|
HS Code |
352281 |
| Name | Methyl 3,5-Dihydroxybenzoate |
| Synonyms | 3,5-Dihydroxybenzoic acid methyl ester |
| Cas Number | 39515-51-6 |
| Molecular Formula | C8H8O4 |
| Molecular Weight | 168.15 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 109-112 °C |
| Boiling Point | 344.7 °C at 760 mmHg |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC(=O)C1=CC(=CC(=C1)O)O |
| Inchi | InChI=1S/C8H8O4/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4,9-10H,1H3 |
| Density | 1.38 g/cm³ |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, keep tightly closed |
As an accredited Methyl 3,5-Dihydroxybenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of Methyl 3,5-Dihydroxybenzoate, sealed with a screw cap, labeled for laboratory use. |
| Shipping | Methyl 3,5-Dihydroxybenzoate is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It should be handled with care and in accordance with local, national, and international regulations for laboratory chemicals. Appropriate hazard labels and documentation accompany the shipment to ensure safe transport and delivery. |
| Storage | Methyl 3,5-Dihydroxybenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat and direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature and protect from moisture. Ensure labeling is clear and compliant with safety regulations, and handle only with proper personal protective equipment. |
Applications of Methyl 3,5-Dihydroxybenzoate in Industrial ManufacturingMethyl 3,5-Dihydroxybenzoate delivers precise performance as a specialty intermediate across multiple chemical sectors. The compound supports advanced synthesis needs for downstream manufacturers, complying with strict industry protocols for quality and traceability. Below we outline core industrial application tracks, with specific compliance, dosage, process positioning, and end-use formulations. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisAPI manufacturers incorporate this compound as a protected phenolic intermediate in the synthesis of several small molecule drug scaffolds. Its chemical structure aids selective modifications through ester hydrolysis or aromatic substitution during early or late-stage synthesis. The compound’s high purity guarantees reliable downstream transformation, meeting stringent requirements for regulated pharmaceutical processes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Cosmetic Antioxidant and Preservative ProductionPersonal care formulators employ this compound as a key intermediate for custom esters and phenolic antioxidants in formulations designed for skin creams, lotions, and sunscreens. Its controlled reactivity allows for consistent phenol-based preservative synthesis, supporting batch-to-batch reproducibility to comply with cosmetic industry certifications. Downstream manufacturers value its robust purity and trace-characterization for finished product safety validation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Polymer Additive and Crosslinker PrecursorManufacturers of specialty resins and performance coatings use this compound as a monomeric additive where the phenolic group enhances resin crosslink density or heat resistance. The substance is reactive toward epoxy, urethane, or polyester networks, supporting unique performance tuning in advanced polymer matrices. Tight molecular weight and impurity profiles help facilitate controlled polymerization and meet industrial polymer quality requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Agrochemical Intermediate for Herbicide and Pesticide FormulationAgrochemical synthesis plants use this material for introducing specific hydroxybenzoate moieties in selective herbicide or fungicide molecules. It serves as a protected scaffold, facilitating efficient construction of target pesticides while maintaining overall synthetic throughput. The product’s purity supports trace residual control for compliance with agricultural chemical regulations and allows reliable conversion during multistep preparations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Methyl 3,5-Dihydroxybenzoate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Every batch of Methyl 3,5-Dihydroxybenzoate rolling off our production lines has a story rooted in chemical discipline and persistent refinement. Crafting this compound demands precision and a solid grasp of process control. In our experience, attention to detail during the methylation phase affects not just purity, but also downstream usability. This product, sometimes known as methyl gentisate, stands out with a chemical structure featuring two hydroxyl groups positioned on the benzene ring. From raw material handling to silica filtration, sticking to robust methodology trims by-products and keeps consistency. Over the years, we built our competency through repeated scale-up, troubleshooting clogging reactors, and continually refining solvent ratios.
There’s a reason the model we settled on for our flagship batches is based on C8H8O4, with the IUPAC name being methyl 3,5-dihydroxybenzoate. Ensuring a purity threshold over 99% w/w requires rigorous selection of methylating agents and a careful approach to manage reaction temperature and moisture content. Side reactions, like over-methylation or oxidation, don’t just hurt yield—they complicate purification. We install redundant checks throughout distillation and drying, because traces of unintended esters can hamper downstream synthesis. It’s these technical realities that shape the product our clients trust.
Chemists often reach for Methyl 3,5-Dihydroxybenzoate when synthesizing complex aromatics, including pharmaceutical precursors and specialty dyes. Its two free phenolic groups, combined with the ester functional group, give it a reactivity profile that stands apart from more basic benzoic acid esters. We see researchers rely on it during etherification steps, and medicinal chemists build on its scaffold to develop biologically active compounds. Over time, as we talked to clients in both academia and active pharmaceutical ingredient (API) production, the demand for high-purity lots became clear. Even a trace of isomeric benzoates or residual acid can throw off reaction pathways.
Manufacturers like us don’t approach these conversations from a distant view. We walk the same floors where spills must be cleaned, and we learn firsthand which filtration tricks boost throughput. Years ago, we lost a major client after HPLC analysis picked up a contaminant we hadn’t seen before. After that, we upped QC frequency and invested in better spectral fingerprinting. Issues like elevated water content or minor chloro-compound contamination taught us that every parameter matters. From experience, the reliability of the input sets up the reliability of the entire synthetic run.
A molecule may seem simple on paper, but years of batch records tell a different story. Unlike ordinary methyl benzoates, the 3,5-dihydroxy variant introduces new complications and opportunities. The dual hydroxyls offer more functionalization options, and the meta arrangement produces unique reactivity that chemists prize for multi-step synthesis. We’ve seen plenty of curiosity about how this compound compares to methyl 2,4-dihydroxybenzoate or methyl 4-hydroxybenzoate. Each isomer changes both reactivity and selectivity, and our process keeps positional isomers to undetectable traces. Maintaining this selectivity during esterification is one thing that sets us apart from quick-turnover traders.
Specifically, our product’s water-soluble fraction stays below 0.2%, critical for scale syntheses in non-aqueous environments. Through aggressive vacuum drying and careful handling, we keep Karl Fischer readings tight. Melting point sits consistently at 164-166°C. These small differences make or break yield, especially for customers running large-scale transformations or pilot plant studies. Manufacturing at scale reveals that even trusted suppliers can slip on basics like proper container sealing or silica dust filtration—mistakes we learned to avoid by overhauling our post-production routines. We don’t substitute packaging quality: moisture-proof liners and inert gas flushing are standard at our site.
Most buyers come to us with a set vision for their batch: pharmaceutical R&D, dye intermediates, polymerization catalysts, or even veterinary medicines. The applications list keeps growing, but several sectors use this molecule in unexpected ways. For example, we collaborated with a specialty pharma firm building kinase inhibitors. Minor inconsistencies in hydroxyl purity caused the whole downstream pathway to fail regulatory purity cutoffs. By tuning our crystallization step and doubling up on thin-layer chromatography, we let their chemists run multi-gram-scale coupling without extra purification hoops.
Another client once fed our product into a supramolecular chemistry project, working on hydrogen-bonded frameworks for molecular sensing. Here, the precise location of the hydroxyls was critical to their host-guest chemistry. Using product from another source, their crystal arrays wouldn’t form. On switching to our material, they reported sharply improved results in both NMR and X-ray crystallography. Interactions like these remind us of the ripple effect that technical details have all the way down an application line.
Years in the chemical industry teach a simple lesson: generic claims and commodity-grade production lead to headaches down the road. Many industry players buy bottom-barrel methyl esters for cost-saving, but we’ve seen the result when a stray impurity turns synthesis on its head. Having a vertical line into both lab and process-scale reactors, we validate every batch using fast and robust techniques: HPLC, ^1H NMR, FTIR, and elemental analysis. Consider, too, the impacts of solvent residues. Leftover toluene or DMF from less controlled processes may not cause issues in bulk paint chemistry, but for pharmaceutical or electronic uses, even ppm levels matter. We've handled recalls where the contamination traced back to insufficient washing steps or reused equipment. These stories shape the way we approach day-to-day choices on the production floor.
We focus not just on delivering premium chemical but on transferring knowledge to our customers, who often face their own regulatory audits. Strict adherence to GMP protocols forms the backbone of our facility—documentation is not lip service for us. We run mock inspections so that if any agency visits, we’re ready. Traceability helps us as much as it helps our clients—we use batch-level logging for reagents and track lot progression from start to finish. During production upsets, we can roll back on the timeline and pinpoint deviations, which saves not just time, but trust.
As an original manufacturer, we see more than formulas and batch numbers. Environmental stewardship forms a lasting theme in our business decisions. Methyl 3,5-Dihydroxybenzoate production, if unchecked, brings risk of phenol emissions and corrosive waste streams. We treat wastewater through activated carbon filtering and two-stage neutralization before discharge. We've trained our floor staff to spot and report leaks at the earliest sign—a lesson learned after a minor incident years back, where phenolic vapors required an evacuation and subsequent process change.
Waste reduction isn’t a catchphrase for us. In synthesis cycles, we recover and recycle methanol and minimize venting by investing in robust distillation gear. Plant-level audits focus on solvent loops, aiming to shrink our resource footprint. We partner with licensed waste officers in our jurisdiction, handing over non-recoverable residues for environmentally sound destruction. For years, we faced challenges with older infrastructure that slowed hazardous waste handling times, and in response, we commissioned a full upgrade to automated waste transfer skids. It paid off not just in local compliance, but in team morale.
Courses and guidelines outline the safe management of aromatic esters, but the shop floor reveals the real pitfalls. Methyl 3,5-Dihydroxybenzoate powders can pose inhalation risks if handled in bulk. From hard-won experience, we enforce double-bagging in cleanrooms and pulse high-efficiency particulate air (HEPA) filtering during transfer. In the early years, we underestimated dust migration and ended up cleaning residues from places nobody expected. We’ve since invested in better containment bins and standard operating procedures for every shift.
Operator training forms a pillar of our safety culture. We regularly refresh hazmat certification for every technician and rotate spill control exercises throughout the year. Our staff learned the hard way that over-reliance on automatics leads to gaps—old equipment setups had fewer safeguards and once let a spill go undetected. Digital checklists and real-time logging sharply improved accuracy and cut incident rates. In our warehouse, storage policies reflect the moisture sensitivity of the product. We keep stocks in temperature- and humidity-controlled rooms, avoiding stacking and monitoring for slow leaks.
Deciding between Methyl 3,5-Dihydroxybenzoate and similar compounds means comparing feats beyond the datasheet. A common alternative, methyl 2,4-dihydroxybenzoate, reacts very differently under cross-coupling or etherification conditions. That distinction matters if a customer’s route depends on specific hydrogen bonding or further derivatization. The meta placement of hydroxyl groups allows different ring substitutions than para or ortho isomers, opening new space for structure-activity explorations.
Technical comparisons surface in real time on the line. If clients report color changes in solution or unexpected by-products, we run quick side-by-side tests. These in-process checks differentiate lots from various competitors. Over the years, we learned that differences invisible to the naked eye—say, slight isomeric impurities—cause visible setbacks in research and production. We tuned our own synthesis processes by following up on every customer complaint, correlating them to minute shifts in starting material or reaction timing.
The market keeps shifting. Demand for higher-purity methylated aromatics has spiked, especially with tightening pharma requirements and greater emphasis on green chemistry. Advanced process analytics feed directly into our strategy here—investment in in-line NMR and automated reactant feeds lets us stay reliable as scales change. We receive more queries about residual solvent profiles and environmental documentation. Scrutiny boosts our vigilance and motivates us to keep tweaking everything from raw material procurement to post-synthesis handling.
Automation, digital quality assurance, and tighter process modeling have driven our recent efficiency improvements. Product traceability links directly to computational records, archiving years’ worth of test results. These changes cut response times when a client flags a possible out-of-spec lot. We remember using paper records and manual recalculation, a practice that often left us hunting for missing details during customer calls. Now, a digital trail lets us answer questions directly and with evidence, supporting not only compliance but customer trust.
Chemical manufacturing rewards consistency and punishes shortcuts. Each lot of Methyl 3,5-Dihydroxybenzoate undergoes scrutiny, from the reagent bins to the final packing line. Real learnings come from fixing problems—not just reading the literature or following baseline procedures. Equipment hiccups, process deviations, and customer complaints all serve as feedback loops that drive us to improve. Work becomes routine only because we invest in systems that let us see errors before they grow. Research teams and production lines function better with chemical lots that behave as expected.
Growth in industry depth comes not through broad claims, but from reliability built on direct experience. Whether a client runs one kilogram or an entire truckload, the impact of consistent and carefully made material ripples through every new molecule or application. By learning from setbacks and leaning into technical challenges, we keep Methyl 3,5-Dihydroxybenzoate a trusted choice for those who depend on certainty. Direct communication, open-door troubleshooting, and a tradition of technical rigor continue to drive our approach as a manufacturer at the intersection of hands-on chemistry and industrial reliability.