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2,3-Diaminophenol

    • Product Name 2,3-Diaminophenol
    • Alias Resorcinol diamine
    • Einecs 220-550-7
    • 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
    VTB
    Specifications

    HS Code

    778479

    Iupac Name 2,3-Diaminophenol
    Molecular Formula C6H8N2O
    Molar Mass 124.14 g/mol
    Cas Number 615-22-5
    Appearance Light brown to beige solid
    Melting Point 152-154 °C
    Solubility In Water Slightly soluble
    Pka Approximately 8.8 (phenolic OH)
    Pubchem Cid 78659
    Smiles C1=CC(=C(C(=C1)N)N)O
    Inchi InChI=1S/C6H8N2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H,7-8H2
    Synonyms 2,3-Dihydroxyaniline; 2-Amino-3-hydroxyaniline; m-Phenylenediaminol
    Hazard Statements Irritant

    As an accredited 2,3-Diaminophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,3-Diaminophenol is supplied in a 25g amber glass bottle with a sealed cap, labeled with hazard warnings and handling instructions.
    Shipping 2,3-Diaminophenol should be shipped in tightly sealed containers, protected from moisture and light. Transport in accordance with local, national, or international regulations for hazardous chemicals. Ensure proper labeling, provide safety data sheets, and use secondary containment to prevent leaks. Handle with care, avoiding exposure, and store in a cool, well-ventilated area during transit.
    Storage 2,3-Diaminophenol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store in a chemical storage cabinet suitable for hazardous materials, and clearly label the container to ensure proper handling and identification.
    Application of 2,3-Diaminophenol

    Applications of 2,3-Diaminophenol in Industrial Manufacturing

    We supply high-purity 2,3-diaminophenol directly to global industrial manufacturers, addressing specialized needs across controlled chemical synthesis. The following sections detail practical applications where our material integrates into downstream processes, highlighting compliance, formulation, and resulting product classes as used by end-producers.

    1. Hair Dye Intermediates for Oxidative Hair Colorants

    2,3-Diaminophenol serves as a targeted intermediate for advanced oxidation hair color formulations, supporting the development of permanent and semi-permanent hair colors that deliver controlled dark tones and nuanced shades. The aromatic diamine structure ensures predictable color performance through oxidative coupling with primary color bases and modifiers under ammonia- or MEA-controlled alkaline conditions. Industrial producers value this molecule for its contribution to fade resistance and shade customization in final dye formulations.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • U.S. FDA 21 CFR 73.2396 (Hair Dye Components)
    • Health Canada Cosmetic Ingredient Hotlist
    • ISO 22716:2007 (Cosmetic GMP)

    Typical usage ratio

    • Ranges from 0.05% to 1.0% by weight in final coloring creams or lotions, with actual content determined by target color intensity, color base, and auxiliary ingredients.

    Downstream process integration

    • Blended directly into aqueous alkaline dye base mixtures during the formulation stage, followed by controlled pH adjustment and stabilization prior to packaging. Incorporated alongside primary and coupling agents before final product emulsification.

    Final product types

    • Permanent oxidative hair dyes
    • Semi-permanent hair colorants
    • Professional salon hair coloring products
    • At-home boxed hair color kits

    2. Synthesis of Photographic Developing Agents

    In photochemical applications, 2,3-diaminophenol is introduced as a precursor for tailoring organic developing agents, especially where high contrast and controlled grain structure are required. Its stable reduction-oxidation capacity allows the formation of fine-tuned aromatic developer compounds under controlled pH and temperature, ensuring compatibility with both black-and-white and reprographic processing lines. Unique to this segment, the material enables reliable developer regeneration and consistent image reproduction in specialty film and print processing.

    Industry compliance standards

    • ISO 18911:2010 (Imaging materials—Storage stability of processed films)
    • ANSI/NAPM IT9.1 (Photographic Films—Stability)
    • RoHS compliance where required for electronic imaging systems

    Typical usage ratio

    • Added at 0.1%–0.3% by weight in stock developer solutions; dosage varies based on film emulsion type, required density scale, and process cycle time.

    Downstream process integration

    • Charged alongside other developing agents (hydroquinone, metol) during developer solution preparation, often dissolved under mild heating and agitation before filtration into processing tanks.

    Final product types

    • Black-and-white film developers
    • Photographic paper developers
    • Microfilm processing chemicals
    • Specialty reprographics and x-ray developer kits

    3. Organic Intermediate for Pharmaceutical Synthesis

    Pharmaceutical producers utilize 2,3-diaminophenol as a specialty intermediate for specific API building blocks, particularly in the preparation of tricyclic and heterocyclic compounds. Its amino and phenolic functionalities facilitate controlled amination, cyclization, and protection steps in multi-stage chemical syntheses. Batch-record transparency and full traceability are maintained throughout for regulatory acceptance, with the compound regularly used under cGMP protocols for active ingredient elaboration supporting final drug product manufacture.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • U.S. FDA cGMP (21 CFR Parts 210 & 211)
    • Ph. Eur. 10.0 (European Pharmacopoeia, relevant monographs for intermediates)
    • ICH Q3A/B (Impurities in New Drug Substances)

    Typical usage ratio

    • Utilized at 0.5–5.0 molar equivalent per reaction step, adjusted per target yield, stoichiometry, and impurity control strategy.

    Downstream process integration

    • Introduced to reaction vessels during amination or cyclization stages, typically under inert gas, solvent-mediated, and temperature-controlled conditions. Frequently subjected to in-process QC analysis (HPLC, GC) before further synthetic steps.

    Final product types

    • Tricyclic antidepressant API intermediates
    • Aromatic heterocycle building blocks for anti-cancer drugs
    • Precursor units in CNS pharmaceutical synthesis

    4. Specialty Polymers and Functional Resin Modification

    High-performance resin manufacturers leverage 2,3-diaminophenol to introduce functionalized amine groups into custom polymer chains, enhancing nucleophilic reactivity and modulating end-use resin properties. Industrial processes employ it as a co-monomer or chain modifier, particularly in polybenzoxazines, phenolic resins, and certain specialty epoxy systems—achieving designed thermal, electrical, or mechanical profiles for niche electronic, adhesive, and composite applications. Well-defined input controls guarantee formulation reproducibility and regulatory shipment requirements.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 compliance for polymer substances
    • UL 94 (Flammability of Plastic Materials)
    • EN 45545-2 (Fire protection on railway vehicles—for transport resins)
    • TSCA (Toxic Substances Control Act, U.S. polymer registration)

    Typical usage ratio

    • Dosed at 0.3%–1.5% by weight of total monomers, depending on required crosslink density and targeted polymer performance metrics.

    Downstream process integration

    • Added during resin pre-polymerization or in chain extension phases, often under nitrogen and at specified thermal profiles, to ensure uniform incorporation and ultimate functional group distribution in the polymer backbone.

    Final product types

    • High-temperature resistant polybenzoxazine resins
    • Flame-retardant phenolic resin-based laminates
    • Specialty epoxy adhesives for electronics
    • Antistatic and conductive composites
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    Competitive 2,3-Diaminophenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding 2,3-Diaminophenol: Quality from a Chemical Manufacturer’s Perspective

    Every gram of 2,3-Diaminophenol that leaves our facility carries the knowledge and dedication of those who work with chemicals on a daily basis. Manufacturing this compound goes beyond mixing and reacting—it takes careful raw material sourcing, experienced handling of delicate reaction conditions, and respect for the uses that drive customers to choose it over other amine derivatives. From years spent on the production line to long hours in the lab, the story of 2,3-Diaminophenol starts with practical experience meeting market demand.

    Product Profile: 2,3-Diaminophenol

    Our 2,3-Diaminophenol, recognized by its CAS number 91-66-7, appears as a fine, off-white to light brown powder. Consistency in particle size and appearance doesn’t just make packaging neat; it reflects the control exercised throughout the synthesis and purification process. We hold purity around 99%—a value confirmed by HPLC analysis at every batch release. Residual moisture is regularly checked and maintained at low levels, usually below 0.5%. Customers often mention how this impacts storage stability and how it reduces headaches when they use it as an intermediate in further synthesis.

    We don’t treat 2,3-Diaminophenol as just another aromatic amine. Its chemical structure—two amino groups adjacent to the phenol ring—gives it a reactivity profile not matched by isomers or simple anilines. For industry, that structural difference changes the pathway and yield of downstream products.

    Practical Uses: Not Just a Raw Material

    Some in the dye industry know 2,3-Diaminophenol as a key intermediate for specific triazine and azo dyes. In our own facility, we’ve run test reactions with customers looking to synthesize metal complex dyes for textile or ink applications. The ortho orientation of the amino groups leads to more stable metal-ligand complexes. Feedback from these customers often supports what journals describe—dyes produced from this compound offer better resistance to washing and light.

    Beyond dyes, our technical staff has engaged with companies developing pharmaceutical and photographic products. The phenolic group introduces an extra handle for selective modification, giving rise to more than a dozen downstream molecules in the pharma sector. From our own failures during R&D, we’ve seen how choosing an incorrect isomer cuts overall yield and complicates purification. That explains why, after extensive in-house benchmarks, research clients tend to favor our 2,3-Diaminophenol for new molecule synthesis rather than its more common cousin, 2,4-diaminophenol. The ortho variation simply reacts differently in classical coupling or nucleophilic substitution steps.

    Another interesting use involves chelating agents and antioxidants. Chemical engineers in battery and electronics manufacturing look for consistent chelation strength and reliable electron-donating properties. Having run our own stability and compatibility tests, we’ve found the two amino groups next to the phenolic moiety interact confidently with metal ions and free radicals, opening up uses in corrosion protection and stabilizers for polymers.

    What Sets Our 2,3-Diaminophenol Apart

    Most industrial customers don’t ask for a generic diaminophenol—they specify the 2,3 version because of tighter reactivity controls in their process. We’ve made both batch and continuous process improvements to limit byproduct formation. Amidine, benzoquinone derivatives, and polycondensed tars form easily if temperature and pH wander. Our operators learn to keep the exotherms in check, and we monitor during reaction and post-treatment for color, melting point, and impurity level. Investing in automated environment control and routine GC-MS screening helps us ship product with tight specifications.

    It’s also easy to underestimate the downstream consequences of small differences in how 2,3-Diaminophenol is handled between production and application. Unlike 2,4- or 3,4-diaminophenol, the ortho compound tends to oxidize faster if left exposed to light or air. We use nitrogen purging and dark HDPE containers for bulk shipments, not as a marketing claim but as a solution to customer-preventable degradation. Our logistics team once documented a multi-tonne shipment that browned during cross-country rail transport, only to identify the issue as a container seal breach.

    Customers often ask about handling differences compared to other diaminophenol isomers. 2,3-Diaminophenol tolerates mildly acidic to neutral conditions better than meta or para versions when dissolved, which is why dye and pharma factories stick with it when using acid or buffer washes. Process chemists comment that its solubility makes washing out byproducts easier and shortens work-up time. We’ve measured this ourselves during pilot scale runs, and the less time required for recrystallization means operators can process larger batches with fewer solvent cycles.

    Challenges and Solutions in Production

    Reliable production of 2,3-Diaminophenol means paying attention to sourcing, synthesis, purification, and logistics. The nitro-reduction step—a major part of its synthesis—presents risk and complexity. Temperature swings trigger side-reactions; impure starting material sabotages selectivity. We source our nitrobenzene derivatives direct from refineries—no trading intermediaries—so we control quality from ground up. Over time, we have shifted away from outdated iron/acetic acid reduction to catalytic hydrogenation, not only for greener practice but for measurable decrease in heavy metal traces. Customers in pharma especially benefit from this, since their regulatory teams demand supplier data on trace metals.

    Separation and purification also involve more than simple filtration. 2,3-Diaminophenol, like other ortho-aminophenols, tends to form oily byproducts if not handled with precision during neutralization. We use staged solvent extraction, tailored to each lot’s impurity profile, guided by real-time analytics in the plant. It’s the details—solvent choice, extraction ratio, even glassware cleanliness—that define outcome. Our team reviews any deviation during weekly round tables to pinpoint faults and tweak protocols as needed.

    Application-Based Feedback Drives Quality

    Our chemists don’t just synthesize and send product out. They support application trials, set up sample programs, and adjust process parameters based on direct customer feedback. Dye makers in Asia once reported a faint batch-to-batch color drift. After site visits, we linked it to a non-obvious trace contaminant in a precursor shipment. Fast response, transparency, and customer-site technical support earned continued trust and repeat business—not just a contract. This hands-on, feedback-driven approach lets us refine each lot, not just settle for “good enough” process conformity.

    Some of the most valuable insights come from small and mid-size R&D-driven customers rather than corporate labs. In one case, a photochemical start-up pointed out that our prior drying step left invisible residues, impacting their quantum yield tests. We didn’t dismiss the feedback. Instead, we upgraded to a new vacuum dryer configuration, running extra analytics on both moisture and volatile content. Results showed clearer downstream performance, and the customer responded with a contract extension.

    Comparing 2,3-Diaminophenol with Other Aromatic Amines

    Too often, buyers lump all aminophenols together, missing how small molecular differences affect both chemical performance and process economics. 2,4- and 3,4-diaminophenol have their place, yet their electron distribution and steric layout shift reactivity in condensation and coupling reactions. In our pilot trials, the ortho orientation in 2,3-Diaminophenol gives distinct color depth and brightness to dyes—not simply a matter of shade, but a result of how the electrons delocalize and how the amino groups interact with metal ions and reactants.

    In pharmaceutical intermediates, these differences show up as diverging reactivity in amide formation and ring closure strategies. Structural analysis labs who test both compounds report faster, more complete coupling when using our ortho product versus a meta or para. Feedback from their process teams points to cleaner HPLC profiles and easier downstream purification, something we see in our own QC results.

    Our customers also point to storage and shelf-life. While 3,4-diaminophenol stands up longer to open air, it doesn’t dissolve as quickly in some solvents, nor does it provide the same dye fastness in metal-complex applications. Making product selection with process in mind, not just price or “aminophenol” label, results in fewer recalls and less waste on the customer side.

    Environmental and Regulatory Considerations

    Chemical manufacturing means managing both product stewardship and compliance. We track not just final assay but also waste output, worker exposure, and downstream environmental impact. Regulations for aromatic amines keep tightening as authorities review more health and ecological data. By shifting to cleaner hydrogenation and closed handling, we keep our emissions and operator exposure under control.

    Suppliers in other regions who cut costs with less-controlled processing sometimes let pollutants slip through. Over the years, a few customers have returned to us after facing custom seizures or regulatory nonconformity for imported bulk diaminophenol. Our documented traceability and routine submission to national authorities supports client-required registration where necessary.

    Some clients target eco-labels for their finished goods—textiles, for example. We assist them with paperwork and documentation on amine-purity, heavy metal testing, and certificate requests. Going beyond regulations isn’t just a chore for us; it smooths the path for our clients and often ends up as a competitive advantage.

    Customer Stories: Field Applications and Lessons Learned

    One global textile manufacturer shared their experience switching to our 2,3-Diaminophenol after dealing with variability from multiple sources. Dye bath analysis, after transition, showed measurable boost in color uniformity and lower need for post-process adjustments on finished cloth. Their purchasing manager later told us that the headaches and rework costs fell, making their purchasing decision less about upfront price and more about steady, reliable feedstock.

    A different story came from an electronics customer looking for antioxidant additives. Initial tests with a standard aminophenol failed to meet their oxidation resistance targets, resulting in performance issues during aging trials. Our technical team stepped in, providing tailored storage advice and supplementary product training. Together, we looked at packaging, humidity control, and real-world test runs on their line. Adjusting both application process and raw material selection brought performance up to specification.

    Pharmaceutical innovators who work under tight cost and purity constraints have given us some of the sharpest process optimization challenges. One customer, producing a key drug intermediate, required not just consistently high purity but regulatory-grade documentation. We facilitated custom retesting, additional certificates, and even a brief on-site audit. That project pushed our team to new levels of transparency and product traceability.

    Innovation and R&D

    We maintain regular dialogue with industry and academic groups. Participation in cooperative research and market studies gives us insight into where 2,3-Diaminophenol demand trends. Some development cycles run for years—chelation agents for energy storage, novel brightening agents for specialty inks, synthesis of advanced APIs. We engage in early trial supply, offer pilot-scale runs, and gather detailed feedback to refine our process.

    Recent R&D has focused on developing crystalline forms that improve solubility and shelf life. We’ve published preliminary findings at industry conferences, pointing to tangible gains in process throughput and handling safety. These investments in process development don’t just provide talking points—they actively cut costs, reduce waste, and enhance downstream uses for our clients.

    The Road Ahead: Commitment and Continuous Improvement

    Our experience with 2,3-Diaminophenol shows that manufacturing isn’t static—it evolves with each batch, each partnership, each process tweak born from client input or regulatory demand. As restrictions on aromatic amines evolve and markets move toward sustainable, higher-purity intermediates, we adapt. Our culture values feedback loops, field visits, and open dialogue.

    We push ourselves to anticipate bottlenecks and industry changes by keeping lines open to both frequent buyers and innovative start-ups. In the long run, quality and customer service outlast simple volume sales or cost-squeezing. Every process audit, customer trouble ticket, and technical request serves as another opportunity to improve. Working from the manufacturing floor up means listening, learning, and acting on what partners and clients need today and tomorrow.

    While supply chain pressures and shifting end markets add complexity, our approach—grounded in years of production experience and field knowledge—lets us rise to the challenges. Decision makers who depend on reliable, high-quality 2,3-Diaminophenol find value in this commitment. We remain dedicated to delivering what clients actually need, learning from every batch, and continuing to grow with every challenge faced.