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HS Code |
872895 |
| Product Name | 3-Amino-3-Azabicyclo[3.3.0]Octane Hydrochloride |
| Cas Number | 111078-34-9 |
| Molecular Formula | C6H13N2Cl |
| Molecular Weight | 148.64 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 210-215°C (dec.) |
| Solubility | Soluble in water |
| Purity | ≥98% |
| Storage Temperature | 2-8°C |
| Synonyms | 3-Aminoquinuclidine hydrochloride |
| Chemical Structure | Bicyclic amine hydrochloride salt |
As an accredited 3-Amino-3-Azabicyclo[3.3.0]Octane Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle with a secure screw cap, clearly labeled for laboratory use. |
| Shipping | 3-Amino-3-Azabicyclo[3.3.0]Octane Hydrochloride is shipped in a tightly sealed container, protected from moisture and light. The packaging complies with relevant hazardous material regulations and includes appropriate labeling. Transport is typically arranged via ground or air freight with all necessary documentation to ensure safe and legal delivery. |
| Storage | 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature (15–25°C). Avoid sources of ignition, acids, and incompatible materials. Always follow safety guidelines and local regulations for proper chemical storage and handling. |
Applications of 3-Amino-3-Azabicyclo[3.3.0]Octane Hydrochloride in Industrial ManufacturingAs the direct manufacturer of 3-Amino-3-Azabicyclo[3.3.0]Octane Hydrochloride, we supply this compound into several high-value industrial sectors where stable performance, regulatory conformity, and process reliability determine downstream usability. Our technical support and rigorous QC protocols are attuned to the nuanced requirements of downstream formulation, upholding compliance benchmarks and ensuring consistent integration across specialized manufacturing environments. Below, we detail specific deployment scenarios based on verified industrial practices and documented application pathways. 1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Drug SynthesisDownstream pharmaceutical companies employ this compound as a structural fragment in the synthesis of central nervous system (CNS) therapeutics, particularly in the manufacture of tropane alkaloid analogues for anti-Parkinsonian and anti-addiction drugs. The material’s defined stereochemistry and high purity grade meet the requirements for multi-step synthetic processes within GMP-accredited facilities. Industry compliance standards
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2. Building Block in Custom Synthesis for Contract Research Organizations (CROs)CROs specializing in medicinal chemistry utilize this hydrochloride salt as a rigid bicyclic amine building block for small-molecule library generation. The compound’s defined chirality and high water solubility make it amenable to parallel synthesis and rapid analog development under high-throughput conditions. Industry compliance standards
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3. Intermediate for Advanced Agrochemical FormulationsMajor agrochemical manufacturers incorporate the material in the targeted synthesis of new-generation pesticide actives, exploiting its bicyclic azabicyclo core as a precursor for selective insecticidal and fungicidal agents with improved biostability. The compound’s nonvolatile hydrochloride form aligns with safety and emission controls in technical grade production facilities. Industry compliance standards
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4. Functional Intermediate for Performance Polymer AdditivesSpecialty polymer producers exploit the amine functionality and unique bicyclic structure during chain extension or end-capping in polyamide and polyimide production. The hydrochloride salt form reduces volatility and enables cleaner feed in melt-phase or solution-phase polymerization lines, contributing to enhanced mechanical and thermal stability in engineering polymers. Industry compliance standards
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5. Reagent for Chiral Selector Synthesis in Analytical ChromatographySpecialty analytical reagent manufacturers use this bicyclic amine as a protected precursor for synthesizing chiral selectors applied in HPLC column packing. Its rigid structure facilitates the development of enantioselective stationary phases, supporting the pharmaceutical and agrochemical industries in chiral impurity quantification and batch release testing. Industry compliance standards
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In our day-to-day work as a chemical manufacturer, we’ve watched the role of specialty amines evolve steadily. Among these, 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride stands out. We turn out this material in batches where purity and uniformity make the difference between a successful downstream process and costly rework. The model we supply carries a reputation for consistent, reliable performance, which did not happen by relying on off-the-shelf approaches. Instead, we built up our protocols after years of feedback from chemists who use these intermediates in real industrial settings, not just on paper.
Many projects in medicinal chemistry or materials research trace their roots to people searching for compounds with unique reactivity or rigidity in structure. 3-Amino-3-azabicyclo[3.3.0]octane hydrochloride, with its bicyclic core, meets the criteria. Unlike open-chain amines, its ring system brings steric bulk and conformational lock. We have seen first-hand how pharmaceutical projects benefit when the required building blocks behave predictably. Some customers step through combinatorial libraries a dozen times a quarter, taking new leads from virtual screening to reality. This compound gives them a versatile handle—amines ready to react, but a backbone that doesn’t twist.
Experienced chemists have a long list of reasons for preferring hydrochloride salts for certain tasks. We chose hydrochloride for more than just tradition: it offers solid handling properties, good shelf-life, and easier quantitative dosing in water or polar solvents. This is no minor point for those running parallel reactions—if each dose is measured correctly, workup becomes routine, and robust parallel synthesis is possible. In our plant, we keep a tight grip on process water content and crystal morphology. Our product carries minimal solvent residues while avoiding troublesome polycrystalline clumping. The resulting white to off-white crystalline powder offers a level of purity our QA teams back up with real data, not wishful thinking.
Talk to a few process chemists and you’ll hear story after story of how a few tenths of a percent impurity can ruin a run. We don’t chase paper specs for the sake of marketing. Batch quality means checking for residual starting amines, remaining solvent traces, and identifying any side-products from ring opening. We use HPLC and NMR for every lot. Our standard model presents a minimum purity by HPLC, not just by NMR or titration. Over the years, we have fielded calls from clients probing every specification, from melting point to counter-ion content. That dialogue has pushed us toward tighter control at every step. We validate each process change, because we’ve learned that even the smallest upstream drift in precursor storage can affect downstream stability.
While published literature has covered the general reactivity of azabicyclo compounds, our customers often break new ground with each project. Medicinal chemists lean on this compound in early-stage hit-to-lead campaigns. The amine group enables coupling with acyl chlorides or sulfonyl halides. Materials scientists see potential in its rigidified structure for crosslinkers or specialized polymer backbones. Peptide chemists value the way it shapes rigidity into their peptide templates. In practice, orders come from both small labs trialing ten grams and larger clients synthesizing hundreds for scale-up.
What sets this compound apart is not just the core itself but the way it resists side reactions that plague less robust bicyclic amines. Months of bench-scale and pilot-scale feedback taught us the criticality of trace water—some projects stall at gram scale due to gradual hydrolysis if the salt is not managed carefully. Moisture control runs deep in both shipping and storage for this product. We ship each batch with proper desiccant and train our warehouse teams to handle it quickly from reactor to packaging.
Plenty of amines see daily use in labs, yet most can’t substitute for a 3-azabicyclo core. Chain amines flex, leaving downstream conformational control to chance. Acylations built on a simple diamine can end up scrambled. With our 3-amino-3-azabicyclo[3.3.0]octane hydrochloride, ring strain locks the structure and atom positions, handing chemists a more defined scaffold to build on.
We’ve sent material for head-to-head trial alongside lower-purity grades from other sources. Customers came back after exploratory runs, pointing to fewer by-products and cleaner isolation steps with our grade. We keep a close eye on particulates and insolubles, since a single inclusion particle can spell trouble for high-throughput screens. Rather than push out uneven quality, we rework out-of-spec material—recyclable whenever possible—to avoid passing the problem on down the supply chain.
Our experience with upstream supply has taught us never to take consistency for granted. Early on, we learned tough lessons from single-source precursors. Now, whenever we qualify a new supplier, we spend just as much time on stability studies as on warehouse audits. Cyclization steps demand precision, so our process chemists take pride in their ability to keep formation and isolation steady, even if raw material costs fluctuate or weather complicates logistics.
As a result, our records show each adjustment, from reaction temperature windows to quench sequence on a per-batch basis. This approach has allowed us to find the sweet spot for crystallization time. Too slow, and solvent picks up colored side-products; too fast, and you get size irregularity, making bulk handling less reliable. After scale-up, we’ve managed mother liquor recycling and worked out the right drying technique, so the product leaves our doors ready for direct use in the downstream step.
Research chemists care about how smoothly a compound reacts and how cleanly it comes through workup. For the teams scaling up a lead, questions get more practical: Is the batch processable? Does the product store stably? We answer these concerns by running stability trials under real shelf storage and shipping stress. We monitor color, melting range, and hydrochloride content monthly. On the bench, the powder handles easily, resists caking, and dissolves with predictable exotherm profile. Those little details matter—especially at kilo scale, where a small shift in solubility or hygroscopicity produces major process headaches.
In shipping, we’ve faced everything from humid coastal warehouses to winter freeze–thaw cycles. Our packing team has learned to use triple-layer sealed liners and outer drums with both impact and moisture resistance, holding up under rough transit. Feedback from global partners has helped us refine these practices, so every delivery arrives with the material in the same condition as it left our QA check.
We keep hearing from people who have been burned by unreliable supply or hidden quality issues from opaque channels. As the manufacturer, we take responsibility for owning both the production traceability and open discussion of what’s possible—and what isn’t—at every step. Our technical teams respond directly, cutting past distributor confusion. When a researcher calls with an issue or a request, that feedback goes to the front line and shapes our next batch runs. We host regular video consultations, walking through certificates, impurity profiles, and sometimes even troubleshooting unusual applications. Over the years, this open-door approach has paid dividends both for our team and for every scientist taking a risk on a new project.
If all amines were interchangeable, shortcuts would dominate the market. Reality doesn’t match. You only need to look at the failure of several scale-ups that relied on untested substitutes to see why certain bicyclic amines do a job no other can. The backbone present in 3-amino-3-azabicyclo[3.3.0]octane hydrochloride brings reliable, targeted reactivity and predictable behavior under a range of condensation, coupling, and derivatization conditions. We’ve watched dozens of projects move faster and more cleanly, saving time and resources thanks to reduced purification burdens and repeatability between lots.
Each lot carries a printout showing compliance to specifications, but our clients often want more: impurity maps, stress-test results, even documented results from application-specific trials. We provide these as part of our commitment to technical partnership, not just as another order shipped. We take pride in supplying research teams taking risks—not just on a new molecule but on a better way to do chemistry.
Today’s research labs focus on speed, reliability, and transparency. Back when we began making heterocyclic compounds, a slow mail order and a handful of reference spectra was enough. Now, teams demand not just lead time, but guidance in handling, documentation covering every impurity, and backup plans in case of project pivots. We get called in for direct support at times when shipped material finds unexpected problems in application environments that textbooks can’t cover.
We see a growing need for molecule-specific handling guides and transparent process histories. More than ever, researchers want to see not just what’s in the bag but a story that reassures them about every link in the chain. Our team makes those histories available—an in-person culture built around open files and direct phone calls, not endless email threads with third parties. That’s how we’ve managed to grow alongside our customers who demand more than the bare minimum.
Producing specialty amines at scale doesn’t happen in a vacuum. Our site operates under strict waste and emission rules. We treat all effluent streams, and the solvents we recover from the hydrohalide salt step go back into later round batches wherever viable. Our operations don’t chase price through shortcuts; instead, we invest in waste reduction, energy savings, and safer material handling. Environmental health and safety is not an afterthought—it’s checked daily, and lessons from each lot roll forward into process improvements.
Because we manage our own process from start to finish, it keeps us close to every detail, from emission permits to packaging waste. The discipline in batch records doubles as a source for regulatory audit backup and helps us adjust each process after the fact, allowing us to meet both compliance standards and pragmatic customer need.
3-Amino-3-azabicyclo[3.3.0]octane hydrochloride delivers a robust, reliable base structure for creative chemical work. The combination of hydrochloride salt form, ring rigidity, and high batch-to-batch purity makes it more than just another amine in a sea of similar names. Over years of production experience, we’ve built up practices that support customer innovation—consistent manufacturing, direct support, and open collaboration with each project lead. We manufacture this compound to be reliable, understood, and backed by real process data, making it a practical tool for the chemist, not just a line in a catalog.
In every step, we put the knowledge gained from being the manufacturer into action. Each batch carries not just the right purity, but the right story, documentation, and support our customers have learned to expect. Our insights and attention to detail make a difference on the lab bench, in the production suite, and throughout the supply chain. That’s the difference our plant brings—and the reason our partners return with new projects and higher standards each year.