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HS Code |
411585 |
| Iupac Name | 2,3-Dihydro-1-benzofuran-5-ylmethanol |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.18 g/mol |
| Cas Number | 40716-66-3 |
| Appearance | White to off-white solid |
| Melting Point | 49-52 °C |
| Solubility In Water | Slightly soluble |
| Smiles | C1COC2=CC=CC(=C2C1)CO |
| Inchi | InChI=1S/C9H10O2/c10-6-7-1-2-8-5-11-4-3-9(7)8/h1-2,10H,3-6H2 |
| Pubchem Cid | 324623 |
| Logp | 1.3 |
As an accredited 2,3-Dihydro-1-Benzofuran-5-Ylmethanol 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 2,3-Dihydro-1-Benzofuran-5-ylmethanol, sealed with a polypropylene cap and tamper-evident label. |
| Shipping | 2,3-Dihydro-1-Benzofuran-5-ylmethanol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packages are clearly labeled with hazard and handling information. Shipping complies with local, national, and international regulations, ensuring safe transit. Typically, the chemical is transported via ground or air with appropriate documentation and temperature control if needed. |
| Storage | Store **2,3-Dihydro-1-Benzofuran-5-ylmethanol** in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers. Keep container tightly closed and properly labeled. Protect from direct sunlight, moisture, and extreme temperatures. Handle using appropriate personal protective equipment and avoid prolonged exposure. Follow all relevant safety and regulatory guidelines during storage and handling. |
Applications of 2,3-Dihydro-1-Benzofuran-5-Ylmethanol in Industrial ManufacturingAs a specialized producer, we supply 2,3-Dihydro-1-Benzofuran-5-Ylmethanol for advanced chemical synthesis across multiple industrial sectors. The following application scenarios highlight real downstream integration and end products, with segment-focused process, compliance, and formulation data for commercial manufacturers. 1. Pharmaceutical Intermediate for Central Nervous System (CNS) CompoundsLarge-scale pharmaceutical manufacturers employ 2,3-Dihydro-1-Benzofuran-5-Ylmethanol as a functional intermediate in the synthesis pathway of CNS-active drug molecules. Its specific hydroxymethyl substitution supports key condensation and acylation steps in producing benzofuran-based drug scaffolds, particularly within anti-anxiety and anti-epileptic research pipelines. Controlled environments handle the compound in dedicated synthetic blocks, monitored for batch consistency and traceability in regulated markets. Industry compliance standards
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2. Fine Fragrance and Aroma IntermediatePerfumery chemical producers use 2,3-Dihydro-1-Benzofuran-5-Ylmethanol to synthesize proprietary aroma molecules with a unique woody-floral character. Its reactivity enables alkylation and acetalization routes yielding high-impact fragrance blocks, which find consistent application in mid to high-end fragrance formulations. These processes adhere to international flavor and fragrance material safety assessments within purpose-built synthesis suites. Industry compliance standards
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3. Agrochemical Synthesis Building BlockLeading agrochemical enterprises integrate 2,3-Dihydro-1-Benzofuran-5-Ylmethanol into herbicide and fungicide active ingredient synthesis. The hydroxymethyl group enables efficient etherification and halogenation steps, supporting differentiated mode-of-action discovery programs. All reaction sequences respect stringent regulatory controls for trace impurities and downstream chemical compatibility, critical for agricultural registration dossiers. Industry compliance standards
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4. Specialty Polymer Modification for Advanced MaterialsAdvanced polymer manufacturers use 2,3-Dihydro-1-Benzofuran-5-Ylmethanol as a customization agent in synthesizing linear and branched copolymers. The benzofuran ring and hydroxymethyl functionality introduce tailored flexibility and improved thermal behavior when grafted into specialty plastics or resins used in electronic encapsulants and engineered elastomers. Integration takes place in controlled polymerization reactors with robust analytical monitoring. Industry compliance standards
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As a company with years of direct involvement in benzofuran chemistry, our team approaches the production of 2,3-Dihydro-1-Benzofuran-5-Ylmethanol with deep respect for product consistency and safety. Every shift on the plant floor underlines this—not just chemical transformations, but also a hands-on familiarity with the quirks this compound can present. Factory work informs more than just paperwork; it shapes how we refine each step, catch aberrant smells or odd reaction heat, and tweak processing conditions after noticing a slight change in a starting material’s quality.
Drawing on this background, we structure our workflow around practical demands from labs and industrial partners. This material, often found under CAS number 4382-46-1, continues to carve out its role in fields like medicinal chemistry, fragrance design, research applications, and specialized material development. Every drum and container that leaves our facility reflects the lived-in caution and precision that advancing chemical manufacturing still demands in an era of high-throughput production.
2,3-Dihydro-1-Benzofuran-5-Ylmethanol stands out in the benzofuran family for its unique attachment of a methylol group at the 5-position. In the lab, this feature creates new paths for chemical modification. Medicinal chemists use it to build molecules that benefit from the polar alcohol, while flavor and fragrance developers sometimes rely on its benzofuran backbone as a jumping-off point.
Our material typically arrives as a crystalline solid, clear to pale in color, with a characteristic mild odor. Moisture content and impurity levels shape how researchers approach their synthesis. That’s why experienced chemists prefer a vendor able to produce lots with low water, minimal metal contamination, and negligible byproducts—which is far less simple than it sounds. Any facility with old lines or inconsistent solvent handling will run into trouble. From experience, storing this compound in tightly sealed containers in cool, dry conditions avoids shelf degradation and keeps downstream reactions predictable.
We do not view batch release as just another checklist. Knowing that medicinal teams and analytical chemists rely on exact composition, we test not just for assay and basic identity, but routinely look for residual solvents, trace reaction byproducts, and even isomeric impurities. Long-term experience has shown that even small fluctuations in isomer ratio—especially from older, out-of-spec benzofuran stocks—can jeopardize reproducibility in multistep syntheses. This is why each batch lot undergoes rigorous checks for NMR, IR, and chromatography fingerprints developed in-house.
From the ground up, this compound’s main value comes from the combinatorial site at the methylol group. Synthesis teams often use it as a protected benzofuran for reactions needing selective deprotection later. In practical process chemistry, this intermediate frequently appears in routes toward pharmaceuticals, fungicides, or high-value aroma chemicals. We see requests from customers working on methods for building heterocyclic scaffolds—places where regular benzofurans can’t deliver the right reactivity or solubility.
Toolkits for research often require grams to kilos of this alcohol, depending on their trial scale. Teams reaching pilot scale for a potential drug or a fragrance accord write us about increasing batch quantities, and share production constraints. We keep technical discussions direct. Sometimes, project chemists run into difficulties dissolving or purifying the product, so we draw on analytical data from our own purification suites. Having material that handles well under both flash chromatography and preparative HPLC saves time for everybody involved.
Compared to more commonplace benzofuran derivatives, the selective reactivity of the 5-hydroxymethyl group often solves bottlenecks for clients chasing higher efficiency downstream. Organic synthesis rarely unfolds without surprises—solvent choices, catalyst tolerance, pigment contamination—all these play a part. Drawing from batches gone wrong in the past, we advise partners on what solvent switches can clean up a streaky TLC, or how careful pH management keeps the crystalline form stable during scale-up.
It’s tempting to lump this methylol benzofuran together with a host of structurally similar compounds. The difference usually comes down to the handle provided by the alcohol group. For teams synthesizing larger systems, the site provides anchoring for chain extensions, selective oxidation, or cyclization approaches flat benzofurans struggle to support.
For plant operators, the challenges of this molecule stand apart from those of simple benzofuran or even alkyl-substituted variants. Consistent purification makes a difference, because the combination of polar functional group and aromatic ring encourages side products that can co-elute or resist basic workup. Factory teams swapping between methyl, methylol, and methoxy derivatives learn to adjust extraction protocols and drying times, or else risk multi-day holdups during critical production windows.
From a hazard and handling standpoint, 2,3-Dihydro-1-Benzofuran-5-Ylmethanol doesn’t fit the same trouble spots as reactive aldehydes or corrosive oxidants, but its solubility profile means older containers exposed to air can pick up water or trace acids—both of which wreak havoc on certain synthetic routes. Warehouse and shipping crew follow tight protocols to avoid such pitfalls and preserve both shelf stability and downstream performance.
Since moving from smaller lab-based lots to commercial scale, our plant team has rolled through more than one overhaul of reactor configurations, feed systems, and drying regimens. Years of tracking yield losses and flagged quality checks point to solvents, not merely raw material quality, as the trickiest variable. Winter shifts teach lessons about how humidity creeps into lines, and cleaning regimes require discipline through early-morning maintenance cycles. We take pride in simple steps: logging dry-down temperatures, calibrating probe accuracy, and rechecking key chromatograph standards.
Batch records go well beyond compliance—they highlight where our people have spotted signs of off-spec product days or weeks before quality control would have flagged it by numbers alone. Tank operators, with years on the floor, walk us through subtle changes in product feel, slight discoloration, or even foaming patterns on stirring. That kind of vigilance has brought our reject rate for benzofuran intermediates far below what we encountered a decade back.
On customer calls, we share these lessons. Chemists often ask where batch differences show up. Sometimes, older samples from other sources give inconsistent NMR readings because of batches with small levels of peroxidation. We work to prevent this by tuning inert gas blanketing on every fill, not just bulk containers. Every material moving through our chain gets tracked, from drum to decanting, to maintain a chain of custody that serves more than just paperwork—it keeps users confident that what shows up on their bench matches what we made in plant.
Material purity comes up in every project meeting. At our facility, we use a suite of analytical tools—NMR, mass spectrometry, UV-Vis, and HPLC—to confirm that our 2,3-Dihydro-1-Benzofuran-5-Ylmethanol measures up batch over batch. The team tuning these instruments has worked on hundreds of runs, so they catch low-level impurities that might slip through basic screening. Purchasers running sensitive downstream chemistry know to compare peaks with standards rather than trusting limits set in old catalogs.
Solvent handling sometimes takes more attention than reaction chemistry itself. Residual pyridine, DMF, or trace acid leftover from synthesis can interfere with downstream reactions, so we maintain active washing protocols and keep solvent trays under scrutiny. This drives analytics to focus on not just main peaks but minor ones that history shows might cause later crystallization or reactivity hiccups during your own workup.
For delivery, we set containers to fit downstream use. Customers running bench-scale reactions need less packaging fuss, so small glass bottles get lined, capped, and double-sealed. Bulk users working on pilot synthesis rely on metal drums or lined kegs that get flushed, dried, and packed under nitrogen. These details emerge not in boardrooms, but on the filling lines, where a single crack or gasket failure can spoil an otherwise fine synth.
Every new customer request opens a fresh window into how this molecule serves different fields. Pharmaceutical developers talk through key controls for impurities at the alcohol position, while academics doing structure-activity relationship studies might need help scaling a method that works at 50 mg up to 50 grams. Over the years, conversations flagged a recurring issue: certain downstream derivatizations produce polysubstituted byproducts if trace oxidant remains from upstream processing. Our staff helps troubleshoot these, pulling from years running small-lot derivatizations or analytic re-checks to get clean outcomes.
For companies focusing on green chemistry, this molecule’s roots in benzofuran chemistry suggest alternatives to more cumbersome synthetic routes involving heavy metals or chlorinated reagents. We support such teams by providing certificates made possible by our own process audits, not by outside consultants or generic certificate programs. The result: project chemists see less cross-contamination and more predictable behavior in their own reactions, and troubleshooting doesn’t require deciphering a maze of third-party standards.
Working directly with fragrance chemists, we have seen the import of subtle off-notes emerging from trace isomers. Teams benchmarking aroma profiles feed back which samples best align with their desired olfactory notes, then we refine purification. In one case, a global firm traced a recurring taint in their blend to an impurity at less than 0.2%. Because our facility already had split-batch chromatography set up, delivering a tailored cut in the next production cycle required only internal cross-checking, rather than outsourcing—and cut both downtime and cost.
Direct experience drives upgrades. Where older plants often ran a fixed recipe, we tweak our own synthesis, extraction, and workup processes month by month. Switching to more gentle drying at key steps preserved both yield and stability. Adding additional inline pH meters ahead of crystallization flagged early changes due to microcontaminants, which once eluded the best off-line titration. Our internal logbooks point to reduced spike occurrences for peroxidation since tightening inert atmosphere requirements at the fill stage.
Operator retention matters. Chemists and process team members who have seen hundreds of controls in action notice the smallest trend—a slightly hazier Mother Liquor or barely off-color flake in the filter cake. Management keeps open communication with operators on every shift, holding debriefings after each run. Learning and safety move together. We run regular cross-training on emergency response not because regulations demand it, but because past incidents have shown the value of muscle memory and clarity under pressure, especially with higher volumes coming through the plant.
Supply chain shocks can throw off any manufacturing process, but we saw the greatest improvements in quality by locking core input vendors for precursors rather than shopping for spot purchases. Tracking every shipment’s certificate and batch code is not glamorous, yet it’s the difference between a rework day and a release day at the plant. Customers note faster confirmation of lot traceability on their end, which has led to growing requests for direct sourcing instead of blends provided by brokers. Sourcing direct brings peace of mind, especially for teams meeting higher GMP or research reproducibility standards.
Synthetic chemists regularly share pain points caused by off-quality intermediates. Reactive alcohols sometimes pick up atmospheric CO2 or trivial contaminants, ruining groups downstream. We’ve learned to anticipate these issues by optimizing every step from reaction quench to final filtration, so downstream project chemistry runs remain on schedule and fewer setbacks pop up late in a campaign.
For materials manufacturers, concerns about trace metals—particularly iron or copper—shape which purification and filtration procedures we run. Blind spots in quality checks can result in random catalytic activity, especially when customers run transition metal-catalyzed cross-coupling or similar chemistry. As a result, we set up periodic targeted screening for nickel, iron, copper, and zinc, then adjust filtration or chelation based on what emerges. This practical trouble-shooting means less downtime for formulators or process engineers who depend on consistent starting material.
Shipping and handling errors remain an ongoing reality, but years of tracking have allowed us to overhaul protocols so that product arrives unscathed. Air- and moisture-tight seals, shock-resistant containers for global routes, and climate-controlled staging all keep quality steady. Insights from operators and shipping managers who have unpacked compromised loads now inform packing training for newer staff.
Scaling up to hundreds of kilograms presents challenges distinct from small-batch lab runs. Reproducibility, even more than in minor lots, sets the tone for both our ongoing R&D as well as our day-to-day manufacturing cycles. We prioritize run-throughs that simulate both ideal and less-than-ideal conditions—operators cycle through runs using recycled solvents as well as fresh charge, so everyone recognizes the feel of both best-case and realistic batches.
Many customers serve regulators who want comprehensive data on the entire lifecycle of intermediates. Our lab team, linked with our process staff, updates full logs for every lot—from raw material intake, through process monitoring, to post-release tracking. Knowledge transfer often occurs not through memos, but from post-production discussions over results, allowing for subtle issues to be flagged early.
Bespoke requests arise from advanced R&D teams. To support them, we re-run analytics on archived samples, check shipping protocols on one-off sample sizes, or arrange staggered deliveries to align with project timelines. Because every member of our staff from synthesis to warehousing participates in these requests, even the most unusual compliance or technical queries get addressed without burdening a single project chemist.
Direct feedback from those who rely on pure, predictable intermediates motivates our approach to 2,3-Dihydro-1-Benzofuran-5-Ylmethanol. Having operated the synthesis, managed the plant, and tested the output, there’s no substitute for the real knowledge gained from both successes and setbacks. Material from a convoluted supply chain rarely brings this assurance. Every hour on the floor shifts our perspective—feedback loops are shorter, and fixes happen in days rather than quarters.
Industry-wide, too many teams still settle for resold, gray-market, or blended benzofuran intermediates, only to find that one batch doesn’t react, crystallizes poorly, or produces unsupportable assay numbers. As direct manufacturers, we serve those whose projects depend not just on basic compliance, but on real outcomes. The thicker the partnership and the shorter the distance between operator, QC, and end-user, the smoother the project runs.
Bringing together years of plant experience, feedback from the field, and continuous technical refinement, we continue to craft 2,3-Dihydro-1-Benzofuran-5-Ylmethanol that stands apart for its reliability and fitness for use. We believe close connections between maker and user drive both innovation and safety, ensuring the molecule continues to open new doors in research, industry, and product design.