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HS Code |
689975 |
| Cas Number | 2243-62-1 |
| Molecular Formula | C10H10N2 |
| Molar Mass | 158.20 g/mol |
| Appearance | White to light brown crystalline powder |
| Melting Point | 164-167°C |
| Boiling Point | 360°C (estimated) |
| Density | 1.19 g/cm³ |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.721 |
| Flash Point | 194°C |
| Pubchem Cid | 81559 |
| Synonyms | 1,5-Naphthalenediamine |
As an accredited 1,5-Diaminonaphthalene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,5-Diaminonaphthalene is packaged in a 100g amber glass bottle, tightly sealed, with hazard labeling and supplier information. |
| Shipping | 1,5-Diaminonaphthalene should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Label as hazardous, according to relevant regulations (e.g., DOT, IATA, IMDG). Ensure proper ventilation and temperature control during transport. Handle with appropriate personal protective equipment to prevent inhalation, ingestion, or skin contact. |
| Storage | **1,5-Diaminonaphthalene** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store in a chemical storage cabinet specifically designed for hazardous organic chemicals and ensure proper labeling to prevent accidental mixing or misuse. |
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Purity 99%: 1,5-Diaminonaphthalene with 99% purity is used in the synthesis of high-performance polymers, where it ensures superior mechanical strength and chemical resistance. Melting Point 242°C: 1,5-Diaminonaphthalene with a melting point of 242°C is used in organic electronic material manufacturing, where thermal stability during processing is critical. Molecular Weight 158.20 g/mol: 1,5-Diaminonaphthalene at a molecular weight of 158.20 g/mol is used in dye intermediate production, where consistent batch quality and reproducibility are necessary. Particle Size <10 μm: 1,5-Diaminonaphthalene with a particle size of less than 10 μm is used in advanced pigment formulations, where improved dispersion and color uniformity are achieved. Stability Temperature up to 200°C: 1,5-Diaminonaphthalene with stability up to 200°C is used in epoxy resin modification, where resistance to high-temperature degradation is required. Moisture Content <0.2%: 1,5-Diaminonaphthalene with moisture content below 0.2% is used in pharmaceutical intermediate synthesis, where product purity and yield are maximized. Low Ash Content: 1,5-Diaminonaphthalene with low ash content is used in specialty chemical manufacturing, where impurities are minimized to enhance end-product performance. |
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Chemistry offers tools that help industries push innovation forward, and 1,5-Diaminonaphthalene stands out as one of those hard-working building blocks. This aromatic compound sits firmly in the family of naphthalene derivatives, featuring two amine groups attached to the naphthalene core at the 1 and 5 positions. For anyone who’s handled the physical stuff: it presents itself usually as a grey to brown crystalline powder, and that color change often signals purity changes or the effects of oxygen. Its molecular formula, C10H8N2, puts it in a stable category that doesn’t break down easily under standard storage—an asset for busy research spaces and manufacturing plants.
My first encounter with 1,5-Diaminonaphthalene happened in a college laboratory, back before I knew what went into the performance dye industry or what it took to stabilize polymers in industrial processes. Its smell, slightly musty and chemical, doesn’t exactly impress. But over the years, you start noticing how a single compound finds its way into so many corners of chemical development, from pigments for plastics to specialty coatings. Looking at the melting point, which floats near 209 °C, you realize why this compound stands up during high-temperature reactions. In a world where machinery runs hot and processes demand stability, having a raw material that stays reliable counts for a lot.
In practical terms, 1,5-Diaminonaphthalene finds itself mostly in the business of making dyes, pigments, and advanced organic materials. Organic chemists often call on its double amino groups to spark off reactions—they’re grateful for its ability to form strong bonds with other moieties, especially in the presence of oxidizing agents. If you crack open a chemistry reference guide, you’ll spot this compound listed as a parent structure for some of the world’s most colorfast and light-stable dyes. Yellow, red, and orange pigments that show up in everything from commercial plastics to high-end printing inks often trace their molecular ancestry here.
The world of electronics has also found more uses for 1,5-Diaminonaphthalene, thanks to its application in building electronic polymers and OLED precursors. One of the things I appreciate about its structure is the way it encourages the formation of extended, planar systems in organic semiconductors. That planarity helps these materials transport charge with less resistance. People working in the field of organic electronics know that certain substitutions at the amine sites—possible with this molecule—can tune electronic properties enough to make a real difference in efficiency and durability.
There’s a branch of analytical chemistry that still leans hard on 1,5-Diaminonaphthalene. In more practical terms, labs use it as a reagent for nitrite detection, and for that, specificity matters. This reagent reacts with nitrite under acidic conditions, giving a measurable color response. Water testing labs, food quality inspectors, and environmental scientists trust this method. In a world crowded with options, reaching for the compound that delivers clear, dependable analytical results just makes sense. It frees resources and reduces error, both big wins for any laboratory that’s working under time or funding pressure.
There’s no shortage of diamino-naphthalene isomers, but the 1,5-structure brings a special reactivity pattern to the table. Compare it to 1,8-Diaminonaphthalene: those two amine groups in the 1,8 version occupy opposite ends of the aromatic system, which leads to quite different reactivity in condensation reactions and electronic materials. The 1,5 isomer’s arrangement encourages a more synchronized response during coupling reactions. The result is that you often see stronger, more stable bonding patterns, and the final products have colors that last longer under outdoor conditions or repeated washing.
Take the example of pigment manufacturing. 1,5-Diaminonaphthalene provides better performance in long-term light exposure when compared to some of the meta-substituted or 2,6-isomers, which is a clear benefit for products like outdoor signage or high-performance coatings. The topology also matters for polymer science. When you’re trying to engineer conductive polymers for electronic applications, the position of the amine groups sets up the monomer units more favorably for chain propagation. This subtle difference lets materials scientists hit electrical conductivity targets while boosting stability—nobody wants a polymer film that falls apart after minimal use.
If you’ve ever ordered specialty chemicals, you know about purity anxiety. With 1,5-Diaminonaphthalene, tiny impurities can poison a whole batch of dye or sabotage polymer synthesis. Manufacturers usually offer purities above 98%, which suits most industrial and research needs. Lower grades sometimes come in at 95% for bulk applications, though. Make sure the supplier delivers certificates of analysis; a short-term gain in cost often fails to make up for a lost production run or rejected QA sample. I’ve seen projects nearly derailed by careless substitutions; cleaning up after poorly refined batches costs more than doing it right the first time.
On the physical side, crystalline powder tends to pick up moisture from the air—left too long on a bench, it slowly darkens and clumps. I once learned that lesson the hard way, discovering a jar stuck together after storage in a humid storeroom. Anhydrous conditions or a well-sealed bottle keep the product stable. Another point is toxicity: this compound, like many aromatic amines, can be harmful if handled carelessly. Gloves and a fume hood aren’t only recommended—they’re essential. Good ventilation saves headaches and more serious health problems, especially for those who use it daily.
Modern chemical manufacturing faces hard questions about sustainability. Those questions don’t always have easy answers. 1,5-Diaminonaphthalene doesn’t break down rapidly in the environment, which means manufacturers and users both bear the responsibility of proper disposal. In my experience talking to plant managers, those who treat their waste streams to limit aromatic contamination run into fewer problems with regulators and communities. Composting or simple landfill isn’t an option here. Incineration at authorized facilities remains safest—if imperfect. Workers in the dye industry remember the environmental impact legacy left by dumping aromatic amines; nobody wants history to repeat itself.
On the bright side, some research points toward greener production methods. Bio-based syntheses or catalytic hydrogenation of renewable feedstocks might one day shift the balance away from petrochemical reliance. While this isn’t a reality for most industrial supply chains yet, keeping an eye on cleaner innovation means companies stay ahead of regulations and public expectations. For mid-sized operations, following best practices on recovery and recycling helps keep overheads down while meeting environmental standards.
One thing I’ve noticed about 1,5-Diaminonaphthalene through practical use: its core structure adapts well to chemical modifications. Organic chemists appreciate the ease of introducing sulfonic acids, carboxyls, or other functional groups. This gives downstream manufacturers space to diversify product lines, whether they need more water solubility or special compatibility with other raw materials. The demand for these modifications keeps shifting, especially as electronics and dye industries move toward materials that meet stricter safety and performance benchmarks.
In educational and industrial settings, this flexibility supports both basic research and scale-up manufacturing. Students often encounter the parent structure during advanced organic synthesis labs, where they see firsthand how modifications at the amino positions enable synthesis of more complex molecules. In commercial chemistry, this adaptability isn’t just a nice feature. It lowers costs by shortening development time and simplifying reaction schemes, which keeps products coming to market quickly and reliably. I’ve watched product teams skip months of frustration by choosing a compound that lends itself smoothly to structural changes instead of fighting through poorly reactive intermediates.
In the controlled chaos of a working lab or production plant, standardization and batch consistency turn out to be as important as product innovation. Multiple suppliers offer 1,5-Diaminonaphthalene, some as technical grades and others in high-purity forms. Anyone engaged in scale-up or regulatory submission knows this step can’t be skipped. I once watched a promising pigment project grind to a halt after an unexpected batch-to-batch variation in the starting material changed the color of the final product—nobody wants that call from a disappointed client.
International standards, such as those used for defining heavy-metal limits and residual solvents, support safe use throughout the supply chain. Analytical methods like gas chromatography and HPLC, combined with spectrophotometric analysis, support these standards and safeguard quality. Several big-name third-party labs can audit purity and check for problematic byproducts, which adds an important safety layer. Larger chemical companies often set custom specifications for their own purposes, especially when customers expect certainties in performance for things like device-grade polymers or pharmaceutical intermediates. Suppliers who can hit these targets consistently simply stay in business longer.
Wider trends in the chemical markets shape availability and price for 1,5-Diaminonaphthalene. Dye and pigment cycles create surges and dips. If you track the major industrial pigment lines, sharp upticks in production often follow a rise in demand for colorful, durable plastics or outdoor paints. Electronics and advanced materials companies add more volatility because they seek higher-purity starting materials and accept fewer impurities. These shifts echo in the price records; a string of unforeseen supply interruptions or a spike in energy costs abroad can double prices over a few weeks.
Globalization has made sourcing simpler in one sense: there are more choices now across Asia, Europe, and North America. But more sources also means buyers need to stay informed about capacity expansions and price undercutting from lower-quality suppliers. I’ve watched colleagues chase a lower price point abroad, only to deal with customs, delays, and more rigorous testing requirements when shipments finally clear. The risk equation changes based on the intended use—for research or one-off syntheses, flexibility helps, but for a plant running 24/7, stability and guaranteed specification count for more than minor cost savings.
Let’s talk about the snags most producers and users run into. Handling safety and regulatory compliance matters for 1,5-Diaminonaphthalene every bit as much as for more widely-known industrial chemicals. Direct skin exposure can cause irritation or worse, so equipment and clear handling training cut down on emergency room visits and improve morale. Periodic air monitoring in work areas helps, especially if there’s any chance of dust. Good housekeeping—clean benches, immediate spill removal, correct storage—prevents accidents and loss. I’ve seen organizations save large sums not by big new investments, but simply by focusing on training: it’s a basic rule that pays off quickly.
Disposal and regulatory paperwork need steady attention. Follow the rules on waste tracking, stay aware of local rules on aromatic amine waste, and keep in close contact with disposal contractors who know how to manage complex chemical waste. Some regions label this compound under regulations for hazardous substances, which includes reporting use and storage above certain threshold amounts. Make life easier by keeping records orderly and conducting regular safety audits. Avoid letting problems linger until a regulator’s surprise inspection—a stitch in time really does save nine here.
In the world of specialty chemicals, informed choice drives stability and innovation. Labs, manufacturing plants, and developers share a responsibility to look beyond spec sheets and price lists and consider the full impact of their sourcing. When quality, consistency, and adaptability all line up, 1,5-Diaminonaphthalene still earns its place in a crowded market. From dyes and pigments to cutting-edge electronic materials, its double amine function and stable backbone keep finding new uses, year after year.
Staying open to new methods—greener synthesis, improved purity, safer packaging—ensures ongoing usefulness for this compound. In conversations with industry veterans, one theme comes through clearly: adaptability and transparency from suppliers, plus diligence from buyers, create a working chemical supply chain. For anyone willing to invest time in learning the quirks and strengths of 1,5-Diaminonaphthalene, the rewards range from more vivid products to scientific breakthroughs. The discipline and care invested up front come back many times over in reliable results.
Over the years, the best lessons have arrived outside textbooks. Early on, I worked with a team making high-performance polyimides, and we needed just the right aromatic diamine for a thermally stable film. Lab tests had favored 1,5-Diaminonaphthalene, but our first industrial batch went all wrong—unexpected color, odd mechanical properties. Eventually, a little detective work revealed contamination in the raw material. From then on, our team doubled down on supplier auditing and trusted only those who provided transparent laboratory data. Our yields stabilized, and customer satisfaction improved right along with it.
In a separate stint at an R&D facility focused on printing inks, I watched a chemist troubleshoot a fading issue on outdoor signage. Competitive products weren’t performing well, but trials with naphthalene-based pigments derived from 1,5-Diaminonaphthalene produced results with much better sun and rain resistance. The change didn’t require a major overhaul, just an update to the pigment precursor. That sort of incremental improvement—switching a starting material to boost longevity—says a lot about why this compound still matters, even as flashier materials hit the headlines.
Some challenges won’t disappear quickly. Aromatic amine toxicity remains an issue in manufacturing, and even the most careful user risks exposure if protocols slip. Progress on less-toxic, equally effective alternatives keeps things honest, but nothing so far beats the combination of reactivity, colorfastness, and resilience offered by the 1,5 isomer. Rather than waiting for a perfect substitute to emerge, many organizations double their efforts on training and process improvement. Promptly dealing with emissions, maintaining airtight storage, and following up on even minor exposure incidents sets a lasting standard.
Industry and the research community both benefit from sharing experiences and new data. Open forums, industry conferences, and research publications drive slow but steady improvements in safe handling, greener chemistries, and product performance. In my own work, joining these conversations added real value—I heard about less-obvious pitfalls, clever troubleshooting strategies, and new sources worth exploring. Sometimes, sharing one hard-earned tip can prevent another team from repeating a costly mistake.
Every chemical has its limits, but some keep earning respect for their stability, reliability, and role in making life more colorful and efficient. 1,5-Diaminonaphthalene remains one of those backbone compounds that, through careful handling, reliable sourcing, and practical adjustments, delivers real-world results in products you see and use every day. New regulatory controls and evolving sustainability targets make life harder for many specialty chemicals, but for now, the track record of this diamine means it keeps showing up where toughness and adaptability matter most.
Future advances may improve on older production methods or resolve lingering health and safety issues, but practical know-how, rooted in real experience, keeps adding value today. In a marketplace where suppliers and buyers face tighter margins, quicker expectations, and sharper scrutiny, those able to master the ins and outs of 1,5-Diaminonaphthalene—without cutting corners—stand ready for whatever comes next.