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HS Code |
361444 |
| Chemicalname | Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro- |
| Molecularformula | C7H4ClNO4 |
| Molecularweight | 201.56 g/mol |
| Casnumber | 65656-77-1 |
| Appearance | Yellow to brown crystalline powder |
| Meltingpoint | 221-224°C |
| Solubilityinwater | Slightly soluble |
| Pka | 2.7 (approximate, for carboxylic acid group) |
| Density | 1.7 g/cm³ (approximate) |
| Smiles | C1=CC(=C(C(=C1C(=O)O)Cl)[N+](=O)[O-])O |
| Inchi | InChI=1S/C7H4ClNO4/c8-4-2-3(7(10)11)1-5(9(12)13)6(4)14/h1-2,14H,(H,10,11) |
| Synonyms | 5-Chloro-2-hydroxy-3-nitrobenzoic acid |
| Storagetemperature | Room temperature, keep dry |
| Hazardclass | Irritant |
As an accredited Benzoic Acid,5-Chloro-2-Hydroxy-3-Nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro- is supplied in a 25g amber glass bottle with secure screw cap labeling. |
| Shipping | Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro- is shipped in securely sealed, chemical-resistant containers to prevent leaks and contamination. Packaging complies with international regulations for hazardous materials and includes proper labeling. Transport is typically arranged via ground or air, depending on destination, with documentation and handling per safety data sheet recommendations. |
| Storage | Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro- should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizers and bases. Ensure the storage area is clearly labeled and access is limited to trained personnel. Avoid sources of ignition and direct sunlight. |
Applications of Benzoic Acid,5-Chloro-2-Hydroxy-3-Nitro- in Industrial ManufacturingAs a committed raw material manufacturer, we supply Benzoic Acid,5-Chloro-2-Hydroxy-3-Nitro- globally for advanced downstream industries that require stringent quality controls, consistent supply, and traceable production processes. Below, we detail the most significant industrial applications, focusing on their real regulatory frameworks, technical dosing, process stages, and the specific end products where this intermediate enables advanced performance, compliance, and differentiation. 1. Pharmaceutical Intermediate for Anti-Infective APIsBenzoic Acid,5-Chloro-2-Hydroxy-3-Nitro- serves as a strategic building block in the synthesis of nitro-chlorinated salicylic acid derivatives, which are core intermediates for manufacturing advanced anti-infective Active Pharmaceutical Ingredients (APIs). Our production quality aligns tightly with industry requirements on purity and contaminant profiles, ensuring consistent outcomes during multi-step pharmaceutical synthesis. Customers incorporate this intermediate post-nitration and chlorination phases, directly before ring-closing or amide coupling steps to construct key functional moieties required by leading antibiotic or antifungal molecules. Industry compliance standards
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2. Synthesis Intermediate for Specialty Agricultural ChemicalsDownstream agrochemical producers utilize this compound as a precursor in the synthesis of complex heterocyclic structures for modern crop protection agents, such as selective fungicides or herbicide formulations. Manufacturers rely on our product’s consistent nitro and halogen functionalization, which facilitates subsequent coupling with amines or alkoxides via nucleophilic aromatic substitution, enabling precise targeted molecule construction. Industry compliance standards
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3. Fine Chemical Synthesis for Specialty Dyes and PigmentsManufacturers of high-performance dyes and pigments for the textile, plastics, or ink sectors select this nitro- and chloro-functional aromatic acid to introduce tailored chromophore patterns. Its unique substitution profile expedites azo coupling or condensation with diamines, creating vivid, heat-stable pigment molecules demanded by downstream colorant producers aiming for performance under harsh industrial conditions. Industry compliance standards
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4. Intermediate for Electronic Grade Functional MaterialsProducers in the electronics materials sector integrate this material during the synthesis of specialty resins or small-molecule additives essential for dielectric coatings, circuit board laminates, or optoelectronic layers. The unique combination of nitro, chloro, and hydroxy groups provides sites for downstream ether or ester linkage, enabling robust molecular design for insulation, adhesion, and heat-resistance specifications in finished devices. Industry compliance standards
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5. Building Block for Advanced Polymer AdditivesFormulators of advanced polymeric additives exploit the multifunctional aromatic structure to build antioxidants, UV stabilizers, and flame-retardant masterbatches for engineering plastics and elastomers. The nitro and hydroxy groups enable further functionalization and grafting, incorporated during melt-blend or in-reactor addition to impart enhanced aging performance or fire resistance. Industry compliance standards
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Benzoic Acid, chemically recognized with the specific structure of 5-chloro-2-hydroxy-3-nitro substitution, stands out as more than a variation in a catalog. The manufacturing floor offers a unique close-up view of materials usually hidden behind a wall of technical jargon, datasheets, or commercial gloss. To those outside the plant, it may sound like just another aromatic acid, but this molecule holds a combination of properties that rarely converge in other benzoic acid derivatives.
Years on the production line showed me the small details others overlook. Once the raw materials are prepped, reactions run in carefully tuned vessels, under keen-eyed oversight. Each batch hands back a clear lesson: the right mix of chloro, hydroxy, and nitro placements on the benzoic scaffold allows us to produce a compound that answers to the changing needs of research labs, specialty materials, and formulators. The time spent optimizing yields and purity pays off every time we open up a fresh drum—crystals form predictably, moisture stays at bay, and off-tones in color or odor rarely slip through when protocols are followed closely.
Many outsiders view benzoic acids as interchangeable except for their catalog numbers or minor substituent tweaks. From a synthesis standpoint, adding a single chlorine group at the 5-position is far from cosmetic. The structure created is not easily swapped for bulk alternatives. Working with chlorinated hydroxy-nitrobenzoic acid teaches that small adjustments shift a product’s chemical tone entirely—solubility changes, reactivity responds, storage and shelf life get influenced. Every molecular position holds weight beyond the chemistry textbook.
Those in R&D, fine chemicals, or pharmaceutical intermediates recognize how the nitro group at the 3-position and hydroxy at the 2-position unlock different reactivity patterns in downstream synthesis. Chlorination further tunes electron density, impacting both the selectivity of coupling partners and the kind of protection/deprotection steps a process chemist can deploy. By preparing this compound to high purity and controlling trace contaminants, we make sure it doesn't just serve as a base chemical, but becomes an enabling tool in the hands of those building complex molecules.
Over the years, I have seen the difference between a batch that barely passes standard testing and one that lays the groundwork for robust, reliable downstream reactions. Impurities in sensitive positions can ruin costly experiments, gum up reactors, or drag down yield for our customers. That is why our team sweats the details—filtration steps, temperature control, precise measurement of reagents. In the case of Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro-, such care amplifies both chemical stability and predictable performance in reactions.
Chemical manufacturers walk a tightrope between maximizing output and keeping integrity. Skimming on purification or overlooking process optimization to squeeze every gram sometimes looks tempting, but the market quickly notices a drop in consistency. From my experience, customers are patient with delays, less so with unexplained variations. We invest in robust analytical protocols—melting point verification, chromatography, spectroscopic confirmation—and share this data so partners can trace each lot’s history back to the feedstock. These controls mean end users don’t face surprises midway through their own synthesis, and manufacturers can identify and fix root causes if anomalies arise.
Walking through the application corridors, I see the requests come in from sectors ranging from pharmaceutical intermediates to specialized resin modification. Research teams working on active pharmaceutical ingredients often seek intermediates with precise functionalization because standard benzoic acid won’t provide the same reactivity or selectivity. The hydroxy and nitro groups in this product direct reactions in predictable ways; for instance, nucleophilic aromatic substitution and electrophilic additions behave much differently than in less substituted benzoic acid siblings.
Polymer chemists sometimes need this compound to alter polarity or reactivity in proprietary resins, while pigment manufacturers ask for it to introduce chromophoric diversity or tune dye fastness in advanced materials. Some developers in fine chemical synthesis, especially where regulatory scrutiny demands traceable raw material quality, choose our lot-controlled, multi-checked batches to avoid hidden bottlenecks under scale-up. With more unique substitutions, the options for arsenal in heterocycle construction or fragment coupling in modern medicines grow.
Early in my career, I thought difference between an off-the-shelf and a specialty benzoic acid would barely matter to end users. Seeing feedback firsthand, I learned customers care if a product dissolves at the precise rate, crystallizes reliably after solvent exchange, or resists discoloration under their reaction sequences. They notice the lot with unexpected impurity and come back to review our process checks. That accountability keeps us improving, batch after batch.
Every plant run brings up tricky problems. Benzoic Acid derivatives are no exception. During scale-up, introduction of chloro and nitro groups can cause stubborn side products, and filtration stages may slow down as solids clump or hinder solvent recovery. Environmental teams keep us sharp—chlorinated byproducts challenge safe disposal and require thorough tracking. Each stage from reaction, wash, and dryout has teams watching for signal changes or anything drifting from historical patterns. We can’t afford to operate without understanding both the immediate chemistry and long-haul logistics.
We rely on process data built from years of strict documentation and operator training. It’s not uncommon to halt the line over ambiguous chromatography peaks or new IR signatures—even if that puts pressure on timelines. Down the road, those moments pay off, as trust grows between our plant team, internal QC staff, and customers who depend on us as a manufacturing partner, not just a supplier. Years watching the same vessels, heat traces, and control panels reveal how small adjustments in one shift leave fingerprints on product quality months later.
Among the spectrum of benzoic acid products, most people start with the unsubstituted parent compound. Enterprises often try 2-hydroxy or 4-nitro benzoic acids for their broader availability or lower price points. Experience shows such products lack some of the unique characteristics this structure brings to a synthesis. The combined substituents—chlorine, hydroxy, and nitro—balance each other both in physical handling and downstream transformation.
Chloro substitution at position 5 cushions the acid’s reactivity compared to the more common 4-chloro alternatives seen in less specialized markets. The 2-hydroxy positioning boosts hydrogen bonding potential, giving more handle in both solvent selection and crystal form determination. Placement of the nitro group tunes the site-selectivity for coupling reactions not available with simple mono-substituted benzoic acids. Chemists working with our product tell us side product profiles decrease, color development stays under control, and downstream isolation takes less time.
Cost and purity become part of the everyday calculation. Bulk suppliers focus on the tenths-of-a-dollar advantage, but long-term partnerships depend on traceable batches and troubleshooting support. I have worked through unexpected shifts in raw material lots, equipment resolutions, or market supply. The investments in quality control, new reactors, and standard operating procedure (SOP) evolution underpin the quiet confidence users have in each drum. They keep coming back because the extra checks show up in reproducible results.
We live in a climate where regulatory and quality standards grow tighter each year. Transforming raw feedstocks into highly functionalized benzoic acids holds practical and legal weight. Responsible manufacturers face routine inspection for recordkeeping, process safety, and output limits on potential waste streams. For compounds containing both nitro and chloro groups, safe handling must become ingrained in culture, not just policy.
As production heads, we enforce workplace controls—ventilation maintained by physical audits, spill protocols drilled and revisited, and new operators paired with experienced staff who understand both hazard and nuance. Labels and safety data become living documents, updated as our R&D teams tweak solvents, introduce automation, or commission new gear. Processes running well today can still surprise tomorrow, so adaptation and humility matter. Engaging with downstream partners on safe storage, handling, and accidental release planning goes beyond the letter of compliance. It returns dividends as stronger partnerships rather than arm’s-length commercial exchanges.
Questions from safety officers and regulators often push us to verify batch consistency for not just composition but also potential impurities or breakdown byproducts. Nitrophenol traces, for example, must be cut below reportable thresholds; our protocols reflect years adjusting filtration media and solvent sequences to catch these early. Third-party audits—though stressful—catch issues blindspots and help align us with the latest compliance shifts.
Older colleagues talk about chemical production as just a matter of maximizing throughput and minimizing raw material cost. The arc of this business now points toward responsible stewardship—energy efficiency, closed-loop solvent cycles, and minimizing hazardous byproducts. Making Benzoic Acid with multiple sensitive functional groups nudges us toward better solvent recovery, process heat integration, and improved emissions capture.
Our facility invested in process analytics that reduce batch variability, cut rework, and limit off-spec disposal. Operators bring up small ideas for improvement—piping reconfigurations, smarter agitation speeds, switching oxidation catalysts—and those lead to measurable gains in safety and sustainability. Customers increasingly favor suppliers who put environmental metrics up alongside technical metrics. We respond by sharing not only certificates of analysis but also waste reduction and energy input data when requested.
Collaboration with customers remains the strongest path to mutual improvement. Most feedback arrives in the form of new application requests or troubleshooting help. Fine adjustments—sample particle size, tracking a downstream color shift, accommodating custom packaging—emerge through years of direct dialogue. Knowing which batch went to which customer on which day, and following up on feedback, creates a two-way street for innovation.
Benzoic Acid, 5-Chloro-2-Hydroxy-3-Nitro- becomes not just a product, but a test of our ability to adapt production to changing research and market needs. Early adopters in specialty medicines or advanced materials set the bar—can we match their purity demand, speed up a turnaround, or shift a crystallization solvent to avoid an environmental issue? Streamlining batches for smaller run sizes, frequent clean-outs, and greater changeover times challenge every department, but reinforce the value of direct feedback.
A continuous improvement loop often homes in on what might seem like small details in other plants—grinding noise during drying could point to particle size changes, stirrer wear shifts dissolution profiles, or subtle changes in seasonal humidity impact filter beds. We document each point, meet as cross-functional groups, and use shared insight to keep every batch on spec.
Distributors and resellers can talk about a product’s theoretical utility, but only the manufacturer witnesses the challenges and learning shaping each container shipped. Sourcing specialty chemicals directly from the origin brings with it not only technical documentation, but also an earned understanding of actual plant variability, supply chain disruptions, or even the realities inside the reactor and centrifuge. This confidence passes through in daily operations—where to screen for late-breaking contaminants, how to recalibrate drying times, how to rotate stock to avoid degradation.
The language may be more technical coming from us, but the intent remains: more controlled production, fewer surprises, and a personal stake in every kilogram leaving the plant. Whether a customer’s success means a groundbreaking medicine, a new industrial coating, or an improved dye, feedback loops through the plant. Lasting partnerships start with an open channel between manufacturer and end user. When users experience fewer headaches and less variability, the value of buying close to the source becomes clear.