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HS Code |
237542 |
| Product Name | Methyl (4-Hydroxymethyl)Benzoate |
| Cas Number | 23160-72-9 |
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.18 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 80-83 °C |
| Boiling Point | 325.6 °C at 760 mmHg |
| Density | 1.26 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | COC(=O)C1=CC=C(C=C1)CO |
| Inchi Key | FLYHRFQOHSYBST-UHFFFAOYSA-N |
| Storage Temperature | Store at 2-8 °C |
| Purity | Typically ≥98% |
| Refractive Index | 1.563 |
As an accredited Methyl (4-Hydroxymethyl)Benzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of Methyl (4-Hydroxymethyl)Benzoate, tightly sealed with a screw cap and labeled clearly. |
| Shipping | Methyl (4-Hydroxymethyl)benzoate should be shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. The packaging must comply with local and international regulations for chemical transport. Ensure proper labeling and documentation, and ship via a reliable courier specializing in hazardous or laboratory chemicals, if applicable. |
| Storage | Store Methyl (4-Hydroxymethyl)benzoate in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it separated from strong oxidizing agents and acids. Ensure proper labeling and secure the storage area to prevent unauthorized access. Avoid moisture and store at room temperature or as recommended on the safety data sheet. |
Applications of Methyl (4-Hydroxymethyl)Benzoate in Industrial ManufacturingAs a direct manufacturer, we supply Methyl (4-Hydroxymethyl)Benzoate to specialized industry sectors where its performance and compliance profiles meet high downstream standards for regulated product manufacturing. Presented below are key application segments based on proven end-market integration, with in-depth information on compliance, formulation, production, and finished goods for each industrial channel. 1. Active Pharmaceutical Ingredient (API) Intermediate in Small Molecule SynthesisPharmaceutical manufacturers leverage Methyl (4-Hydroxymethyl)Benzoate as a selective intermediate for building complex active compounds, particularly in the synthesis of anti-hypertensive agents and antiviral scaffolds. The precision reactivity of the hydroxymethyl group facilitates subsequent targeted functionalizations within GMP-controlled batch and continuous flow processes that underpin regulated API production. Industry compliance standards
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2. Fine Chemical Intermediate for UV Absorber ManufacturingManufacturers of ultraviolet absorbers in specialty polymers and coatings rely on our material’s hydroxymethyl functionality to introduce reactive linkages in the synthesis of benzotriazole and benzophenone-based UV-stabilizing additives. Strict quality specifications ensure suitability for downstream automotive, packaging, and construction applications demanding durability and weather resistance. Industry compliance standards
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3. Fragrance and Flavor Ester Precursor in Food-Contact ApplicationProducers in the flavor and fragrance sector select our compound for controlled esterification reactions that generate targeted aromatic esters used in food-contact plastics and indirect flavor carriers. Its regulated profile supports application in packaging materials compliant with food safety testing, enabling aromatic compound release without cross-contamination. Industry compliance standards
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4. Monomer Precursor in Specialty Polyester and Polycarbonate SynthesisSpecialty resin producers deploy our product as a functional monomer precursor to introduce hydroxymethylbenzoate units into the backbone of engineered polyesters and polycarbonates, improving polymer flexibility and providing sites for further crosslinking or functional modification. Controlled reactivity enables process stability and ensures batch reproducibility across high-spec resin lots. Industry compliance standards
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5. Intermediate for Agrochemical SynthesisActive substance manufacturers in the crop protection sector employ Methyl (4-Hydroxymethyl)Benzoate as a building block for the synthesis of specific fungicide and herbicide actives. Its reactivity provides strategic entry points for incorporating bioactive pharmacophores, facilitating downstream product formulations subject to land and environmental stewardship protocols. Industry compliance standards
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As a chemical manufacturer with decades of work behind us, we’ve processed countless batches of fine organics across the years. Methyl (4-Hydroxymethyl)Benzoate doesn’t just appear on a spec sheet for us—it starts as raw materials entering the facility, moves through reactors run by real chemists, and leaves our doors carefully controlled for both purity and utility. It’s not about chasing the latest buzzword in specialty chemicals. It’s about consistent, deliberate results, and supporting those who rely on predictable, repeatable intermediates for their own synthesis and formulations.
Our approach rests on a technical and practical foundation. Regular sampling, in-process controls, hands-on verification—the most advanced instrumentation means little without seasoned operators who know the smell of a well-run methylation, who recognize what a clear endpoint looks like. We value the disciplined practice of solid chemistry, which builds trust over time between supplier and end-user, researcher and producer.
Methyl (4-Hydroxymethyl)Benzoate, by structure, occupies a useful spot in the benzoate family. For us, the importance comes down to its functional groups: an aromatic ring, an ester, and a primary alcohol, each lending versatility for further chemical transformation. We select feedstocks for quality and trace them through each batch, not just because regulators require it, but because a missed impurity or rushed reaction step can spoil purity or lead to process headaches for our customers. Each drum or bottle leaving our facility carries this underpinning of conscious selection, careful preparation, and practical oversight.
The chemical itself sometimes appears in fine white crystalline form, easily handled but requiring mindful storage due to its mild hygroscopic tendency. We produce it most consistently in kilogram-to-ton scale, standardized for research and commercial use. Batch-to-batch reproducibility matters, because a process built today in a research lab may grow into tomorrow’s full-scale plant. We support customers with open data—certificate of analysis, impurity profile, residual solvent screen—not merely to tick boxes, but to answer the exact questions real chemists ask about process efficiency and analytical confidence.
Listing out numbers does little without an understanding of why they matter. In practical work, the minimum purity for Methyl (4-Hydroxymethyl)Benzoate typically exceeds 98%. For us, that’s not a slogan; it’s a result of re-crystallization steps, drying under vacuum, and careful packing to avoid contamination between orders. Moisture content draws special attention, given the presence of a primary alcohol group. We run routine Karl Fischer titrations and advise on correct drying or storage conditions. Color, appearance, odor—these tell experienced users a great deal even before an assay result is available.
Contaminants such as unreacted starting materials, methyl (4-formyl)benzoate, or methyl (4-carboxymethyl)benzoate must stay below detection limits, not only for the integrity of downstream reactions but also to avoid unintended catalytic effects or off-flavors in certain applications. Our batch records detail solvent residues, heavy metals, and commonly encountered processing-related byproducts, because regular process monitoring finds unexpected results long before troubleshooting begins.
Few chemical intermediates appear in isolation—they serve as stepping stones toward larger targets in organic synthesis, pharmaceutical research, fragrance design, or advanced materials science. In our regular client requests, Methyl (4-Hydroxymethyl)Benzoate fills roles as a protected intermediate for benzylic transformations, as a precursor in custom ether and ester syntheses, or as a scaffold for introducing diverse substituents on the aromatic ring.
Some of our pharmaceutical clients leverage the stability of the methyl ester moiety, modifying the alcohol group to obtain prodrugs or advanced building blocks. In fine chemistry, the compound becomes a launch point for selective oxidation to aldehydes or acids, or as a handle for further C—C, C—N, or C—O bond formation. Our conversations rarely revolve around simple use descriptions. We’re often troubleshooting specific coupling or catalytic steps, discussing the behavior under different solvents, or supporting analytical teams searching for impurity spikes at tight detection limits.
Lab and production teams benefit from understanding how this compound plays with common solvents and environmental conditions. Though it appears fairly stable under dry, dark storage, exposure to ambient humidity or excess heat can trigger clumping, minor degradation, or loss of activity for sensitive reactions. Early batches in our plant years ago revealed migration of trace acid or peroxide impurities, so we implemented airtight containers and inert gas fills for longer-term lots. Customers working in pilot and kilo-scale settings will see advantages in simple jar or drum packaging, but we always recommend grinding only under clean, dry atmosphere to avoid excess moisture uptake.
The industry offers a crowded field of benzoate esters, often with small structural tweaks that carry big consequences for reactivity or downstream performance. We’ve worked with methyl 4-methylbenzoate, methyl 4-formylbenzoate, and simple methyl benzoate itself. The unique draw of Methyl (4-Hydroxymethyl)Benzoate is that dual reactivity: the methyl ester provides a baseline of chemical stability, while the hydroxymethyl group is highly amenable to functionalization. Methyl 4-formylbenzoate lacks that alcohol versatility, and methyl benzoate strips away substituent reactivity altogether.
From our process viewpoint, Methyl (4-Hydroxymethyl)Benzoate slots in where chemists need that precise mix of reactivity and stability. It handles reductions, oxidations, and protection strategies with fewer side reactions than isomers or structurally similar esters. Our teams have observed shorter reaction times in etherification and improved yields in peptide coupling work compared to alternative substrates.
The molecule can step in as a synthetic “chassis” for dye, UV absorber, and flavor and fragrance development. We receive feedback regularly from development chemists who saw increased selectivity in their routes, specifically due to this dual-functional-group arrangement on the aromatic core. This sets it apart, especially when adapting lab-scale literature routes to pilot or commercial processes, where small impurity shifts or laborious purifications can disrupt entire projects.
Most of our clientele are practical chemists, engineers, or product developers, interested in more than just a drum or jar delivered to their site. We treat every inquiry as a two-way street, responding to requests for exact spectral data, Lot-to-Lot reproducibility analysis, or special packing to suit automated feed systems. We’ve built collaborative communications with formulation teams, troubleshooting reaction anomalies and offering access to our internal library of method development notes.
Several large-scale customers have shared stories about scaling transformations from grams to hundreds of kilograms—success depended on not just the raw material supply, but reliable solubility data, impurity traps, and detailed working procedures. We give practical advice on reaction vessel materials, solvents, and filtration choices, not canned recommendations, since our teams have encountered—sometimes painfully—how changes in process water or atmospheric conditions can shift product performance.
We stand by our responsibility as stewards of both chemical safety and the environment. Our site investments include improved wastewater treatment and secondary containment, particularly because compounds bearing aromatic and ester groups like Methyl (4-Hydroxymethyl)Benzoate present specific treatment challenges. Air emissions and effluent monitoring do more than keep us compliant; they let us detect process anomalies early, feeding back into continuous improvement.
Transport and handling policies meet international standards to prevent accidental release or degradation during shipping. We keep up-to-date with evolving regional and global regulations, and provide compliance documentation that truly reflects batch-specific performance, not just a generic template. For customers facing stricter jurisdictional requirements on purity, trace metals, or residual solvents, we tailor production to align with those needs, discussing any trade-offs or technical solutions as partners rather than just as suppliers.
We often receive requests for “standard grade” or “high-purity grade” and always make it clear: the difference comes not just from the label, but from the way we handle raw materials, control the synthesis, and carry out purification. Real-world syntheses are rarely perfectly clean. Side reactions can creep in—a small step left unchecked can create persistent byproducts or carryover materials that affect future batches. Rigorous physical removal, targeted chemical conversions of byproducts, and real scrutiny in drying and packaging create the difference between routine and truly reliable output.
Take batch consistency. Since lab and production teams might run decades of similar chemistry, the smallest changes in solubility, color, or melting point catch experienced hands quickly. We contend with those variables each day—if a process cools too quickly, crystals might trap mother liquor. If drying pulls too hard at high temperature, product can start to yellow or degrade. These hands-on realities shape the way we refine protocols, rather than simply setting broad specs and walking away.
Process troubleshooting isn’t a once-a-decade event; it forms part of our culture. Whenever a client signals a shift in impurity profile or a drop in downstream yield, we collaborate to reproduce and resolve the result quickly. Sometimes it’s a matter of mineral content in a fresh supply of water—other times, it requires changing the point of reagent addition or swapping out filtration phases. Our in-house teams contribute time and knowledge freely, because small interventions at this stage prevent wasted effort, material, and energy at later points.
A specific example from several years back involved an overseas client scaling up an alkylation step. Minor color formation and impurity drift were holding back their quality and throughput. Our teams helped adapt the isolation and washing sequences, supplied fresh data sheets, and confirmed new drying and packaging routines. Their batches moved into full-scale production, and our ability to fine-tune support at the source became a regular talking point throughout their organization.
While synthetic chemistry often moves in cycles—old methods returning to favor as feedstocks and pricing shift—our place as producer keeps us testing and optimizing routes. We experiment with catalysts, novel protection strategies, greener solvent systems, and continuous process intensification, with an eye on both efficiency and safety. Methyl (4-Hydroxymethyl)Benzoate synthesis lends itself to step-economical approaches and avoids some of the harsher reagents common to related compounds.
A recurring trend among our partners is the push for sustainable practices. Minimal solvent use, less persistent waste, energy-efficient reactions—our product development groups stay in close consultation with both customers and regulatory experts when adapting synthesis to use safer reagents or more benign environments.
Some recent upgrades involved switching to a new catalytic system, cutting reaction time and waste while boosting final purity. Less workup not only means improved environmental performance, but also less opportunity for loss or contamination—techniques we now carry forward into multiple lines of fine aromatic compounds.
Independent verification always trumps marketing claims. We encourage partners to scrutinize our products: run their own NMR, HPLC, GC-MS, FTIR; cross-check our COAs against internal standards; provide feedback which we feed directly back into our production and QA systems. Some clients have flagged minor peaks or outliers that escaped earlier screens, and our willingness to revisit the data and reinforce controls helped solidify trust rather than shake it.
Long-term stability and reproducibility come through habits, not one-off inspections. We run stability checks, track data trends, and keep samples on reserve for traceability later on if issues crop up years down the line. We welcome partners from universities, established manufacturers, and small startups alike to not only use but question our process and results. These open channels strengthen both product quality and broader working relationships.
Each order or technical inquiry builds our shared knowledge. We consider our laboratory notebook as much a company asset as our production lines or analytics bank. If a customer points out a faster filter method or flags a subtle side reaction, we capture and review the learning. Our team shares this experience across departments—from synthesis to purification, QC, logistics, and support—each reinforcing the value of attention to detail at every stage.
The more we collaborate, the better both parties understand how process, product, and application intersect in the real world. Especially in an industry where failures and surprises often teach stronger lessons than quick wins, the foundation of trust rests on integrity in production, transparency about capabilities, and a history of learning from both success and shortfall.
Sourcing chemicals directly from the manufacturer closes knowledge gaps, shortens supply lines, and strengthens accountability. Many customers come to us after difficult experiences with intermediaries or resellers who cannot trace back questions, resolve quality issues, or adjust to unique operational needs. By working from the ground up, we offer more than just material supply—we solve, support, and improve together.
Supply disruptions, evolving product regulations, and changes in end-use needs all illustrate why partnering with an accountable producer saves time and resources over the long run. Our facility and team are accessible for audits and questions, and we believe in real discussions about lot traceability, alternate syntheses, or packaging adjustments, not boilerplate emails sent from a distant broker.
Demand for reliable and versatile benzoate intermediates continues to develop across research and industry sectors. Our journey with Methyl (4-Hydroxymethyl)Benzoate stands as an example of how experience, practical controls, and close cooperation underpin not only strong product supply, but also shared advancement in the chemical field. We invite ongoing dialogue, data sharing, and technical learning, certain that the best outcomes come from hands-on production and open collaboration between those who know the work at a fundamental level.