|
HS Code |
312147 |
| Product Name | 4-Chloro-2-Methylphenylboronic Acid |
| Cas Number | 374222-97-6 |
| Molecular Formula | C7H8BClO2 |
| Molecular Weight | 170.40 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 123-126 °C |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in DMSO, methanol, and slightly soluble in water |
| Smiles | CC1=C(C=CC(=C1)Cl)B(O)O |
| Inchi | InChI=1S/C7H8BClO2/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4,10-11H,1H3 |
| Storage Temperature | 2-8°C, keep container tightly closed |
As an accredited 4-Chloro-2-Methylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic screw-cap bottle labeled "4-Chloro-2-Methylphenylboronic Acid, 25 grams, CAS: 61676-60-8." Label includes hazard and safety information. |
| Shipping | 4-Chloro-2-Methylphenylboronic Acid is shipped in tightly sealed containers, typically under inert gas or desiccants to prevent moisture exposure. Packed in accordance with regulatory standards for hazardous chemicals, it is transported via ground or air, labeled with appropriate hazard warnings, and accompanied by a Safety Data Sheet (SDS) for safe handling. |
| Storage | 4-Chloro-2-Methylphenylboronic Acid should be stored in a tightly sealed container, away from direct sunlight and moisture, in a cool, dry, and well-ventilated area. Store at room temperature, avoiding exposure to strong oxidizing agents and acids. Protect from air and humidity to prevent degradation. Label containers clearly and handle using appropriate personal protective equipment. |
Applications of 4-Chloro-2-Methylphenylboronic Acid in Industrial ManufacturingAs a direct producer of 4-Chloro-2-Methylphenylboronic Acid, we partner with manufacturers in specialized chemical sectors that require reliable, high-purity intermediates for targeted applications. The material features prominently as a critical coupling component in advanced organic synthesis, supporting the development of high-value products in regulated industries. Below, we detail its practical use across major downstream fields, supported by established formulation protocols and compliance expectations. 1. Pharmaceutical Intermediate Synthesis (API Manufacturing)Pharmaceutical production leverages this boronic acid as a coupling partner during Suzuki-Miyaura reactions to construct complex biaryl motifs frequently found in anti-tumor, anti-inflammatory, and CNS-active small molecules. Process chemists rely on this reagent for fragment assembly in pre-final synthetic steps, where regulatory traceability and impurity management shape every input selection. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis (Active Ingredient Manufacturing)Manufacturers of advanced crop protection agents employ 4-Chloro-2-Methylphenylboronic Acid in the synthesis of custom biaryl building blocks for herbicides and fungicides, often utilizing Suzuki coupling to achieve unique substitution patterns. This input supports innovation in active ingredient portfolios where patent protection depends on precise aromatic modifications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemical Manufacturing (Organic Semiconductors and OLEDs)Producers within the electronics sector utilize this boronic acid to construct custom biaryl, biphenyl, and polyaromatic systems found in organic semiconductors, specifically in high-performance OLED emitter and hole-transport material synthesis. The precise reactivity profile of this input enables tight molecular weight control vital for device consistency. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Chemical Building Blocks (Custom Fine Chemical Synthesis)Custom chemical producers incorporate 4-Chloro-2-Methylphenylboronic Acid for the strategic assembly of high-value fine chemicals used in dye intermediates, advanced monomers, and specialty ligands. Its selectivity and compatibility with transition metal-catalyzed cross-couplings provides critical differentiation in synthesizing complex biphenyl frameworks for further downstream functionalization. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Active Material Precursor for Advanced Material R&DResearch-driven material science and specialty research divisions leverage this boronic acid to design and synthesize target biaryl or heteroaryl structures that serve as building blocks in advanced materials, including molecular sensors and functionalized nanoparticles. Here, process control, documentation, and batch reproducibility are critical for application in prototyping and pilot-scale innovation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-Chloro-2-Methylphenylboronic 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
Flexible payment, competitive price, premium service - Inquire now!
Years of hands-on synthesis work have shown one thing consistently: impurity management drives successful reactions. After logging countless production runs on 4-Chloro-2-Methylphenylboronic Acid, we’ve learned that purity means more than a simple specifications page. Trace metals linger from poorly cleaned vessels, isomeric contaminants sneak in through rushed crystallization, and moisture seeps into hurried packaging. This compound, due to its reactive boronic acid group, amplifies every stray ion and water molecule in your glassware. So, we polish every batch through tightly-controlled filtration lines, monitor residual solvents down to low ppm, and check each lot’s water content with Karl Fischer titration. This isn’t a checkbox exercise—downstream headaches for your Suzuki couplings pile up fast. We stake our name and our workflow on cleaner, more predictable raw material so you don’t end up purifying side products out of your final API intermediates.
Chemists mostly refer to this product by its IUPAC name, but for routine lab work we catalog our key model under the short title: 4-Chloro-2-Methylphenylboronic Acid—CAS 3845-13-2. Over the years, we have focused on producing crystalline, free-flowing material in pale white or off-white color. A true quality batch stays dry and packs firmly into a bottle with no clumping or yellowing around the cap. Molecular weight sits at 170.42, a number that rarely shifts when formulation is monitored by modern NMR and GC-MS equipment. Melting point sits firmly between 190–195°C; consistent melting is a simple but powerful way to spot cross-contamination.
Many customers come to us after struggling with batches that reek of halogen impurities or odd, bitter-smelling breakdown byproducts. We treat waste streams aggressively to prevent environmental carryover and do not recycle previous reaction residues into fresh product. Upstream, batch records log every change in pressure, temperature, and pH so we can literally trace each bottle back to its reactor. Spec sheets confirm at least 99 percent purity by HPLC or GC—it’s tempting to shave this number to fluff yields, but that always comes back in the form of difficult separations and frustrating loss of active reagent downstream.
Those who have spent time on the bench know boronic acids fill a particular need. This molecule is no exception, popping up in cross-coupling chemistry, medicinal libraries, and even some innovative advanced materials. The 4-chloro-2-methyl pattern keeps the aromatic ring tuned just right for Suzuki-Miyaura couplings—a textbook reaction for building biaryl bonds in pharmaceutical intermediates. When aryl chlorides and methyl substituents get stacked just so, chemoselectivity holds strong. Adding boronic acids of lesser purity drags down palladium catalyst lifetimes, gums up columns, and lowers the yield batch on batch.
We get calls from process chemists looking to optimize coupling reactions, especially where downstream deprotection, methyl migration, or oddly sticky impurities pop up. Our product’s reliable shelf life and narrowly-defined melting point stand out when you’re trying to scale up a complex synthetic route—too much water or trace metals can literally grind a run to a halt. We’ve seen high-throughput screening efforts succeed only after switching out inferior boronic acids for a more rigorously controlled source. Library synthesis in medicinal chemistry, where tens or hundreds of derivatives crowd a plate, benefits enormously from a steady, predictable boronic acid at the foundation.
A lot of suppliers sell generic boronic acids, including regular phenylboronic acid and o- or p-chloro- or methyl analogs. What chemists sometimes miss is how small structural tweaks ripple through the entire synthetic process. Our product sports both a chloro and a methyl on the ring—a combination boosting reactivity and selectivity in many couplings. The electron-withdrawing chlorine on the para position tames over-reactivity, while the ortho methyl adds a subtle steric shield, protecting against unwanted polymerization or undesired side-reactions.
Another routine question comes up: why not just buy a bulk, cheaper 4-chlorophenylboronic acid or a generic methyl analog? Through actual scale-up trials, we’ve tracked better conversion rates and fewer isolation headaches in heterocycle and biaryl formation with this dual-substituted version. Gas chromatography traces show a remarkably clean product profile—far fewer side peaks, minimal unknowns, and no broad humps near the baseline. This means less spent solvent, less time on column purification, and fewer surprises in later synthetic steps. Bulk-grade materials sound attractive on a per-kilo basis until your project grinds to a halt troubleshooting sticky, low-converting reactions caused by inconsistent boron loading or trace halogen scrambling.
If you’ve ever opened a jar of boronic acid that clumped up hard or yellowed at the rim, you know stability is more than a specification—it’s earned through cleanroom practices, smart packaging, and truckloads of silica gel. We found early on that moisture-sensitive packing made a huge difference, even during brief handling on the plant floor. No matter your fancy desiccator, carton, or barrier bag, real-world stability testing on our batches proved that the right blend of packaging and storage temperature keeps product flowable for months.
A key issue: boronic acids gradually pick up water from the air, eventually forming sticky masses that resist redissolution or turn glassy. Our approach keeps every bottle double-sealed, flushed with inert atmosphere, and hand-labeled with manufacturing date and batch number. Quality checks weeks and months later show crystal form and melting point stay steady, no creeping haze or off odors. For customers running multi-year research programs, this kind of shelf-life reliability matters when you don’t want to recalibrate each new bottle or lose product to hydrolysis.
Strict health and safety standards have evolved alongside our production lines. Open handling of fine powders carries real-world risks: dust inhalation, accidental mixing with incompatible solvents, minor but manageable skin irritation from boronic acids. Clear labeling, accessible data, and simple PPE protocol—gloves, dust mask, eye protection—keep our workers and downstream labs safe. Trace contaminants, often ignored by traders, get flagged and isolated on the production floor before anything leaves our site.
From direct hands-on experience, we refuse to compromise on plant hygiene. It’s easier to schedule regular equipment teardown and sanctuary cleaning than to risk recall or destroy contaminated batches. If an off-spec run appears, we track back to the root cause before restarting anything; this isn’t just policy, it’s practical, hard-won knowledge. Problems found with supplier material purity get shared openly with our partners, so issues are solved before reaching your bench.
Independent third-party testing can complement internal QC, but meticulous in-house analytics remain our foundation. Routine proton and carbon NMR check for ring substitution patterns, confirming no isomerization or unintended byproducts. FTIR and GC routinely validate structure and purity, with cross-checks against retained reference standards from every batch run. If there’s any unexplained signal or ghost peak, full investigation follows before clearing a batch for shipment.
Many mid-sized manufacturers automate away some QC, letting small aberrations slip through. We deploy direct supervision on all analytics because chemistry remains stubbornly unpredictable at scale. Consistent purity, confirmed by in-line and off-line checks, stands as our differentiator—the result of investing in experienced staff and robust instrumentation rather than penny-pinching peroxide quench protocols or skipping final melt checks.
Like every manufacturer handling halogenated starting materials, we face the challenge of waste streams. The classic production route to 4-Chloro-2-Methylphenylboronic Acid involves reactions that, if handled carelessly, generate halide-rich aqueous layers or solvent waste. Our approach centers around real containment and treatment—multi-stage neutralization, high-efficiency solvent recovery, and careful monitoring of effluent. Environmental audits from both regulators and our own staff push us toward cleaner solutions. This includes targeted solvent swaps to less toxic options, bulk solvent recycling, and even the physical reduction of packaging waste along the production line.
We know claims of “green chemistry” ring hollow unless backed by specific actions. Year-on-year, we track measurable improvements: reduced halogen content in water discharge, solvent use per kilo product down, and recovered waste streams that are actually reused rather than dumped. Small steps—using lower-volume reactors when possible, staging reagent addition rather than all-at-once mass transfer, and continuous process improvement—add up to cleaner, leaner facilities over time.
Supplying 4-Chloro-2-Methylphenylboronic Acid goes beyond filling an order sheet. Process chemists face a pressure cooker of project deadlines, variable feedstocks, and shifting project scopes. Labs who buy from us know we take their feedback seriously. If a researcher faces a late-stage problem—reaction quenching, unexpected color, product fouling—we dig through batch records and analytics reports, not just offer a refund or swap. True support comes from knowing how small details in production filter down to bench-scale complications.
On real-world collaborations, we share detailed batch verification and offer witnessed third-party QC when requested. Customers gain access to technical documentation, impurity profiles, and advice on storage or dissolution protocols. Offering smaller, precisely weighed lots, or even custom packaging, follows directly from lab user requests—not a one-size-fits-all approach, but a practical response to feedback designed to eliminate as many barriers as possible to seamless synthesis.
Over the last decade, demand for substituted phenylboronic acids has shifted from bulk commodity to specialized, often small-lot requirements. Drug discovery teams, materials scientists, and university labs want reliable supplies for both small-scale screening and intermediate kilogram production. Order cycles have tightened, expectations for batch-to-batch consistency have gone up, and tolerance for off-grade supply keeps shrinking.
We listen to requests for improved documentation, faster delivery, or alternate particle sizes. Some projects want crystalline powder to reduce static electricity during formulation; others request larger granules for dust minimization in automated dosing setups. We have responded by varying our product preparation methods, including additional drying or careful milling, but never at the cost of reduced purity.
Competition comes from large multinational chemical suppliers and quick-turnaround online resellers. Our differentiation comes from batch traceability, in-person technical support, and reliability over price. Researchers tell us that a marginal increase in upfront cost pays back in time saved troubleshooting unpredictable chemistry or sifting through poorly documented material records.
Raw material supply disruptions are not theoretical—recent years have shown how tight margins in international trade, transport delays, and upstream regulatory hurdles can wipe out months of planning. Alternative sourcing, stockpiling, or working with obscure traders often brings new problems: inconsistent quality, missing paperwork, unclear impurity background. We spool up production on flexible schedules, using warehoused raw materials sourced from vetted suppliers only. Sudden increases in demand, whether due to a research breakthrough or competitor shortfall, mean ramping up reactor time and opening new shifts—realities we’re ready for.
From decades of experience, we know shortcuts in sourcing or documentation produce ripple effects for both us and our customers. Careful materials vetting, rigorous supplier qualification, and frequent plant audits ensure we avoid surprises—rogue contaminants, out-of-spec batches, and unreliable inventory levels. Doing it right takes time, costs more, and requires skilled staff, but ultimately leads to lower rates of returns, fewer customer complaints, and a reputation worth having in a tight-knit market.
The best advances in product quality, handling, and packaging result from direct lab feedback. We regularly invite partners to visit, review production logs, and suggest new approaches. Recent upgrades—vacuum-sealed container designs, more robust moisture barriers, and improved leak testing on bulk drums—arose from field reports of minor handling issues or product degradation after extended storage. Every lot shipped spurs a feedback loop, allowing us to tweak, refine, and renew standard practices based on what real chemists actually encounter in use.
Open channels between our technical support team and customer labs keep us grounded in chemists’ day-to-day needs. Conferences, supplier audits, and collaborative problem-solving sessions generate new packaging ideas, faster analytical checks, and time-saving documentation. Most importantly, these discussions highlight emerging issues, including new catalyst systems, solvent compatibility challenges, or evolving drug regulatory standards.
Day-to-day, the practical value of 4-Chloro-2-Methylphenylboronic Acid shows up in reaction vessels across pharmaceuticals, agrochemicals, and advanced materials. The certainty gained from consistent quality, trusted origin, and reliable documentation turns experimental chaos into productive work. We have seen teams push forward new cross-coupling campaigns or scale up gram-to-kilogram synthesis with fewer setbacks and measurable savings in labor costs.
Process chemists rely on fast onboarding, immediate access to completed analytical reports, and honest notification of any recall or delay. Rapid response to replacement orders or rush requests supports the rapid pace of modern research. By providing not just a product, but the backing of experienced manufacturing, transparent records, and technical insight, we give labs an edge in both speed and outcome certainty.
Practical, hands-on expertise trumps abstract claims. Every batch of 4-Chloro-2-Methylphenylboronic Acid produced here comes from experience earned on the plant floor and tested in actual customer labs. By focusing on purity, consistency, and direct technical backing, we deliver more than just raw material—we provide the foundation for confident, efficient advanced chemistry. The real measure of value lies in customers returning not just for a product, but for lasting solutions that keep research projects on track and productive from first reaction to final product.