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HS Code |
259540 |
| Chemical Name | N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid |
| Molecular Formula | C17H14N2O8S2 |
| Molecular Weight | 454.43 g/mol |
| Appearance | Solid, usually powder |
| Color | Light yellow to brown |
| Solubility | Soluble in water |
| Melting Point | Decomposes on heating |
| Cas Number | 81-10-5 |
| Synonyms | Acid Yellow 99, Acid Yellow G, Acid Yellow GG, Acid Yellow NGR |
| Usage | Dyestuff, analytical reagent |
| Storage Conditions | Store in a cool, dry place |
| Stability | Stable under recommended conditions |
| Ph | Acidic aqueous solutions |
| Odor | Odorless |
| Hazard Classification | May cause eye, skin, and respiratory irritation |
As an accredited N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid in a sealed, amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12MT packed in 480 fiber drums, each 25kg net, palletized for safe transport of this chemical. |
| Shipping | **Shipping Description:** N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid is shipped in tightly sealed containers to protect from moisture and light. It should be transported at ambient temperature, following all relevant chemical safety regulations. Proper labeling and documentation are required. Avoid contact with incompatible materials and handle carefully to prevent spills or exposure. |
| Storage | N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid should be stored in a tightly sealed container, protected from light, moisture, and air. Store at room temperature in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Properly label the container, and avoid exposure to excessive heat. Follow all safety guidelines and local regulations for chemical storage. |
| Shelf Life | Shelf life of N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid: Stable for 2 years if stored cool, dry, and sealed. |
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Purity 98%: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with purity 98% is used in dye manufacturing processes, where it ensures consistent chromatic intensity and minimal byproduct formation. Water solubility: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with high water solubility is used in textile dye baths, where it promotes uniform fiber coloration and enhances dye uptake efficiency. Molecular weight 456.45 g/mol: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid at molecular weight 456.45 g/mol is used in analytical chemistry as a calibration standard, where it provides reliable molecular quantification and detection sensitivity. Melting point 285°C: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with melting point 285°C is used in high-temperature ink formulations, where it maintains pigment stability and prevents decomposition during processing. Particle size ≤10 µm: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with particle size ≤10 µm is used in advanced coatings applications, where it delivers smooth surface finishes and consistent pigment dispersion. Stability temperature up to 180°C: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid stable up to 180°C is used in thermal printing systems, where it retains color integrity and resists degradation under heat. Sulfonic acid group content: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with high sulfonic acid group content is used in the synthesis of reactive dyes, where it enhances dye-fiber bonding and wash fastness. UV absorption maxima at 335 nm: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid exhibiting UV absorption maxima at 335 nm is used in photoactive material research, where it supports efficient UV light harvesting and optical signal amplification. Chemical stability in acidic media: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with chemical stability in acidic media is used in industrial wastewater treatment, where it sustains its molecular structure and provides robust pollutant removal. High affinity for protein fibers: N-(4-Aminobenzoyl)-2-Amino-8-Naphthol-3,6-Disulfonic Acid with high affinity for protein fibers is used in specialized leather dyeing, where it enhances penetration and long-lasting coloration. |
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Production floors often favor brevity, but in research and manufacturing, the full chemical name matters. N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid, a mouthful in any language, has earned a spot in dye and intermediate chemistry thanks to its balance of functional groups. This product’s structure—anchored by two powerful sulfonic acids and two amines—gives it versatility in synthetic coloring and specialty chemical synthesis. Seeing it in action at our facility, one appreciates how its unique combination of the naphthol ring, sulfonic acids, and aminobenzoyl group shapes its performance in industrial reactions.
Decades of steady output have taught us a fair amount about the challenges and rewards of manufacturing N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid. Unlike simpler aromatic sulfonic acids, this compound asks for careful orchestration at each reaction step. Our plant emphasizes stepwise sulfonation and protection-deprotection techniques to avoid unwanted byproducts. Each batch presents a lesson in solvent selection and temperature control, especially to keep both yield and purity where they ought to be. Years spent refining our process let us meet tight specification windows, with high-purity output that holds up under third-party analysis—something end-users in sensitive dye syntheses have come to expect.
Granular, free-flowing crystals or powders—our finished product sometimes shows minor texture differences from lot to lot. These shifts don’t affect active content or performance, but we monitor them to support downstream process uniformity. We’ve installed advanced drying and milling systems to hold moisture levels steady and avoid caking during transport or storage. Handling this compound in bulk calls for specialized equipment, as it can take up moisture and, rarely, clump if ambient humidity spikes. Our packaging engineers constantly tweak methods to keep product movement frictionless, from silo loading to final bagging and sealing.
Most users meet N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid midway through a more complex synthesis, where it acts as a key naphthol-based intermediate. Typical demand comes from the production of acid or reactive dyes, often those destined for wool, nylon, or silk. Its robust solubility in water and strong ion-exchange performance let it participate in fast-coupling reactions, especially those calling for ammonium or diazonium salt intermediates. In operations focused on specialty pigments or azo dye synthesis, our grades consistently deliver the repeatable reactivity color chemists look for.
Other standard aromatic naphthol derivatives fail to offer the same balance of amine reactivity and sulfonic acid stability. Those less optimal candidates can show drifting reactivity or leave end-users with higher exhaust losses or shade inconsistencies across dyed lots. By contrast, our N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid, with its dual amine configuration, holds coupling partners in solution and responds rapidly even under variable pH conditions. This has let some customers cut out stabilizing agents or buffers in their own formulations, simplifying process control—a theme that surfaces often in our technical exchanges.
Manufacturers in this space have experimented with related molecules, especially other aminonaphthol sulfonic acids differing at the position or number of amine or sulfonate groups. Take 6-amino-2-naphthol-3-sulfonic acid, which we also make in a dedicated unit. This material covers a swath of the same diazo-coupling landscape but lacks the particular aminobenzoyl attachment found on the product discussed here. That absence has cost implications downstream. For example, those seeking deeper, more neutral dye shades find that the aminobenzoyl bridge delivers tighter color fastness and higher wash stability. Side-by-side technical tests reveal that the shift to our primary material consistently leads to sharper dye uptake and more even coverage on synthetic fibers.
Process chemists looking for reliable performance sometimes hesitate when substituting with alternative naphthol sulfonic acids, especially where high-purity requirements limit the tolerance for secondary byproducts. Many substitute products leave behind more unreacted starting materials or spawn off-color tints in finished dye baths. Years ago, we fielded frequent requests from partners hoping to swap in other naphthylamines or simpler monoamines, only for them to circle back once end-product testing highlighted the limits of those alternatives. In practical terms, N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid keeps earning its way back into sophisticated dye and pigment processes for this reason.
Keeping our production in step with the broader chemicals industry has meant continuous investment in both process control and environmental management. N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid doesn’t just leave our plant as powder or slurry; we integrate traceable batch records and analytical data packs for every shipment. Our on-site quality labs use chromatographic and spectrophotometric techniques to track purity, detect isomers, and signal any drift from established standards. This diligence matters not only for regulatory audits but also for clients engaged in high-volume coloring where consistency translates to profit.
The chemicals sector faces tighter scrutiny around effluent and emissions. Manufacture of sulfonic acids, especially those as structurally complex as this one, generates side streams in both organic and inorganic phases. We treat these streams with tailored wet oxidation and advanced filtration, minimizing waste and capturing valuable byproducts when feasible. Local authorities tour our facility regularly, taking samples, auditing bonds and tanks, and reviewing logs. Strong environmental stewardship forms part of our brand reputation, and we have invested in third-party audits to verify our process claims. Our practices align with accepted industrial hygiene and worker safety guidelines, as much for internal peace of mind as for external compliance.
Over time, our technical teams have forged open channels with clients in the dye, pigment, and specialty chemical sectors. These partnerships help us understand recurring pain points in color synthesis: consistency from batch to batch, filterability during downstream processing, and resistance to light or water after fixation on textiles. By staying close to our users—not just through datasheets but through site visits and troubleshooting—we keep seeing fresh applications for the product. Users deploying sophisticated fiber blends or novel polymers have looped us in as early as pilot trials, allowing our skilled chemists to help adapt product grade or offer real-world handling advice.
One example that stands out involved a partner in the automotive textile industry. They needed a deeper navy shade with low migration during heat-setting. Our joint lab team dug into pH and ionic strength adjustments throughout their process, eventually fine-tuning the application method. Achieving that optimal shade owed much to the dual amine chemistry of N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid, which locked in the diazo partner and resisted degradation even under intense thermal exposure. Every season brings new technical requests like these, and each one pushes us to keep learning and improving.
Sustainability isn’t just a marketing slogan here. We track raw material sourcing for our core inputs—napthols, sulfonating agents, and amines. Where possible, we leverage suppliers who adopt safer practices and renewable utilities. In downstream manufacturing, the switch to greener solvents and water-based cleaning cycles has helped cut overall water consumption by about fifteen percent during the last fiscal year. Sometimes the most meaningful changes come from suggestions made by the folks running the reaction vessels and distillation columns—a practical proof that sustainable practices align best with input from those closest to production challenges.
We have explored closed-loop wastewater treatment, especially for wash water following crystallization and drying. These new systems return treated water to non-critical cooling and washing steps, further slashing the plant’s freshwater demand. If dye manufacturers downstream follow similar paths, the impact multiplies across global supply chains. Pioneering these measures satisfies not only regulatory expectations but upholds our promise to future chemists and communities alike.
The world’s supply chains have faced turmoil—from pandemic disruptions to freight bottlenecks. Logistics for a specialty chemical like N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid need more than the usual haulage arrangements. Safe shipping requires antistatic packaging and moisture-barrier liners to cope with swings in ocean humidity or warehouse temperature. Our distribution teams have adapted by coordinating direct runs, avoiding excessive handoffs or temperature cycling that could compromise batch quality. Clients sometimes request smaller, more frequent shipments to minimize site storage. We have responded with investments in automated bagging systems and flexible inventory management to meet this need.
During global shortages of various upstream chemicals, we’ve leaned on our experience in substitution. For instance, when a supply crunch hit a particular amine precursor, we carried out extensive bench tests to confirm that alternative sources or slight recipe changes did not cause drift in final product quality. Rigorous validation at this stage spares end-users downstream headaches involving shade migration or mechanical instability in their dye baths. We have made it a point to share these test results proactively, giving partners confidence in both our product reliability and our problem-solving mentality.
Most of the world knows N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid through its established role in synthetic dye chemistry. Current laboratory efforts, though, are opening new avenues. Specialty chemical firms are investigating its suitability as a coupling partner in advanced polymer synthesis, especially those aiming for tunable optical properties in films used for electronics and coatings. Our own research cell collaborates with academic and industrial groups, exchanging protocols and sharing structure-reactivity data to chart new territory for this molecule. Real-world problems—heat aging in printed circuits or field-stable coloration on synthetic fabrics—drive much of this work.
Medical and diagnostic sectors occasionally ask about specialty batches for research on chemical markers and contrast agents. We have seen lab-scale demonstrations where the compound’s dual sulfonic acid groups help solubilize conjugates in aqueous media, supporting rapid development without extensive salt additives. While regulatory clearance for pharmaceutical use lags behind industrial dyes, signs point to additional growth as research standards and analytical tools improve. For those of us making the product, this represents both a challenge and an incentive—a push to keep our own methods nimble and flexible.
End users now expect transparency on everything from the carbon footprint to detailed analytical test reports. In response, we rolled out real-time digital batch data for interested partners. These moves let us bridge the conversations between purchasing teams and R&D laboratories. From factory tours given to university students and multinational dye makers alike, conversations always circle back to one theme: chemistry stands still for no one. We accept every critique and every new question as part of a cycle of improvement—key to holding up our end in the global specialty chemicals network.
Customer feedback drives our annual investments, whether in digital controls for improved batch tracking or in educational outreach that helps procurement agents and researchers understand how our processes impact their own. Shift supervisors note recurring themes in feedback calls—requests for tighter spec windows, eco-friendlier intermediate grades, and traceability for certification audits. Meeting these needs means sustained technical training for line staff and ongoing upgrades to both lab and production equipment. These realities shape our annual operating budget and keep our technical documentation evolving with the times.
For us, making N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid never feels routine. Workers calibrate dosing pumps daily in the sulfonation room, adjusting to minute shifts in raw material titer or reaction pH. Forklift operators train specifically for this product's denser packs, and laboratory techs double-check each sample to thread the needle between reaction completeness and minimal byproducts. Longtime employees say you only really understand the chemistry after a season or two in the process trenches, troubleshooting clogs or adjusting vacuum levels during drying. These stories filter through to our process improvement meetings, giving real shape to what at first seems like just another fine chemical in the catalog.
By engaging up and down the supply chain, we recognize both the challenges and opportunities that come with this specialty product. While we take pride in our ability to scale batches consistently, every year brings its own unique puzzles, whether in source material purity, shipping logistics, or end-user application tweaks. This hands-on perspective informs how we support customers, refine internal processes, and keep a sharp eye on both safety and sustainability. In this way, our relationship with N-(4-Aminobenzoyl)-2-amino-8-naphthol-3,6-disulfonic acid remains a living, learning experience—one rooted in hard-won manufacturing knowledge and a commitment to continual growth.