Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

5-Formylfuran-3-Boronic Acid

    • Product Name 5-Formylfuran-3-Boronic Acid
    • Alias 5-Formylfuran-3-boronic acid
    • Einecs 831-740-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    963443

    Product Name 5-Formylfuran-3-Boronic Acid
    Cas Number 848184-24-5
    Molecular Formula C5H5BO4
    Molecular Weight 139.91 g/mol
    Appearance Off-white to light yellow solid
    Purity Typically ≥95%
    Smiles B(C1=COC=C1C=O)(O)O
    Solubility Soluble in DMSO, DMF
    Storage Temperature 2-8°C (refrigerated)
    Synonyms 5-Formyl-3-furanylboronic acid
    Chemical Class Furan boronic acid derivative

    As an accredited 5-Formylfuran-3-Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Formylfuran-3-Boronic Acid, 1g, supplied in a sealed amber glass vial within a protective screw-cap container, labeled with hazard information.
    Shipping **Shipping Description for 5-Formylfuran-3-Boronic Acid:** 5-Formylfuran-3-Boronic Acid is shipped in tightly sealed containers under an inert atmosphere, protected from moisture and light. It is packaged with cushioning materials to prevent breakage. All packages comply with relevant chemical transport regulations, with necessary labeling for safe handling and prompt delivery. Safety datasheets are included.
    Storage 5-Formylfuran-3-boronic acid should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry place, preferably in a refrigerator (2–8°C). Protect the compound from light and incompatible substances, such as oxidizers, to maintain its stability and purity.
    Application of 5-Formylfuran-3-Boronic Acid

    Applications of 5-Formylfuran-3-Boronic Acid in Industrial Manufacturing

    As a direct manufacturer of 5-Formylfuran-3-Boronic Acid, we supply this specialty boronic acid to downstream producers in high-value segments where its unique functionalities are essential for targeted synthesis and advanced intermediate formation. The following application scenarios reflect established, real-world uses based on industry-accepted processes and standards.

    1. Pharmaceutical API Intermediate Synthesis

    5-Formylfuran-3-Boronic Acid serves as a crucial building block for Suzuki-Miyaura cross-coupling in the multi-step synthesis of innovative heterocyclic drugs, particularly within anti-infective and CNS drug pipelines. Downstream pharmaceutical manufacturers incorporate this compound at the aldehyde stage to facilitate C–C bond formations, supporting diversification of functional groups while adhering strictly to regulatory compliance, batch-to-batch analytical traceability, and impurity profiling.

    Industry compliance standards

    • ICH Q7 Guidelines on Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP / EP / JP monographs for intermediates and APIs
    • 21 CFR Part 211 U.S. cGMP for finished pharmaceuticals
    • EDQM CEP and Drug Master File (where applicable)

    Typical usage ratio

    • Employed at 0.7–1.3 molar equivalents relative to halogenated aromatic substrates in coupling steps; dosage tailored using in-process HPLC analysis for minimal excess reactant.

    Downstream process integration

    • Added during the Suzuki coupling or related palladium-catalyzed cross-coupling stage following prior halogenation of a substrate, most often after solvent swap or crystallization steps to ensure phase compatibility.

    Final product types

    • Non-pyrazole heterocyclic active pharmaceutical ingredient intermediates
    • Advanced CNS or anti-infective drug candidates
    • Specialty pharmaceutical building blocks

    2. Fine Chemical Synthesis for Functionalized Furan Derivatives

    Producers of advanced electronic chemicals and photoinitiators utilize 5-Formylfuran-3-Boronic Acid to construct functionalized furan derivatives, which demand precision in purity and consistent aldehyde group reactivity. This material enters processes that require controlled boron chemistry, producing intermediates crucial for next-generation materials used in device fabrication, OLEDs, and light stabilization.

    Industry compliance standards

    • ISO 9001:2015 quality management systems for specialty chemical manufacture
    • REACH (EC) No. 1907/2006 registration for non-pharma downstream applications
    • SEMI standards for electronic material purity
    • Internal corporate raw material purity specifications (minimum 98% GC/HPLC)

    Typical usage ratio

    • Used at 2–5 wt% in furan ring-functionalization reactions; ratio adjusted based on analytical monitoring of limiting reagents to balance cost and conversion rates.

    Downstream process integration

    • Introduced during the C–C or C–O coupling reaction phase, typically following pre-activation of coupling partners, under inert atmosphere to ensure boronate stability throughout the process chain.

    Final product types

    • High-purity photoinitiator intermediates
    • Conductive and charge-transport furan derivatives
    • OLED precursor chemicals

    3. Agrochemical Active Ingredient Development

    Agrochemical R&D and manufacturing facilities employ 5-Formylfuran-3-Boronic Acid as a core intermediate in the elaboration of boron-containing and furan-functional crop protection agents, especially for the structure-activity optimization of new herbicidal and fungicidal candidates. The boronic acid moiety introduces selectivity and binding efficiency, while the formyl group enables further derivatization under mild conditions.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials and formulations
    • ISO 17025 accreditation for agricultural testing laboratories
    • Regulation (EC) No. 1107/2009 on the marketing of plant protection products
    • OECD TG 417 & 420: chemical safety and toxicology assessments

    Typical usage ratio

    • Applied at 0.5–1.2 equivalents to the primary aryl halide for diversifying agrochemical leads; precise ratio determined by route scouting and toxicological profile optimization.

    Downstream process integration

    • Fed into the key coupling stage following core skeleton assembly—usually after acylation or oxidative transformation, bridging to boron coupling chemistry for scaffold diversification.

    Final product types

    • Novel herbicidal and fungicidal pre-active intermediates
    • Regulatory submission samples for agrochemical registration
    • Reference standards for metabolic fate studies

    4. Material Sciences: Advanced Polymeric Structures

    In material science laboratories and specialty polymer manufacturing, 5-Formylfuran-3-Boronic Acid acts as a monomeric or crosslinkable functional group source for developing boron-infused, furan-based specialty polymers. Its dual functionality provides sites for condensation polymerization and subsequent modification, supporting the design of advanced materials with enhanced chemical resistance or electronic properties.

    Industry compliance standards

    • ASTM D638 and D882 for mechanical property testing of films and plastics
    • ISO 14001:2015 environmental management standards in polymer production
    • RoHS (2011/65/EU) compliance for electronics-related polymers
    • Customer-specified purity and residual monomer thresholds

    Typical usage ratio

    • Used at 1–10 mol% as a functional co-monomer in polycondensation; loading rate set according to desired crosslinking density and property profile in the resulting copolymer matrix.

    Downstream process integration

    • Charged during the initial monomer blending and pre-polymerization step, ensuring direct incorporation into the backbone or side-chain structures; post-polymerization modification possible under controlled oxidation or reductive conditions.

    Final product types

    • Boron-modified aromatic polyesters
    • Electronically active furanic copolymers for sensors and flexible electronics
    • Chemically resistant polymer resins for specialty coatings

    5. Organic Synthesis R&D and Reference Material

    Academic and contract research laboratories employ 5-Formylfuran-3-Boronic Acid for mechanistic studies, method development, and standardization applications, particularly where controlled aldehyde and boronate chemistry is required for calibration, kinetic studies, or structure elucidation within analytical and synthetic organic chemistry.

    Industry compliance standards

    • GLP (Good Laboratory Practice, OECD Principles)
    • ISO/IEC 17025 for reference material quality
    • Institutional research safety and chemical inventory protocols

    Typical usage ratio

    • Applied at stoichiometric or sub-stoichiometric amounts (0.1–1.0 eq.) depending on the experimental design, typically scaled from milligram to multigram quantities.

    Downstream process integration

    • Used as a starting material or standard in reaction sequence benchmarking, mechanism elucidation, and analytical method validation, often dissolved in dry DMSO, THF, or DMF immediately before use to control reaction conditions.

    Final product types

    • Custom reference standards
    • Synthesized calibration solutions for HPLC/GC-MS
    • NMR and FTIR characterization samples
    Free Quote

    Competitive 5-Formylfuran-3-Boronic 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Insight into 5-Formylfuran-3-Boronic Acid: A Manufacturer's Perspective

    Experience Behind the Synthesis

    Day in, day out, we handle the chemistry behind complex organics, and few compounds have stirred as much industry buzz as 5-Formylfuran-3-Boronic Acid. Manufactures who see beyond conventional reagents notice the quiet potential in furan-based boronic acids. Decades on the production floor have taught us to judge both purity and process friendliness, not just basic chemical specs. This molecule stands out because of the unique furan ring, which brings a new level of reactivity and compatibility.

    Our own processes emphasize strict moisture control and clean, oxygen-free conditions. The real trick comes from the boronic acid group—we have to ensure both the aromatic ring and the acid function stay intact. That balance doesn’t always come easy, and producers who fail to account for batch size or inconsistent reaction temperature see the yields take a hit. Consistent product comes from time spent tweaking, not just following textbook routes.

    On Specifications and Consistency

    Across our production halls, the eyes of chemists focus on every gram. We start by vetting raw furan materials to eliminate potential aldehyde impurities up front. High-performance liquid chromatography keeps us honest—there’s no shortcut here, every batch gets full spectra trawling. Typical purity ranges upward of 97%, though some syntheses push above 99% when downstream applications demand it.

    Moisture content causes headaches if left unchecked. That’s especially true since boronic acids display sensitivity and form boroxines if storage conditions slip. We always keep final dried product under argon in sealed amber bottles, guarding against the subtle but steady degradation you get under ordinary air.

    Particle size distribution can quietly disrupt customer reactions. We have seen that careful recrystallization, combined with precision drying, leads to both manageable powders and smoother weighing on the bench. While these details seem minor, process engineers spot the difference the first time they move from bulk drum to pilot vessel. The powder flows without caking and disperses easily—our staff have spent enough hours scraping clumped intermediates to appreciate the impact.

    Usage Based on the Demands of Modern Chemistry

    Years working with researchers in pharmaceutical and materials science have given us a front-row view of 5-Formylfuran-3-Boronic Acid’s practical strengths. Its real value becomes clear in Suzuki-Miyaura coupling reactions—this boronic acid brings a rare combination of electronic activation with a flexible furan core. Med chem teams notice that the furan-aldehyde motif enables rapid structure-activity exploration along new chemical space, letting lead optimization move faster.

    Developers in solar materials and organic electronics seek out aromatic boronic acids, but our experience has shown that furan-based variants behave differently from simple phenylboronic acids. With 5-Formylfuran-3-Boronic Acid, conjugation through the furan ring can enhance electron mobility and stability in finished devices—a claim supported both by peer-reviewed studies and feedback from research consortia we support directly through material grants.

    Incorporating this compound into existing synthetic routes often needs careful pH control and deoxygenated solvents to avoid side reactions. We’ve noticed that automated liquid handling systems benefit from stable, dry product—the ingredient doesn't sludge up lines or settle unpredictably in storage silos. Projects that scale from bench to plant run smoother since the material resists moisture and stays free-flowing under controlled environments.

    Comparing Subtle Chemistry: What Sets This Compound Apart

    The chemical market is awash with standard boronic acids, yet few meet the subtle requirements of both process chemistry and innovative design. Many request phenylboronic acid initially, only to find the electronics just don’t deliver for advanced pharmaceutical routes or next-generation polymers. Our team has repeatedly seen clients switch mid-stream after early-stage testing. With 5-Formylfuran-3-Boronic Acid, the electron-rich furan not only makes couplings more efficient under mild conditions but also introduces structural motifs nearly impossible with benzene-based analogues.

    In trying to substitute with other compounds, some attempt using 2- or 3-substituted furanyl boronic acids. Yet only the 5-formyl variant offers the right balance. Synthetic chemists appreciate that the aldehyde functionality unlocks further downstream derivatization. We’ve fielded many calls from process teams needing orthogonally protected aldehyde sites, and this molecule answers that challenge efficiently. In our hands, its stability remains superior during both transport and bench work—the boronic acid group does not hydrolyze prematurely, given tight control during synthesis and storage.

    Having seen the entire lifecycle—from reaction planning, dried solid transfer, to post-synthesis workup—the practical benefits go further than abstract structure. Where others deal with inconsistent off-white clumps or pungent odors from poor handling, we provide a reliably crystalline product with low residual solvent. These differences matter out in the plant or in automated laboratories, avoiding both reprocessing and extra QC testing.

    It isn’t simply about purity testing on paper. Some competitors overlook the loss-on-drying stage and ignore microcontaminants. Over time, customers report failed couplings or trouble in scale-up, leading to higher costs and downtime. The extra work we put in with clean inert transfers and batch-level feedback loops becomes visible downstream, saving whole projects from last-minute troubleshooting. None of this comes easy; it flows from ongoing effort, not wishful thinking.

    Working with End Users: Lessons from Real Applications

    Over years, our technical support has walked end users through transitions from commodity products to this targeted boronic acid. Synthesis chemists testing new heterocyclic drugs asked for advice on scale-up—not just how to stir or filter, but which apparatus fit best with our powder’s granularity. Materials scientists developing furan-based oligomers for organic LEDs needed feedback on the best dissolution routine and what solvent systems matched the product’s solubility profile.

    In a prominent example, one customer struggled with batch inconsistency from a competing supplier. Their automated peptide synthesizer suffered from inconsistent pickup rates due to unpredictable clumping. Our switch led to normalized batch yields and steadier spectral purity after installation of our tight-seal packaging. Such challenges rarely show up in literature, but we track feedback and adapt. From improved drum liners to vacuum-sealed sachets for smaller research lots, we make handling easier for operators who spend hours at the bench.

    In the world of pharmaceuticals, minor impurities can derail an entire clinical program. We invest in round-table discussions with R&D leaders to keep contaminant limits tight. Dissolved oxygen monitoring and inline pH adjustment systems grew directly out of these conversations; practical changes matter more than theory alone. This direct link between plant floor experience and end user needs sharpens every run and every batch inspection report.

    Addressing the Big Challenges

    One recurring issue in boronic acid chemistry is shelf life. Too many stories circulate about degraded lots from bulk shipping or unsealed store rooms. Boroxine formation wrecks batch consistency, introduces unwanted byproducts, and can clog filters during reaction workup. Our production team responded by refining moisture monitoring and switching to higher-barrier packaging. These changes, raised during bi-weekly staff meetings and confirmed through stability trials, reduce frustration downstream. While some insist that boronic acids must be used quickly after purchase, our practice shows that careful preparation gives a longer usable window, often stretching several months past industry standard.

    Extraction and post-reaction workup often introduce impurities not visible on initial testing. Rigorous cleaning of glassware and solvent selection, paired with our low-residual solid, minimize loss and reprocessing cycles. Scaling up from grams to multikilograms reveals bottlenecks others might ignore at small scale. Steam lines, dust controls, and solvent recovery all see attention during tech transfer—cutting corners just passes trouble down the chain. Our internal troubleshooting checklists, formalized over many projects and pilot campaigns, bring these problems to light ahead of customer complaints.

    Working closely with upstream suppliers means fewer unwanted trace metals make it into high-value pharma runs. A run with substandard boronic acid risks downstream purity failures—each rework or disposal affects both cost and environmental impact. We reached out to campaign partners in raw material supply, setting stricter specs and regular audits, driving out inconsistent batches that lead to ‘surprise’ trouble months later.

    Supporting Next-Generation Innovation

    Academic partners push the limits of molecular design, and we supply them with reliable lots for one-off syntheses in medicinal chemistry. Several grant-funded labs have credited the furan-aldehyde motif’s compatibility for their ability to reach new heterocycles or macrocycles. Importantly, our technical notes come from lab-grown knowledge, built over years as we watched which routes handled scale-up better or allowed easier purification.

    Device manufacturers building on organic thin-film transistors learned, after some failed attempts, that the furan core’s electronic properties only shine when starting materials haven’t seen a moisture dip or acid contamination mid-shipment. To this day, our feedback from a major OLED startup keeps us testing small modifications: tweaks in crystal habit, shifts in solvent combinations, changes in post-drying atmospheric conditions. These constant improvements enable new functional coatings and advanced catalysts, responding quickly to shifts in technology demand.

    Patent activity globally now tracks new compounds built from well-characterized boronic acids. Our insights, gathered from close feedback with small-molecule drug developers and electronic material teams, make clear that new motifs succeed only when starting materials behave as expected. It takes more than shipping a drum and sending an invoice; the collaboration from sample R&D up to commercial scale launches depends on reliable support, answering late-night process questions, and troubleshooting obscure lab headaches as they arise.

    Manufacturing with Purpose: Beyond the Label

    Chemical manufacturing is more than a matter of filling orders and printing certificates. We see outcomes in every recertification request and every customer phone call looking for help after hours. The challenges of 5-Formylfuran-3-Boronic Acid production pushed us to rethink plant layout, drying cycles, even the way we plan storage expansions. The product doesn’t just flow from a production scheduler—it shapes the way the team manages scheduling, equipment cleaning rotas, and downstream logistics planning.

    Even the smallest handling decisions—choice of container, timing between drying and sealing, or checks on cap tightness—ripple out to the end user. It takes time and hard lessons to recognize which details end up influencing whether a research campaign succeeds or fails. Each time we pilot a new batch, the process team doesn’t just mark off a list: they watch for minor shifts in powder flow, test for unplanned polymorphs, and review how every yield change shows up at the kilogram scale.

    We find ourselves troubleshooting right alongside research chemists as their projects progress. From scaling up initial gram samples to supporting continuous runs for production, the needs shift—large drums for plants, tightly sealed vials for discovery labs, intermediate options for mid-stage scale-ups. Our continual dialogue with users drives incremental but meaningful change in how we approach every run, and sometimes the only sign of our improvements comes in a satisfied researcher reporting a seamless coupling or a device team reaching an efficiency milestone months ahead of schedule.

    Driving Improvement, Batch by Batch

    Quality never comes by accident. Our crews begin every production run with a checklist built on the last campaign’s lessons and the latest user feedback. Each shift logs anomalies, tracking real-world changes in product properties. Not every challenge gets solved overnight: at times, shifts in upstream solvent supply force a pivot in handling, or a spike in bulk demand demands re-examination of our drying protocols. Cross-team problem-solving among QC, operations, packaging, and shipping staff remains fundamental, keeping us ready for both sudden surges and routine cycles.

    Failures, too, teach. Moisture intrusion detected through a stray air leak led to overhauling our entire final packaging area a few years back. Incorrect cap choices, identified by observing minor product caking after long transit, prompted a new round of liner evaluations. Even after extensive investment in monitoring and training, fresh challenges appear. Direct, careful attention to each step has become habit, not exception.

    Customer trends never stand still—demands for smaller, preweighed lots or enhanced batch traceability grew from marketplace needs, not internal brainstorming. Annual feedback surveys and open forums with both large-scale and boutique customers give us new ideas each year. By acting on feedback, we help users who really understand how small shifts in chemical handling drive costly project delays or costly instrument shut-downs. The crew behind the tanks and hoods shares in those wins and setbacks, knowing that each improvement carries forward.

    The Real Mark of Progress

    Progress can be subtle, not always dramatic. In our chemical work, switching from generic boronic acids to 5-Formylfuran-3-Boronic Acid introduced more complexity—a cost in time, effort, and training. Yet the stories returning from the field make clear what’s at stake: more robust product at the front line, confident scale-up for new pharmaceutical routes, and smoother development cycles for advanced functional materials. Each change, tested and proven across dozens of runs and through collaboration with both laboratory and production end users, reflects a hard-earned step away from “good enough” toward truly reliable and flexible starting materials.

    The spirit of reliable chemical manufacturing isn’t captured in catalogs or glossy flyers. It comes across in customer notes, late-night troubleshooting calls, and the careful, persistent dedication that brings every lot from raw intermediate to finished, precisely packaged product. 5-Formylfuran-3-Boronic Acid keeps teaching us new lessons—about process control, fine handling, and the vast space of opportunity still to be explored in modern synthesis. For manufacturers and users alike, that’s where the true value lies.