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HS Code |
283279 |
| Product Name | 3,5-Dimethoxybenzoic Acid |
| Cas Number | 99-68-3 |
| Molecular Formula | C9H10O4 |
| Molecular Weight | 182.17 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 178-182°C |
| Boiling Point | 369.1°C at 760 mmHg |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.286 g/cm3 |
| Smiles | COC1=CC(=CC(=C1)OC)C(=O)O |
| Inchi | InChI=1S/C9H10O4/c1-12-7-3-6(9(10)11)4-8(5-7)13-2/h3-5H,1-2H3,(H,10,11) |
| Pka | 4.3 |
| Refractive Index | 1.547 |
| Storage Temperature | Store at room temperature |
| Synonyms | m-Carboxyveratrole, 3,5-BDMA |
As an accredited 3,5-Dimethoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle securely sealed, labeled with "3,5-Dimethoxybenzoic Acid," product code, lot number, and hazard warnings. |
| Shipping | 3,5-Dimethoxybenzoic Acid is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is typically packed according to standard chemical safety regulations, labeled clearly for identification, and transported as a stable, non-hazardous solid. Ensure storage in a cool, dry place away from incompatible substances during shipping. |
| Storage | 3,5-Dimethoxybenzoic acid should be stored in a tightly sealed container, away from moisture and strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Protect the chemical from direct sunlight, heat sources, and incompatible substances. Proper labeling and secure storage are essential to ensure chemical stability and laboratory safety. |
Applications of 3,5-Dimethoxybenzoic Acid in Industrial ManufacturingAs a direct producer of 3,5-Dimethoxybenzoic Acid, we support a focused range of downstream sectors that rely on this intermediate for technically specific processes. Each industrial scenario below outlines validated applications, integrating formulation detail, regulation adherence, and processing context for professional procurement and technical teams. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 3,5-Dimethoxybenzoic Acid as an acylation intermediate to form substituted benzoic acid derivatives that serve as key building blocks in the synthesis of anti-tumor, anti-inflammatory, and central nervous system drug candidates. The compound routinely enters the process at the stage of amide formation, where precise molar equivalency ensures high purity for subsequent functionalization steps or coupling reactions. Production adheres strictly to quality-system validated batch records and traceability, with in-process control to confirm conversion rates and impurity profile before transfer to downstream purification. Industry compliance standards
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2. Liquid Crystal Material PrecursorsThe electronics and display industry incorporates this compound as a monomeric precursor in the synthesis of conductor and non-conductive aromatic esters for advanced nematic and smectic liquid crystal formulations. Manufacturers rely on the controlled reactivity of its dimethoxybenzoic acid group for introducing rigidity and precise polarity in the final mesogen structure, which directly impacts electro-optic response and alignment layer compatibility in high-specification LCD modules for industrial and automotive panels. Industry compliance standards
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3. Agrochemical Active Ingredient ManufacturingAgrochemical companies use this acid as a specialized intermediate in constructing ring-substituted aromatic scaffolds for herbicide and fungicide actives. The presence of dual methoxy substituents supports selective halogenations, alkylations, or etherifications, offering process chemists a way to fine-tune activity and degradation profiles of the resulting pesticide molecules. Industrial processes precisely control feed ratios and reaction sequence to achieve target bioactivity without residual contamination. Industry compliance standards
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4. Dyes and Pigment Intermediate ProductionThe colorant industry employs this chemical as a precursor in multi-step syntheses for metal-complex dyes, azo dyes, and high-stability organic pigments, especially where electron-donating groups enhance color fastness or improve solubility characteristics. The acid is typically introduced at the controlled condensation or coupling stage to guarantee chromatic properties and infrared absorption profile required in specialty inks and industrial coatings. Industry compliance standards
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5. Polymer Additive and Modifier SynthesisThe specialty polymer sector integrates this raw material as a functional monomeric acid to introduce polar groups or increase UV stability in chain-extended aromatic polyesters, polyamides, or specialty polyimides. Processing lines apply it at precision-calibrated dosing to achieve targeted molecular weight, glass transition temperature, and enhanced weatherability in engineering polymers destined for high-durability uses, including electronics housings and optical films. Industry compliance standards
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Talking about 3,5-Dimethoxybenzoic Acid, you step straight into a story of craftsmanship at the reactor—no supply chain jugglers, just straightforward, accountable work. Our factory team has worked hands-on with aromatic carboxylic acids for years, and every batch we produce reflects that embedded knowledge. We see the differences in how a raw material is weighed, how tightly a temperature profile is run, or how subtle tweaks in agitation reveal themselves later at quality control.
Let’s not dress it up: 3,5-Dimethoxybenzoic Acid isn’t one of those high-turnover commodities that fill out a catalog for the sake of it. In our plant, it’s a regular part of the synth line, often produced in multi-step campaigns to match real-world demand rather than on hope or speculation. This matters especially in a specialty intermediate like this, where downstream users actually call us up with genuine technical queries based on their next reaction, not marketing hype.
You notice right away: 3,5-Dimethoxybenzoic Acid (CAS 50-84-0, C9H10O4) isn’t your average benzoic derivative. The presence of the two methoxy groups at the 3 and 5 positions creates properties that matter on the shop floor. Unlike simply methylated or unsubstituted benzoic acids, those two ether oxygens alter both the acid’s electron behavior and its crystal structure. This shifts melting points and, for certain customers, influences everything from solvent selection to crystallization step yields.
Most of our clients are in fine chemicals, agrochemical research, or pharmaceutical intermediates. They appreciate that we keep specifications tight: purity consistently above 99% by HPLC, low moisture step-dried under nitrogen, and elimination of chloro or nitro impurities below 0.1%. Real batch data matters because trace impurities can swamp a synthesis downstream or block a catalyst, and those headaches often land back at our technical desk.
Direct manufacturing control also lets us deviate from “textbook” methods and adapt the process as supply chains shift. For example, when regional regulations affected the import of some phenolic precursors, our process developers found new sourcing and adjusted chemo-catalytic steps. We managed to lower residual sulfur and amine side products, which often sneak in from cheaper raw input sources. Customers who’ve worked with low-grade material made in distant plants tell us they see fewer purification issues with our product. They get a predictable melting point (around 182-185°C) and no smearing in the TLC lane—small details, but crucial on the benchtop.
We see a fair bit of confusion from buyers who treat every benzoic acid as interchangeable, but practical chemistry tells another story. 3,5-Dimethoxybenzoic Acid isn’t a substitute for, say, 4-methoxybenzoic acid or even simple benzoic acid when specificity of function or substitution pattern comes into play. The electron-donating effect of having two methoxy groups in positions 3 and 5 sets up reactivity for downstream C–C coupling or for making custom esters or amides. Medicinal chemists call us specifically because they’re working on modifications of natural products, where regioselectivity and the behavior of the aromatic ring matter for the biological end-point.
In our plant, the main output goes to companies developing building blocks for drug candidates. These groups often pursue SAR (structure-activity relationship) studies, logging dozens of analogues, each requiring strict reproducibility. Our QC team knows that batch-to-batch consistency is not academic—it’s central to making sure a promising route doesn’t collapse due to background contaminants. The molecular structure of 3,5-Dimethoxybenzoic Acid shields critical sites from unwanted side reactions during protection-deprotection steps in peptide or nucleoside synthesis. This is why it stands apart from 2,5- or 3,4-dimethoxybenzoic acid analogues in practical application.
Synthesis of 3,5-Dimethoxybenzoic Acid at scale involves running O-methylations either directly on hydroxybenzoic acid or through a sequence of selective protection and methylation using agents like dimethyl sulfate or methyl iodide, depending on the grades required and local environmental standards. The isolation steps seem simple on paper—crystallization from water and recrystallization from ethanol—but at production scale, reproducibility demands more. Slow cooling rates reduce occluded solvents, batch agitation must be tight, and filtration in an inert atmosphere keeps out particulate guests.
Product packaging is often more than just a drum or a bag. Customers who need analytical quantities for early R&D work expect 5g vials, while scale-up groups may buy by the kilo. We answer detailed questions about long-term stability, thermal decomposition, and compatibility with downstream solvents. We keep close track of shelf-life because even a conscientious lab can run into color changes or caking if the acid pulls in water during humid storage—one reason we always recommend keeping containers tightly closed and in a dry environment.
Some expect benzoic acids to behave predictably in organic solvents, yet subtle differences cause big process headaches. 3,5-Dimethoxybenzoic Acid dissolves well in hot ethanol or acetone but shows weak solubility in cold water and alkanes. This trait helps purification by recrystallization, making it a solid choice for those working on multi-step syntheses. Downstream, the acid group lends itself to esterifications or amidations, and the methoxy patterns change the rate at which those reactions run—sometimes speeding up, sometimes requiring a longer reaction window compared to their monosubstituted cousins.
Because we run our own scale-ups, the process team regularly records deviations in color, odor, or crystal habit as an early warning system. Customers have commented on the lack of off-spec burnt smell or discoloration that plagues batches made with older equipment or recycled solvents. Thermal stability up to about 195°C before decomposition allows for robust handling during stepwise syntheses, unlike some lower-grade material where color changes tip off decomposition or trace catalyst poisoning.
Our experience tells us that buyers who consult us are not just looking for a number on a COA—they want to know which lot numbers worked best for similar processes, what side contaminants show up at scale, and the best solvent/recrystallization pairs. Hearing that a pharmaceutical API developer saw yield drops due to slight shifts in methoxy content or unexpected color bodies drives us to keep the process lean, tuned, and open to customer feedback. We sometimes invite clients to audit our plant. Watching our people test wet cakes or dry filter cakes, instead of relying purely on instruments, changes how they think about process tolerances.
Some of our closest partners in process development have shifted their specs after learning how even minor downstream changes—like switching a condenser material or running a different grade of ethanol—impacted their own purity metrics. We invite such interactions because, at the end of the day, making 3,5-Dimethoxybenzoic Acid is as much about shared expertise as it is about producing white powder with a specific melting point.
If you look at closely related products like 2,5-dimethoxybenzoic acid or 4-methoxybenzoic acid, differences emerge right away. Single-methoxy derivatives tend to show higher melting points and stronger acids thanks to the absence of the second electron-donating group. Some customers imagine any dimethoxy pattern works the same, but shifts in substitution pattern lead to pronounced changes in chemical reactivity and process yields. For instance, ortho-substitution can create more reactive or less stable intermediates than the meta-substitution found in 3,5-dimethoxybenzoic acid.
Bulk manufacturers sometimes chase lower prices by using generalized clean-up methods for “any benzoic acid derivative.” We learned the hard way that treating each isomer as fungible will always cost more over the long run through rework or lost batches. This is why we keep different glassware, filtration lines, and solvent tanks for our core benzoic intermediates; trace mixing leads to fouling in later steps and, worst of all, wasted product for the end user. That’s a cost nobody wants to pass on.
Our chemists and operators pay real attention to how wastes are minimized, how solvents are recycled, and how energy usage is reduced. For 3,5-Dimethoxybenzoic Acid, we’ve optimized the methylation step for greener agents and introduced solvent recovery loops that keep emissions low. These are decisions that traders don’t face, but as actual manufacturers, we invest because every percent gained is a risk avoided in the future: fewer regulatory knock-backs, less off-grade material, and steadier pricing downstream. We trace each lot from raw input to final drum or vial, and customers see this as an antidote to faceless bulk chemicals sourced from shadow suppliers.
We publish data points not because anyone demands them, but because experience proves how quickly a bad input source or uncontrolled side product can derail downstream production and the reputation that goes with it. Over time, making these decisions under our own roof has brought in repeat customers from R&D accelerators to established big pharma and crop-science groups. They see that we make adjustments based on chemistry, not arbitrage.
We welcome feedback and sometimes get suggestions from customers who notice tiny benefits from using a slightly different granulation or drying schedule. These may seem minor, but at scale, small surprises add up to big headaches, so we’ve learned to batch-test and report openly. This culture of direct dialogue is born out of practical necessity—every batch of 3,5-Dimethoxybenzoic Acid might travel a different process path through the plant, depending on order size, but our standards remain constant.
Standard process tracking doesn’t always catch subtle fluctuations in color or particle size. That’s why our staff rely on both fine-tuned analytical equipment (HPLC, NMR, mass spec, FTIR) and the “chemists’ sense”—a result of years standing at the reaction flask, smelling, observing, and adjusting. Direct communication with application scientists creates a feedback loop that benefits every future batch. If a customer sees faster dissolution when switching lots or encounters less foaming in their reactors, we log it and ask for more details, calling them back, not just replying by email.
Recent global shifts in environmental law, worker safety, and cross-border logistics make it clear that only hands-on manufacturers—those who control process, compliance, and documentation—stand a chance of long-term survival. For 3,5-Dimethoxybenzoic Acid, being able to supply traceable, consistent pure material, with clean paper trails and batch records, is not a virtue signal but a necessity for audited pharma and specialty chemical sectors.
We keep abreast of documentation requirements; real lab notebooks back up every certificate, and batch data stretches years. That’s not the case with goods that travel through networks of brokers and aggregators. Our direct oversight gives customers the confidence to scale up their own syntheses confidently, whether their goals are a single kilogram or multi-ton scale.
The reality for a chemical manufacturer is that 3,5-Dimethoxybenzoic Acid is more than just a molecule—it’s a test of process discipline, technical integrity, and customer relationships. Every detail, from raw material selection, through stepwise reaction control, down to packaging under dry nitrogen, plays into the outcome that researchers and formulators depend on.
Over decades, working directly with our end users, we see that expectations have only gotten higher. Customers want to know how a substance is produced, not just what it’s called. They want assurance in every drum, vial, or kilo that it performs the way their data demands. That trust comes only from those who make, not those who trade.
We welcome those conversations—direct, technical, and honest. In the world of specialty chemicals, that’s what sets real manufacturers apart, and for 3,5-Dimethoxybenzoic Acid, it’s what drives us to keep improving, one batch at a time.