|
HS Code |
271895 |
| Chemical Name | 3-Bromo-2-methoxy-5-trifluoromethylpyridine |
| Molecular Formula | C7H5BrF3NO |
| Molecular Weight | 256.02 g/mol |
| Cas Number | 884494-36-6 |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | Approx. 184 °C (estimate) |
| Density | 1.66 g/cm³ (estimate) |
| Solubility | Soluble in organic solvents such as DMSO and dichloromethane |
| Purity | Typically ≥ 97% |
| Smiles | COC1=NC=C(C=C1Br)C(F)(F)F |
| Inchi | InChI=1S/C7H5BrF3NO/c1-13-7-5(8)2-4(3-12-7)6(9,10)11 |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited 3-Bromo-2-methoxy-5-trifluoromethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with a secure screw cap, labeled "3-Bromo-2-methoxy-5-trifluoromethylpyridine, 5 grams," including safety and hazard information. |
| Container Loading (20′ FCL) | 3-Bromo-2-methoxy-5-trifluoromethylpyridine is loaded in 20′ FCL using sealed drums, palletized, with proper labeling and safety precautions. |
| Shipping | 3-Bromo-2-methoxy-5-trifluoromethylpyridine is shipped in tightly sealed, chemically resistant containers under ambient temperature. The package complies with relevant hazardous material regulations, clearly labeled with hazard and handling information. Ensure protection from physical damage, moisture, and direct sunlight during transit. Shipping documentation includes safety data sheets and regulatory compliance certifications. |
| Storage | Store 3-Bromo-2-methoxy-5-trifluoromethylpyridine in a tightly sealed container, away from direct sunlight and moisture, in a cool, dry, and well-ventilated area. Keep it separated from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and use appropriate chemical storage cabinets, such as those designed for organic chemicals or halogenated compounds. |
| Shelf Life | 3-Bromo-2-methoxy-5-trifluoromethylpyridine is stable for at least two years when stored under recommended conditions, tightly sealed. |
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Purity 98%: 3-Bromo-2-methoxy-5-trifluoromethylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Melting Point 52–55°C: 3-Bromo-2-methoxy-5-trifluoromethylpyridine with a melting point of 52–55°C is used in solid-state process optimization, where it facilitates controlled crystallization. Molecular Weight 276.03 g/mol: 3-Bromo-2-methoxy-5-trifluoromethylpyridine at a molecular weight of 276.03 g/mol is used in medicinal chemistry, where it provides precise mass balance in compound design. Particle Size < 50 µm: 3-Bromo-2-methoxy-5-trifluoromethylpyridine with particle size below 50 µm is used in formulation development, where it enhances dissolution rate and uniform dispersion. Stability Temperature up to 90°C: 3-Bromo-2-methoxy-5-trifluoromethylpyridine with stability up to 90°C is used in high-temperature reaction protocols, where it maintains structural integrity under processing conditions. HPLC Assay ≥99%: 3-Bromo-2-methoxy-5-trifluoromethylpyridine with HPLC assay ≥99% is used in analytical research, where it guarantees product consistency and reproducibility of results. |
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Some compounds have a long road from development to practical use, and 3-Bromo-2-methoxy-5-trifluoromethylpyridine stands out as a prime example in the specialty chemicals arena. Our own team has been hands-on with this pyridine derivative for several years, shaping both our process technology and our understanding of its application potential. The chemical structure brings together bromine, a methoxy group, and a trifluoromethyl group on a pyridine ring—each part leaving its own fingerprint on reactivity and suitability for downstream chemistry, particularly in pharmaceutical synthesis and agrochemical research.
This molecule (CAS: 875781-19-8) occupies a unique space in our product line. We synthesize it using refined halogenation and methylation steps in our reactors, followed by close attention in purification to minimize trace impurities—details only growers and real users care about, but which set apart a process-committed manufacturer from pack-and-ship rebaggers.
Other pyridine derivatives rarely balance the electron-withdrawing power of both bromine and a trifluoromethyl group alongside the push from a methoxy substituent at the 2-position. That balance matters on the bench, as chemists often need to create intermediates for complex molecules where site-selective reactivity or metabolic stability are concerns. A trifluoromethyl group shifts the electron density further than a simple methyl, for example, while bromine at the 3-position offers a reliable handle in Suzuki or Buchwald-Hartwig coupling reactions. Not all analogues deliver the same mix of reactivity and selectivity—some overreact, others resist transformation or introduce problematic byproducts downstream.
Day-to-day experience in our facilities has taught us there’s no substitute for tight control over water, trace halides, and metal residue in pyridine derivatives—especially those headed into medicinal chemistry labs. Each kilogram we produce runs through batch chromatographic purification, then undergoes GC-MS and NMR verification. We routinely achieve purity above 98%, and even after shipment to international partners, we’ve observed this level maintained thanks to our moisture-barrier drums and proper inert gas blanketing.
Unlike broader commodity chemicals, specialty heteroaromatics such as 3-Bromo-2-methoxy-5-trifluoromethylpyridine require dedicated equipment. Some of our neighbors in the field try to run operations in multipurpose lines, but contamination risks from previous campaigns are real. Our reactors and centrifuges only see this product or its close relatives, which means we can keep cross-contaminants down below recognized detection limits. That makes a difference if you’re formulating sensitive intermediates in a pipeline where regents interact or in proprietary crop protection trials where trace unknowns can skew results.
Most of the demand we see for this compound comes from early-stage pharmaceutical synthesis. Med chem teams often use the bromo group for cross-coupling to append a wide variety of aryl or alkyl fragments—essential in generating analog libraries during lead optimization. The presence of both the methoxy and trifluoromethyl groups helps tune lipophilicity and metabolic fate, which can give an edge in the preclinical phase if the right balance is struck between permeability and clearance.
Beyond pharma, agricultural R&D groups have picked up on the unique properties of this scaffold. Our in-house experiments with structure-activity relationship (SAR) profiles confirm a rise in bioactivity when the trifluoromethyl sits at the 5-position compared with 4-position analogs. As a functional intermediate, it offers synthetic flexibility for designing molecules with enhanced persistence in the field and reduced environmental mobility—a consideration especially relevant now with tightening crop protection standards.
From a bench perspective, 3-Bromo-2-methoxy-5-trifluoromethylpyridine behaves robustly under both conventional and microwave heating. Many transition-metal catalysts tolerate the electron-deficient ring, and the methoxy group rarely succumbs to unwanted cleavage. We’ve managed successful scale-ups to multi-kilogram batches without noticeable shifts in reactivity or byproduct profiles, signaling both process stability and reliability for customers pushing from grams to pilot-stage work.
Compared to seemingly similar halopyridines like 3-bromo-5-trifluoromethylpyridine or 3-bromo-2-methoxypyridine, this molecule shows higher chemical stability during storage and handling, provided the moisture barrier remains intact. Many end users underestimate the impact of humidity or exposure to strong acids, which can draw out hydrolysis or deactivation issues down the line. After some early setbacks with less-protected packaging, we switched over fully to aluminum-lined containers—seemingly small changes, but they dramatically cut down on off-spec feedback from overseas.
Another practical difference comes during hydrogenation and reduction steps. Our teams have noted that the trifluoromethyl group at the 5-position makes it more resistant to reduction than the same group at other positions. That increased resistance allows for more aggressive conditions elsewhere in a synthetic route without damaging the core scaffold. Such insight only comes after years of test reactions and failed pilot runs—not something you get by reading catalogs.
Cost-wise, the specialized feedstock and stepwise synthesis make this a more expensive compound per kilo than simpler pyridines or bromopyridines. We have invested heavily in process control, safety monitoring, and staff training for handling brominated and fluorinated reagents. Each improvement in yield or reduction in waste, driven often by in-house data from repeated runs, translates into tangible stability in price and supply—a factor every development chemist stuck with sudden shortfalls appreciates.
No chemical product reaches the market without its share of hiccups. In the early days of production, we ran into issues with residual bromine in final product, which affected downstream reactivity, especially in sensitive palladium-catalyzed steps. Manual tweaking of quenching routines and double washes allowed us to hit unreactive bromide backgrounds without compromising yields.
Scale translates differently than literature conditions suggest: higher viscosity, heat transfer complexities, and sometimes unexpected side reactions. We have seen trace side reactions that only reveal themselves during long-term storage—minor impurities under analytical detection at shipping, but noticeable after months at a customer’s warehouse. Adjusting to this reality, we started extending our own long-term stability studies, going well beyond the typical three-month windows, and reporting our findings directly to long-term buyers, building trust that doesn’t rely on flashy promises or overloaded data sheets.
Every batch speaks for itself. By following feedback from regular customers—pharmaceutical and agricultural research labs—we tune both process and service. It’s not uncommon for chemists to ring us up with complaints about clogging lines or off odors. Most of these cases, we traced back to incompatible solvents or mixing with residual acids in customer tanks, issues we now warn about in every shipment report.
Handling pyridine derivatives with halogen and fluorine content demands more than token compliance. Over the past decade, we have installed real-time emissions monitoring and closed-loop scrubbers, not only to meet regulatory standards but to avoid building up risk liabilities downstream. This commitment helps us minimize worker exposure and community complaints—a reality for chemical plants surrounded by growing populations.
Waste treatment plays a critical role in supporting responsible manufacturing. Through spent catalyst reclamation and solvent recovery systems, we have driven down both unit cost and environmental impact. This approach paid off when a sudden tightening of local EPA standards forced less-prepared firms off the market; our plants continued smooth operation without scrambling or emergency shutdowns. We know a healthy operation depends on long-term investments that protect both the workforce and the company’s future.
We also keep up-to-date SDS files and run scheduled drills for spills or inhalation exposure, training crews to manage the risks of accidental releases of potent halogenated pyridines. This isn’t paperwork—it directly impacts turnaround times and emergency outcomes, contributing to a decades-long run of zero major incidents.
The specialty chemicals market brings its own brand of uncertainty. Sourcing halogenated and fluorinated building blocks sometimes faces delays owing to tightened controls, political wrangling, and global logistics hiccups. Seasonal scrambles often drive up lead times and prices, especially around the turn of the financial year or during plant shutdowns for regulatory audits—or when a competitor goes offline due to a safety incident.
We navigate this volatility by building redundancy in our own supply chain and working on secondary synthesis routes. Raw material dual-sourcing, stockpiling during low-demand windows, and keeping close communication with freight partners help us keep shipments steady for research and pilot production partners. Experienced teams know to warn customers earlier when some grades of starting materials run short, preferring backorder transparency over unreliable promises.
The ability to maintain consistent quality and supply for a specialized compound like 3-Bromo-2-methoxy-5-trifluoromethylpyridine depends less on the scale of the business and more on constant attention to operational details—resource allocation, rigorous documentation, training, and ongoing dialogues with users whose needs shift project by project.
Trust is a currency that takes years to earn and minutes to lose, especially in regulated sectors like pharmaceuticals and engineered agriculture. We’ve studied cases where batch failures or poorly characterized intermediates caused chain reactions across entire research programs. Transparent communication, actual batch samples, and site audits (whether virtual or onsite) help potential partners gauge our level of control and responsiveness. The most loyal customers often started with a small qualifying order before moving to regular procurement; they stayed because the consistency, not discounts or big claims, matched their project needs.
Firms that rely on traders or spot-market resellers often run into unpredictable delays, paperwork bottlenecks, or documentation worries. Firsthand production, supported by traceability documents, allows our buyers to be confident answering to auditors or regulatory inspectors. We don’t separate product from process or from the people who monitor purity readings or troubleshoot equipment in real time.
Experience tells us that the right information—chemical fingerprint, impurity profile, shelf-life data—counts more than generic product flyers. Buyers in discovery chemistry or late-stage development have expressed more appreciation for real-time support and aftersales troubleshooting than any static list of properties on a website.
Space for improvement always exists, so every year brings new process experiments and small modifications. Continuous feedback loops from customers have spurred us to push boundaries—testing alternative solvents, finetuning reaction sequences, and automating more steps for safety and reproducibility. We continue to invest in pilot reactors that simulate production at practical scales, capturing unseen issues before they reach customer labs.
Growing interest in greener chemistry has motivated our R&D teams to explore biocatalytic or less halogen-intensive synthetic steps—sometimes at the expense of margins, but with an eye on future compliance and market access. Experience in this industry has proven again and again that adaptability and openness—not standardized checklists—make or break long-term partnerships.
The journey of 3-Bromo-2-methoxy-5-trifluoromethylpyridine from synthetic scheme to practical utility shows how much real-world knowledge, process control, and direct customer feedback shape a specialty chemical’s value. This compound, with its well-considered substitution pattern, supports innovation in both pharmaceutical and agrochemical research—not through generic claims, but through the reliability, quality, and experience of hands-on production teams.
Customers who value more than a batch number seek chemical partners who share their drive for repeatability, transparency, and incremental progress. Our most rewarding projects come from these shared goals, building up a reservoir of knowledge and technical expertise that continues to serve every new batch, every troubleshooting call, and every improvement to the next generation of complex molecules.