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HS Code |
770907 |
| Chemical Name | 2-Chloro-5-Methylphenylboronic Acid |
| Synonyms | 2-Chloro-5-methylbenzeneboronic acid |
| Cas Number | 936060-36-1 |
| Molecular Formula | C7H8BClO2 |
| Molecular Weight | 170.41 |
| Appearance | White to off-white solid |
| Melting Point | 176-181 °C |
| Purity | >97% |
| Storage Temperature | 2-8 °C |
| Solubility | Soluble in DMSO, Methanol |
| Inchi | InChI=1S/C7H8BClO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4,10-11H,1H3 |
As an accredited 2-Chloro-5-Methylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package features a white screw-cap bottle, labeled with “2-Chloro-5-Methylphenylboronic Acid,” CAS number, and safety information. |
| Shipping | 2-Chloro-5-Methylphenylboronic Acid is typically shipped in sealed, chemical-resistant containers to prevent moisture ingress and contamination. It is handled as a solid, often packed with desiccant, and shipped under ambient or cool conditions. Appropriate labeling and documentation, including safety information, accompany the shipment per relevant chemical transport regulations. |
| Storage | 2-Chloro-5-Methylphenylboronic Acid should be stored in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Recommended storage temperature is room temperature or lower (2-8°C). Ensure proper labeling, and avoid exposure to air to prevent hydrolysis or degradation of the compound. |
Applications of 2-Chloro-5-Methylphenylboronic Acid in Industrial ManufacturingAs a dedicated manufacturer of 2-Chloro-5-Methylphenylboronic Acid, we support key partners in specialized chemical sectors where this boronic acid derivative fulfills stringent process and quality requirements. Below, we highlight the principal downstream industrial applications, each defined by distinct process integration, compliance standards, formulation guidance, and final product types. 1. Pharmaceutical Intermediates: Sartan Antihypertensive SynthesisOur material enters the pharmaceutical sector as a boron-containing building block in the Suzuki-Miyaura cross-coupling route, supporting the synthesis of intermediates for sartan-class antihypertensive drugs such as valsartan and olmesartan. It enables the formation of key aryl-aryl bonds in the biphenyl tetrazole substructure, a defining motif in this therapeutic class. Stringent trace-level impurity and residual boron control remain critical for subsequent API processing and batch release for regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Agrochemical Synthesis: Arylated Herbicide IntermediatesThis boronic acid derivative plays a strategic role in crop protection manufacturing, particularly in constructing arylated intermediates used in selective herbicide APIs. Downstream partners employ the material in palladium-mediated coupling steps to assemble complex aromatic fragments, resulting in active molecules with desired selectivity for broadacre and specialty crops. Residual catalyst and byproduct elimination steps in this segment must align with pesticide residue guidelines set by major agricultural regulatory bodies. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemicals: OLED Material Precursors2-Chloro-5-Methylphenylboronic Acid is adopted in the advanced materials sector as a molecular building block for the production of custom aryl-based ligands and conjugated molecules essential for OLED (organic light-emitting diode) device manufacturing. Its high purity and controlled boron content ensure defect-free electronic properties in display and lighting applications. Precise stoichiometry, ultra-trace metallic contamination limits, and solvent compatibility define quality assurance at this stage. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Chemical Manufacturing: Fine Chemical Intermediates for Performance AdditivesIndustrial users in the specialty chemical segment utilize 2-Chloro-5-Methylphenylboronic Acid to construct intermediates that confer specific performance attributes to end-use additives for coatings, lubricants, and engineered fluids. The boronic acid moiety supports precise aryl-aryl bond formation, giving rise to functional organic fragments that enhance anti-wear, UV-resistance, or adhesion characteristics within tailored additive systems. Stability, consistency, and purity assessments align with the needs of high-performance industrial environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Manufacturing 2-Chloro-5-Methylphenylboronic Acid presents a daily test in balancing technical precision with reliable output. In our facilities, each batch comes out of the reactor following close supervision to detect and control byproducts, stubborn traces of metal, and other complications that can introduce noise into downstream reactions. Over years spent tuning the Suzuki coupling process and monitoring crystallization, I have learned that shaving fractional impurities from every batch is what separates reliable phenylboronic acids from inconsistent or unreliable supply. Chemists across small-molecule pharma, agrochemical research, and flavor science hold every minor impurity against their process performance, so our monitoring catches sulfated, oxidized, or hydrolyzed traces that build up over time. Our process relies less on textbook purity hurdles and more on hands-on troubleshooting from operators who have learned what a bad batch smells or granulates like. That sort of experience shapes how we fine-tune process points, starting with raw material qualification and ending with a strong, shelf-stable acid.
2-Chloro-5-Methylphenylboronic Acid stands out for its distinct substitution pattern—chlorine and methyl positioned where they direct Suzuki–Miyaura cross-coupling in a way that plain phenylboronic acid or other regioisomers do not. That isn’t academic. The automatic substitution comes from the way chlorine at the second position blocks undesired side forms and the methyl group tweaks reactivity so newer ligands in modern palladium complexes shine. That’s a practical advantage for process chemists searching for selective bond formation under challenging conditions. Our product usually appears as a solid, white to light beige, reliable enough for accurate batching, yet not sticky or hygroscopic. The real difference traces back to the purity and process traceability, which research teams say helps when scaling from millimole to kilogram. Structural fingerprints—like the particular melting point, HPLC purity, and absence of residual solvents—reflect our control strategy, rather than listing a generic grade.
In the field or lab, the use of this acid isn’t limited to generic coupling. Medicinal chemists deploy it in the core steps when introducing functionality onto complex heterocycles or bridging challenging fragments. For those synthesizing kinase inhibitors, the boronic acid’s reactivity can make or break a key step. Our customers working on advanced intermediates report inconsistent yields if they deviate from a narrow pH window or if the starting boronic acid picks up halide contamination during warehousing. This isn’t a talking point so much as a lesson learned from returns and troubleshooting with end users on pharma process lines. Agrochemical researchers cite its role in creating selective herbicide analogs where contamination alters bioactivity, which directly hits the bottom line with wasted pilot runs.
Our batches routinely undergo additional drying cycles and packaging under nitrogen, so the free acid doesn’t degrade or form boroxine. Typical lab-grade acid, sometimes supplied through broad-market distributors, rarel preserves both high purity and consistent water content. That’s a gap we close by integrating real-time analytics in drying rooms and handling lines. Such attention to technical detail arises directly from scale-up customers who need predictable behavior in kilo-batches for first-in-plant scale or pilot launches. Impacts go beyond the flask: waste stream volumes can shrink when the input meets specification because purification can be dialed back. Insights like these don’t come from spec sheets but from day-to-day communication with process chemists and bench scientists.
A crowded portfolio of boronic acids means plenty of choices. Yet the 2-chloro, 5-methyl pattern carves its own path, beyond just the substitution map. It shows a balance between electronic activity and steric hindrance, translating to fewer side products and cleaner conversion in coupling reactions—notably in demanding arylation stages. We see customers shifting away from 4-chloro or 2-methyl variants after encountering solubility problems or byproducts that complicate downstream isolation. Some switch to our product upon seeing lower retention of halide or methyl impurities, which can induce off-color byproducts or sticky chromatography fractions.
From hands-on track record, robustness comes not only from chemical theory, but the actual feel and odor of the batches—problems like smoky odor or off-white color flag incomplete purification or degradation. Our focus has always been that problems caught early in the production floor save hours for R&D, where a chemist won’t waste time tracing variable results back to their batch’s origin. We hear from clients who run longitudinal studies across years, and trace erratic yield blips to off-prime sources, rather than intrinsic chemistry. It matters most in regulatory filings where full traceability charts are required. If the boronic acid batch deviates from its standard spectral profile, it triggers exhaustive extra work in regulatory departments for DMF or technical dossier updates.
Production model lines run on batch-based reactors, supported by solvent recovery systems and controlled airflow, not just for environmental compliance but to stabilize the boronic acids before packaging. The raw materials reach us only after multi-point qualification—chlorinated aromatics and trialkyl borates checked for residual halides and peroxides. Our operators routinely log batch times and intermediate color changes, since boronic acid reactions can turn quickly with minor deviations in air or humidity. Through years at the controls, we’ve refined additives and drying cycles: the acid responds better to incremental solvent drips rather than a one-shot addition. This attention impacts crystal habit, downstream filtering, and—very practically—reduces caking for end users during weighing or transfer.
Specifications for our batches typically include HPLC purity exceeding 98.5%, melting point ranges within two degrees, low residual metal content, and tightly controlled moisture. These targets arise not because a lab manager asked for them, but because too many hours were lost to long reaction workups or re-runs due to drifting melting points or slow-dissolving byproducts. Our team chose to run extra drying cycles and invest in NMR cross-validation after seeing that benchtop purity sensors alone missed trace defects, especially after humidity spikes. Our vision of specification traces back to customer process feedback, and less to generic industry norms. Crystalline material is easier to dose, and lot uniformity saves hours of calibration.
Stability isn’t about a label promise, but the chain of choices—from plant drying to drum packaging and shipping. Every time a container crosses a humidity boundary, there’s a risk: boronic acids can cake or degrade if they pick up water or if temperature swings wildly. Our workers double-bag and flush containers with dry nitrogen, based on hard-won lessons from lost batches in early years. Trucking in monsoon conditions taught us the value of overpacking and locating dry storage as close to outbound lanes as possible. Customers benefit when every drum provides extended shelf life and batch-to-batch consistency, avoiding mid-campaign product failures.
We maintain logs for each batch, including the unique visual cues—a pale beige tinge or uneven texture often signal issues before lab numbers confirm them. Operators rely on direct handling feedback rather than trusting numbers alone. We found over time that losing track of minor handling incidents—such as power failures that stall air handling—can quietly influence degradation rates. Our best performances followed tight communication between plant, warehouse, and customer, rather than relying on rigid protocols. Customers dealing with scale-up or regulatory filings often ask for handling narratives, and we provide actual event logs, not generic claims.
Beyond spec sheets and technical datasheets, stories from real manufacturing campaigns carry more weight. Several of our larger pharmaceutical clients have transformed medicinal chemistry programs by switching to our 2-Chloro-5-Methylphenylboronic Acid after frustration with inconsistent crystallinity and variable purity from general-market sources. A case comes to mind where a mid-sized pharma company in scale-up hit a wall sourcing consistent acid for a kinase inhibitor series. They traced repeated chromatography issues back to variable free chloride content and resolved those by switching to our controlled drying protocol. The reduced need for extra purification not only improved labor productivity but also saved on solvent costs and hazardous waste.
Agricultural researchers reiterate similar themes: one group reformulating an herbicide precursor faced inconsistent reactivity with catalog boronic acids. Subtle differences in methyl and chloro positioning challenged regioselective arylation. Direct feedback led our team to increase pack size flexibility and add mid-batch sampling, which improved the uniformity for their process and minimized out-of-spec batches. Those operational adjustments surfaced not from company-wide memos but from detailed calls with research chemists breaking down synthetic bottlenecks.
Production doesn’t always follow plan. Unexpected humidity, unstable intermediates, and batch-to-batch deviations create headaches daily, so process improvements target issues as they emerge. Equipment upgrades—like vapor-locked filtration systems—directly respond to caking and moisture pick-up complaints. Adjusted time intervals in the crystallization tank grew out of operator feedback regarding unfiltered fines and product sticking to tank walls. Each tweak follows from day-to-day technical discussions with chemists, not just SOPs or Six Sigma worksessions.
Supply chain uncertainty constantly threatens steady supply. Only by building buffer inventory and qualifying multiple raw material vendors do we deliver consistently; we learned that the hard way after a regional solvent plant outage ground an entire campaign to a halt. Experienced teams anticipate bottlenecks and reduce cycle variation by turning these disruptions into workable contingency plans. Manufacturing boronic acids often means shipping special drums or pails to climate-sensitive zones. We selected heavy-duty liners and real-time tracking based on end-user demands after repeated heat exposure damaged incoming material. These solutions aren’t showpieces—they result from field failures and operator-driven learning.
Today’s chemical landscape demands full traceability. Our export customers preparing for regulatory hearings—whether in pharma or agro sectors—push for documented batch histories, QA data, and deviation logs. Only full record-keeping, from raw material testing through to packaging, supports the claims we make about our 2-Chloro-5-Methylphenylboronic Acid. Trace metal levels, certificate of analysis, and on-demand supplementary COA documentation all get generated in-house, not provided by an external agency. These aren’t just compliance items; they materially assist with troubleshooting complex syntheses and regulatory audits.
We manage regular updates to analytical methods, shifting to mass-spec or NMR when standard wet-chemistry methods catch less than 100 ppm of specific impurities. Every customer gets the version history of our testing regimen because a surprise impurity in an earlier batch can leave them scrambling in mid-trial. This level of transparency, while resource-intensive, reflects both our operational philosophy and ongoing industry trends toward more rigorous filings. By delivering not only physical product but also the record and rationale of each process step, we limit downstream surprises and foster long-term partnerships.
2-Chloro-5-Methylphenylboronic Acid unlocks synthetic routes considered bottlenecked or too risky for traditional boronic acids. We’ve watched as process teams gain more flexibility in coupling complex or sensitive starting materials—they count on our finely produced acid helping them introduce unique aryl groups without sacrificing yield or purity. For research groups, switching to this specific acid sometimes eliminates entire steps, reducing both cycle times and cost. It’s not uncommon for clients to bring forward requests for slight tweaks to crystal size or package tonnage, enabling their teams to bypass unnecessary reworking or fiddly filtration.
Some fields—such as specialty materials—have just started to adopt this acid for applications in advanced polymers or select functional coatings. Here, batch uniformity and traceability matter even more, since end-point quality relies on predictable reactivity. Experience tells us that process simplicity enables new product launches, helping researchers avoid delays due to raw material insecurity. Thus, the acid not only fills a gap for pharmas and agro players but also opens creative approaches in adjacent high-tech sectors.
We keep our competitive edge by learning directly from recurring issues, whether they stem from equipment wear, raw material inconsistency, or end-product handling. Every improvement in reactor cleanout, solvent recycling, or drying room management has roots in field complaints and logistics breakdowns. Hands-on engagement—rather than managerial dictation—drives those shifts. A real-world example: upgraded drum closure systems arose after two seasons of transit failures led to degraded boronic acid in hot, humid regions.
Cross-disciplinary squads routinely analyze returns and failed batches, not just to find immediate fixes but to permanently reduce causes of quality loss. These teams feature operators, lab analysts, and field-facing chemists, creating solutions that last beyond just one campaign. Implementing feedback loops between shipping, QA, and synthesis improves reliability—customers can trace back every kilo to its origins. From upgraded filtration mesh specification to real-time digital batch logs, process changes earn their keep only through repeat field verification.
The story of our 2-Chloro-5-Methylphenylboronic Acid isn’t about catalog claims. The value lies in lessons learned batch by batch, on the plant floor and in technical debriefs with user teams. Only years of incremental change drive lasting improvements—whether in product purity, physical handling, or regulatory readiness. The proof comes in uninterrupted campaigns, compliance on demand, and collaborative development with research teams. Choosing this chemical from a hands-on manufacturer means gaining not only a reagent, but the depth of experience supporting every gram delivered.