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HS Code |
370237 |
| Product Name | 3-(Methylthio)Phenylboronic Acid |
| Cas Number | 1053575-33-7 |
| Molecular Formula | C7H9BO2S |
| Molecular Weight | 168.02 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 110-114°C |
| Purity | ≥97% |
| Solubility | Soluble in DMSO, MeOH, slightly soluble in water |
| Smiles | B(C1=CC=CC(=C1)SC)(O)O |
| Inchi | InChI=1S/C7H9BO2S/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5,9-10H,1H3 |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | 3-(Methylthio)benzeneboronic acid |
As an accredited 3-(Methylthio)Phenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle with a screw cap, clearly labeled "3-(Methylthio)Phenylboronic Acid," including safety and handling instructions. |
| Shipping | 3-(Methylthio)Phenylboronic Acid is securely packaged in sealed containers to protect against moisture and contamination. It is shipped following standard chemical transport regulations, including appropriate labeling and documentation. Handling precautions and Material Safety Data Sheets (MSDS) are included to ensure safe transit and delivery. Temperature control may be applied if required by regulations. |
| Storage | 3-(Methylthio)Phenylboronic Acid should be stored in a tightly sealed container, protected from moisture and light. Store at room temperature or lower, away from strong oxidizing agents and incompatible substances. Ensure good ventilation in the storage area. Avoid extended exposure to air, as boronic acids can degrade. Handle under dry, inert atmosphere if possible for optimal stability and longevity. |
Applications of 3-(Methylthio)Phenylboronic Acid in Industrial Manufacturing3-(Methylthio)Phenylboronic Acid serves as a key intermediate for high-value chemical syntheses in a select group of precision-driven industries. Below, we provide detailed industrial application scenarios, focusing on real manufacturing sectors utilizing this raw material, along with compliance requirements, typical ratios, downstream production steps, and principal finished goods. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies employ 3-(Methylthio)Phenylboronic Acid as a coupling partner in Suzuki-Miyaura cross-coupling reactions, essential for building biaryl motifs in targeted therapies, oncology agents, and research-stage small molecule APIs. The high purity and consistent lot-to-lot quality allow for precise integration into multi-step syntheses. Our facility ensures all production lots meet stringent impurity and trace metal controls required in regulated drug substance pathways. Industry compliance standards
Typical usage ratio
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2. Crop Protection Active Ingredient ManufacturingAgrochemical manufacturers utilize 3-(Methylthio)Phenylboronic Acid as a pivotal synthon in the synthesis of phenylthio-substituted herbicides, fungicides, or insecticides. The compound’s boronic acid moiety is leveraged in scalable coupling reactions essential for constructing diversified agrochemical scaffolds, ensuring high field activity and environmental stability. Industry compliance standards
Typical usage ratio
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3. OLED and Specialty Electronic Chemical SynthesisProducers of organic light emitting diodes and advanced display components source 3-(Methylthio)Phenylboronic Acid for use in the development of functional biaryl-thioether molecules, essential for high-end emissive layers and charge-transporting motifs. Purity and metal trace levels are critical to avoid quenching in final device performance. Industry compliance standards
Typical usage ratio
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4. Advanced Chemical Research and Custom SynthesisContract research organizations and specialty synthesis manufacturers employ 3-(Methylthio)Phenylboronic Acid in the development of novel compounds for medicinal chemistry, library synthesis, and advanced material research. The compound supports the rapid exploration of new biaryl scaffolds, photonic structures, and sulfur-functionalized moieties, which are subsequently evaluated for performance or biological activity. Industry compliance standards
Typical usage ratio
Downstream process integration
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Every kilogram of 3-(Methylthio)Phenylboronic Acid that rolls off our reactors reflects a journey of chemical precision, hands-on problem-solving, and real industry experience. This isn’t a commodity that gets bought and flipped through a chain of resellers — this is a carefully developed molecule, produced on-site in a facility built for innovation and reliability. Our mission as a manufacturer has always been rooted in delivering exactly what advanced synthesis demands, every time. Through years of handling boronic acids, we have gained the perspective needed to tackle purity, stability, and scale-up challenges that so often compromise downstream applications.
Mainstream labs and global tech companies routinely tell us: reproducibility drives meaningful research. That’s been our guiding star through every development batch of 3-(Methylthio)Phenylboronic Acid. Our process chemistry teams optimize each reaction to keep impurity profiles low and batch consistency high, so that when chemists push forward with Suzuki-Miyaura couplings or fine electronics assembly, they’re never left asking, ‘Was it the reagent or the process?’ Knowledge from multiple campaigns — not just from a single batch — shape the way we purify, dry, and handle this compound. We understand the material’s sensitivity to air and moisture, and this informs every step, from the last quench to the final sealing in export-ready containers.
Our commercial line for 3-(Methylthio)Phenylboronic Acid responds to a simple fact: different disciplines require different specifications. Whether supporting kilogram-scale pharma synthesis or furnishing milligram lots to R&D teams, we’ve structured our own production streams. Common requests focus on the model number CAS 6165-68-0. Typical batches reach purity levels above 98% by HPLC, backed by in-house spectrometric and chromatographic confirmation. Moister content and residual metals factor into our monitoring, which means our clients can trust downstream complexation without risking catalyst poisoning. We pack, store, and ship in formats that fit both glovebox and warehouse workflows, having learned that material quality means little if supply logistics break the chain.
It’s tempting to see boronic acids as interchangeable, but the specifics of each functional group tell us otherwise. Our 3-(Methylthio) derivative delivers the nuanced reactivity that comes from its sulfur substituent. In many modern synthetic schemes, this methylthio group opens new routes to thioether-containing targets — from advanced pharmaceutical intermediates to compounds used in organic electronics. Our own researchers have published process notes where this modification streamlined cross-coupling steps, showing improved yields under milder baseline conditions versus less tailored boronic acids. We’ve also found that the shelf life and purity retention of our batches outstrip mass-made resellers’ products in side-by-side stability tests. That resilience under normal handling conditions supports smoother lab operations and reduces loss from degradation or spontaneous hydrolysis.
Producing 3-(Methylthio)Phenylboronic Acid at scale didn’t start with textbook reactions — it began in pilot reactors, with glassware stained from the first generation of small-batch runs. That history matters. We’ve seen how minor tweaks in solvent, agitation, or temperature shift the impurity profile or crystallization efficiency. For example, our switch to a greener workup solvent system not only met internal sustainability benchmarks, but also improved overall yield and made the product easier for our partners to handle downstream. The implications here go beyond compliance or environmental reporting — it’s the type of result that only a team running their own reactors would find, since direct observation led to refining our protocols.
This kind of feedback loop — from production to lab, and from our customers back to us — drives continuous improvement in a way matched only by hands-on chemical manufacturing organizations. It’s the reason our support team fields practical questions, like how our acid behaves in certain palladium catalyst systems, or what the actual shelf life looks like under humid conditions. As a manufacturing group, there’s nothing more gratifying than hearing from a researcher at a global pharma company, reporting that the reagent held up perfectly through multi-step syntheses that would’ve broken down a lower-tier product.
This isn’t just another entry in a long catalogue of specialty chemicals. Direct customer feedback, case studies, and published literature have shown that 3-(Methylthio)Phenylboronic Acid enables innovation in multiple fields. In pharmaceutical development, the methylthio substituent on the phenyl ring allows for rapid diversification of lead compounds by direct cross-coupling, supporting medicinal chemists on tight discovery timelines. Our material features in applications that push the boundaries of small-molecule synthesis — constructing libraries so that overlooked functional groups can be explored, or unlocking late-stage diversification for structure-activity relationship studies.
Beyond pharma, our 3-(Methylthio)Phenylboronic Acid appears in the hands of material scientists working on new conducting polymers. The sulfur modification grants electronic materials tunability, allowing teams to alter their properties for specific device needs. These end uses have specific requirements: high-purity starting points so that subsequent polymerization steps don’t incorporate contaminants, and robust handling so the acid doesn’t decompose before it hits the reactor. Our plant’s output remains centered on these expectations, and we continue to refine both micro-scale and bulk-scale deliveries to keep pace with what applied R&D needs.
Many companies source complex reagents through bulk intermediaries and repackage under their own label. Our approach diverges at every stage. We operate reactors specifically sized for fine-tuning transformations like selective methylthiolation and subsequent boronation. Control of temperature, pH, and reaction time remains under direct supervision of experienced process chemists, not remote contractors or third-party packagers.
Handling boronic acids requires strict control over air and water exposure due to hydrolysis risk — a lesson hammered home years ago after we lost a series of early batches to simple humidity. Through that learning, we invested in climate-controlled packaging rooms and trained staff to minimize exposure during all steps, from vacuum transfer to final drum filling. Each lot receives full traceability, from raw material order to finished drum, so that any question about process or contamination can get a straight answer from a chemist who worked on the batch itself.
Every operator in our plant tracks subtle cues — from exotherm behavior to the color hints at endpoint — that never make it into academic writeups. This tacit knowledge anchors our reliability. Years ago, troubleshooting a pressure anomaly during the boronation step led us to re-examine our nitrogen sparging setup. The resulting adjustment reduced batch-to-batch pressure variance, decreased side product formation, and ultimately increased product yield, all without introducing new variables for our end users. These types of improvements emerge from direct, long-term engagement with every tool, not from outsourcing or theoretical design.
Customers often believe that all boronic acids on the global market come off a single pipeline, with no real differences between producers. We’ve disproved this idea through controlled side-by-side stability studies. For example, a reference batch produced by a third-party supplier developed visible discoloration and lost 20% assay after three months at 25°C, while our in-house produced 3-(Methylthio)Phenylboronic Acid maintained 98% purity. Rigorous control of post-synthesis drying and inert gas handling achieves this, rather than a lucky storage period. For chemists — whether pharma, materials, or academic — this difference means fewer surprises with chromatography, more straightforward purification, and greater trust in reported yields.
Our technical teams log every deviation, anomaly, or question received about a particular batch. It’s not enough to have the best analytical numbers on a certificate; we aim to back those numbers with responsive, technically fluent support. Some clients work through high-throughput workflows with automation — in those cases, we’ve adjusted particle size or optimized packaging for robotic handling, building flexibility based on our own process control at every stage.
Success stories come straight from chemists who’ve pushed the boundaries on tough coupling reactions. One pharmaceutical team reported that by switching to our 3-(Methylthio)Phenylboronic Acid, their screening runs eliminated unexpected byproducts that had appeared with commercial generic sources. They traced the difference to lower levels of residual chloride and a tighter specification on the methylthio position, variables we watch closely during our own synthesis. Academic groups, too, report that the robust color and texture of our product matches their past success metrics, streamlining reproducibility efforts. These stories close the loop on our feedback process, informing the next run and the next improvement cycle.
Generic phenylboronic acids cover many synthetic needs, but niche applications benefit from the added functionality at the 3-position. For example, regular phenylboronic acid may fall short in select cross-coupling reactions where electronic modulation or steric hindrance from the methylthio group tips yields or selectivity in the desired direction. We’ve had customers in both pharma and materials science trade comparison data, showing that in certain catalytic regimes — particularly under mild warming or base — this methylthio-modified acid creates less side reaction and sticks more reliably to the desired product profile.
In direct production, our line keeps a narrower focus. Each impurity, from trace metals to high-boiling solvents, goes under the same scrutiny as our pharma-grade boronic acids. With generic boronic acid producers, clients sometimes describe a lack of transparency or indifference to purity levels that don’t meet their technical specs. We recognize that every deviation off target in starting materials can ripple through to the final compound, so process control remains our obsession — not because a spec sheet says so, but because customer applications keep showing us how minor changes save weeks in troubleshooting and downstream analytics.
No piece of equipment sits idle in our plant unless it delivers actionable data. We staff our analytical group with chemists who understand both the synthesis and the limitations of each analysis. Spectrometers, chromatographs, and titrators never become compliance theater or a check-the-box exercise — they guide real production decisions. Issues such as carryover from previous campaigns or subtle crosstalk between synthetic steps can escape the attention of a contract lab, but manufacturers like us catch them in real-time, with knowledge born of accountability for every finished drum.
Operator experience matters as much as machinery. Our senior process techs know more about reactor tuning and temperature ramping than any SOP could spell out. Years of hands-on learning — managing reactive intermediates, monitoring endpoint signals, fine-tuning filtrations in real time — all contribute to a finished material that meets the standards of the world’s top research groups and manufacturing teams. Direct feedback from customers, especially around previously unexplained inconsistencies, keeps our plant’s culture focused on learning-by-doing rather than abstract theory.
From the bench to the plant floor, challenges in developing or scaling a custom coupling reaction often come down to the reliability of key building blocks like 3-(Methylthio)Phenylboronic Acid. Material quality can mean the difference between a stalled project and commercial success. Take, for example, electronic material companies looking for precise control of the band gaps in their polymers. Often, project timelines hinge on the delivery of a stable, pure methylthio-modified boronic acid that won’t contaminate or disrupt subsequent steps. Our direct manufacturing control allows us to respond to requests on adjusted purity grades, solvent content, or custom packaging, rather than sending these needs up the chain to slow-moving traders or repackagers.
The same responsiveness keeps pharmacology teams moving forward. Chemistry teams focused on rapid iteration for SAR studies need grams to kilos of specialty acids, sometimes with tight delivery windows. By owning our own production process and managing logistics from raw materials to the dock, we can fulfill tailored shipments quickly, sidestepping the long lead times and speculative inventories that can come with layers of distribution. Direct relationships with the end users mean troubleshooting assistance actually comes from people who made the batch, not from a support script.
Precision manufacturing is driven by a relentless need to adapt. Every audit, every customer critique, and every lost batch turns into a lesson for future runs. Our plant’s QA meetings run directly with the same staff who handle the reactors and analytics, closing the gap between quality intent and operational practice. This direct connection — absent from distributor-based models — lets us chase incremental improvements, whether shrinking a batch’s impurity profile, adjusting the isolation window, or fine-tuning particle handling for automated synthesis lines.
Surprises sometimes come from unlikely places. Two years ago, a newer operator noticed a microcrystalline build-up during filtration that previous teams had written off as unavoidable. By running a detailed review and targeted experiments, we isolated its root cause: a process control temperature oscillation during a late-stage neutralization. The next campaigns ran without the build-up, delivering cleaner, free-flowing product with less downstream cleaning required. These hands-on improvements arrive not through outside suggestion, but through keeping every aspect of production intimate and responsive.
Our continued investment in in-house expertise, analytics, and flexible production enables us to offer 3-(Methylthio)Phenylboronic Acid with a level of reliability, stability, and purity that directly supports synthetic innovation. Unlike broadly traded commodities, every gram carries the weight of years spent refining, scaling, handling, and reworking the same chemistry until it fits the needs of advanced synthetic applications and production processes. We appreciate that every missed spec can ripple outward, stalling projects or skewing results. Our approach — grounded in hands-on know-how and long-term partnerships — consistently delivers a product that lives up to the demands of research-intensive industries around the globe.