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HS Code |
414196 |
| Chemical Name | 5-Tert-Butyl-2-Methylfuran-3-Carboxylic Acid |
| Cas Number | 93477-04-6 |
| Molecular Formula | C10H14O3 |
| Molecular Weight | 182.22 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 118-120°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥97% |
| Structure | Furan ring with tert-butyl at position 5, methyl at position 2, and carboxylic acid at position 3 |
| Storage Conditions | Store at room temperature, protected from light and moisture |
| Inchi | InChI=1S/C10H14O3/c1-7-6-8(10(11)12)13-9(7)5-10(2,3)4/h6H,5H2,1-4H3,(H,11,12) |
| Smiles | CC1=CC(=C(O1)C(=O)O)C(C)(C)C |
| Synonyms | 5-tert-Butyl-2-methyl-3-furoic acid |
As an accredited 5-Tert-Butyl-2-Methylfuran-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g chemical is supplied in a sealed amber glass bottle, labeled with the name, CAS number, and safety information. |
| Shipping | 5-Tert-Butyl-2-Methylfuran-3-Carboxylic Acid is shipped in tightly sealed containers, protected from light and moisture. Standard chemical shipping protocols are followed, including appropriate labeling and hazard documentation. The package should be handled with care, avoiding exposure to heat or ignition sources, and transported according to local, national, and international regulations. |
| Storage | **5-tert-Butyl-2-methylfuran-3-carboxylic acid** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Store at room temperature or as recommended by the supplier. Ensure proper labeling and prevent exposure to excessive heat or direct sunlight. |
Applications of 5-Tert-Butyl-2-Methylfuran-3-Carboxylic Acid in Industrial Manufacturing5-Tert-Butyl-2-Methylfuran-3-Carboxylic Acid serves as a high-value intermediate in several advanced manufacturing streams. Our facility produces this compound under strict quality control to support specialized chemical synthesis in industries driven by innovation and regulatory compliance. Below, we detail key application areas supported by documented industrial practice. 1. API Intermediate for Oncology Drug SynthesisPharmaceutical producers use this material as a building block in synthesizing advanced heterocyclic compounds with antitumor activity. It enables site-specific functionalization in complex organic synthesis schemes underpinning active pharmaceutical ingredients (APIs) for targeted therapies. Production teams incorporate the compound at the cyclization stage, allowing precise control of side-chain architecture required for patent-protected molecules. Industry compliance standards
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2. Functional Monomer for Specialty PolyimidesHigh-performance polymer manufacturers implement this acid derivative as a functional monomer modifier in polyimide synthesis. Its branched alkyl group introduces bulk and improves heat deflection properties in insulating films and molded parts. The raw material supports batch and continuous imidization processes for specialty dielectric and mechanical materials in electronics. Industry compliance standards
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3. Precursor for Agrochemical SynthesisCrop protection manufacturers employ our compound as a precursor in the synthesis of novel substituted furan compounds with herbicidal and fungicidal properties. Integrators optimize carboxylic acid reactivity for selective esterification and amide coupling to achieve crop-specific performance under regulated residue limits, meeting market demand for innovative actives. Industry compliance standards
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4. Advanced Material for Organic ElectronicsManufacturers developing high-mobility organic semiconductors utilize the acid as a precursor for tailored conjugated polymer synthesis. Its steric and electron-donating effects fine-tune charge transport properties in thin-film applications. Solid-state device fabrication integrates the compound for advanced OTFT, OLED, and sensor architectures demanding precise compositional control. Industry compliance standards
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Generations of organic synthesis have taught us one consistent lesson — reliability springs from experience, repetition, and a strong focus on process. Crafting 5-tert-butyl-2-methylfuran-3-carboxylic acid requires more than following a recipe; each batch draws from a blend of laboratory insight and large-scale practice. Instead of treating our product as just another chemical, we see it as a result of countless individual steps, decision points, and technological advances in heterocyclic chemistry.
The essence of the compound lies in its structure: a furan ring stabilized with both a tert-butyl and a methyl group, anchored by a carboxylic acid function at the 3-position. This arrangement goes beyond simple molecular assembly. We’ve run these reactions at all scales — from gram reactions under glass, to kilo-scale transformations in jacketed reactors. Each iteration taught us more about controlling temperature, pressure, and the reactivity of furan intermediates, all while ensuring that the sensitive carboxylic acid group remains unaltered and accessible.
Crystallization forms a pivotal stage in our manufacturing process, sharpening both purity and consistency. Users working downstream, whether in pharmaceutical research or advanced materials, often report that the reliability of our carboxylic acid form cuts down on separate purification steps, saving time and resources. Our product’s distinct melting point, spectral profile, and physical appearance come from this rigorous hands-on process, not from a third-party intermediary.
Years in the lab have shown that 5-tert-butyl-2-methylfuran-3-carboxylic acid holds strong appeal for those seeking aromatic substitution patterns differently than pyrroles, thiophenes, or simple furan acids. The alteration at the 5-position with a tert-butyl group offers extra steric bulk, a feature chemists often value when pushing reactions away from undesired oxidation pathways or tailoring molecules for biological screening. In straightforward coupling or amidation reactions, the methyl and tert-butyl groups help shield the furan core. This can limit side reactions, drive selectivity, and ultimately impact yields.
More than one industrial partner has noted the speed and reproducibility with which this acid incorporates into their target molecules, particularly in the synthesis of intermediates for active ingredients. The carboxylic acid group offers versatility — easily forming esters, amides, and other derivatives without the risk of furan ring opening, a problem sometimes encountered with less stabilized analogues.
After decades working with the furan scaffold, we’ve dialed in our operating windows. Our typical product comes as a crystalline solid, its stability confirmed through repeated cycling and long-term storage tests. Infrared and NMR analyses nailed down batch-to-batch reproducibility. The melting point consistently falls within a narrow expected range; water pickup and loss assessments ensure little deviation over transit and storage. Technical personnel and purchasing managers both rely on measured lot data, presented without hype or guesswork, to inform their own quality systems.
Yet chemistry doesn’t stop at the certificate of analysis. Real samples, representative aliquots drawn from the main lots, go out for customer evaluation before full shipments. Feedback from formulation chemists and lead optimization specialists drives process improvements. If a batch drifts from specifications, real-time corrections — not batch rejection — define our response. Our catalysts, solvents, and glassware get tracked and cleaned with a directness that sidesteps theoretical promises and focuses only on practical outcomes.
With every order and conversation, direct users highlight specific needs met only by this acid. Practitioners choose it not for branding but for concrete performance advantages. Unlike basic furan-3-carboxylic acid, which can succumb to addition reactions at unprotected positions or display unpredictable reactivity during further derivatization, the tert-butyl and methyl groups on our molecule create a much tougher, less reactive background. Less byproduct, fewer incompatibilities, and a tighter focus on the intended transformation — that’s the difference felt in the flask and at scale.
Other aromatic acids, such as benzoic or pyridine carboxylic derivatives, lack the same set of electronic and steric properties. We’ve repeatedly seen that substitution with tert-butyl provides both solubility in common organic solvents and a degree of crystalline order which aids in filtration and drying steps. Methylation at the 2-position, on the furan ring, also tunes the electron distribution. As a result, acyl chloride formation and subsequent couplings proceed with fewer surprises, and purification steps are more straightforward for many end users.
No chemical manufacturing process escapes periodic scrutiny, process deviations, or supply chain complexity. For this molecule, the biggest technical challenge comes from sourcing high-purity precursors and controlling the oxidation of the furan — a ring notoriously sensitive to both air and light. In our reactors, we’ve invested in oxygen-scavenging technology and made use of closed system reactors, minimizing exposure. Operators check intermediates using on-line spectroscopy, so process interruptions get flagged early.
Scale-up sometimes exposes unseen bottlenecks; heat transfer and mixing, easy at bench scale, can go awry in a hundred-liter setup. To combat uneven temperature gradients or precipitation in transfer lines, we’ve installed redundant in-line temperature sensors and custom agitation systems. Each improvement reflects not just engineering inputs, but also the feedback from colleagues tasked with scraping crystallizer filters in real time.
Product loss at any stage — from overnight drying to long-distance shipping — translates into real cost. Seal integrity and packaging type matter as much as the chemistry within. We shifted away from porous liners to screw-top lab jars, confirming with shipping simulations that product reaches the customer as a free-flowing crystalline powder, not compacted or degraded by transit humidity.
Chemical safety forms a thread that winds through every batch. Our in-house team trains not just on regulatory rules but also on hands-on control of volatile intermediates and neutralization of byproducts. Whether for an internal batch or a shipment overseas, documentation meets regional safety requirements — not with empty legal language, but practical data for safe handling. Customers and regulators alike want traceable lot history and manufacturing transparency. We give them both, from raw precursor origin all the way through to post-packaging residue checks. The goal: no surprises for the lab tech receiving the product, or the shipping specialist handing it off.
Feedback loops drive progress. Ongoing collaborations with pharmaceutical clients, agrochemical start-ups, and research departments deliver sharper insights every quarter. We set up pilot projects where clients openly report any process hiccups, helping us tweak our operations. For example, one development group needed a larger batch for early toxicology screening and struggled with re-dissolving the acid in their chosen solvent. A direct exchange of samples and technical notes led us to pre-mill a portion of the batch, adjusting particle size for their workflow, without broad changes to our full production stream. The responsiveness typical of research-scale manufacture now finds a seat at our larger reactors, blending adaptability with consistent output.
Researchers using 5-tert-butyl-2-methylfuran-3-carboxylic acid often aim to create target molecules featuring complex substitution patterns impractical using standard aromatic acids. Customization starts with our ability to control substitution purity at the starting material level and tracks through to the delivery of a product tailored for advanced downstream chemistry — whether amide coupling, esterification, or a protected derivatization step.
Transparency in manufacturing isn’t a catchphrase, it’s a daily obligation. Customers increasingly seek more than basic data or technical guarantees. From the origin of starting materials to the specifics of our quality controls, we document every significant variable in the process. Our laboratories publish real chromatograms and spectra to guide user QC, not just summaries lifted from generic texts. If a customer reports an anomaly — say, an unexpected melt or off-odor — we pull retained samples and run side-by-side analytics.
We’ve invested in IT infrastructure linking site operations to order tracking and customer service, taking the guesswork out of order timing and delivery. Customers receive pre-shipment notifications, documentation, and — when requested — access to our in-house technical support team, who are trained not just in sales, but in the underlying chemistry.
Producing heterocyclic acids at scale does create waste streams and resource consumption. Our engineers and chemists work together on process intensification, solvent recycling, and byproduct minimization projects. Where industry tolerates 95% yields, we push further through small-batch trials, product work-up modifications, and real solvent reuse. Over the past five years, process emissions dropped by more than a quarter following switchovers to closed-system distillation and targeted filtration upgrades.
A push for greener chemistry motivated a change from heavy-metal-based catalysts to alternative, more benign transition metal systems. While initial adoption incurred higher raw material cost, downstream benefits in waste reduction and workplace safety soon vindicated the extra investment. Internal audits and emerging customer questions about chemical traceability only prioritized such changes — not as buzzwords, but as part of daily progress.
Despite the complexity, those of us involved in manufacturing 5-tert-butyl-2-methylfuran-3-carboxylic acid prefer a straightforward approach: candid communication, data-driven support, and a constant willingness to adapt. Whether you run a kilo-scale campaign for a pilot program or test new routes on the benchtop, our experience forms the foundation of a dialogue rooted in actual production, not theoretical marketing.
We encourage partners to ask hard questions, request samples, and walk through the process as closely as practical. Each bottle reflects both scientific detail and real-world flexibility. Order cycles, batch retention, and quality verification all get the same scrutiny, regardless of project size. As chemical professionals, we stand ready to meet your process needs, answer technical questions with clarity, and continue to refine a product that others may treat as a mere catalog item. Our legacy comes not from one-liner product listings, but from years of hands-on trial, technical dialogue, and honest feedback.
In the years since rolling out commercial production of 5-tert-butyl-2-methylfuran-3-carboxylic acid, we’ve worked through evolving regulatory requirements, shifting customer priorities, and a growing commitment to laboratory safety. Each improvement was informed by experiment, not speculation, and by long-term relationships with demanding customers. Whether supporting pharmaceutical discovery, new material synthesis, or specialty intermediate production, our commitment is grounded in those daily incremental gains and shared experience.
As the field of chemical development continues to grow and adapt, we recognize our own role not just as a supplier, but as a participant in your research and production story. We invite current and prospective users to share process insights, challenge our assumptions, and partner on specific improvements — all toward making the most of a unique, versatile molecule whose value emerges most clearly in active use. Our promise: no shortcuts, open exchange, and a continuous focus on tangible performance.