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HS Code |
994130 |
| Chemical Name | 2,5-Dihydroxybenzoic Acid |
| Synonyms | Gentisic acid |
| Molecular Formula | C7H6O4 |
| Molar Mass | 154.12 g/mol |
| Cas Number | 490-79-9 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 203-205 °C |
| Solubility In Water | Slightly soluble |
| Pka Values | 2.38, 11.40 |
| Structure | A benzene ring with hydroxy groups at positions 2 and 5 and a carboxylic acid at position 1 |
| Pubchem Cid | 346 |
| Odor | Odorless |
As an accredited 2,5-Dihydroxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,5-Dihydroxybenzoic Acid is packaged in a sealed 100g amber glass bottle with a clear chemical label and hazard symbols. |
| Shipping | 2,5-Dihydroxybenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be labeled as a chemical substance and handled according to safety guidelines. Shipments typically include safety data sheets and are transported in compliance with relevant regulations for chemical materials, ensuring safe delivery to the destination. |
| Storage | 2,5-Dihydroxybenzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from excessive heat, moisture, and direct sunlight. Proper labeling and secure shelving are recommended to minimize contamination and ensure safe handling. |
Applications of 2,5-Dihydroxybenzoic Acid in Industrial Manufacturing2,5-Dihydroxybenzoic Acid supports multiple specialized manufacturing sectors with critical functions in synthesis, formulation, and process control. As the direct producer, we deliver consistent quality for advanced integration in demanding industrial workflows. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies use 2,5-Dihydroxybenzoic Acid as an intermediate for the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and certain antibacterial compounds. The substance participates in key condensation and esterification reactions, serving as a precursor for various complex aromatic molecules. Production runs require stringent traceability, precise pH adjustment, and maintenance of high-purity throughout crystallization to meet drug master file (DMF) submission criteria. Industry compliance standards
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2. Analytical Chemistry and MALDI-TOF Matrix Component ProductionManufacturers of mass spectrometry consumables incorporate 2,5-Dihydroxybenzoic Acid as a matrix component in matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) analysis kits. Its chemical characteristics promote efficient energy absorption and controlled ionization of biomolecules. Accurate formulation, including fine-milling and impurity control, is essential to minimize signal interference and ensure reproducibility across research and clinical diagnostic laboratories. Industry compliance standards
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3. Fine Chemical Synthesis of Dyes and PigmentsDye and pigment manufacturers utilize 2,5-Dihydroxybenzoic Acid as a functionalized aromatic building block in the production of specialty azo compounds. Its ortho-dihydroxy moiety enables specific diazotization and coupling reactions, resulting in colorfast pigment structures suited to textile and ink industries. Raw material integration demands strict control of side reactions, particularly during diazotization, and final pigment evaluation for purity, tone, and dispersibility. Industry compliance standards
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4. Corrosion Inhibitor Additive in Industrial Metal ProcessingCorrosion inhibitor formulators select 2,5-Dihydroxybenzoic Acid for its chelating properties in aqueous and solvent-based systems designed to protect ferrous metals. Its integration improves formation of passive films, reducing acid attack during pickling, cooling water treatment, and industrial cleaning processes. Consistency in grain size, solubility, and absence of metallic contaminants are required for efficacy and compatibility in various environments. Industry compliance standards
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5. Polymer Modification Agent for Functional Polymer DevelopmentAdvanced materials manufacturers incorporate 2,5-Dihydroxybenzoic Acid as a modifying monomer or end-group in the synthesis of specialty polyesters and polyamides. Its dihydroxy functional groups enable step-growth polymerization, instilling improved hydrogen bonding capacity and enhancing the chemical resistance or adhesive properties of the resulting material. Controlled dosing, polymerization at set temperature ranges, and rigorous post-polymerization purification are essential to meet physical and chemical property specifications of high-performance plastics. Industry compliance standards
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6. Food Additive and Preservative Synthesis (Indirect – Not Direct Food Use)Food ingredient producers employ 2,5-Dihydroxybenzoic Acid as a starting material in the synthesis of preservative agents and antioxidant components, where permitted under relevant food additive regulations. The compound undergoes controlled esterification, yielding derivatives with improved solubility and performance in fat-containing systems. All handling and final product testing occur in dedicated lines to avoid cross-contamination and meet food-grade purity requirements. Industry compliance standards
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Throughout our years in the chemical manufacturing sector, the demand for reliable and precisely produced 2,5-dihydroxybenzoic acid (also widely called gentisic acid) has remained steady. As production lines evolve, so do the expectations for purity, crystalline form, and dependability. Large-scale synthesis at our facilities places a premium on control at every step, from raw material selection to final packaging. This compound stands out thanks to its broad use across pharmaceuticals, specialty chemicals, and life sciences research.
Every batch of 2,5-dihydroxybenzoic acid leaving our site upholds purity levels above 99% (HPLC), supported by batch-level testing for moisture, heavy metals, and any trace organic contaminants. Attention to these precise details shapes the baseline for developing consistent downstream formulations. Researchers and industrial formulators have come to expect this level of integrity because even a minor fluctuation in impurity can throw off the results of a lab trial or production process. Our controlled crystallization methods prevent variation from lot to lot, keeping performance expectations predictable.
Drawing on years operating reactors and purification columns, we refine our specifications not just to check regulatory demands but to meet real-world needs voiced by formulators and analysts. Chemically, our 2,5-dihydroxybenzoic acid comes as a white to off-white crystalline powder, with a minimal moisture content maintained by our proprietary drying system. Solubility in water and alcohol presents practical benefits for solution preparation — a point added to by the steady pH behavior in typical dissolution environments. The melting point remains sharp, with minimal spreading, reflecting structural homogeneity.
We keep metal content — lead, arsenic, and mercury — lower than the detection thresholds common in pharmacopoeias. Because some processes are highly sensitive to metal ions, neglecting these trace contaminants leads to batch failures, which our process control systems are built to prevent. Over time, customer requests for tighter optical clarity and specific sieve fractions drove us to adjust our powder milling and sieving equipment. Laboratory feedback cycles quickly into the production routine, bridging the gap between scale-up and bench-scale experimentation.
In practice, gentisic acid sees the most volume in pharmaceutical intermediates, especially for analgesic-antipyretic synthesis and as a characterizing standard in analytical chemistry. The compound’s ability to scavenge oxygen radicals — due to its ortho-dihydroxy substitution on the benzene ring — creates opportunities in food and cosmetic antioxidant blends, though the main markets remain lab-based and industrial. Clients working on chromatographic matrix materials, MALDI-TOF mass spectrometry preparations, and biosensor prototypes all draw from our standard lots.
Researchers emphasize reproducibility. The fine microstructure of our crystals, preserved during bulk packaging, plays a subtle yet important role here. Powders ground too finely can clump or pick up atmospheric moisture quickly, while coarser crystals risk inconsistent dissolution. Over many production cycles, we tuned our protocols to balance these competing demands, giving customers the right flow and handling profile for tablet pressing, solution mixing, or analytical weighing.
Our team understands that no line runs perfectly unless every input and every reaction condition remains under careful scrutiny. The starting benzoic acid derivatives need tight purity controls, and our reactors rely on precise temperature and pH monitoring. Over-oxidation can introduce unwanted hydroxybenzoic isomers, which sap reaction yield and complicate crystallization. Vigilance in this stage—especially during scale-up—saves both time and the bottom line.
Once the initial reaction completes, controlled precipitation isolates gentisic acid. Washing steps strip away mother liquor and dissolve out highly soluble byproducts, while our filtration equipment handles the fine particle slurries efficiently. The final product undergoes vacuum drying on trays set to carefully calibrated temperatures. This avoids thermal degradation and undesirable polymorphic changes. In one production cycle, attempts to rush drying with excess heat led to off-color product and repeat purification. That mistake reinforced our practice of favoring patient, staged drying, which now produces a consistently bright, chemically faithful output.
Quality assurance goes further than chemical analysis. Our operators take samples at multiple points within each run. Collected material undergoes FTIR scans, HPLC purity profiling, and water content checks before any product gets into the packaging room. Here, double-wrapped, moisture-proof containers limit exposure before shipment. A misstep in closure technique—like a shipment we sent in the rainy season years ago—taught us to over-engineer rather than accept package integrity risks. Small details, learned through troubleshooting and customer feedback, set long-term standards in a manufacturing environment.
As chemists, we handle several dihydroxybenzoic acid isomers, but the position of hydroxyl groups makes all the difference in their performance. Our 2,5-dihydroxybenzoic acid, with its functional groups at the meta and para positions, offers distinct reactivity compared to 2,3- or 2,4-dihydroxybenzoic acid. Structural nuances affect not only antioxidant capacity but also metal chelation and electronic properties. In pharmaceutical applications, incorrect isomer choice changes synthesis pathways dramatically, and our technical team often works with formulators to verify they match the intended structure.
Compared to ordinary benzoic acid, 2,5-dihydroxybenzoic acid allows more hydrogen bonding, which enhances solubility in polar solvents. 4-Hydroxybenzoic acid, a popular cosmetic preservative, shares the aromatic core but lacks the dual radical-quenching ability offered by two adjacent hydroxyls. For mass spectrometry, especially matrix-assisted laser desorption/ionization, our material’s purity and particle uniformity set it apart from grades designed for bulk chemical processes. Years spent cleaning contamination from alternate sources have made our clients wary of trace impurities—a difference we can document, batch by batch, with precise testing.
Supplying a specialty compound at scale forces a continuous search for process improvements. Impurities from upstream benzene derivatives can linger at parts-per-million levels, and new analytical equipment grants us sharper detection than we had decades ago. Operators attend regular training on managing equipment drift and chemical handling safety. Solvent recovery, a focus both for cost and environmental footprint, pushes our distillation engineers to recover near-complete input material. As regulations on process emissions grow, our waste gas scrubbing and effluent treatment plants keep pace.
One production year, an unexpected supply chain hiccup stalled access to a key solvent. Alternative routes flared up stability problems and unfamiliar byproducts. This detour underlined the value of rigorous documentation and redundancy in sourcing—but also the disadvantage of relying on short-term cost savings at the expense of process experience. Today, any procurement change goes through technical review, then undergoes limited pilot batches before adoption.
Shipping and storage present their own hurdles. Customers on different continents request varying particle sizes and packaging. Frequent shipments by sea risk moisture incursion and temperature swings. Desiccant loads, improved liners, and vacuum-sealed drums now buffer these risks. Previously, powder caking led to customer complaints that forced us to overhaul our inventory management practices. Real-world usage, not lab-based assumption, sets the bar for process discipline.
Our customer base, stretching from pharmaceutical labs to specialty polymer houses, holds us to high standards for service and technical dialogue. It’s not enough to simply sell a chemical compound; clients turn to manufacturers that back up each order with data, feedback, and transparent discussion. Shifting global regulations in chemical handling, worker safety, and environmental stewardship mean production never stands still. Our own practices grew from early lessons—be it an unexpectedly reactive impurity or a shipment damaged by careless loading.
Traceability sits at the heart of our operation. Every drum and bag carries a hand-logged lot number, with full QA profiles traceable from starting reagents to finished material. This not only helps in regulatory reporting but also arms our collaborators with the confidence to defend their product development in audits and scale-ups. Chemical manufacturing can invite trouble when corners get cut; maintaining robust records and routine cross-checks keep our culture centered on accountability.
Analytical chemists and process engineers are quick to report shifts in their experience with a lot. Slow dissolving powder signals particle aggregation, perhaps from thermal stress in shipment, while off-odors or discoloration usually point to degrade during prolonged storage. Our technical team routinely travels to customer sites, not to advertise, but to listen and learn from those putting 2,5-dihydroxybenzoic acid into real process streams and analytical methods.
No production challenge holds for long when lessons turn into new SOPs and operator training. Early mistakes with filter sizing, which led to fines passing into product, gave way to staged multi-mesh screening and particle-size tracking. Adjustments in crystallization temperature curve, prompted by seasonal humidity swings, now flow from real-time sensor data rather than static batch recipes. Distributors expect flexible shipment volumes, but manufacturers must balance stockpile size against shelf-life.
Technical support teams connect directly with R&D, shortening the feedback loop from lab bench or tablet press to synthesis control. When a customer flagged micro-level inconsistencies in powder density, short of outright batch rejection, we recalibrated our milling lines. Many of our team members recall batches lost to miscalculated drying times or premature container closure. Each scenario cemented the best ways forward, seeded from direct results rather than abstract best practices.
Responding to demand for greener solutions, solvent recovery rates now exceed 98 percent in our reactors, and waste minimization motivates both maintenance routines and technology upgrades. Customers in the EU and North America request specific documentation on manufacturing environmental impact. Our on-site treatment plant processes all liquid wastes, monitored using both legacy and cutting-edge analysis tools. Regulations may shift, but building systems for process continuity secures longer-term resilience for both our clients and our own team.
The steady march of technology in pharmaceuticals, biotech, and materials science brings new uses for 2,5-dihydroxybenzoic acid into view. Instrumental analysis, especially in proteomics, leans on reliable matrix materials for sensitive detection methods. Next-generation polymers sometimes incorporate this compound for tailored degradation or binding properties. Each application tightens requirements on purity, physical form, or trace constituents, spurring us to evolve our process technology. We invest in up-to-date measurement tools not just to satisfy present needs, but to anticipate what synthesis, analysis, and manufacturing may demand next.
Feedback from partners across the globe—whether in a pharma pilot plant or academic R&D team—drives our technical progression. A chemist pointing out spectral drift or unexpected impurity profiles early can change a production approach for all clients. The best practices we now use to achieve homogeneity, reproducibility, and regulatory conformity grew directly from confronting, then solving, each new bottleneck.
Day-to-day chemical production rarely aligns with textbook simplicity. Every drum of 2,5-dihydroxybenzoic acid reflects accumulated trials, operator diligence, and customer feedback. Specification sheets and certificates back up each claim, but informal notes, batch records, and recalls of hiccups in routine also inform how the next lot gets made. Value in chemical manufacturing comes from knowing where things go wrong, and building better after each revue. Partnerships with end-users fuel continuous improvement—the lessons of the past anchor the reliability delivered with every order.
While 2,5-dihydroxybenzoic acid may seem a simple aromatic acid to some, its industrial story reveals ongoing adaptation, steady learning, and an unwavering focus on quality born of necessity and collaboration. Our team takes pride in this legacy, knowing every improvement springs from the needs and insight of those who handle our product every day.