|
HS Code |
356968 |
| Chemicalname | 3-Methoxybenzoic Acid |
| Casnumber | 586-38-9 |
| Molecularformula | C8H8O3 |
| Molecularweight | 152.15 g/mol |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 108-111°C |
| Boilingpoint | 280°C (decomposes) |
| Density | 1.24 g/cm3 |
| Solubilityinwater | Slightly soluble |
| Pka | 4.08 |
| Smiles | COC1=CC=CC(C(=O)O)=C1 |
| Inchikey | PHWUMDCKRJQQDU-UHFFFAOYSA-N |
| Synonyms | m-Anisic acid, meta-Anisic acid |
| Flashpoint | 166°C |
| Refractiveindex | 1.563 (predicted) |
As an accredited 3-Methoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "3-Methoxybenzoic Acid, 100g." Includes hazard symbols, CAS number, lot number, supplier name, and batch date. |
| Shipping | 3-Methoxybenzoic Acid is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with international safety regulations for hazardous chemicals. During transit, it is clearly labeled and handled as a non-flammable, low-toxicity solid, ensuring secure and safe delivery to laboratories or industrial users. |
| Storage | 3-Methoxybenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Properly label the container and keep it away from food and beverages. Use appropriate personal protective equipment when handling or transferring the chemical. |
|
Purity 99%: 3-Methoxybenzoic Acid with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures reliable reaction yield and product consistency. Melting Point 180°C: 3-Methoxybenzoic Acid with melting point 180°C is used in organic crystal engineering, where defined phase transitions enable controlled crystallization processes. Molecular Weight 152.15 g/mol: 3-Methoxybenzoic Acid with molecular weight 152.15 g/mol is used in drug design research, where precise molecular mass supports accurate dosage formulation. Particle Size <100 µm: 3-Methoxybenzoic Acid with particle size less than 100 µm is used in fine chemical blending, where uniform dispersion enhances homogeneity in mixtures. Stability Temperature up to 200°C: 3-Methoxybenzoic Acid with stability temperature up to 200°C is used in high-temperature polymer modification, where thermal stability maintains chemical integrity during processing. Solubility in Ethanol 20 g/L: 3-Methoxybenzoic Acid with solubility in ethanol 20 g/L is used in analytical standard preparations, where solubility promotes accurate solution-based assays. Low Water Content <0.1%: 3-Methoxybenzoic Acid with water content below 0.1% is used in moisture-sensitive reactions, where minimal hydration prevents unwanted side reactions. Spectral Purity (HPLC) 98%: 3-Methoxybenzoic Acid with spectral purity (HPLC) of 98% is used in reference material calibration, where certified purity allows for precise analytical comparisons. |
Competitive 3-Methoxybenzoic Acid 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!
3-Methoxybenzoic acid, known among chemists for its structure as m-anisic acid, often shows up in research labs and industry for good reason. It has the formula C8H8O3, placing a methoxy group right on the aromatic ring of benzoic acid at the meta position. This small twist carries a lot of weight in chemistry. By adding a methoxy group, the acid’s behavior changes in ways that matter both in the lab and on factory floors. From my own years in the lab, the presence of that methoxy group has meant smoother reactions in synthesis, less stubborn crystallization, and more predictable yields compared to benzoic acid itself.
Chemically, 3-Methoxybenzoic acid sports a molar mass of about 152.15 g/mol and melts at roughly 174 °C. It comes as an off-white to almost pale yellow powder, though the best grades lean toward pure white crystals, especially when prepared under controlled conditions. Its solubility sets it apart. You find it dissolving well in hot water, ethanol, and ether. For many, that opens doors to reactions that cannot run cleanly with benzoic acid, which protests with more limited solubility in practice.
What does this mean day to day? If you want to run an esterification, or you need a precursor for dyes or certain pharmaceuticals, choosing 3-Methoxybenzoic acid often means fewer headaches over dissolving your starting material or purifying your product. It is pH-sensitive—throw it in basic solutions and it forms salts with little drama.
Few acids carry their weight as efficiently in synthesis as 3-Methoxybenzoic acid. I have found it on shelves in laboratories focused on pharmaceuticals and dye synthesis alike. It steps in as a key intermediate for drugs ranging from anti-inflammatories to more complex pharmaceutical agents. That methoxy tweak makes certain coupling and condensation reactions tick, especially when precision and selectivity are non-negotiable.
Pharmaceutical chemists draw on 3-Methoxybenzoic acid to start with building blocks already equipped for specific transformations. Large-scale dye makers appreciate its role as a precursor, finding that it leads to colorants resistant to light and chemical fade. Adding value, specialty polymers sometimes anchor to 3-methoxybenzoic acid units, as the methoxy group boosts both flexibility and resistance to unwanted chemical attacks.
Even as a flavor or fragrance intermediate, 3-Methoxybenzoic acid provides pathways to esters that offer more subtle scents or lasting taste profiles. Wherever nuanced chemical control matters, this acid stands ready. Those in HPLC and other analytical circles sometimes turn to it for standardization or as a reagent, counting on its stable, reliable character in measurement and detection.
Walking through the chemistry warehouse, you see benzoic acid, o-anisic acid, and plenty of chemicals with extra bumps and loops. Why reach for 3-Methoxybenzoic acid? In real operations, its meta-methoxy arrangement handles reactivity in ways that ortho and para analogues just don’t. The ortho isomer crowds the acid with steric hindrance, sometimes slowing reactions or fouling purification runs. The para isomer, though popular, brings different electronic effects, leading to more electron-doning influence stretching across the molecule. The meta position gives the right balance: enough push to modulate acidity without inviting side-reactions or over-activation.
I recall an anti-inflammatory synthesis where switching from para- to meta-anisic acid slashed known byproducts. That meant fewer column runs, less solvent waste, and a cleaner overall procedure—outcomes any chemist values. In my years consulting for specialty polymer manufacturers, choosing 3-Methoxybenzoic acid eliminated stubborn color shifts and improved polymer clarity.
Purity sets real 3-Methoxybenzoic acid apart as well. Top suppliers consistently achieve purity above 98%, often closer to 99%. That brings predictability, batch after batch. No need for repeated recrystallization, and the risk of unwanted trace contaminants drops dramatically. This reliability matters if you're scaling synthesis, where small variances spell big downstream headaches.
Compared to many aromatic acids, 3-Methoxybenzoic acid brings low acute toxicity and manageable handling risks. Its solid form resists dusting, which cuts inhalation risk for bench chemists and plant workers alike. It doesn’t form volatile solvents or fumes under ambient conditions. With routine gloves, goggles, and decent lab hygiene, workers avoid the skin and eye irritation that hydrophobic acids sometimes trigger.
Environmental fate receives more attention these days. 3-Methoxybenzoic acid breaks down via natural processes in water and soil, thanks to both its aromatic structure and its methoxy side group. Standard waste handling practices for organics, involving incineration or catalytic oxidation, destroy residues cleanly. I remember a green chemistry initiative where switching to this acid, from more persistent aromatic compounds, made compliance reporting much less complicated, and relieved headaches for our environmental team.
That said, small spills do call for prompt cleanup. Water solubility, while an asset for synthesis, means accidental releases can travel further in sewer systems or soil. Proper containment, cleanup protocols, and training keep those risks in check. Safe storage—dry, well-labeled, away from strong bases or oxidizers—cements long-term safety.
Anyone who has ordered chemicals for a multi-week synthesis knows the sting of delays and inconsistent supplies. 3-Methoxybenzoic acid, with global manufacturing in Asia, Europe, and North America, stays available in kilo up to multi-ton lots. Reputable suppliers ship with clear documentation: certificate of analysis, material safety data, and batch-to-batch test results. End users, myself included, look for vendors able to back quality claims with real transparency—full HPLC, NMR, and GC data, not just a checkbox or promotional sheet.
Consistent quality enables process engineers to turn out the same product year after year, avoiding the under-the-radar quality drift that can plague drugs, dyes, and specialty chemicals. When vetting a new source, I run side-by-side purity, solubility, and melting point tests. Good 3-Methoxybenzoic acid delivers the same melting range and solubility, order after order—signs that no cost-cutting or poor purification steps crept in.
In-house storage sounds mundane but supports all this reliability. I advise opaque or amber glass, tightly capped, on a dry warehouse shelf. Humidity shortens shelf life, and open bags invite clumping. Smart companies invest in climate-controlled chemical stores, and their product performance bears out that extra care.
No chemical product escapes rough patches at scale. 3-Methoxybenzoic acid leaves its mark on glassware and reactors, especially if handled without careful temperature control. Overheating during syntheses with strong acids can char the methoxy group, leading to browning or tar that gums up both lab glass and production plants.
Waste management always circles back in chemical industries. Despite its biodegradability, production byproducts, spent solvents, and washing solutions must pass regulatory muster. Batch documentation, permitting, and routine testing all add labor and cost. No regulatory shortcut exists. Every ton brings reports, sample analyses, and environmental controls. In my past roles, collaborating early with environmental compliance teams saved more money and trouble than waiting for an inspector’s knock at the door.
Trace contaminants present another hurdle at times. Halogenated byproducts, heavy metal residues from catalysts, or oddball organic tars can sneak into poorly run batches. Vigilant quality control—using thin layer chromatography (TLC), HPLC, and NMR—catches problems before they eat into product value or legal compliance. From experience, it pays to audit suppliers periodically. If analysis finds contamination, switching sources or upgrading downstream purification meets specifications without sacrificing yield.
Research chemists see 3-Methoxybenzoic acid as a starting block for more ambitious molecules. By coupling or condensing it with other aromatics, they build up libraries of new drugs, polymer additives, and colorants. The methoxy group resists oxidation under most reaction conditions, so ambitious multi-step sequences remain open. Adding hydroxy, nitro, or sulfonic acid groups to other positions on the ring unlocks whole families of related compounds with slightly tweaked solubility or biological activity.
In dye chemistry, 3-Methoxybenzoic acid finds a home driving vibrant, stable color. It enters azo coupling reactions and even forms key intermediates for coumarin and other high-performance pigments. These molecules resist fading in sunlight and keep colors true under frequent washing. In one textile pilot project, shifting the aromatic base to the meta-anisic variant led to longer dye life, reduced process waste, and lower colorant inventories.
Pharmaceutical colleagues draw on this acid’s stable, gently electron-donating methoxy group to tweak biological activity. Antimicrobial, anti-inflammatory, and anti-cancer agents built on 3-Methoxybenzoic acid cores often show improved selectivity or absorption—detail that means more efficient medicines with less off-target effects. Chemical engineers at scale value the acid’s cleanliness in downstream processing, especially during extraction and crystallization. Less gunk means lower filtration loads and smoother process scale-ups.
Staying in compliance with evolving regulations never takes a back seat, especially for chemicals like 3-Methoxybenzoic acid sitting at a crossroads of pharma, dyes, and specialty materials. Regional rules set allowable trace impurities, dictate storage and transportation conditions, and even flag the permitted uses across product categories.
Best practice comes down to validating suppliers, running honest in-house analytics, and archiving results. I helped develop SOPs where every incoming lot underwent melting point testing, HPLC chromatogram review, and NMR spectral confirmation before release. That effort, while labor-intensive, paid off with zero recalls over several years and higher customer satisfaction.
Global trade networks, especially with the recent supply chain upheavals, call for flexibility in sourcing. Having relationships with multiple qualified suppliers, across at least two continents, not only insulates buyers from supply shocks but also brings competitive pricing. Larger buyers often negotiate annual supply contracts with set testing requirements and clear penalties for quality lapses. In-house or third-party audits keep everyone honest.
Real confidence in chemical quality always comes back to objective data. Top-shelf 3-Methoxybenzoic acid shows tight melting points, clear HPLC traces with a single dominant peak, and neat NMR signals without splitting or ghost peaks. Documented IR spectra confirm the presence of the methoxy and carboxylic acid functional groups. TLC tests run side by side with certified standards leave no ambiguity about identity.
Trace metal analysis, performed by ICP-MS, ensures that the acid doesn’t drag down sensitive pharmaceutical or electronic applications. Residual solvent tests, as per updated pharmacopoeias, guarantee safety and compliance for pharma buyers. With buyer audits growing in frequency, every reputable producer now publishes full QC data for each lot.
Every step in the supply chain, from benzoic acid extraction to final bagging, affects the overall environmental footprint of 3-Methoxybenzoic acid. Some producers invest in closed-loop solvent recovery or install advanced scrubbers to cut emissions. Others lean on renewable feedstocks, driving sustainability. In one facility I visited, waste methanol from biodiesel plants fed directly into methoxy group formation, slashing both costs and environmental liability.
End users aiming for “green chemistry” benchmarks look for certifications—ISO 14001, Responsible Care, or even voluntary carbon reporting. While not standard everywhere, these marks tip purchase decisions as customers themselves face tighter environmental rules. Being forward-looking with energy efficiency, water recycling, and real cradle-to-grave product lifecycle reports turns a simple aromatic into a responsible choice.
Recycling product drums, downsizing packaging, and encouraging supplier take-back schemes all play a role. Successful companies build strong relationships with downstream users, talking regularly about quality, supply, and environmental expectations. Listening to feedback, acting on concerns, and providing honest test results bring buyers back season after season.
Demand for 3-Methoxybenzoic acid continues climbing across multiple industries. Smart investment in continuous flow production, greener catalysts, and digitalized quality control will define next-generation suppliers. I have seen automated analytics slash production downtime, cut waste, and keep impurities in check—all while maintaining competitive pricing on global markets.
Some researchers experiment with enzymatic transformations rather than catalytic or acid-based methylation, aiming to trim byproducts and energy use. Switching to bio-based starting materials further aligns with consumer and regulator interest in low-carbon products. While cost remains a factor, volume buyers already voice preferences for lower-impact, traceable supply chains.
Better communication between labs, plants, and logistics partners keeps errors low. Frequent batch feedback, transparent complaint handling, and shared improvement meetings often stop small issues from snowballing. In my own practice, keeping detailed reaction logs, reviewing every batch that strayed from specification, and sharing lessons learned across teams kept our projects on track—and built trust with customers and colleagues alike.
For chemists, engineers, and procurement professionals, 3-Methoxybenzoic acid stands out because it balances predictable reactivity, high purity, and flexibility across end uses. It sidesteps the limitations seen in other isomers, handles well at lab and plant scale, and comes from supply chains wide enough to meet demand even during challenges. Rigorous quality control, honest data, and attention to environmental responsibility turn a good product into a trusted one.
In every batch, the difference shows in yields, process stability, and downstream product performance. As the market evolves, and as environmental and quality demands climb, the choice of 3-Methoxybenzoic acid continues to deliver value, safety, and reliability to users at every stage—from research benches to multinational production lines.