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HS Code |
629618 |
| Product Name | N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride |
| Cas Number | 36643-41-5 |
| Molecular Formula | C13H17ClN2 |
| Molecular Weight | 236.74 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 209-212°C (decomposes) |
| Solubility | Soluble in water and methanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, protected from light and moisture |
| Synonyms | N-Methyl-N-(1-naphthyl)ethane-1,2-diamine hydrochloride |
| Iupac Name | N-methyl-N-(naphthalen-1-yl)ethane-1,2-diamine hydrochloride |
| Smiles | CN(CCN)C1=CC=CC2=CC=CC=C21.Cl |
As an accredited N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of N-Methyl-N-(Naphthalen-1-Yl)ethylenediamine hydrochloride, labeled with hazard warnings. |
| Shipping | N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Typically transported as a solid, it must comply with chemical safety regulations. Ensure appropriate labeling and packaging, and use secondary containment if necessary. Store and ship at room temperature unless otherwise specified by the manufacturer. |
| Storage | N-Methyl-N-(Naphthalen-1-yl)ethylenediamine hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure that storage complies with local chemical safety regulations and label the container clearly. |
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Purity 99%: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 198°C: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with a melting point of 198°C is used in organic compound crystallization processes, where it provides improved thermal stability during purification. Molecular Weight 265.81 g/mol: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with molecular weight 265.81 g/mol is used in drug formulation research, where it enables accurate dosage calculations and reproducible formulations. Stability Temperature up to 120°C: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with stability temperature up to 120°C is used in chemical synthesis under mild heating conditions, where it maintains structural integrity without decomposition. Hydrochloride Salt Form: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride in hydrochloride salt form is used in analytical biochemistry applications, where it facilitates enhanced water solubility and rapid dissolution. Particle Size < 50 µm: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with particle size below 50 µm is used in catalyst preparation processes, where it enables uniform dispersion and maximized catalytic surface area. Storage Stability 24 months: N-Methyl-N-(Naphthalen-1-Yl)Ethylenediamine Hydrochloride with 24 months storage stability is used in long-term reagent inventory management, where it reduces material degradation and inventory turnover rates. |
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N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride has started carving its place in labs that push the boundaries of organic synthesis and drug discovery. I remember the first time I came across this compound—a colleague in medicinal chemistry pointed out its role as part of an innovative route to developing diverse scaffolds for small molecule drugs. It’s the kind of insight that sticks with you, especially after years spent dealing with the same old amines that offer few surprises.
What stands out about this substance is the presence of both a methylated amine and a naphthalenyl group, each providing benefits that aren’t commonly found in one molecule. The naphthalenyl ring boosts pi-stacking and aromaticity, traits that influence how compounds interact with biological targets. The methyl group changes the electronic character of the amine, affecting reactivity and solubility in ways researchers leverage when they want to fine-tune their syntheses.
Strict standards matter in chemistry; labs depend on consistency. This compound typically comes in a fine, white powder form, with purity levels exceeding 98%. That high degree of confidence means fewer failed reactions or contaminants clouding results. I’ve seen projects derailed by a few percentage points of impurity in specialty amines—costing days of troubleshooting. Here, reliable quality means researchers spend less time double-checking their materials and more time testing ideas.
It dissolves easily in common polar solvents, which simplifies protocol adjustments. Most bench chemists prefer working with hydrochloride salts because you can weigh them out without worrying about humidity affecting measured quantities. Stability under room temperature makes shipping and storage straightforward. These details may not make headlines, but they save real time and money for research teams.
The boom in medicinal chemistry has highlighted the value of building blocks like N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride. Its mix of lipophilicity and reactivity offers options for those looking to modify receptor ligands, enzyme inhibitors, or experimental tools for mapping out protein surfaces. In drug discovery labs, it often surfaces in efforts to introduce rigidity and aromatic character into small molecules—a strategy that sometimes nudges a weak lead compound across the line into a promising candidate.
I’ve met scientists who rely on this compound to introduce secondary amines into complex cores, adjusting charge states and tuning how molecules distribute themselves within biological systems. You see these hands-on adjustments play out during SAR (structure-activity relationship) studies, where each tweak to an amine or an aromatic ring teaches the team something new about what their molecule can do. Looking at patent filings, drug candidates or bioactive tools with motifs derived from naphthyl-ethylenediamines appear more often each year.
Beyond pharma, specialty chemical manufacturers also keep stocks for constructing fluorescent probes, ligands for organometallic chemistry, or as intermediates in specialty dyes. I remember troubleshooting a reaction where another naphthalenyl-based diamine failed to react selectively; shifting to the methylated version brought the process under control because the change in electron density helped moderate reactivity. These are moments where design meets experience—inventiveness reinforced by having the right material on hand.
This compound doesn’t stand in isolation. Dozens of amines crowd chemical catalogs, ranging from simple ethylene diamine to heavily substituted aromatic diamines. Price, availability, and solubility often drive choices in routine settings. In the case of N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride, its distinctive hybrid structure gives you clear reasons to favor it over blander options.
Working with standard aliphatic diamines, I’ve noticed they often bring unwanted basicity or lack the right kind of rigidity for binding studies. When you need aromatic stacking or want to introduce steric bulk near a functional site, the naphthalenyl group makes a visible difference in both NMR and biological testing. Adding a methyl group onto the amine shifts outcomes in subtle ways, often improving selectivity or solubility at precisely the point where other analogs struggle. Methyl groups can also slow down metabolic breakdown by cytochrome P450 enzymes in mammals, hinting at new avenues for medicinal optimization.
Sometimes, colleagues try to swap in other substituted naphthylamines, hoping for similar outcomes, but without the methyl, those analogs often give less tractable reactivity. I’ve seen documented cases where the methyl tweak opened successful reaction channels or allowed more predictable purification. There’s satisfaction when something as minor as a methylation changes the playing field entirely.
Over coffee, practical chemists rarely talk about “enabling technologies” or buzzwords. Rather, they share specifics—how a compound tolerated tricky coupling partners or how its hydrochloride form avoided endless column runs. These stories, spread between groups or shared at conferences, weigh more than catalog promises. They create expectations about reliability and help shape the unwritten standards people lean on.
One story stands out: a custom synthesis specialist described saving half a week by switching from a basic naphthalenyl ethylenediamine to this methylated salt. The experiment needed exact stoichiometry and minimal side reactions. The old material absorbed water and clogged up glassware; the new batch ran smoothly and cleaned up easily. No abstract terms can substitute for that kind of direct impact on workflow and morale.
Even the most reliable compounds run into real-world obstacles. Shipping regulations on amines, local import controls on specialty chemicals, or supply chain delays can halt even the most well-planned projects. With this molecule, the major concern isn’t usually toxicity—it’s access. Many suppliers have variable lead times or credit restrictions, which slow research in smaller labs or start-ups.
Colleagues sometimes address this by pooling orders or relying on regional distributors with established stocks. Localized resellers can bridge the gap, although this solution only works in places with mature markets and reliable oversight. Open communication with vendors helps too—clarity on batch consistency, typical yields, and storage conditions improves planning. Labs benefit from periodic reviews of their chemical inventories and supplier relationships to avoid unpredictable delays.
Recycling and re-purifying off-the-shelf compounds rarely makes sense with this kind of specialty material, as you risk introducing contaminants that can cascade into experimental failures. The lesson here is that strong partnerships with trusted suppliers matter more than shaving pennies off the per-gram price. Products come and go, but a reputation for high-quality chemicals keeps chemists coming back.
Reliable raw materials underpin reproducible science. Years of troubleshooting in academic and industry settings have shown how quickly projects stall over invisible issues with reagents. Purity and well-characterized identity remain essential, especially when working at molecular margins where small changes can derail big ideas.
N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride stands out through more than just technical purity. Its unique combination of features makes it a go-to for those designing new molecular architectures or needing a predictable amine for scaffolding. Each published study, patent, or grant report built on sturdy material reinforces trust not just in the product, but in the system that supplies it. Skimping at this stage often leads to unnecessary setbacks that could be avoided by starting with better building blocks.
Access to advanced chemicals shouldn’t depend on geographic location or institutional size. There’s still a gap between large, resource-rich labs and smaller outfits that lack bulk ordering power. I’ve seen creative workarounds, from academic consortia pooling orders to negotiating shared inventory platforms. Regional science funding can make a difference by subsidizing access to specialized chemicals or standardizing price structures.
Efforts to make material sourcing more transparent—public batch records, openly available certificates of analysis, and robust supply chain information—all promote research integrity. Labs feel more secure taking scientific risks if they know their basic materials won’t vanish or change unexpectedly within a year. Those gains translate into both greater efficiency and more confidence in reported findings.
Greater demand brings up questions about sustainability and long-term stewardship. Specialty chemicals, especially ones containing aromatic hydrocarbons, draw scrutiny about their environmental footprint and safe handling. High-purity hydrochloride salts aren’t especially hazardous compared to many industrial solvents, but responsible labs invest in proper waste disposal and careful recordkeeping.
Some companies have already begun looking at greener synthesis methods or alternate purification steps to shrink the environmental toll. In my time consulting for a contract research organization, I saw the shift away from obsolete, high-waste processes accelerate as both regulations and moral standards rose. The challenge is finding a balance between meeting modern scientific needs and reducing environmental impact. Progress here grows from close collaboration between suppliers, industry watchdogs, and the scientific community.
Interest in molecules like N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride rises as drug screening and synthetic methodology advance. As omics technology and artificial intelligence converge with traditional bench chemistry, demand for robust, versatile building blocks is set to grow. Speaking from experience, each time a new screening platform goes live, a wave of new structure-activity explorations follows—drawing on compounds that deliver both reliability and flexibility.
I’ve watched collaborations between computational chemists and synthetic teams accelerate hit-to-lead workflows, updating chemical inventories in near real-time to suit rapidly shifting research questions. In these dynamic environments, stockouts or unexpected changes in reagent quality can cost more than just money—they disrupt whole months of planning and innovation. A stable supply of high-performing amines often spells the difference between a routine synthesis and a breakthrough series of experiments.
Laboratories never grow tired of having reliable options. What I appreciate about N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride is how it bridges gaps—fitting seamlessly into a range of protocols, whether students are running undergraduate experiments or professionals are building new pharmaceutical candidates. I recall a training session where new researchers flagged how easy it was to transition from stockroom to scale-up bench without changing procedures or troubleshooting unexpected quirks.
Experienced chemists remember the days of improvising with whatever was on hand. The current landscape rewards careful planning, and compounds like this one reinforce the culture of preparation. Protocols annotated with details about which supplier batch performed best, or which run gave the cleanest spectra, circulate through teams for a reason—they keep science moving ahead. The more researchers learn from each other's small successes and failures, the sharper the collective edge becomes.
The internet now serves as one giant lab notebook—forums, preprints, and open-access chemistry databases create new expectations for knowledge sharing. I’ve seen research teams build custom digital archives of their own experience with compounds like N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride, noting quirks in reactivity or long-term storage quirks that others might miss. These shared insights fill gaps left by official catalogs or safety data, making it easier for the next lab to avoid old pitfalls.
Collaborative problem solving and regular communication between labs, suppliers, and independent auditors have driven positive changes in how specialty chemicals are produced and distributed. Transparency on impurities, clear documentation, and prompt responses to technical questions contribute to an atmosphere where trust grows through proven reliability. Scientists know when they’re being listened to, and they reward that respect by remaining loyal customers.
Discovery grows from tried-and-tested materials, not wishful thinking. As the field of synthetic and medicinal chemistry continues to take on more complex targets, demand for creative building blocks will only rise. N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride has earned its reputation not through flashy marketing or abstract claims but through its quiet track record of practical utility.
Looking at the future, I see this class of molecules featuring more prominently in chemical biology, novel sensing applications, and new types of organic materials. Success here won’t come from luck; it will come from a commitment to quality, transparent sourcing, and open dialogue between everyone involved in the supply and use of fine chemicals.
Each year, new students and scientists enter labs eager to make their mark. Reliable reagents empower them to take risks, learn by doing, and share what works. N-Methyl-N-(naphthalen-1-yl)ethylenediamine hydrochloride doesn’t close off possibilities; it opens doors to methods and discoveries that build on the best of what’s come before.
Reflecting on the growth of the scientific supply community, I realize how everyone—veterans, new hires, suppliers, and reviewers—feeds into the shared goal of making discovery more dependable. That’s what helps move science, and society, ahead.