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(2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide

    • Product Name: (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide
    • Alias: Voriconazole impurity 5
    • Einecs: 821-578-9
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: sales3@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    276476

    Iupac Name (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide
    Molecular Formula C13H13F2N5OS
    Molecular Weight 341.34 g/mol
    Cas Number 188416-36-7
    Appearance White to off-white solid
    Melting Point 148-150 °C
    Solubility In Water Slightly soluble
    Smiles CC(C(=O)N)SCC1=NN=CN1C2=C(C=C(C=C2)F)F
    Optical Activity Chiral compound (2R,3R configuration)
    Storage Conditions Store at 2-8°C, protected from light
    Pubchem Cid 10409428

    As an accredited (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled with chemical name and safety information, containing 10 grams of the compound.
    Shipping This chemical, (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide, is shipped in tightly sealed containers, protected from moisture and light. It is transported in compliance with all chemical safety regulations, using appropriate labeling and documentation. Temperature and handling precautions are followed to ensure product stability and safety.
    Storage (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide should be stored in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerator temperature). Ensure the storage area is well-ventilated and away from incompatible substances such as strong oxidizers. Proper labeling and adherence to safety protocols are essential for safe handling and storage.
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    Certification & Compliance
    More Introduction

    (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide: A Direct Perspective from the Factory Floor

    Understanding the Chemical’s Purpose and Real-World Applications

    Inside our own production halls, (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide stands out as a specialty molecule, one we have learned to approach with a level of respect thanks to its unique profile. Unlike the more commonplace building blocks we see in everyday synthetic work, this compound bridges subtlety and function. The presence of the 2,5-difluorophenyl group alongside the triazole moiety gives it a character that drives its use forward in pharmaceutical synthesis, particularly where precision and specific activity profiles are called for.

    Our chemists talk most about the interplay between structure and results. Here, the compound’s two chiral centers unlock opportunities for enantioselective synthesis routes. The result is not just another intermediate, but a useful synthon that can—and does—impact development pipelines for antifungal agents, antimicrobial research, and more advanced chemical discovery efforts. Based on requests from research teams and long-term customers, we know this molecule’s place is most often in the preclinical phase of pharmaceutical development, or in tailored projects for fine-tuning lead candidates.

    What Sets This Compound Apart in Production and Handling

    Integrating two fluorine atoms on the aromatic ring isn’t as trivial as it looks on paper. Fluorination brings about challenges—both in the synthesis phase and downstream handling. Our plant learned this through some hard lessons, adjusting to the right reaction conditions to maximize selectivity and purity while minimizing byproduct formation that comes with poorly controlled halogenation. Having two fluorine atoms on the phenyl group creates a different electron distribution compared to mono-fluorinated derivatives. Over time, batch records reflect this: fewer impurities when you nail down the correct catalyst loads and temperature profiles. Many chemists consider this just another job, but our engineers remind us that controlling those variables separates reliable suppliers from those who just buy and resell stock lots.

    The thioamide motif featured in this structure doesn’t just change reactivity for the sake of academic novelty. In our own blending tanks, we see firsthand how this functional group influences overall solubility and the way downstream protection and deprotection steps unfold. Simple mistakes in timing—adding reagents just a few minutes too early or changing the stirring speed—can mean hours of extra work trying to recover the batch or managing waste streams. This personal experience shapes our process, and we can point to real changes in operational discipline based on feedback cycles between lab and plant floor.

    The Triazole Connection—Industry Trends Meet Daily Routine

    Triazoles have long held a place in pharmaceutical and agrochemical chemistry. The triazole ring in this molecule marks a strategic move, allowing our clients to target a different spectrum of bioactivity. In our conversations with formulation chemists, they point to the inherent stability of triazoles, not just in the theoretical sense but in day-to-day shelf-life concerns and during bioassays. Compared with other five-membered heterocycles, 1,2,4-triazoles like the one here ride that line between reactivity and resilience. It means we often hear fewer complaints about degradation or handling hazards than we did with older imidazole analogs.

    Upstream, assembling the triazole unit isn’t exactly cheap, and some processes generate waste that would be a headache without investment in proper scrubbing equipment and solvent recovery. We bit the bullet on this equipment years ago, after one of our effluent streams failed to meet internal quality benchmarks. No customer cares about that story except when end-use purity starts to slip, or compliant documentation is demanded during regulatory review. Our systems now keep emissions below strict local guidelines—a real-world investment that comes back to us in repeat orders. Keeping triazole residues under control cuts headaches for both our technicians and regulatory affairs team.

    Tangible Benefits and the Production Reality

    From our point of view, working with this compound provides clear advantages for R&D partners and advanced manufacturing programs. Feedback loops help us avoid chasing after impractical yields or tolerating unstable intermediates. The two chiral centers yield enantiomerically pure material when processed using our chiral HPLC separation methods coupled with tight batch monitoring. The difference becomes evident in downstream assays, as our partners routinely meet target activity and pharmacokinetic profiles with fewer surprises. Structural analogs that omit fluorine or swap the triazole for something else tend to miss that sweet spot of balance between reactivity and durability.

    Compared to products like 3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide without difluorophenyl substitution, we see meaningful leaps in chemical behavior during kinetic studies. The partial electron-withdrawing effect of the difluorophenyl group modifies not just activity but also oxidation resistance, impacting not only shelf-life but speed to project milestones. These are not just academic details—orders fulfilled for time-sensitive programs depend on these differences, and our schedule reflects the pressure to deliver reliable product with each cycle.

    Addressing Raw Material & Environmental Challenges

    Securing high-quality starting materials for multi-functional molecules like this one has grown more challenging. Difluorobenzene isn’t always readily available, and prices of feedstock fluctuate based on upstream supply chain disruptions. We maintain relationships with certain fluorine chemistry partners who understand our strict quality expectations. Quality control teams batch-test every lot before it even enters our reactors, having seen too many costly downstream issues from subtle contamination or improper storage in the past. Each impurity, especially those that can’t be tracked by a basic GC method, invites extra cost or makes whole batches unmarketable.

    Our facility doesn’t just think in terms of output but pay close attention to environmental impact. Solvent use, especially in fluorination and triazole formation steps, brings with it responsibility for treatment and recycling. We rely on modern scrubbing units, modular distillation setups, and advanced analytical equipment to confirm discharge is within safe limits. Chemists here double-check plant modifications, sometimes shutting down lines for days just to introduce safer waste-handling protocols or new monitoring tech. This savings repeats over years, as regulatory thresholds become stricter and fines for even minor violations rise. Real-world investments in cleaner production translate into stable partnerships with multinationals who care about sustainability beyond CSR reports.

    Handling and Storing the Compound: What Experience Taught Us

    Years spent moving drums and bags of this product have taught plant teams and warehouse staff that temperature control and clean handling make a tangible difference. The molecule may appear robust on paper, but heat or humidity swings can accelerate hydrolysis or subtle breakdown that a typical user wouldn’t notice until product quality slips downstream. Our process ships out only after passing a battery of in-house and third-party analyses—NMR, HPLC, moisture content, plus repeat chiral purity tests. Storage in climate-controlled facilities, with regular inventory rotation, keeps waste minimized and customer complaints at bay.

    From one memorable incident, we realized even trace cleaning agents left over from a previous clean-in-place cycle reacted unexpectedly with unprotected triazole. Standard operating procedures changed overnight: additional flushes, more frequent swabbing, and trace analysis each month. These changes sound like small things, but they matter. The result has been a drop in off-spec returns and positive feedback from both domestic and export clients with high QA scrutiny. Staff buy-in is high because the link between careful handling and fewer problems is clear and direct.

    Differences That Matter—Direct Comparisons

    Every project starts with a choice: simple structural analogs or value-added specialty products like this one? Our clients who tried less-substituted phenyl derivatives saw that missing fluorines shrink biological windows and drop metabolic stability in animal models. They come back for (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide because it stands up to their toughest studies. Given the trend to design for both potency and ADME optimization, we hear that this scaffold often gets coded into early-stage libraries not just by default, but because it accelerates lead optimization.

    Assessments performed by partner labs confirm that difluoro- functionalization doesn’t just tweak logP or binding profile, but also lengthens half-life and reduces rates of oxidative degradation when compared side-by-side with mono-fluorinated or non-fluorinated relatives. Many off-the-shelf options skip the chiral integrity—producing single racemates or, worse, uncharacterized mixtures. We refuse to cut corners that way. With tools built for rigorous enantioselective production, we provide batches that avoid those pitfalls, translating to cleaner biological data for downstream clients. Our operational transparency gives procurement teams a reason to return beyond punch-list price checks.

    Collaboration, Speed, and Real-Life Impact

    Our team finds that speed of delivery counts as much as purity or documentation. New projects can’t afford six months of waiting, or the logistical headaches that come with shifting sources mid-development. To keep pace, our production line employs both batch and continuous synthesis, shifting capacity up or down based on quarterly forecasts. Personal relationships with vetted logistics carriers matter more than abstract promises—every lost shipment or customs mishap means lost credibility. It’s not uncommon for a member of our technical staff to personally supervise a new client’s first order, walking them through documentation, shipping conditions, and support protocols. The goal is frictionless integration into their workflow.

    Frequent communication between our process chemists and customer R&D teams leads to minor modifications or improvements—sometimes a tweak in crystallization solvent, adjustment to packing, or a new analytic certificate the client’s regulator demands at the eleventh hour. Every such move comes from listening closely, not just pushing stock. Some clients come with rush requests for clinical project deadlines. We slot these into the schedule, mobilizing extra shifts or reallocating reactors as needed. Having walked through last-minute scale-ups and pilot programs, we value honesty about what can be achieved and how delays can be addressed with real solutions—not canned apologies.

    Intellectual Property, Data Integrity, and Trust Built Over Time

    IP concerns weigh heavily on industrial partners. The specific substitution pattern of (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide serves as a safeguard for exclusivity routes in pharma R&D. Our in-house documentation and confidentiality agreements create a shield for our clients’ discoveries. Chain of custody remains airtight from synthesis to shipping. Once, a client flagged data inconsistencies with a competitor’s batch. We opened our own records, cross-checking chromatography and spectral files, finding not only the source of the problem but a faster route to confirming authenticity. This willingness to open the factory books—warts and all—builds trust, leading to contracts that last through shifts in the external marketplace, mergers, and regulatory changes.

    Analytical transparency is part of our company’s DNA. Regular audit cycles, both internal and external, keep the team focused. All deviations are logged and addressed, no matter how minor. Suppliers who can’t step up with robust data integrity documentation rarely last long in our supply chain. We share methods, calibration lots, and certificates without hesitation when requested by our clients, supporting their own filings and project timelines. Every batch that leaves our facility arrives with a paper trail that stands up to due diligence, technical review, or audit—something our partners have come to expect, especially those from regulated markets.

    Continued Investment in Quality at Every Step

    To keep up with demand and regulatory scrutiny, our company invests heavily in quality controls for (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide. From semi-automated reactors allowing precise temperature gradients, to hand-titration points overseen by veteran chemists, small details stack up to make a tangible difference in the outcome. Quality assurance for each lot means more than ticking boxes—it’s a constant interplay of science, gut feeling, and accumulated factory wisdom. During scale-up runs, we see subtle changes in yield and impurity profile, which our analysts spot before issues reach the client.

    Sterility and contamination control receive equal attention. The team learned from a past contamination scare—traced later to a new filter model used by one of our solvent suppliers. We now trace every incoming component, requalifying at regular intervals and updating the SOPs immediately if anomalies emerge. Plant managers prioritize staff retraining and update process manuals when needed, with solutions often coming not from boardroom decisions but from observations made during night shifts or maintenance checks.

    In short, everyone in our company—from line operators to senior chemists—recognizes the interconnected roles we play in delivering this compound reliably. Every credible fact or success story rests on decades of chemicals industry experience, capable hands in synthesis, and openness to improvement.

    Supporting Clients with Solutions that Make a Difference

    For us, supplying (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide has never been about simply filling a catalog line. Partners bring us problems: solubility headaches, processing bottlenecks, or tricky regulatory timelines. Our commitment is to share what we know with those needing real solutions—whether that means an extra analytic test, a customized logistic fix for temperature-sensitive shipments, or the rapid mobilization of technical support when a batch must meet an unexpected deadline.

    Facilities are kept open to visitors—something that has changed the tone of many partnerships. Prospective clients show up to check how we operate, sometimes bringing their own analysts for third-party review. Some have ended up redesigning their own internal handling steps after seeing our in-process controls and documentation. The learning is always two-way; we’ve adopted tweaks from client best practices, sometimes just based on a conversation over the laboratory bench.

    Every kilogram produced here reflects both the technical challenge of chiral, polyfunctional intermediates and the lived expertise of a manufacturing team that understands what it means to deliver on expectations. No client wonders who actually made their material, and the feedback comes straight to us—good, bad, or challenging.

    Perspective that Grounds Future Progress

    Manufacturing (2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-2-methyl-4-(1H-1,2,4-triazol-1-yl)thiobutanamide goes deeper than technical expertise or compliance. Every challenge faced, from sourcing feedstock to late-night troubleshooting when a tank alarm goes off, shapes not just our process but the confidence clients have in our product. Building on real-world experience, we continue to adapt to changes in the regulatory field and the shifting demands of pharmaceutical innovation. The daily reality remains clear: only by standing behind each batch—with facts, transparency, and open lines of communication—can we maintain the trust earned from years of consistent supply and partnership.

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