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1,8-Bis(Dimethylamino)Naphtalene

    • Product Name 1,8-Bis(Dimethylamino)Naphtalene
    • Alias Proton Sponge
    • Einecs 208-973-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    536809

    Chemical Name 1,8-Bis(Dimethylamino)Naphthalene
    Other Names Proton Sponge
    Molecular Formula C14H18N2
    Molar Mass 214.31 g/mol
    Appearance Yellow solid
    Melting Point 124-127°C
    Boiling Point 138-140°C at 0.2 mmHg
    Density 1.10 g/cm³
    Solubility In Water Insoluble
    Pka 12.34 (for conjugate acid)
    Cas Number 3333-07-3
    Smiles CN(C)c1cccc2c1c(N(C)C)ccc2

    As an accredited 1,8-Bis(Dimethylamino)Naphtalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled "1,8-Bis(Dimethylamino)Naphthalene," including safety and handling instructions.
    Shipping **1,8-Bis(Dimethylamino)Naphthalene** is typically shipped in sealed, airtight containers to prevent exposure to air and moisture. The containers are clearly labeled according to hazardous material regulations. The chemical is transported as a solid, under cool, dry conditions, and handled in accordance with standard safety protocols for corrosive and irritant substances.
    Storage 1,8-Bis(dimethylamino)naphthalene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry, and well-ventilated area, away from oxidizing agents and acids. Store at room temperature and avoid direct sunlight. Label appropriately and follow all relevant chemical safety guidelines.
    Application of 1,8-Bis(Dimethylamino)Naphtalene

    Applications of 1,8-Bis(Dimethylamino)Naphtalene in Industrial Manufacturing

    As a direct manufacturer, we supply 1,8-Bis(Dimethylamino)Naphtalene to specialized industrial customers integrating this compound in demanding downstream processes. Our product supports high-value applications across several mature sectors with strict technical and regulatory controls.

    1. Strong Non-Nucleophilic Base for Pharmaceutical API Synthesis

    Process chemists rely on this compound as a proton scavenger and strong organic base in the synthesis of active pharmaceutical ingredients, especially in reactions involving sensitive functional groups or where strong inorganic bases lead to side reactions or decomposition. 1,8-Bis(Dimethylamino)Naphtalene participates in condensation, alkylation, and acylation steps supporting high purity and yield in GMP pharmaceutical manufacturing. Its use is typically subject to cleaning validation and minimized residuals in the final API.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP General Chapters & API Monographs relevant to synthesis impurities
    • EU GMP Annex 2 for medicinal substances
    • FDA 21 CFR parts 210/211 (United States)

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to acidic sites; adjusted according to substrate acidity and process scale

    Downstream process integration

    • Introduced in reaction vessel for condensation or substitution reactions, often quenched and removed by aqueous extraction during work-up, with strict removal from final API crystallization

    Final product types

    • Small molecule APIs (e.g., cardiovascular agents, oncology products)
    • Pharmaceutical intermediates
    • Specialty drug substances requiring high base selectivity

    2. Catalyst and Base in Agrochemical Active Ingredient Manufacturing

    1,8-Bis(Dimethylamino)Naphtalene finds application in the large-scale synthesis of crop protection agents, particularly where base-sensitive intermediates and selective deprotonation are required. Its use mitigates side reactions, contributing to higher selectivity in the synthesis of modern herbicides and fungicides. Downstream processes favor this compound due to its ability to function at low stoichiometry and to be effectively separated from target molecules.

    Industry compliance standards

    • FAO/WHO specification for active ingredients
    • ISO 9001 certified production practices for agrochemicals
    • REACH registration for manufacturing and importation in the EU
    • China GB and Ministry of Agriculture standards for pesticides

    Typical usage ratio

    • 0.2–1.5 equivalents per functional group, dependent on route step and yield optimization studies

    Downstream process integration

    • Employed during base-mediated alkylation or cyclization phases; inclusion during pilot and production scale-up followed by separation during aqueous work-up and downstream purification

    Final product types

    • Systemic fungicide actives
    • Triazine and sulfonylurea herbicides
    • Insecticidal intermediates

    3. Deprotonation Agent in Advanced Electronic Material Synthesis

    This base serves in the controlled deprotonation of aromatic or heteroaromatic systems for the manufacture of organic electronic intermediates, including OLED, OPV, and organic transistor materials. Its strong basicity with low nucleophilicity enables formation of key reactive intermediates while minimizing unwanted side reactions that would impair device performance. The compound’s use requires batch records to ensure trace levels do not interfere with electronic properties.

    Industry compliance standards

    • ISO 9001/14001 (Quality and Environmental Management)
    • RoHS Directive (European Union Restriction of Hazardous Substances)
    • Semi S2/S8 environmental, health, and safety guidelines
    • Internal QC protocols for electronics-grade intermediates

    Typical usage ratio

    • 1.0–2.2 equivalents relative to the aromatic or heteroaromatic substrate, tuned for reactivity and impurity profile

    Downstream process integration

    • Base is charged prior to or during lithiation or borylation steps; removed during work-up via extraction and residue monitoring prior to advanced purification stages

    Final product types

    • OLED emitter building blocks
    • Organic photovoltaic (OPV) monomers
    • Polymeric semiconductors for display technologies

    4. Proton Sponge for Analytical Reagent and Reference Standard Production

    Analytical and research laboratories incorporate this compound in the preparation of reagent-grade buffers and as a titration base where minimal interference is critical. Its high proton affinity underpins calibration standard manufacturing and formulation of diagnostic kits. Stringent batch documentation controls impurities and ensures reliable analytical performance.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and calibration laboratories)
    • National Institute of Standards and Technology (NIST) traceability for reference materials
    • GLP (Good Laboratory Practice) for reagent production environments
    • Internal SOPs for analytical grade chemicals

    Typical usage ratio

    • 0.1–1.0 equivalents depending on buffer capacity or titration endpoint requirements

    Downstream process integration

    • Added directly to buffer formulations or titration mixtures; removed or neutralized during final preparation or left as a defined component in analytical standards

    Final product types

    • Analytical titration standards
    • Diagnostic reagent kits
    • Buffer solutions for spectroscopy and chromatography
    Free Quote

    Competitive 1,8-Bis(Dimethylamino)Naphtalene 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.

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    Certification & Compliance
    More Introduction

    Outstanding Chemistry Begins with 1,8-Bis(Dimethylamino)Naphthalene

    The Craft Behind Our 1,8-Bis(Dimethylamino)Naphthalene

    In the real world of chemical manufacturing, 1,8-bis(dimethylamino)naphthalene does not just exist as a reagent pulled from a catalog. Each batch carries the experience, practical know-how, and relentless attention to detail accumulated through decades in the lab and on the shop floor. Known by many as “Proton Sponge,” this compound stands out because of its unusual molecular structure: two dimethylamino groups fixed in close proximity at the 1 and 8 positions of the naphthalene ring. That proximity, forcing charges to fight for space, is the secret to its incredible basicity, one of the highest among organic amines. It’s a tool that turns routine reactions into elegant solutions.

    Getting the Model Right

    Chemists who have used various grades of this material know that quality starts long before the powder or crystal reaches the container. Control over the synthesis pathway determines more than just purity; thorough removal of byproducts and control of moisture content matter for air- and moisture-sensitive work. We have worked for years refining the process: ensuring rigorous exclusion of water and oxygen during both production and storage, and pulling the material through purification steps that leave nothing behind that might cause side-reactions or degrade shelf life. The most reliable source of high basicity and minimal contamination comes from a process designed and run by hands that have learned over time what really counts—results in the user's lab.

    Typically, you'll receive a white to off-white crystalline solid, melting in a narrow range near 159°C, well above room temperature. That solid packs one of the most potent organic bases into a form that’s easy to handle for precision dosing in reactions without the volatility and hazards seen with many alkali metals or alkoxide reagents. We ship material that’s immediately ready for use, straight from our nitrogen-purged vessels to your flask, limiting degradation on the shelf or during shipping.

    Knowing Its Edge

    We see firsthand that the true difference between 1,8-bis(dimethylamino)naphthalene and other common organic bases is more than a number from a catalog. With a pKa of its conjugate acid around 12.1 in water, and even higher in organic solvents, this compound handles protons others cannot. The two amino groups, held close by the naphthalene structure, shield and stabilize any extra proton. This makes it keen to grab even the most weakly bonded hydrogen, letting chemists pull off transformations that would otherwise stall or require harsher techniques.

    Other popular bases like triethylamine, pyridine, or even 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) cannot match this combination of basic strength and selectivity. Our customers often bring us transformations that demand high basicity without the unwanted nucleophilicity that ruins more sensitive targets. 1,8-bis(dimethylamino)naphthalene consistently gives them a way forward where other bases give up, such as deprotonating very weak acids or stabilizing fleeting intermediates in catalytic cycles.

    Routine Applications in Our Own Practice

    We've seen it firsthand: in peptide synthesis, choosing our 1,8-bis(dimethylamino)naphthalene can make the difference between a failed coupling and clean, high-yielding product. In many organic transformations—especially those involving weakly acidic protons—lesser bases simply stall out, leaving valuable time and resources wasted. Our teams and long-term collaborators routinely employ this compound for selective dehydrohalogenation, formation of carbanions, or scavenging trace acids from sensitive preparations.

    Even more impressive, proton sponge gives you reactivity without the fingerprint left by nucleophilic bases, which too often lead to unwanted side reactions or complex purification. Those engaged in designing pharmaceuticals, new materials, or exotic ligands have come to rely on the silent efficiency of this molecule: a sharp, clean abstraction of protons with no messy footprints. It supports high-throughput screening, challenging synthesis setups, and all scales of operation. The feedback from research chemists is clear: the reliability of our manufacturing process helps keep their results consistent from experiment to pilot plant.

    Why Chemists Keep Coming Back

    Many have tried alternatives—strong alkoxides, powdery hydrides, and even conventional amines. Each time, the same story rises: purity and process consistency make or break hard-won research. Our strict control during manufacturing sets our product apart. We test each lot using high-sensitivity titration, nuclear magnetic resonance, and advanced chromatography. Every batch includes analytical certificates based on actual test data, not just book specifications. Problems due to trace contamination, residual solvents, or gradual decomposition rarely show up for our customers, thanks to tight quality control from raw materials to finished product.

    Chemists in academia and industry alike have told us our proton sponge cannot hide poor technique or substitute for creative problem-solving, but it sure won’t be the limiting factor in their research. Process chemists count on it during scale-up to deliver repeatable, reproducible results, even under the more challenging conditions of pilot and full-plant runs. Where reformulation or troubleshooting is often the order of the day, 1,8-bis(dimethylamino)naphthalene often ends up as the reliable old friend that quietly gets the job done.

    Comparing With Other Strong Organic Bases

    We often hear the question: “Why use 1,8-bis(dimethylamino)naphthalene instead of other strong organic bases?” It's an honest question and a crucial one in method development. While DBU and DBN are strong, their bicyclic structure brings greater nucleophilicity, which occasionally interferes with sensitive electrophilic functional groups. Sodium hydride and potassium tert-butoxide offer brute strength, but present more handling risks and can promote side reactions.

    Our proton sponge combines basicity and low nucleophilicity in a way you rarely find elsewhere, making it uniquely suited for work that requires clean abstraction of protons from stubborn acids. Where hydrolysis, ring-opening, or racemization need to stay tightly controlled, our experience shows no competitor provides a similar level of confidence or reproducible outcome. In routine dehydration of amides, formation of sensitive carbanions, or elimination reactions involving weak leaving groups, chemists using our material gain an advantage you can see in each flask or reactor.

    Nuanced Practices: Crystallization, Handling, and Longevity

    As hands-on producers, we do more than just pack and ship. Each batch passes through meticulous purification—multiple recrystallizations under inert atmosphere, for example—to drive down impurity profiles and achieve near-theoretical yields. We know some chemists will keep the material on the shelf for months between uses; that's why we use moisture-proof, light-blocking packaging and intentionally minimize changes in crystal size, making consistent weighing and dissolving easier.

    We always advise that users handle the material in a glovebox or under dry nitrogen whenever practical. Experience has shown even brief exposure to ambient air, especially on a humid day, can dull performance over time. We've also invested in testing the effect of small doses of acid scavengers or stabilizers on shelf life, identifying which additives can extend usable life while not interfering with sensitive chemistry. That attention to physical handling echoes back into the lab, reducing the headaches of spoiled reagents or puzzling side reactions.

    Real-World Challenges and How We Respond

    Life in chemical manufacturing never runs as smoothly as theory would suggest. Raw material variability, minor changes in process temperature, or hiccups in solvent quality can all affect outcomes. We’ve met these challenges by investing in continuous monitoring—keeping real-time logs of temperature, pressure, and atmospheric conditions throughout each run. Automated alerts notify our crew to watch for deviations, and experience guides the decisions on in-process corrections. By adapting quickly, we minimize waste and keep the product aligned with what seasoned chemists expect from our name.

    We've also learned the hard way that not all purification solvents or finishes deliver the same downstream results. Each time we run a lot destined for material-sensitive users—especially those in drug discovery or catalyst development—we ramp up the analytics, looking for overlooked side products or trace metals. Open communication with our customers keeps us focused on what really matters for them. In cases where users reported mysterious byproducts or yield drop-offs, careful back-and-forth let us tweak purification conditions to fully address their issues.

    The Chemistry Beyond the Bottle

    Our fascination with this molecule does not end at manufacturing. Seeing how chemists leverage its extreme basicity offers daily reminders of why we stay in this business. 1,8-bis(dimethylamino)naphthalene helps push the boundaries of modern synthesis. Methods for activating inert C–H bonds, accelerating challenging cross-coupling reactions, and stabilizing short-lived transition states have all benefited directly from this base. Researchers digging into new ligand scaffolds or improving selectivity in medicinal chemistry projects find the basicity profile of proton sponge reshapes what’s possible on the bench.

    Customers exploring green chemistry appreciate the lack of heavy metals, ease of waste treatment, and controllable reactivity. Its crystalline solid form cuts down on worker exposure to noxious fumes, compared to aggressive liquid or gaseous bases. Process chemists like its clean removal after reactions—simple extraction or crystallization steps sweep it away, leaving few residues in the product stream.

    One story from our own partnership network stands out: a team building a new diagnostic probe ran into persistent acid-catalyzed hydrolysis in their labeling step. Competing bases brought side reactions, but switching to our 1,8-bis(dimethylamino)naphthalene gave them product yields that enabled full-scale trials and later a commercial launch. Their success proved the point: consistent, highly-purified base in hand can mean the difference between a stalled project and a scientific breakthrough.

    Anticipating Tomorrow’s Chemistry

    As synthetic techniques evolve, we see new challenges in custom functional group installation, process intensification, and even energy-efficient scale-up. We stay ahead of these by collaborating regularly with research chemists and production managers at leading institutions, listening intently for the bottlenecks they face. Their toughest requests drive our internal R&D forward—whether it means further tightening impurity profiles, minimizing trace water content, or supplying custom particle sizes for automated reactors.

    Our technical support team, composed of chemists who have run reactions and fixed problems with their own hands, stays available for troubleshooting. If a user runs into unexplained color change, odd melting behavior, or lower basicity than expected, we consult directly. Often, over the years, issues traced back to incorrect storage, accidental exposure, or incompatibility with stabilizers found in other reagents. We aim to help users get the most out of every gram they use.

    Long-term, we invest in refining both the synthetic route and post-processing—experimenting with greener solvents where possible, boosting overall efficiency, and working to minimize environmental footprint. Each improvement flows back to the customer, making research smoother and scale-up less risky.

    What Makes Our 1,8-Bis(Dimethylamino)Naphthalene a Staple

    In the chemical industry, reputation sticks to every lot that leaves the plant. The details—how well the product tolerates air and humidity, the ease of weighing or solution preparation, the documentation included with every shipment—add up fast. Those who have experienced supplies from re-packagers or third-party vendors often return to us for peace of mind: the traceability, the hands-on support from real chemists, and the assurance that they are starting with the best possible material for their work.

    We spend as much effort tracking feedback as we do running reactors. We follow up with labs new to the product, learning how their specific workflow interacts with our solid. In response, we’ve tailored packaging and shipping to suit a global set of climates and use cases. Our long-term users benefit from continuous process improvements, and the next generation of chemists inherits a reliable foundation for pushing deeper into the unknowns of molecular synthesis.

    Few compounds in the organic toolkit match the versatility and strength of 1,8-bis(dimethylamino)naphthalene. Our experience shows that prioritizing batch-to-batch consistency, practical handling, and customer-driven solutions fosters more successful chemistry—reaction after reaction, project after project.

    Embracing Real-World Impact

    Chemical manufacturing exists to serve curiosity and practical need—new drugs, lighter materials, smarter catalysts, greener processes. The best raw material can make even bold ideas work out in the lab, and the wrong one brings unnecessary reruns and high costs. By keeping our focus on high-quality production, transparency about our process, and honest conversation with users, we help the scientific community trust that this basic building block will rise to each new occasion.

    From isolating delicate intermediates or cleaning up product streams, to supporting the scale-up of next-generation pharmaceuticals, our version of 1,8-bis(dimethylamino)naphthalene stands as a dependable partner. Behind every batch shipped lies a commitment to reproducibility, chemical purity, and real expertise—backed by people who know what’s at stake in every synthesis.

    Anyone committed to challenging chemistry deserves a foundation built with equal rigor. Our manufacturing efforts aim to supply just that foundation, again and again, reacting to what users demand rather than pushing commoditized product into the market. In a field where small details define outcomes, our proton sponge continues to prove essential, quietly shaping countless advances throughout science and industry.