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HS Code |
355446 |
| Chemicalname | 5-(bromomethyl)-2-(trifluoromethyl)pyridine |
| Molecularformula | C7H5BrF3N |
| Molecularweight | 240.02 g/mol |
| Casnumber | 1072954-94-1 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.65 g/cm3 (estimated) |
| Smiles | C1=CC(=NC=C1C(F)(F)F)CBr |
| Inchi | InChI=1S/C7H5BrF3N/c8-4-5-1-2-6(7(9,10)11)12-3-5/h1-3H,4H2 |
| Refractiveindex | 1.47 (estimated) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Storageconditions | Store at 2-8°C, protect from light and moisture |
As an accredited 5-(bromomethyl)-2-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5-(bromomethyl)-2-(trifluoromethyl)pyridine, sealed with a PTFE-lined cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL container loading: Securely packed drums of 5-(bromomethyl)-2-(trifluoromethyl)pyridine, labeled, palletized, and compliant with chemical transport regulations. |
| Shipping | 5-(Bromomethyl)-2-(trifluoromethyl)pyridine is shipped in a tightly sealed, chemical-resistant container, protected from light and moisture. The package is clearly labeled as hazardous, in compliance with international regulations for transport of chemicals. Appropriate documentation and safety data sheets are included. Shipping may require temperature control and will be via certified carriers. |
| Storage | **5-(Bromomethyl)-2-(trifluoromethyl)pyridine** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, oxidizing agents, and incompatible substances. Store under inert atmosphere (e.g., nitrogen) if possible to prevent decomposition. Ensure proper labeling and follow all relevant safety and regulatory guidelines. |
| Shelf Life | Shelf Life: 5-(bromomethyl)-2-(trifluoromethyl)pyridine is stable for at least 2 years if stored sealed, dry, and protected from light. |
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Purity 98%: 5-(bromomethyl)-2-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Melting Point 55-58°C: 5-(bromomethyl)-2-(trifluoromethyl)pyridine at a melting point range of 55-58°C is employed in organic electronics manufacturing, where it facilitates uniform film formation. Stability Temperature 25°C: 5-(bromomethyl)-2-(trifluoromethyl)pyridine stable at 25°C is used in agrochemical development, where it maintains reactivity during storage and formulation. Water Content ≤0.5%: 5-(bromomethyl)-2-(trifluoromethyl)pyridine with water content ≤0.5% is utilized in fine chemical synthesis, where it reduces hydrolysis risk and product degradation. Density 1.65 g/cm³: 5-(bromomethyl)-2-(trifluoromethyl)pyridine at a density of 1.65 g/cm³ is used in material science research, where it enables precise volumetric dosing and reproducibility. Molecular Weight 260.02 g/mol: 5-(bromomethyl)-2-(trifluoromethyl)pyridine, having a molecular weight of 260.02 g/mol, is used in heterocyclic compound design, where it allows for accurate stoichiometric calculations. Particle Size ≤10 µm: 5-(bromomethyl)-2-(trifluoromethyl)pyridine with particle size ≤10 µm is used in catalyst formulation, where it provides enhanced dispersion and reaction kinetics. |
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Every time a new synthetic target passes across the lab bench, finding a stable, trustworthy building block saves time and opens doors for chemists. As a manufacturer producing 5-(bromomethyl)-2-(trifluoromethyl)pyridine, we see it up close—that reliable performance means more than glossy words in a brochure. Our clients, mainly from the pharmaceutical research field and the advanced agrochemical development sector, request this compound because it brings flexibility and efficiency to making complex molecules.
The model and composition carry significance for daily users, not just spec sheets. Each batch of our 5-(bromomethyl)-2-(trifluoromethyl)pyridine offers a pinpoint blend of reactivity and manageability. With a molecular formula of C7H5BrF3N and a molecular weight of around 256.02 g/mol, it strikes a balance between handling and downstream versatility. We pay attention to factors like crystallinity, absence of caking, and a manageable melting behavior. Our purity range typically exceeds 98 percent, based on HPLC and NMR confirmation, making the product suited for demanding downstream chemistry.
What sets this pyridine derivative apart is the inclusion of both a bromomethyl group and a trifluoromethyl group on the same aromatic ring—these choices aren’t a matter of chance. The bromomethyl group provides a practical site for nucleophilic substitution or cross-coupling, key for constructing carbon–carbon or carbon–heteroatom bonds. This reactivity can shorten synthetic routes. The trifluoromethyl group, by contrast, adjusts pKa, boosts metabolic stability, and shifts electronic properties of finished products, especially in medicinal and plant-protection chemistry.
From our own manufacturing floor, we know the bulk of demand for this molecule comes from early-stage pharmaceutical and crop protection research. Synthetic chemists are always chasing newer, more effective scaffolds. The compound’s design speaks directly to this need. It allows functionalization on the pyridine ring, pushing forward analog development and structure–activity relationship studies. Common pharmaceutical projects use this intermediate when they are optimizing bioactive molecules for enzyme inhibition, receptor binding, or metabolic fine-tuning.
Colleagues in the crop science sector often request the product for development of herbicides or fungicides. The balance the molecule strikes finds use when a project needs a moderate leaving group and a handle for late-stage derivatization. It enables construction of custom heterocycles, pyridine-based acids, or ether derivatives that have patent-protected activity and environmental compartmentalization properties.
Many pyridine-based methyl halides exist, but only a few boast the distinctive blend of a bromomethyl and a trifluoromethyl group. Compared to 2-(trifluoromethyl)pyridine alone, the product opens more routes for forming C-N, C-O, or C-C bonds through nucleophilic substitution at the bromomethyl site. Contrast it further with 5-(chloromethyl)-2-(trifluoromethyl)pyridine—the bromine atom’s size and polarizability yield higher reactivity in many coupling reactions. In batch work, we see customers reduce reaction times and improve yields on pilot scale. This isn’t an abstract claim but feedback from process chemists who adapt their conditions on the fly and send us real-world data.
Standard 2-(trifluoromethyl)pyridine lacks easy functionalization at the 5-position. There is no halogen handle, which limits options for side-chain introduction—a gap our product neatly fills. It bridges a common problem for process development chemists needing both electronic tuning (via trifluoromethyl) and further elaboration (via the bromomethyl)—especially valuable under pressure to deliver analogs for SAR studies or fine-tune physical properties like solubility or membrane permeability.
Experience tells us lab-scale standards don’t automatically translate to smooth scaling. We’ve engineered our synthesis for repeatability and waste control, using processes designed to minimize formation of unwanted byproducts or side-reactions, such as overbromination or ring halogenation. Rigorous temperature monitoring prevents exotherms. During work-up and purification, the batch is never exposed to untreated moisture or air longer than necessary. We send representative retention samples to analytical labs within hours of synthesis—tight time controls ensure what customers receive matches the original certificate of analysis.
You can’t ignore safety with halomethylated heterocycles. The bromo group demands closed handling and precise dosing. Over the years, our shift toward sealed glass or coated-metal reactors made a clear difference in yield and personal protection. Each drum or bottle comes with tamper-proof seals and batch traceability. Customer audits regularly verify our in-house training programs—well before we ever ship lots, our operators follow a process-oriented workflow, logging each critical control point electronically. This helps clients sleep easier. If a problem arises anywhere downstream, batch traceability helps with root-cause analysis and regulatory compliance.
Our sales and support teams keep their ears open for feedback beyond the purity and assay numbers. Researchers cite the handling profile—our batches resist hygroscopic clumping, retain free-flowing texture, and don’t need extended prepping before use. This comes directly from batch management—manipulating humidity at every stage and packaging immediately after QC approval. In rare cases, researchers identify subtle matrix effects in formulations or slight color differences between lots. These aren't just filed away; we adapt our protocols to maintain color, texture, and flow across scales.
One shared concern: occasional trace halides or moisture affecting downstream cross-couplings, especially in high-throughput screening. We keep these under control through dynamic purging, three-step drying, and periodic customer audits. If any user flags something—even as minor as shifts in NMR integrals or drifting melting points—our technical staff investigates, retests, and communicates findings directly. We believe in transparency over reputation-building.
Our location in the value chain matters. We don’t just ship material; our technical staff regularly consults on compatibility questions, synthetic troubleshooting, and custom adaptation of the bromomethyl motif. Drug discovery teams often probe regiochemical preferences—our own R&D runs pilot reactions, offering insights on how minor solvent tweaks or reflux changes alter selectivity. This builds a two-way knowledge loop, informing our next round of process improvements and industry best practice recommendations.
Worldwide, regulatory trends keep an intense spotlight on trace impurities, recycling, and environmental stewardship. Our process rigorously tracks materials and byproducts. We recover solvents, minimize purged mother liquors, and avoid halogenated waste streams. Whenever a new regulation emerges in the US, EU, or Asia, we adapt—not just for compliance, but to build confidence with science-led buyers who ask tough questions about sourcing and bioburden. Environmental, social, and governance criteria aren’t hypothetical—they influence supplier choices across the pharmaceutical and specialty chemical value chain.
Challenges don’t end upon dispatch. In emerging markets, the logistics chain introduces risks—temperature cycling, extended transit, and customs delays can test physical stability. To protect the product, we use high-barrier, tamper-proof containers matched to batch size. Temperature-monitoring indicators ride with shipments. Local partners have been trained on repackaging, resampling, and reclamation protocols to pre-empt desiccant failure or accidental breach. Quick follow-up with customers ensures each lot remains fit-for-use across oceans and months.
Complex regulatory patchworks demand proactivity. Global pharmaceutical regulations demand traceability for every precursor, not only the final molecule. We retain all production and analytical documentation, aligned with ISO and Good Manufacturing Practice standards where applicable. Auditors—whether in pharma, agrochemical, or specialty chemical supply chains—drill deep on validation, waste handling, and contamination histories. Our teams host site visits, share long-term trending data, and respond to market and regulatory feedback instead of relying only on formal paperwork.
From repeated interactions with R&D labs, we see demand shifting toward more highly functionalized heterocycles in the coming years. Chemists need tools that streamline DMPK optimization, enable rapid analog expansion, and respond to stricter regulatory curation. The unique blend of the trifluoromethyl and bromomethyl groups positions our pyridine as more than just a link in a synthetic chain—it anchors much of the analog expansion and tweaking, particularly in fields chasing first-in-class candidates or patent-protected chemistries.
Market pressures also nudge suppliers toward greater sustainability and transparency. Authenticity claims mean less if traceability and full analytical disclosure lag behind. Our teams continuously upgrade batch documentation, integrate digital tracking, and encourage independent secondary testing. As next-generation drugs and crop agents grow more intricate, intermediates must keep pace. We invest in new reactor platforms, smarter in-line monitoring, and faster cycle times—all to shorten concept-to-batch lead times and uphold reliability.
Manufacturing 5-(bromomethyl)-2-(trifluoromethyl)pyridine doesn’t boil down to purity figures alone. It takes hands-on technical expertise and a visible supply chain to support both breakthrough science and ongoing industrial production. Researchers value a supplier who treats quality concerns with the same urgency and candor they bring to their own work. Continuous, open exchanges with industry chemists drive both our process improvements and our reliability.
No two projects use this intermediate in the same way. Some process development teams handle tons, others a few grams, but all care about reproducibility and accountability along the value chain. From mitigating handling hazards to delivering evidence-based support for research groups, our commitment lies in practical, science-backed manufacturing. The days of faceless, commodity-focused intermediates have given way to a world where buyers expect trust as much as a clean assay.
Over time, our direct engagement with users reveals new directions and applications—fueling future improvements to both synthesis and supply. As demand grows for tailored, function-rich intermediates, we remain ready to solve real-world challenges alongside the creators who rely on us.