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HS Code |
154096 |
| Name | Iminodibenzyl |
| Chemical Formula | C13H11N |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 70-73°C |
| Boiling Point | 346°C |
| Cas Number | 494-19-9 |
| Density | 1.14 g/cm³ |
| Solubility In Water | Practically insoluble |
| Synonyms | Dibenzazepine |
| Pubchem Cid | 6956 |
| Smiles | c1ccc2c(c1)N=CC3=CC=CC=C23 |
| Inchi | InChI=1S/C13H11N/c1-3-7-11-13(9-5-1)14-12-8-4-2-6-10(12)11/h1-9H |
As an accredited Iminodibenzyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Iminodibenzyl is supplied in a 100g amber glass bottle with a secure screw cap, labeled with product details and hazard information. |
| Shipping | Iminodibenzyl is shipped in tightly sealed containers to prevent contamination and moisture exposure. The packaging complies with chemical safety regulations, including clear hazard labeling. During transport, it is handled as a non-hazardous material but kept separate from incompatible substances, stored at a cool, dry location away from direct sunlight and ignition sources. |
| Storage | Iminodibenzyl should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Avoid exposure to moisture and direct sunlight. Proper chemical storage protocols should be followed to prevent contamination, spills, or accidental release. Always label containers clearly and store at room temperature. |
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Purity 99%: Iminodibenzyl Purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation and consistent drug quality. Molecular Weight 193.26 g/mol: Iminodibenzyl Molecular Weight 193.26 g/mol is used in organic synthesis processes, where defined molecular mass supports accurate formulation and predictable reaction outcomes. Melting Point 123–125°C: Iminodibenzyl Melting Point 123–125°C is used in solid-state processing, where controlled melting behavior provides uniform blending with other compounds. Stability Temperature up to 200°C: Iminodibenzyl Stability Temperature up to 200°C is used in high-temperature polymer applications, where thermal stability maintains structural integrity during manufacturing. Particle Size <10 µm: Iminodibenzyl Particle Size <10 µm is used in catalyst preparation, where fine particle distribution enhances surface area and reaction efficiency. Viscosity Grade Low: Iminodibenzyl Viscosity Grade Low is used in solution-phase reactions, where low viscosity promotes easier mixing and improved reagent diffusion. Solubility in Ethanol: Iminodibenzyl Solubility in Ethanol is used in analytical chemistry protocols, where solubility facilitates efficient sample preparation and analysis. |
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Among chemical compounds rooted in medical and industrial history, iminodibenzyl stands as a trusted backbone for a range of applications. Many researchers, chemists, and pharmaceutical partners already recognize its subtle yet critical place in the world of chemical synthesis. My first exposure to iminodibenzyl came during graduate school when our organic chemistry group traced the history of tricyclic antidepressants. We marveled at the way this compound, with its characteristic fused-ring structure and nitrogen bridge, quietly shaped decades of progress. Professionals value this molecule not only for what it offers on paper, but for the efficiency and reliability borne out over years of continuous use in labs and factories.
Iminodibenzyl’s chemical name might intimidate some at first glance, but unpacking its structure isn’t too complicated. Chemists will describe it as “10,11-dihydro-5H-dibenz[b,f]azepine.” At its core sits a tricyclic system built from two benzene rings fused through a seven-membered azepine. That configuration sounds dry until you realize it’s the essential architecture underpinning a variety of blockbuster drugs and specialty molecules. It presents itself as a white to slightly yellowish powder, often stable under standard laboratory conditions with a melting range typically reported between 72 to 76 degrees Celsius.
What separates this model from closely related compounds? For a start, the nitrogen bridge within the azepine ring delivers a unique flexibility to chemical modification. This means experimenters and manufacturers don’t wrestle with unpredictable reactions as often, as the bridged structure maintains clarity during substitutions, oxidations, and reductions. In my lab experience, the predictability of the molecule simplifies experimental planning. You don’t waste precious time troubleshooting side-reactions or purification issues, so process development runs smoother than it does with many polycyclic compounds.
Most discussions tie iminodibenzyl directly to the synthesis of tricyclic antidepressants, like imipramine and its analogs. Many established antidepressant drugs trace their molecular family line straight back to this compound. As a starting scaffold, it enables the assembly of various therapeutics targeting serotonin and norepinephrine reuptake. This isn’t just a detail for medicinal chemists; patients all over the globe benefit from the groundwork laid by early research into iminodibenzyl.
Beyond its pharmaceutical legacy, iminodibenzyl also supports advances in dye manufacture, photochemistry, and sensor technology. Industrial chemists appreciate its ability to form stable derivatives under controlled conditions. Some labs apply it in structure-activity relationship studies, using the core skeleton to probe how subtle changes in molecular electronics impact bioactivity or photophysical properties. Especially for early-stage discovery work, the flexibility to introduce substitutions at multiple positions without unraveling the framework becomes a real advantage.
A question I hear from students and younger chemists: How does iminodibenzyl stack up against more widely invoked tricyclic compounds, like dibenzazepine or dibenzocycloheptene? I like to answer by pointing to a few practical distinctions. The nitrogen bridge in iminodibenzyl’s central seven-membered azepine ring provides distinct resonance and reactivity. Most notable, it’s less prone to ring cleavage or hydrolysis during standard procedures – a constant headache for anyone who’s had to run late-night chromatography to separate breakdown products.
Furthermore, iminodibenzyl’s nitrogen can serve as a convenient platform for both alkylation and acylation, expanding the chemical toolbox. Analogous compounds sometimes miss this capability, forcing more roundabout synthesis routes. I remember one specific project on receptor ligands where, after several frustrating weeks, our team found iminodibenzyl handled our desired transformations with less byproduct than its oxygen or sulfur-containing cousins. Streamlined handling means less waste, less solvent, and a lighter touch on the environmental impact—practical wins for any operation.
Its melting point falls in a range that supports easy recrystallization and purification without exotic equipment. And compared with highly substituted aromatic scaffolds, the relatively simple core minimizes impurities in commercial batches. Realistically, anyone running kilo-scale synthesis seeks out molecules that keep costs low and purification straightforward. That’s the edge of iminodibenzyl over more ornamented, less stable frameworks.
Many supply chain managers feel the pinch of volatility in specialty chemicals. Pandemic logistics, energy disruptions, and shifting compliance rules all threaten steady access to staple intermediates. Iminodibenzyl’s status as a robust platform mitigates some of this unpredictability. It’s persisted in global commerce for decades, with suppliers in Europe, Asia, and North America continuing to meet quality benchmarks without dramatic price shocks.
Once, during a raw material shortage that disrupted several key precursors, our small biotech operation leaned on iminodibenzyl as a fallback scaffold. Reliable delivery prevented research from stalling out. The compound tolerates a range of storage and shipping conditions, so the headaches of temperature excursions or humidity exposure take a backseat. Product consistency holds, batch to batch, matching pharmaceutical-grade standards required by regulatory agencies. That stability becomes all the more important when facing stricter traceability requirements and international audits.
Production of pure iminodibenzyl calls for skilled hands and a proper understanding of safety. The standard lab synthesis involves cyclization steps followed by careful extraction and purification. Labs with decades of experience consistently report product purity upwards of 98%, matching demanding research and pharmaceutical applications. Handling invariably brings safety into focus. Proper ventilation, dust control, and chemical storage prevent accidents and keep operations running smoothly.
A persistent myth claims iminodibenzyl is tough to handle or store for extended periods. In practice, standard containment and labeling procedures suffice. Over the years, the teams I’ve worked with stored tightly sealed containers in cool, dry conditions for years without any reported degradation or significant color change. Routine analytical checks, like melting point determination and thin-layer chromatography, confirm ongoing stability.
Every chemical project today rests on a solid grasp of environmental and occupational safety. Iminodibenzyl features moderate toxicity, so direct inhalation, ingestion, or prolonged skin contact are discouraged. That said, responsible operations report minimal incidents when staff follow standard lab PPE and disposal protocols. Proper waste management routes material through incineration or approved hazardous chemical disposal, rather than dumping in mixed municipal waste.
From an environmental lens, minimizing byproduct formation during synthesis and refining purification methods go a long way in shrinking the ecological footprint. In my group’s pilot work on alternative solvents, green chemistry principles shaved off nearly half the need for chlorinated solvents. Safer handling protects both workers and communities. Companies routinely pass regulatory audits by integrating staff training with robust environmental monitoring—experience proves these approaches keep iminodibenzyl a routine, rather than risky, part of operations.
Medicinal chemistry and drug manufacturing increasingly rely on stringent controls traceable through every supply chain link. Agencies worldwide demand transparency in sourcing, production, handling, and transportation of critical intermediates. Iminodibenzyl has successfully weathered changing regulations due to its limited volatility, identifiable analytical fingerprints, and long history of compliant synthesis.
Quality assurance goes beyond routine melting point checks or simple mass spectroscopy runs. Analytical chemists typically rely on nuclear magnetic resonance (NMR) and infrared (IR) spectroscopic analysis, supplemented with high-performance liquid chromatography (HPLC) to confirm purity and identity. These instruments spot even minor contaminants long before products progress to the next manufacturing step. Any operation still relying on spot-check analysis or inconsistent reporting risks falling behind—not only on compliance but on customer trust.
Look at publications spanning the past fifty years, and you’ll see the recurring role of iminodibenzyl in advancing diverse innovations. Large-scale pharmaceutical facilities and small university labs sound a common refrain: reliability breeds innovation. The compound stands at the crossroads between classic medicinal chemistry and forward-looking applications like organic electronics and photoluminescent materials.
During my earliest days running bench experiments, the predictability of iminodibenzyl gave me the confidence to invest time into new synthetic routes. Failures still happened—every scientist has tales of impure fractions or high-pressure syntheses gone awry—but more often than not, the central scaffold performed as textbooks predicted. Our research group managed to design and test new analogs, share reproducible findings with peers, and move from milligram to multi-gram scale without fuss.
Markets change quickly, and cost factors always tag along with chemical advancements. Sourcing reliable intermediates while staying within budget feels like a tightrope act for procurement teams. Packs of iminodibenzyl, from grams up to multi-kilogram drums, present competitive price points compared with newer, less proven tricyclic frameworks. Major suppliers maintain consistent production lots featuring robust lot-to-lot data, linking each batch to certificates of analysis that back up quality claims.
Low price alone doesn’t decide buying choices, but it certainly eases the burden on project managers or startup labs trying to extract maximum mileage from tight research budgets. The added benefit of widespread availability means order fulfillment won’t stall time-sensitive research or production runs. In my procurement experience, the cost savings and supplier reliability surrounding iminodibenzyl usually tip the scales away from flashier—but more temperamental—analogs.
The story of iminodibenzyl doesn’t end with tricyclic antidepressants. Newer research harnesses its structure for custom ligands, library building blocks, and optically active materials. Green chemistry initiatives look toward this type of reliable framework for sustainable synthesis. Labs advance process development by swapping hazardous reagents and solvents for cleaner, safer options, all while making use of this compound’s chemical stability.
Teaching up-and-coming chemists about iminodibenzyl also opens their eyes to the importance of molecular frameworks that perform reliably year in and year out. Too often, students chase the latest “hot” scaffold, overlooking the hard-won lessons embedded in time-tested classics. Real innovation often starts on a foundation laid by molecules like iminodibenzyl. Its framework enables both incremental advances and occasional leaps forward as new reactions and uses come to light.
The modern era puts sustainability and worker safety right at the center of chemical production. Practices built around the established synthesis and application of iminodibenzyl already show how experience-driven standards deliver both performance and lower risk. But there’s always more room to press forward—more environmentally friendly reagents, improved waste reduction strategies, and greater transparency around sourcing.
It’s easy to overlook careful waste management or accidental emissions when loyal intermediates draw little attention. Still, any operation can improve with periodic audits and by seeking out new green chemistry advances. Regulatory professionals encourage investing in analytical upgrades and adopting digital record-keeping—steps that reinforce the trust so central to pharmaceutical and specialty chemical supply chains.
From the vantage point of chemists, formulators, and procurement teams alike, the greatest strength of iminodibenzyl remains its foundation of proven experience. The collective knowledge accumulated through decades of research and production enables more effective troubleshooting, faster scale-up, and sustained regulatory compliance. Laboratories push forward, confident in the tools and insights nurtured by practitioners who have shared both successes and hard-won lessons.
This sense of community—one where experts debate optimal reaction conditions or improved methods of waste handling—preserves the legacy of iminodibenzyl while advancing best practices in modern settings. It’s no exaggeration to say some of the safest, most productive workplaces owe their foundations to shared knowledge passed between generations. Building further value means putting that experience front and center, inspiring both old hands and newcomers alike.
In the shifting landscape of specialty chemicals, some compounds become mainstays for all the right reasons. Iminodibenzyl, with its storied history, chemical resilience, and flexibility, has earned its reputation. Rather than chasing each new trend, chemists and industry players find continued value in the lessons and technology advanced by this reliable molecule. As green chemistry and regulatory rigor shape the industry’s future, those who understand and respect the practical legacy of iminodibenzyl will stand ready to respond—confident that both performance and responsibility can go hand in hand.