|
HS Code |
863825 |
| Iupac Name | methyl 2-hydroxybenzoate |
| Common Name | 2-(Methoxycarbonyl)phenol |
| Cas Number | 119-36-8 |
| Molecular Formula | C8H8O3 |
| Molecular Weight | 152.15 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 222-224 °C |
| Melting Point | 8-9 °C |
| Density | 1.174 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 96 °C |
| Smiles | COC(=O)C1=CC=CC=C1O |
| Inchi | InChI=1S/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H3 |
As an accredited 2-(Methoxycarbonyl)Phenol 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 2-(Methoxycarbonyl)Phenol, tightly sealed, labeled with chemical details and handling instructions. |
| Shipping | 2-(Methoxycarbonyl)phenol is shipped in tightly sealed containers to prevent moisture and air exposure. During transit, it is packaged in accordance with chemical safety regulations, often using secondary containment, and labeled with hazard information. Store and transport at ambient temperature, away from incompatible substances, and in compliance with local and international shipping guidelines. |
| Storage | 2-(Methoxycarbonyl)phenol 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 and bases. Protect from light and moisture. Store at room temperature and properly label the container. Ensure appropriate safety measures are taken to prevent exposure during handling and storage. |
Competitive 2-(Methoxycarbonyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 2-(Methoxycarbonyl)phenol (sometimes known by its CAS number, 3120-74-9) carries the marks of our production process. Years of experience in specialty chemical manufacturing taught us that consistent quality isn’t just a promise—it’s a process. Our teams handle each step, from raw material selection to final purification, with care that comes from real hands-on experience. This chemical shines in fine chemical syntheses and as a key intermediate in various industries, so we pour attention into every lot.
2-(Methoxycarbonyl)phenol, with the structure featuring a methoxycarbonyl group at the ortho-position of the phenol, brings a specific reactivity not seen in its close analogues. The ester moiety tunes its behavior, making this molecule a preferred choice where a protected phenol group is needed or where controlled reactivity can set up more complex transformations. Research chemists favor this structure for its cleaner reaction profiles and selective reactivity, allowing more predictable outcomes in multi-step syntheses.
The daily reality in our plant starts with sourcing reliable phenol and methyl chloroformate. No shortcuts here. Our technicians monitor every stage, using gas chromatography to keep every impurity in check, especially residual starting materials. The quality of the catalyst and the control we keep over reaction temperatures shape the color, purity, and micro-impurity signature of the final product. Our teams wash, extract, and dry with attention born from hundreds of batches—not just confidence in equipment but a respect for the chemistry itself.
Sterile-packed containers ensure the smallest trace of moisture, dust, or residual solvent doesn't compromise the product. We know that even minor solvent residue can cause issues downstream—either stalling a reaction or introducing a shadow of off-target products in later steps. We make sure every drum moves fast from production into dry, ventilated storage, minimizing exposure to air and light, both of which can threaten purity. What leaves our facility reflects not just compliance, but accountability.
People outside the plant may not always see the everyday challenges of delivering a niche molecule like 2-(Methoxycarbonyl)phenol. Fluctuating upstream feedstock prices and shifting purity demands require adjustment, both in sourcing and process optimization. It’s not rare for researchers or industrial users to need a custom particle size, a particular solvent system for dissolution, or slightly tweaked purity thresholds. These needs aren't just tick boxes on a spec sheet—they require real process adaptation and clear communication across production and quality control teams.
Shipping regulations for aromatic esters changed several years ago, mandating extra documentation and compliance checks, so our logistics staff coordinates closely with the supply chain to minimize bottlenecks. Each kilogram represents not just a product, but the accumulated work of dozens of skilled workers and the costs tied to safe transport and handling. These realities shape both price and value, and we address them transparently with our partners.
At first glance, 2-(Methoxycarbonyl)phenol can look similar to methyl salicylate or even plain phenol. The difference shows up sharply in synthetic applications. Methyl salicylate carries a different ester placement, giving quite distinct reactivity and often triggering side reactions chemists want to avoid in pharmaceutical or agrochemical syntheses. Simple esters or unprotected phenols create difficulties, from lower yields to poor selectivity in target transformations. The ortho-relationship of methoxycarbonyl and hydroxyl profoundly influences reactivity, making this compound valuable in Suzuki couplings, selective acylations, and as a key building block in active ingredient pipelines.
Many clients come to us after running into issues using off-the-shelf esters or phenols, only to find they battle low yields, tough purification problems, or unpredictable side reactions. Our 2-(Methoxycarbonyl)phenol stands out because of how tightly we control every parameter—water content, residual metals, particle size distribution, and by-product profile. There’s no one-size-fits-all solution in fine chemistry, so the extra steps we take translate directly into more predictable downstream processes.
Typical specifications cover appearance, assay, water content, and residue on ignition. What’s not always captured on a certificate is the subtle effect of micro-impurities, color stability, or lot-to-lot reproducibility. We see that, especially in research and pharmaceutical manufacturing, minor shifts in impurity profile can derail timelines or even regulatory submissions. For this reason, we invest in both classic chemical analysis and modern chromatographic fingerprinting on every lot, so our customers know exactly what they’re working with each time.
Some users demand higher than 99% assay. Others request low heavy metal content or documentation on solvents not used in the process. Rather than standardizing every batch, we maintain flexibility in our reactors and processing line to meet these needs. This dedication grows from experience—chemists trying to scale up a reaction don’t want surprises from subtle shifts in input material.
The real strength of 2-(Methoxycarbonyl)phenol comes through in application. For several pharmaceutical R&D teams we supply, the molecule acts as a protected phenol, entering multi-step syntheses where selective transformation of the aromatic ring is crucial. This chemical hides the phenol group, allowing other transformations to run with higher control. Later, mild hydrolysis reveals the phenol moiety when desired. This strategy prevents by-product formation, boosts yield, and sidesteps complex purification headaches.
Agrochemical researchers value its selectivity too. We have seen several projects that failed with basic methyl esters due to unselective reactions or instability under mild bases. Substituting 2-(Methoxycarbonyl)phenol unlocked a clean path toward complex herbicide candidates and crop-protection agents. Selectivity, not just basic reactivity, drives up the molecule’s utility. Our technical staff often workshops with customers to troubleshoot problems when substituting other esters for this structure, gathering lessons that feed right back into production improvements.
Handling aromatic esters and phenols brings its own set of safety and environmental issues. We maintain closed-system processing where feasible, minimizing airborne exposure. Real-time monitoring detects traces of methanol, phenol, and CO, ensuring ambient exposure stays well below occupational thresholds. Waste from the manufacturing process undergoes thorough treatment—neutralizing acidic remnants, separating off organics, and recycling solvents where viable.
We collaborate with safety authorities and regularly update staff on transport legislation and safe handling. Our teams train to spot leaks or mishandling before they become real hazards. We learned years ago that investing in on-site containment infrastructure—spill kits, ventilation upgrades, closed drums—prevents not just incidents, but production delays. It’s an upfront cost, but one that earned its place many times over.
Even with decades working with molecules like 2-(Methoxycarbonyl)phenol, the search for process improvements never slows down. Some colleagues in industry look for green chemistry routes—investigating less hazardous solvents or lower-energy reaction conditions. Our R&D teams tested alternative catalysts aiming to reduce reaction waste and improve atom economy. It’s not rare for a subtle tweak in the cleaning phase to lead to brighter color, longer shelf life, or easier filtration.
We keep an eye on recyclability and circular chemistry ambitions, too. Where earlier plants treated waste methyl chloroformate as incineration material, our modern lines recover and recycle it. Progress here isn’t always dramatic, but each efficiency mapped in practice means lower costs, less waste, and less environmental impact. Innovations often begin at the production line, working with operators and lab staff, and then scale up with customer feedback.
Clients, research partners, and end users bring us problems big and small. Sometimes it’s a question about trace metals in the active compound. Other times it’s streamlining packaging to fit automated reactors. These aren’t just theoretical problems—they affect throughput, regulatory approval, and even safety. Open lines of communication help us refine our process, document more clearly, and sometimes adjust our specifications so that batch delivery matches real workplace needs.
A few years ago, we collaborated with a downstream fine chemical plant that developed a new polymer using our material as a building block. They required a much tighter color specification than normal batches due to strict optical requirements. We adjusted our crystallization and filtration method, installing in-line colorimetric monitoring to catch off-spec lots just as they emerged. This experience sharpened both our technical process and our ability to tune to customer needs, letting us avoid repeated delays and rework.
Global events rarely leave the chemical industry untouched. Disruptions in upstream raw materials, shifting regulations, or surges in demand flow downstream fast. During regional transport slowdowns or raw material shortages, our forward planning has meant building buffer stock where possible and qualifying alternative suppliers ahead of time. Each link in the supply chain is mapped and monitored for transparency—the days of guessing about real-time stock levels or waiting weeks for shipment status have passed for us.
Working directly as a manufacturer puts pressure on every part of the process to deliver on time and with full traceability. We maintain detailed process records for every lot that passes through our lines, tracing it from raw materials to finished goods. This helps us spot potential failure points, meet modern regulatory expectations, and make improvements based on real-world demand shifts. Flexibility is as vital as infrastructure—teams react fast to shifts in demand or logistics barriers, usually with solutions that prevent a single late shipment from cascading into bigger problems.
Each drum that rolls down our shipping dock carries with it the result of many years of refinement, teamwork, and customer interaction. The difference this compound brings versus similar aromatics or esters comes from its combination of designed reactivity, reliable supply, and clear communication built between scientists, technicians, and users. The journey from phenol and methyl chloroformate to pure, high-quality 2-(Methoxycarbonyl)phenol involves more than just routine processing—it takes the combined input from everyone along the chain. Every new challenge from our partners sharpens the product, the process, and our resolve to deliver a compound that meets real-world needs, not just theoretical expectations.
With each discussion, trial, and feedback session, priorities change and so do the standards. Pharmaceutical teams working under the tightest regulatory climates set purity bars higher. Polymer innovators ask for cleaner, more consistent batches. Environmental regulators push us to find greener process routes and safer waste-handling solutions. We shape our roadmap to meet these expectations, not just because of compliance, but because we believe our success grows from real-world partnerships and the trust built through direct engagement.
2-(Methoxycarbonyl)phenol may seem like a straightforward product at first glance. But behind each order sits a web of carefully coordinated acts—meticulous process design, firm quality controls, smart logistics, honest communication, and a continual drive for improvement based on the real issues faced by researchers and industrial chemists. This compound’s utility grows out of these foundations, giving users an edge in everything from lab-scale reactions to full production runs. From our plant floors to customer labs, the story of 2-(Methoxycarbonyl)phenol is ongoing, always getting better with every challenge and every batch delivered.