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HS Code |
279895 |
| Iupac Name | 5-Bromo-1-methyl-1H-imidazole |
| Molecular Formula | C4H5BrN2 |
| Molecular Weight | 161.00 |
| Cas Number | 1120-88-9 |
| Appearance | White to off-white solid |
| Melting Point | 65-69°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | Cn1cncc1Br |
| Inchi | InChI=1S/C4H5BrN2/c1-7-3-6-2-4(7)5/h2-3H,1H3 |
| Pubchem Cid | 99948 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | 5-Bromo-N-methylimidazole |
As an accredited 5-Bromo-1-Methyl-1H-Imidazole 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-Bromo-1-Methyl-1H-Imidazole, sealed with a white screw cap and labeled with safety information. |
| Shipping | **Shipping for 5-Bromo-1-Methyl-1H-Imidazole:** This chemical is shipped in secure, chemical-resistant containers to prevent leaks and contamination. Packages comply with international transport regulations, including labeling for hazardous substances if required. Transport may require temperature control and documentation such as SDS. Handle with proper PPE upon reception. Expedited shipping available upon request. |
| Storage | 5-Bromo-1-Methyl-1H-Imidazole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Store at room temperature and protect from moisture. Ensure proper labeling and follow local regulations for chemical storage to prevent accidental exposure or environmental contamination. |
Applications of 5-Bromo-1-Methyl-1H-Imidazole in Industrial ManufacturingAs a direct manufacturer with long-standing production experience, we supply 5-Bromo-1-Methyl-1H-Imidazole for advanced industrial applications, supporting customers across regulated sectors such as pharmaceuticals, agrochemicals, specialty chemicals, and fine chemical synthesis. Below, we present distinct downstream application scenarios, highlighting real formulation specifications, compliance requirements, and process details critical for professional producers. 1. Pharmaceutical Intermediate for Antiviral API SynthesisLeading pharmaceutical companies integrate 5-Bromo-1-Methyl-1H-Imidazole as a heterocyclic building block in the synthesis pathway of advanced antiviral active pharmaceutical ingredients (APIs), notably in nucleoside analogue drugs. Its brominated imidazole core introduces targeted functionalization sites, supporting regioselective coupling reactions essential for leading nucleoside-based therapies. Industry compliance standards
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2. Agrochemical Active Compound PrecursorProducers of agricultural fungicides and systemic agents use 5-Bromo-1-Methyl-1H-Imidazole as a key intermediate in the manufacturing of heterocycle-based agrochemicals. Its methylated imidazole ring serves as a strategic core for subsequent derivatization steps, enabling high selectivity in final actives targeting pathogenic fungi or plant viruses. Industry compliance standards
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3. Building Block in Specialty Dye SynthesisDye and pigment manufacturers utilize this imidazole derivative in the creation of advanced specialty dyes requiring precise electron-donating and -withdrawing substituents. The bromine atom serves as an activation point for palladium-catalyzed arylations, enabling access to unique imidazole-based chromophores for high-stability colorants used in industrial coatings, inks, or optical materials. Industry compliance standards
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4. Intermediate for Active Pharmaceutical Ingredient Sartan Type API SynthesisProducers of antihypertensive drug substances employ brominated imidazole scaffolds in the multi-step synthesis of sartan-class active pharmaceutical ingredients. The compound acts as a critical precursor for the selective construction of biphenyl-tetrazole frameworks via palladium-catalyzed coupling methodologies, supporting the stringent impurity and trace residual management required for cardiovascular end-products. Industry compliance standards
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5. Fine Chemical Synthesis for Research & Custom Synthesis LabsCustom synthesis workshops and R&D laboratories often require 5-Bromo-1-Methyl-1H-Imidazole as a versatile starting point in exploratory heterocyclic chemistry, particularly in the preparation of reference standards, library compounds, or functional materials earmarked for further development. Its defined reactivity profile supports rapid modification using Pd-catalyzed methods as well as nucleophilic substitution routes, with robust quality control on batch-to-batch impurity levels. Industry compliance standards
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Anyone who's spent years on the manufacturing floor—among reactors and distillation columns—knows that every day means looking at raw materials through the lens of reliability. Over time, you develop a kind of respect for certain chemical skeletons, and the imidazole ring easily earns its place. 5-Bromo-1-Methyl-1H-Imidazole stands as a testament to how subtle adjustments in molecular structure decide which direction a synthesis route can take. For producers like us, this molecule isn’t just another entry in the catalog. We have observed its increasing demand, marked by the specific needs of trusted partners in both pharmaceutical and chemical research industries.
This compound draws attention for more than its bromine substitution on the five position or the methyl group on the nitrogen. What users see as a bottle of crystalline powder, we view in terms of batch purity, freedom from colored impurities, chemical stability during warehousing, and ease of weighing on the plant floor. Our process builds in rigorous analytical steps—no shortcuts from batch sampling, drying, to final packing. Each lot meets consistent quality checks, including HPLC purity that reflects the best possible result from our synthesis pathway.
The model most frequently requested aligns with laboratory and pilot production scales. We have consistently delivered products where both bromine and methyl groups appear exactly where chemists expect, confirmed by not just NMR or MS data but by real-world reactivity in their syntheses. We don’t pamper our molecules with exotic stabilizers; our approach values clean chemistry and rigorous handling, keeping water and extraneous halide contamination minimized by controlled drying and storage.
There’s a stark difference between pushing small amounts through a Schlenk line in the lab and turning out kilograms at an industrial plant. We have learned that scaling 5-Bromo-1-Methyl-1H-Imidazole production brings unique challenges, especially when aiming for reproducibility in larger volumes. Over years of optimization, we’ve fine-tuned conditions to limit the formation of side products—namely, overbromination or degradation under elevated temperatures. Our team’s experience here brings confidence to researchers: no batch-to-batch guessing, no surprises in impurity profiles.
From the manufacturing side, this means investing in reliable agitation, exact timing, and solvent controls. Plant workers track humidity and temperature swings and stick to reliable sources for reagents and solvents: no corner-cutting, not if you’re in it for the long-term partnerships.
In practical terms, most customers approach us for applications relating to pharmaceutical intermediate production or for specialized building blocks in organic synthesis. The bromo group at the five position, paired with N-methylation, opens the door to versatile reactivity. It takes well to cross-couplings, allowing medicinal chemists to append a range of aromatic or heteroaromatic partners. Suzuki and Buchwald–Hartwig reactions have become mainstays in their labs. We’ve watched research teams halve their lead-optimization effort by directly introducing this imidazole moiety, saving time on additional synthetic steps.
Other uses include exploring the biological activity landscape—the precise location of the bromine atom and N-methyl group can profoundly influence receptor binding. As direct knowledge grows among medicinal chemists, more nuanced patterns in SAR (structure–activity relationships) surface and feed back into how we approach our own controls. The feedback loop between what we learn from users and what we can do on the manufacturing floor remains one of the most satisfying parts of this job.
It’s easy to list similar imidazole derivatives—3-bromo, 4-bromo, N-unsubstituted counterparts, or fused analogs. But small differences in substitution dramatically change how each fits into a synthetic plan. Over the years, we have handled orders for almost every isomer, from unsubstituted imidazoles to multi-methylated, multi-halogenated rings. The challenge with 5-Bromo-1-Methyl-1H-Imidazole lies in balancing selectivity during the synthesis phase, as bromination on an imidazole ring never truly leaves room for error. The nature of N-alkylation also shifts reactivity patterns; methylation prevents unwanted tautomerization, locks the molecule in a usable state for subsequent couplings, and usually improves solubility compared to the parent imidazole or other N-unsubstituted versions.
Buyers often trial 5-bromo-N-methyl versus 5-bromo parent imidazole or 2-substituted isomers, seeking better activity profiles or process efficiency. Our own hands-on experience says that customers running late-stage alkylation on a 5-bromo imidazole often encounter unpredictable N/N’ selectivity. By starting with an N-methyl variant, you walk past this bottle-neck entirely. This small, foresight-driven choice reduces potential byproducts in scale-up, saves downstream purification effort, and means less frustrations dealing with purification columns that can quickly clog with sticky side products.
For those of us working directly with reactors and filtration assemblies, purity specs are not just a checkbox for documentation. Any deviation in melting point, NMR signal, or residual solvent can ripple out, affecting downstream chemistry and even influencing the safety of pharmaceutical candidates. We have spent years learning how discernment in material handling pays dividends in the end results seen by our clients. Our experience revealed early that wet solvents or partially dried intermediates create more work for our users by causing unexpected byproducts or retention issues during analytical testing.
That’s why our production lines use both automated drying and in-situ purity checks at critical control points. We have repeatedly adjusted our process to keep heavy metal residues (often overlooked in academic-scale work) below industry-accepted limits. Our batch records chart the incremental improvements in yield and purity over time—gains earned through trial, error, and honest feedback from those actually using our chemicals, not just our own internal benchmarks.
The chemical industry faces ongoing scrutiny regarding waste streams, solvent usage, and the sources of its raw materials. We cannot sidestep the concerns about brominated intermediates. Careful control of effluents, trapped volatile byproducts, and solvent recovery make up essential conversations in our plant meetings. We derived value from shifting to greener solvents and switching to catalysts that reduce byproduct formation. Over time, protocols for distillation and material re-use cut our chlorinated and halogenated waste—changes that came from grassroots discussions among our processing team, sparked by direct hands-on observations.
Each decision has a ripple effect not just for us, but for those handling our product downstream. We have found that cleaner chemistry on our end results in safer, more predictable chemistry in the labs of our customers. There’s pride in knowing that our efficiency improvements—largely invisible to outsiders—translate into less hazardous waste generated by the end-user. We share process improvements and sustainability metrics transparently with those who rely on our products, building on mutual trust and responsibility toward the environment we all share.
As a manufacturer, we see the process from raw material to packed drum, not just from catalog to carton. Stability of both the bulk compound and the final packaged product matters a great deal. 5-Bromo-1-Methyl-1H-Imidazole stores well under standard warehouse conditions, but we cycle stock aggressively to limit any risk of degradation, especially in regions with high humidity or fluctuating temperatures. Each batch is sealed with attention to moisture exclusion, and our shipping team maintains a watchful eye for signs of physical distress—caking, discoloration, or oiling off.
Our logistics team has lived through the headaches of customs delays and shipping mishaps, so we equip ourselves with documentation and packaging standards that meet both export regulations and sensitive laboratory requirements across borders. We encourage direct dialogue between our dispatchers and end users when special storage or expedited shipping is necessary, rather than relying entirely on intermediaries who may not appreciate the sensitivity of these chemical intermediates. Regular audits of our shipping practices help us catch problems before they affect the end user's timeline.
Manufacturing at scale brings blind spots. We urge our customers—whether in small startups or established pharmaceutical labs—to share unsolicited feedback, both positive and negative. It’s only after seeing reports of successful scale-ups, identifying minor yield losses, or solving downstream purification snags that we push for process tweaks. More than once, seemingly small feedback—an offhand comment about solubility in an unfamiliar solvent, or trace coloration under certain lighting—spurred real modifications in our plant operations.
Chemists and process engineers rely on repeatable, predictable lots. We track every user concern, collecting data over years, and use this archive to anticipate changes to both our synthetic protocol and packaging. Our technical support teams regularly host internal retrospectives, asking tough questions about variance and how we can further tighten controls. For us, making better 5-Bromo-1-Methyl-1H-Imidazole isn’t about chasing sales, but about building a more dependable partnership where researchers trust that the material will perform the same, every time, no matter the project scale.
We have held rigorous process reviews long before industry buzzwords like “continuous improvement” took root. By tracing every failed batch, each analytical anomaly, and all ambiguous impurities back to their root causes, we learned that constant vigilance pays off. Process changes get logged, discussed across shifts, and pilot-tested before entering routine production. We single out the points that cause energy spikes, delays, or waste, and we make changes with the quiet confidence that comes from direct experience.
Continuous training of our staff, careful equipment maintenance, and responsive troubleshooting define our spirit. Most gains we’ve achieved came not from top-down management memos but by listening to the plant crew: those who stand by the filters, monitor reaction exotherms after hours, and spot the fine specks of off-color in a product tray missed by automated sensors.
The world doesn’t wait for supply chains to catch up. We have ridden the rollercoaster of raw material price swings and shipping crunches. Sourcing high-purity imidazole and bromination reagents meant taking proactive steps with qualified vendors and backing up critical raw stocks. During times of market stress, the difference between a missed delivery and a smooth handover often rests on simple habits—prompt communication, honest updates, and stubborn loyalty to quality over profit margins.
Responding to these pressures, we invested early in digital tracking of our procurement cycles, tighter vendor audits, and batch-to-batch analysis of incoming materials. Any time a supplier shifts their process, even subtly, we adapt our own analytical controls to guard against inconsistent performance in the outgoing product. These lessons are hard-won. By keeping both eyes on the market and two feet planted in day-to-day operations, we keep reliability as our unshakeable bottom line.
The final success of 5-Bromo-1-Methyl-1H-Imidazole depends on more than just what leaves our plant. End users—researchers, formulation chemists, production chemists—hold a stake in how this molecule will drive innovation, bring new therapies forward, or build advanced materials. Our job doesn’t end at delivery. We keep the lines open for support, technical inquiries, and troubleshooting. This shared responsibility enhances safety, improves yields, and ensures the collective progress of all who tap into the potential of this adaptable molecule.
It’s not uncommon for us to revisit production documentation after fielding a crystallization question from a customer, or to create new lot-specific analytical reports for especially sensitive pharmacological work. We operate with a view that both supplier and user move the field forward together, and the history tracked in every batch, improvement, and user note reflects this mutual journey.
Every chemical manufactured in our facility tells a story. The journey of 5-Bromo-1-Methyl-1H-Imidazole reflects years of incremental gains—minimized impurities, controlled particle morphology, and steady yields—earned through dedication to both process and partnership. For the researchers at the bench, each gram represents a chance to push science forward. For those of us on the line producing it, each drum packed with precision represents a bond of trust, built through years of trial, attention to detail, and a promise of reliability.
We continue refining our process, informed by real-world application, customer insight, and a steadfast commitment to stewardship—balancing innovation, quality, sustainability, and the needs of those who depend on us to deliver, every time.