineering drove up demand for higher-purity lots and variant forms (e.g., wet-cake, micronized, or formulated blends). As a direct producer, we tweak drying curves, particle size, and chelating counterions to fit customer protocols. The feedback leads not only to happier research partners, but also to an ongoing cycle of self-auditing and risk reduction across the site.
Skill in producing 4-Cyano-2-Nitrophenolate comes from experience—hours spent troubleshooting, refining, and checking each batch before it ships. With tighter regulatory scrutiny and shifting global standards, we keep pace by enrolling in outside audits and benchmarking our facility’s technical performance against current best practices. From personal engagement, we know researchers and companies value both the science of molecules and the art of reliable supply. It is not enough that the product works on paper; it must work in every setting where new ideas begin.
Current projects include working with cross-disciplinary R&D teams exploring novel electronic materials and advanced imaging agents. These applications present technical questions about scale-up, reactivity, and stability that test our process at each stage. Our production floor operators and technical staff share a commitment to documentation, data-driven improvement, and responsiveness. In fact, our investment in better inline monitoring and remote support grew out of hearing stories from users whose projects depended on one high-stakes delivery, at the right specification, every time.
Serving as a manufacturer in this space demands attention to both molecular details and practical outcomes. 4-Cyano-2-Nitrophenolate finds use in ambitious chemical synthesis, dynamic material innovation, and emerging analytical techniques. Each kilogram delivered reflects many iterations, lessons, and shared problem-solving from both sides of the supplier-user relationship. We pour our manufacturing experience into every order—staying available for technical questions and always learning what matters most to real-world applications.