|
HS Code |
422505 |
| Iupac Name | (1S,4S)-2-methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide |
| Molecular Formula | C6H14N2·2HBr |
| Molecular Weight | 277.02 g/mol |
| Cas Number | 157310-52-2 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water |
| Melting Point | 220-225°C (decomposes) |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | Quinuclidine, methyl-, dihydrobromide (1S,4S); 2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide |
| Smiles | C1CN2CC1C(N2)(C)Br.Br |
| Inchi | InChI=1S/C6H14N2.2BrH/c1-8-5-2-6(8)4-7-3-5;;/h5-7H,2-4H2,1H3;2*1H/t5-,6-;;/m0../s1 |
| Pubchem Id | 13464713 |
As an accredited (1S,4S)-2-Methyl-2,5-Diazabicyclo[2.2.1]Heptane Dihydrobromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
Competitive (1S,4S)-2-Methyl-2,5-Diazabicyclo[2.2.1]Heptane Dihydrobromide 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!
Chemists are always searching for molecular tools that open new doors to precision and creativity in synthesis. (1S,4S)-2-Methyl-2,5-Diazabicyclo[2.2.1]Heptane Dihydrobromide—often simply dubbed as MBD—offers a blend of stability, selectivity, and versatility that helps fuel experiments and industrial workflows alike. This compound stands out because of its well-defined bicyclic structure, which brings a unique set of interactions to the table. Researchers in organic and pharmaceutical labs recognize this not just for being another reagent on the shelf, but for the way it often pulls off results that other amines or salts miss.
There’s something almost tactile about working with a compound as compact and robust as MBD. Its diazabicyclo scaffold packs two nitrogen atoms into a bridged ring structure. Add in the methyl group and the dihydrobromide salt form, and you get a molecule with strong basicity, but lower volatility compared to some alternatives. This not only makes handling easier, it helps control reaction conditions more tightly—a fact that chemists appreciate as they aim for accurate, reproducible outcomes.
Many amine reagents struggle under harsh reaction conditions or leave too many contaminants behind. MBD tends to hold up during long reaction cycles and doesn’t break down as quickly. That stability matters when you’re pushing a synthesis step forward; small gains in purity and yield can add up, whether the end goal is a new experimental compound or a batch destined for clinical evaluation.
Talking with colleagues, I've found people appreciate it when product details cut through the noise. MBD typically appears as a white, crystalline solid with a melting point in the range suited for bench storage. It dissolves well in polar solvents, such as water, methanol, and ethanol. The dihydrobromide form provides extra assurance against air and moisture intrusion, which often extends shelf life and cuts down on frustrating product degradation.
The optical purity—having that (1S,4S) stereochemistry nailed down—can shape the outcome in asymmetric synthesis or catalysis. If you try subbing this in for a less-selective amine, differences show up not only in yields but in how cleanly products emerge from the reaction mix. There’s a grounded reliability in the crystalline form, too. The solid handles well in both milligram and kilogram batches, useful for both academic bench work and commercial application.
Many synthetic routes call for a basic amine that doesn’t complicate matters by adding extra water or unwanted side reactions. MBD delivers here, providing a sterically controlled base that can drive alkylation, acylation, or Michael addition steps. At larger scales, process chemists recognize that the low volatility means fewer headaches about product loss or contamination.
There’s a difference between reading about selectivity and seeing it in action. Researchers looking to create precise stereochemical outcomes, such as chiral pharmaceuticals, rely on the defined configuration of MBD—the (1S,4S) variant in particular. Enzymatic and metal-catalyzed reactions sometimes gain a bump in efficiency and clarity just by switching to this base. For those working with sensitive substrates or intermediates, not having to fight against background reactions saves time and money downstream.
Over the years, I’ve seen labs reach for MBD during tricky multi-step syntheses, especially when chasing new heterocycles or fine-tuning nervous intermediates. Pharmaceutical researchers often speak of its role in asymmetric transformations that other amines can botch. In our own team’s projects, swapping in MBD sometimes helped recover stalled reactions—not because it’s a miracle worker, but because its architecture gently influences the course of the chemistry.
Process chemists often search for something that strikes a balance between performance and convenience. MBD has a knack for keeping reactions on track, and its solid form makes dosing and weighing straightforward—even during scale-up. Industrial teams focused on continuous production lines cite its long shelf life and consistent reactivity as practical assets. By not introducing as much moisture or other secondary products, it leaves less to clean up at the end of the process and less chance for costly reprocessing.
It’s tempting to lump all bicyclic amines together, yet not all perform with the same grace. Where some analogs—like quinuclidine or DABCO—bring their own strengths, MBD’s methyl substitution and dihydrobromide salt create a sweet spot of solubility, base strength, and thermal tolerance. The presence of bromide ions over other common counterions, like chloride or sulfate, can also impact how a reaction proceeds.
Switching from a less-pure, racemic base to the optically pure version found in MBD may cut byproducts and improve yields. In my experience, reactions that lag with more basic or flexible amines often move forward with greater control when MBD steps in. That precision is hard-earned for those aiming at sensitive targets, whether crafting new ligands, adjusting catalyst loads, or preparing enantiomerically enriched compounds.
Other amines with analogous ring systems—say, unmodified diazabicycloheptanes—sometimes create more unwanted reaction pathways or require tougher clean-up. The balance between reactivity and selectivity in MBD often saves hours at the purification bench and helps researchers deliver more useful, characterizable products.
Every chemist knows that product quality reaches further than just ticking off a specification box. Reagent consistency directly supports reproducibility in both research and manufacturing. I’ve worked in labs where one batch of a competitor’s base caused headaches, skewed runs, or forced a rerun of weeks of work. MBD’s lot-to-lot stability cuts down on those moments of doubt, helping teams trust both their data and their outcomes.
There’s satisfaction in working with a material that not only meets purity standards, but often surpasses them. Third-party validation, strong supplier partnerships, and in-house quality checks combine to ensure that what’s delivered matches what was promised. In fast-paced development pipelines, these details translate into higher success rates for compound development and a smoother path through regulatory approval.
Anyone who’s wrestled with hygroscopic powders or volatile liquids knows how much easier everyday work feels with a solid, non-deliquescent salt. MBD doesn't cling to humidity in the lab as some salts might. It stores well in closed containers, on shelves or in flammable cabinets, without demanding a lot of attention or backup precautions. This isn't just a matter of convenience; it preserves the integrity of the product and saves time during inventory checks or replenishment.
Simple storage requirements lower waste and reduce risk of mishaps. In large-scale settings, the ability to store and transport the compound without extensive climate control cuts costs and ensures a reliable flow of materials to the production line. Research labs often cite easy weighing and transfer as surprisingly valuable—no one likes cleaning spills or loss from clingy, sticky powders.
Conversations across the industry keep returning to sustainability and safety. Many teams want to avoid harsh or risky reagents when possible, both for health and environmental reasons. MBD’s mild handling profile and high reactivity allow scientists to streamline protocols, leaving out additional solvents or washes, which add to hazardous waste. That approach not only reduces environmental impact but often speeds up workflows and helps meet regulatory benchmarks for greener practices.
Safer chemical handling benefits researchers daily. Dramatically reducing exposure to volatile amines or uncontrolled reaction heat can mean the difference between a routine day and a safety incident. This compound’s chemistry finds the sweet spot between strength and manageability. Operating with MBD aligns well with modern lab safety guidelines, which mandate both personal safety and responsible stewardship of chemicals throughout their lifecycle.
Stereochemistry often serves as the foundation for performance in organic compounds, especially in pharmaceuticals, catalysts, and specialty materials. The (1S,4S) isomer of MBD brings more than just subtlety; it can determine whether a synthetic project succeeds or fizzles out. Chemists who’ve juggled racemic starting materials—or tried separating byproducts after a non-selective reaction—recognize how valuable predicable enantioselectivity is to their daily efforts.
Pharmaceutical development, in particular, rarely tolerates ambiguity in stereochemical purity. Process optimization around MBD’s configuration opens doors to both greater product quality and deeper insight into mechanisms. Years ago, our team realized how much time could be saved by starting from pure stereoisomers, both in terms of product isolation and in gaining regulatory clarity for later clinical stages.
No chemical product is a silver bullet. Some might argue for cost reductions or seek faster dissolution rates in non-polar systems. Others want even longer shelf lives or more granular control over impurities. Scaling up always uncovers quirks—heat transfer, packing density, or filterability during downstream purification present open questions that require hands-on experience to untangle.
Labs with continuous flow setups sometimes chase amines that won’t clog microreactors or reactor tubes. MBD’s crystalline texture and salt format help, yet every system brings its own set of challenges—so process engineers stay vigilant for improvements. Finding greener, more efficient manufacturing routes, minimizing bromide byproducts, and optimizing recycling of spent materials all represent promising avenues for both supplier innovation and end-user feedback.
Decades of accumulated practice underpin how chemists choose and use specialized reagents. Trust in a compound like MBD comes not just from technical bulletins, but from day-to-day trial and error, troubleshooting, and innovation. Reliable supply and support from knowledgeable partners boost confidence, and encourage more creative exploration of what’s possible in synthesis and scale-up.
Extended conversations at conferences and over lab benches reveal that MBD keeps cropping up in stories where a project pivots—either through overcoming a technical hurdle or finally achieving a tough selectivity target. Those moments, widely shared but hard to quantify, end up driving both adoption and further improvement. There’s still space for open discussion about sourcing, regulatory status, and handling, as new applications continue to expand.
New challenges push the chemical supply community forward. Increased demand for sustainable specialty chemicals prompts more companies to delve into their supply chains and investigate recyclable packaging, improved documentation, and user education. Workshops and open forums help both seasoned and early-career chemists develop a deeper understanding of tools like MBD, sharing hard-won tips and highlighting emerging risks and rewards.
Ongoing research aims to clarify reaction mechanisms and footprints, with open data sharing offering a way to accelerate learning and reduce duplication of effort. Collaboration between manufacturers, academic leaders, and end-users keeps feedback loops active, driving more practical approaches to stewardship and more innovative research directions.
The real reason a product like (1S,4S)-2-Methyl-2,5-Diazabicyclo[2.2.1]Heptane Dihydrobromide keeps gaining momentum is that it bridges technical rigor with daily practicality. For chemists under pressure to deliver high-purity, well-characterized materials—whether for the next new drug, advanced material, or ambitious research project—this compound brings consistency, safety, and selectivity. As labs everywhere keep striving for better, faster, and more sustainable results, compounds like MBD serve as partners in progress, shaped by a mix of thoughtful design, hands-on experience, and honest feedback from experts at every level.