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HS Code |
529710 |
| Product Name | 3-Amino-2-Bromo-4,6-Dimethylpyridine |
| Cas Number | 884494-91-1 |
| Molecular Formula | C7H9BrN2 |
| Molecular Weight | 201.07 g/mol |
| Appearance | Light yellow to brown solid |
| Purity | Typically > 95% |
| Solubility | Soluble in common organic solvents such as DMSO and methanol |
| Smiles | CC1=NC(=C(C(=C1N)Br)C)N |
| Synonyms | 2-Bromo-3-amino-4,6-dimethylpyridine |
| Storage Conditions | Store at room temperature, dry place |
As an accredited 3-Amino-2-Bromo-4,6-Dimethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g sample of 3-Amino-2-Bromo-4,6-Dimethylpyridine is supplied in a tightly sealed amber glass bottle with hazard labeling. |
| Shipping | 3-Amino-2-Bromo-4,6-Dimethylpyridine is shipped in tightly sealed containers, protected from light and moisture. It is packed according to standard protocols for hazardous chemicals, complying with local and international regulations. Proper labeling and documentation are provided to ensure safe handling and transport during shipping. Temperature-sensitive precautions may apply if specified. |
| Storage | Store **3-Amino-2-Bromo-4,6-Dimethylpyridine** in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Store at room temperature, unless otherwise specified by the supplier. Properly label the container and ensure access is restricted to trained personnel to maintain safe handling. |
Applications of 3-Amino-2-Bromo-4,6-Dimethylpyridine in Industrial ManufacturingAs an established original manufacturer, we supply 3-Amino-2-Bromo-4,6-Dimethylpyridine to advanced chemical industries that require reliable input for high-purity synthesis routes. The compound’s unique structure supports several targeted downstream applications, most notably in pharmaceutical intermediate production and crop protection active development. The following sections detail specific use cases based on customer process data and industrial supply experience. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical synthesis workflows employ this pyridine derivative as a crucial step in constructing target heterocyclic scaffolds. Its halogen- and amino-substitution pattern enables selective Suzuki and Buchwald–Hartwig couplings, facilitating the assembly of pharmaceutically relevant molecules such as kinase inhibitors and antimicrobials. Customers implement this intermediate primarily in regulated GMP environments, where traceability and controlled impurity profiles are mandatory. Industry compliance standards
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2. Agrochemical R&D and Active Ingredient PrecursorResearch and development divisions of crop protection manufacturers adopt this pyridine compound to synthesize selective herbicide, fungicide, and insecticide candidates. The building block supports rapid access to 2-bromo amino-pyridine motifs prevalent in many new chemical entities (NCEs). Typical production runs maintain batch records for regulatory compliance and facilitate rapid upscaling from laboratory to pilot scale. Industry compliance standards
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3. Specialty Chemical Additive for Electronic Material SynthesisManufacturers of advanced electronic materials use this compound as a precursor for heterocyclic ligands or as a dopant precursor in organic electronics. Its reactivity suits fine-tuned substitution for creating custom ligands or charge transport intermediates, with strict batch homogeneity required to support device-grade material production. Documentation follows material supplier QC traceability systems for specialty electronics. Industry compliance standards
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4. Intermediate for Veterinary Drug SynthesisCustom active intermediate producers for veterinary drugs use this compound in assembling pyridine-ring-containing actives designed for animal health. Regulatory scrutiny covers trace impurity controls and cross-contamination protocols, especially when running parallel syntheses with other veterinary intermediates. Industry compliance standards
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Working in chemical synthesis day in and day out means handling a steady stream of requests for fine chemicals that push boundaries. Our facility lives and breathes heterocycles, and over time, 3-Amino-2-Bromo-4,6-Dimethylpyridine stands out in the catalog. Chemists ask us about availability for a reason. This pyridine derivative offers versatility in research labs and development seats, especially where custom routes in medicinal chemistry demand a balance of reactivity and stability. Here, we walk through what sets this compound apart and how it earns its keep.
Our usual output for this product lands in the 98% minimum purity range by HPLC, not from over-promising but because separating byproducts at this stage keeps synthetic routes on schedule for our partners. We ship as a pale to off-white crystalline solid, and batches clear moisture checks before bottling. Batches average a melting point between 132°C and 137°C, which matches published ranges for this compound. We choose manufacturing solvents and cleaning agents based on what prevents cross-contamination in downstream reactions. We only certify lots after head-to-head NMR and MS comparison to authenticated references.
Everything about this compound’s handling, right through packaging, takes cues from how it behaves in real benches. The BLG (brominated, aminated, dimethylated) scaffold responds to standard storage but holds up best when kept airtight and away from prolonged light exposure. That’s not marketing—just chemists avoiding headaches of impurity spikes or color change from overlooked material.
Pyrazines and pyridines with similar amino and bromo substitutions can create headaches on scale. Low solubility and tendency for certain polymorphs have led to more than one tense day with a filtration train. This compound’s dimethyl substitution eases the load, allowing more predictable solvation and filtration profiles, which means better outcomes for downstream transformations. For us, this translates into fewer lost hours reclaiming stuck filtration setups.
We run 3-Amino-2-Bromo-4,6-Dimethylpyridine in both glass and stainless vessels depending on campaign volume. That flexibility comes after years of optimization, not guesswork. Each run draws monitoring from our technical crew to ensure bromine incorporation and amino group stabilities, watched by both TLC and NMR checks. Product consistency means our clients rarely circle back for replacements. Repeat orders flow, not because we’re biggest, but because our lot variation stays within trusted bounds.
Demand for this reagent tracks with the health of the custom synthesis and pharmaceutical research markets. Researchers count on the amino group for nucleophilic addition and condensation routes, especially when building more complex heterocyclic scaffolds. The bromo moiety offers a reliable handle for cross-coupling techniques—Suzuki, Buchwald–Hartwig, and Stille couplings all find a platform here. Our customers ask repeatedly for this compound, reporting consistent yield and fewer side products compared to pyridines without the dual methyl and amino substitutions. The electron-donating nature of the methyls stabilizes intermediates during coupling reactions, minimizing unwanted dehalogenation.
Some bench chemists push this intermediate into bioactive structure campaigns, targeting kinase inhibitors, anti-inflammatories, and antiviral lead compounds. Its specific substitution pattern—a combination of 2-bromo and the 4,6-dimethyl—introduces just enough steric bulk to nudge reactivity in a predictable way, avoiding over-activation or unwanted ring opening. This provides an edge over simpler pyridine analogs that lack selectivity during scale-up.
It helps to put this compound in context. Pyridine chemistry covers a lot of ground, but introducing both an amino group and a bromo group in the positions found here turns an ordinary substrate into a selective building block. Products such as 2-Bromo-4,6-dimethylpyridine miss out on the direct functionalization that the amino group brings. Similarly, 3-Amino-4,6-dimethylpyridine (without bromine) fails to offer an easy attachment point for catalytic cross-couplings. From countless scale-ups, it's clear this specific structure leaves open more synthetic doors.
Some labs experiment with cheaper halogenated pyridines only to discover the increased purification steps or stability issues offset any price savings. Through years of working with process chemists, we have seen how the right blend of substitutions saves time in the long run. Our message to R&D directors weighing alternatives: consider finished cost, waste stream, and chemist time, not just catalog price.
Scaling up often exposes deep issues invisible at small batch. Early in our work with this compound, we dealt with batch variability from the choice of brominating agents. Low-quality feedstock introduced trace impurities visible by NMR after crystallization, which later affected downstream product stability. It took several process revisions, along with partnerships with our own raw material suppliers, to pin down a consistent and stable workflow. Reworking the purification, especially to improve recovery for waste management, not only improved yield but also trimmed costs for everyone down the supply chain.
Other roadblocks turned into learning experiences. At gram scale, the product responds well to general vacuum drying. At kilo scale, we learned that improper nitrogen flow during drying led to minute oxidation, shifting lot color. Our operators now follow specific protocols, and no batch leaves unless it matches agreed standards—not because regulations told us to, but because those lessons stick.
Requests for analytical data come with the territory, especially from larger clients and regulatory-facing projects. We maintain full documentation: NMR (proton and carbon), mass spectrometry, melting point, and HPLC traces for every lot. From a manufacturer’s seat, this is the only way to build repeat business. If a compound lacks a reliable fingerprint, it costs everyone real time in troubleshooting. This habit of thorough documentation came about not from trend-chasing, but from direct pressure to reduce cycle times for client validation batches.
Our methods evolve as tools advance. We've moved to digital NMR archiving and centralized all spectral libraries so reference checks run fast. This isn’t just a nice-to-have—it smooths every reorder, saves headaches for our technical service crew, and lets our partners validate before product ships.
Fine chemicals like 3-Amino-2-Bromo-4,6-Dimethylpyridine present a tough balance between production efficiency and environmental footprint. We treat every campaign, large or small, with a consistent eye on solvent recovery and responsible halogen handling. Brominated intermediates, including ours, hold persistent environmental risk if managed poorly. We've set our own internal targets on emission management, adopting methods for selective scrubbing and in-process solvent recycling. These approaches grew out of close calls: solvent mishaps and early batch filtrates forced us to rethink old shortcuts and choose safer, sustainable handling.
End users tend not to see these struggles on their bench. Still, buying from a source that manages waste and treats halogenated effluent provides assurance their own compliance requirements won’t bring last-minute regulatory snags. We update our environmental protocols and share best practices with partners, not just as a courtesy but as a core part of what responsible manufacturing means.
Supply chains for fine chemicals face constant pressure from global raw material swings. We track tight relationships with upstream producers, especially for intermediates such as methylpyridines and brominating reagents. Sporadic price spikes have forced us to expand our supplier base, building redundancy to keep customer lead times predictable. We pass these efficiencies down—ensuring reliable supply is how we maintain strong ties to both long-time and first-time clients.
Downstream, feedback loops tell us what matters during application. Our partners in drug discovery appreciate single-lot consistency, which speeds regulatory documentation. Scale-up for pilot and process chemists runs smoother when each contract batch matches prior experience. As a manufacturer with feet on the ground in every step, we value honest feedback from benches: whether during coupling trials, crystallizations, or final formulation work.
Original research thrives on ready access to well-defined building blocks. Over the years, we've provided this compound to groups in medicinal chemistry, agrochemical sciences, and advanced material synthesis. Each field bends its methods to the strengths of the molecule—some exploit the amino group for diazotization and further function, others perform direct cross-couplings with boronic acids straight from our lot.
Pyridine derivatives rarely offer such versatility without the baggage of reactivity or instability. The bromo-amino-dimethyl set-up simplifies library construction in lead optimization projects. By sharing our own application notes (gleaned from process runs and customer pilot feedback), we cut down on redundant experimentation, helping labs start at a higher level while maintaining rigorous safety standards.
Behind every synth run lies a team—chemists, operators, quality staff—who track thousands of data points and care about every shipment. Our operators have hundreds of cumulative years working with aromatic amines and brominated compounds. When issues come up, we sit together to troubleshoot on real cases, not hypotheticals. That level of care carries through to each bottle, and long-time partners know they can pick up the phone and get an answer grounded in lived experience.
Each time we introduce a new process, senior staff guide hands-on training, and we document process changes so that new team members learn not just the “what” but exactly why each decision makes future runs smoother. Honesty about the risk points—sourcing, process bottlenecks, or even how to handle customer complaints—keeps us accountable to our promise of practical reliability.
3-Amino-2-Bromo-4,6-Dimethylpyridine is not just another line item on a datasheet. For our clients, what matters most is knowing that every shipment reflects decades of problem-solving, process tuning, and hands-on experience with these molecules. The molecular backbone may look straightforward, but what counts is predictable, low-variance material delivered on a timeline without surprises. We see ourselves as partners to R&D teams seeking new therapies, improved crop science, or specialty materials—each application shaped by this unique blend of chemical features.
In our world, reliability grows from each cycle—every scale-up, every repeat order, every phone call to clarify a technical query or troubleshoot an unexpected curveball. This compound has earned its reputation not because it sits at the bleeding edge of novelty but because it anchors so many successful syntheses with few roadblocks and plenty of room for creative chemistry.
Manufacturing 3-Amino-2-Bromo-4,6-Dimethylpyridine means more than producing a commodity. Every lot we send out tells a story of countless adjustments, quality checks, and lessons learned. We take every feedback loop seriously—whether about application-specific performance, documentation for regulatory files, or handling and storage quirks.
True value in chemicals comes not just from purity percentages or technical spec sheets but from real partnership. Our door stays open to customers dealing with novel synthesis routes or new regulatory hurdles, and we keep adapting alongside the researchers we work with.
Every bottle, every shipment, roots itself in this daily back-and-forth: experienced manufacturing meeting hard-driving scientific work. 3-Amino-2-Bromo-4,6-Dimethylpyridine fits into discovery pipelines, process trials, and production projects. Decades at the bench, in the control room, or talking across industry tables remind us that the right compound—reliably made—makes the difference between promising ideas and real-world success.