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3,5-Diaminobenzoic Acid

    • Product Name 3,5-Diaminobenzoic Acid
    • Alias 3,5-DABA
    • Einecs 214-656-6
    • 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

    264288

    Name 3,5-Diaminobenzoic Acid
    Cas Number 99-05-8
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Appearance Off-white to light brown powder
    Melting Point 225-228 °C
    Solubility In Water Slightly soluble
    Density 1.317 g/cm3
    Pka 3.93 (carboxylic acid)
    Iupac Name 3,5-diaminobenzoic acid
    Pubchem Cid 7365
    Smiles C1=C(C=C(C=C1N)N)C(=O)O
    Inchi Key JSCVSSIXZWGDMY-UHFFFAOYSA-N
    Storage Temperature Store at room temperature (15-25 °C)

    As an accredited 3,5-Diaminobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle, tightly sealed with a screw cap, contains white crystalline 3,5-diaminobenzoic acid, labeled for laboratory use.
    Shipping 3,5-Diaminobenzoic Acid is shipped in tightly sealed containers to protect from moisture and contamination. It is classified as a chemical reagent and should be transported in accordance with local, state, and international regulations. Containers must be labeled properly, handled with care, and stored in a cool, dry location away from incompatible substances.
    Storage 3,5-Diaminobenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect from light, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature, away from sources of ignition or heat. Properly label the container and keep it out of reach of unauthorized personnel or incompatible materials.
    Application of 3,5-Diaminobenzoic Acid

    Applications of 3,5-Diaminobenzoic Acid in Industrial Manufacturing

    Our production of 3,5-Diaminobenzoic Acid directly supports advanced synthesis requirements in specialized industrial sectors. Through practical collaboration with downstream customers, we have documented the principal application scenarios below, focused on real manufacturing processes and key market products. Each section demonstrates our commitment to quality assurance, compliance, and formulation expertise.

    1. High-Performance Polyamide Engineering Plastics

    In the engineering plastics industry, producers use 3,5-Diaminobenzoic Acid as a vital comonomer during the polymerization of specialty polyamides, especially those targeting elevated thermal and mechanical resistance. Its meta-structure introduces controlled flexibility and chemical functionalization to the polyamide backbone, directly influencing the heat distortion resistance and dimensional stability of molded components. Formulators set dosing based on the mechanical specifications required for final goods such as electrical insulation parts and precision automotive devices.

    Industry compliance standards

    • ISO 1874-1:2022 (Plastics – Polyamide)
    • UL 94 (Flammability for Plastic Materials)
    • RoHS Directive (EU 2011/65/EU) for electrical/electronic products
    • REACH (EC 1907/2006) registration and risk assessment

    Typical usage ratio

    • 0.5–4.5 mol% of the total diamine formulation, subject to end-use performance targets (higher levels when enhanced thermal resistance and microstructural modification are desirable)

    Downstream process integration

    • Added directly into the aqueous polycondensation step, following salt formation with selected diacid(s); precise stoichiometric adjustment ensures consistent chain length and molecular structure

    Final product types

    • High-temperature nylon resins (e.g., meta-aramid-modified PA66, PA46, custom copolyamides)
    • Precision electrical connectors
    • Automotive under-the-hood components

    2. Reactive Dye Intermediates for Synthetic Textile Fibers

    Reactive dye manufacturers select 3,5-Diaminobenzoic Acid for diazo- and coupling chemistry in synthesis of monoazo and disazo dyes, targeting improved affinity and fastness on wool and polyamide fibers. Unique amine-group spacing enables highly stable chromophore integration, making possible deeper shade intensities and increased wash durability in textile applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Product Class II (dye safety for textiles in direct contact with skin)
    • ZDHC MRSL v3.1 – Zero Discharge of Hazardous Chemicals
    • EN ISO 105 series (color fastness standards on textiles)
    • EU REACH Regulation Annex XVII (restrictions on azo compounds)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to the diazonium precursor in azo dye synthesis (exact proportion adjusted for target dye class and chromophore resonance stabilization needs)

    Downstream process integration

    • Used as a direct substrate in the amination stage or as a coupling agent post-diazotization; advanced chromatography used for in-process QC validation of dye intermediates

    Final product types

    • Reactive dyes for wool, polyamide, and blended textile yarns
    • Azo-based pigments for technical coatings
    • Water-soluble dye powders and granules for industrial textile mills

    3. Specialty Polybenzoxazole (PBO) Fiber Manufacturing

    PBO fiber manufacturers utilize 3,5-Diaminobenzoic Acid as a rigid aromatic diamine precursor, directly affecting molecular orientation and mechanical performance in high-strength fibers. During solution polymerization, the specific placement of amino groups optimizes the rigidity and crystallinity of the resulting polymer chain, contributing to advanced fiber performance in extreme applications such as protective apparel and composites.

    Industry compliance standards

    • ISO 16637:2016 (Protective clothing – PBO fibers requirements)
    • NFPA 1971 (Standard on Protective Ensembles for Structural Fire Fighting)
    • ASTM D3822 (Tensile Properties of Single Textile Fibers)
    • EN ISO 13934-1 (Tensile strength and elongation of fabrics)

    Typical usage ratio

    • 1.0 molar ratio as a main-chain diamine monomer with strong acids (typically 50–60% of the total diamine content, depending on final fiber modulation targets)

    Downstream process integration

    • Introduced in the initial polymerization step with terephthalic acid or similar diacid under controlled dehydration conditions; subsequent solution spinning and thermal annealing performed to achieve target fiber structure

    Final product types

    • High-performance PBO fibers for ballistic-resistant clothing
    • Chemical-resistant protective suits
    • PBO-based woven and nonwoven industrial fabrics

    4. Pharmaceutical Impurity Standards and Process Intermediates

    Pharmaceutical manufacturers source 3,5-Diaminobenzoic Acid as a well-characterized intermediate for targeted active pharmaceutical ingredients, as well as for validation of impurity profiles in regulated manufacture. The material’s precise aromatic structure serves as a structural motif in several heterocyclic drug synthetics, allowing controlled downstream condensation or cyclization. It also functions as a reference impurity in validated analytical methods for pharmacopoeial compliance testing.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF Monograph references for known process-related impurities
    • EDQM CEP (Certificate of Suitability – TSE guidelines)
    • Chinese Pharmacopoeia (ChP) and Indian Pharmacopoeia for intermediate QC

    Typical usage ratio

    • 0.1–1.5% molar ratio based on specific synthetic route and desired yield (adjusted depending on role as intermediate, reference standard, or impurity threshold determination in API batches)

    Downstream process integration

    • Applied in multi-step condensation or cyclization reactions; analytical reference standard introduced during high-performance liquid chromatography (HPLC) and LC-MS validation of APIs

    Final product types

    • Reference impurity standards for pharmaceutical QC labs
    • API precursors for specialty heterocyclic therapeutics
    • Pharmaceutical process documentation materials for regulatory submission

    5. Advanced Epoxy Curing Agents

    Epoxy resin manufacturers incorporate 3,5-Diaminobenzoic Acid as a multifunctional curing agent for specialty reactive systems, particularly where precise control of cross-link density and glass transition temperature is critical. Its aromatic core and ortho-amino configuration contribute to enhanced chemical resistance and mechanical integrity in cured formulations, which are deployed in electronics encapsulation and high-end adhesive production.

    Industry compliance standards

    • IEC 61249-2-21 (halogen-free base materials for electronic assemblies)
    • UL 746E (Polymeric Materials – Curing Compounds)
    • RoHS Directive (EU 2011/65/EU) compatibility for electronics
    • ASTM D1652 (Epoxy Content Determination)

    Typical usage ratio

    • 2–8 phr (parts per hundred of resin); optimal addition rate adjusted for required pot life and cured-state properties

    Downstream process integration

    • Added during resin compounding and mixed under controlled temperature to prevent premature gelation; subsequent casting, coating, or lamination processes performed for component manufacture

    Final product types

    • Electronics encapsulants and potting materials
    • Structural epoxy adhesives for automotive electronics
    • Advanced laminating resins for printed circuit boards
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    Certification & Compliance
    More Introduction

    3,5-Diaminobenzoic Acid: Hands-on Insights from the Plant Floor

    A Closer Look at 3,5-Diaminobenzoic Acid

    Stepping into any plant that manufactures intermediates for dyes, pharmaceuticals, or polymerization processes, materials like 3,5-diaminobenzoic acid carry their weight quietly, but their role shapes the backbone of entire production lines. From reactors to quality control stations, our staff interacts daily with this compound, observing its behavior in real environments. The distinctive arrangement of amino groups on the benzoic acid ring sets it apart—we see this structural difference directly impacting how well the product holds up during synthesis and downstream reactions.

    Why Model and Purity Matter in Real Applications

    In our facility, the grade and specifications take priority because deviations show up fast on production output. This material does not just fill space on a spec sheet; its consistent performance speaks through every batch of colorant, API, or polymer building block that relies on pure and predictable input. Whether targeting a 99% pure crystalline solid or batches purified further for low-impurity pharmaceutical precursors, our operating teams track each intermediary step. Even minor contamination changes tone in azo dyes and lowers efficacy in sensitive active molecules.

    We continuously refine crystallization methods and purification protocols, not only because regulations set the bar, but because the end-users—researchers, formulators, or application chemists—see differences in real work. Fine-tuning particle size and dryness also drives processing speed in automated lines. Inconsistent batches cost hours of troubleshooting, so the consistent character of our 3,5-diaminobenzoic acid means fewer production resets and less waste.

    Experienced Observations: Structure’s Direct Impact

    Not all diaminobenzoic acids act the same. Direct engagement with all three isomers—2,4-, 2,5-, and 3,5-diaminobenzoic acid—brings clear contrasts to light. The 3,5- variant features both amino groups meta to the carboxylic acid, which fundamentally affects how the molecule interacts with acylating agents or condenses with other aromatic rings. In dye manufacture, this geometry tilts color yield and wash-fastness properties, a fact we’ve validated in actual textile trials.

    Difference also emerges in solubility. 3,5-diaminobenzoic acid commonly dissolves well in hot water and polar organic solvents, promoting efficient handling in reactors with reduced risk of clogging or precipitate formation during dosing. In the synthesis of pharmaceuticals, this increased solubility allows chemists to use safer solvents, drop in fewer additives, and maintain clean product separation at scale.

    Usage in Dyes and Pigments—From the Shop Floor’s Point of View

    Routine operations see our 3,5-diaminobenzoic acid vaulting into the dye chain through diazotization and coupling reactions. Workers load product into reactors fitted for both batch and continuous-flow synthesis. In pigment plants, the aromatic scaffold acts as a foundation for building complex colorant architectures, especially those prized for high tint strength and light stability. Delivered purity keeps hues sharp and batch-to-batch color drift in check.

    Sometimes, formulators push for more efficient mordant interaction or altered shade. The meta-orientation gives greater freedom to design specialty dyes with unique tones that tight ortho- or para-arrangements cannot offer. In QA labs, we repeatedly confirm this edge by tracking color development curves and test results in targeted textile runs.

    Pharmaceutical Chemistry: Value Beyond the Bench

    On the pharma end, our plant supports scale-ups from grams to metric tons. Experts exploring new antibacterial agents and non-steroidal anti-inflammatory drug scaffolds show strong demand for this meta-substituted amine. Its arrangement influences bioisosteric replacements and heterocycle synthesis, frequently delivering higher selectivity in condensation reactions.

    Our customers highlight the difficulty of finding reliable intermediates when pilot lots scale to commercial production. They want not only stability but also ease of downstream purification. Years of collaboration with formulation scientists give us a concrete sense of requirements: sharp melting points, defined color, and known impurity profiles improve both synthetic predictability and regulatory confidence.

    Polymers and Specialty Materials—Direct User Experience

    Polymer scientists and resin formulators benefit from the unique positioning of the amine groups. We have observed that 3,5-diaminobenzoic acid can initiate or modify condensation reactions to generate polyamides, imides, or more elaborate ladder polymers. The resulting materials resist thermal and chemical attack with better stability, due to steric effects from the meta substitution.

    Manufacturing staff recognize differences quickly during scale-up. Handling properties—such as dustiness, flow, and wetting—shift with any deviation in process parameters. Long hours spent on the line highlight where bulk density or particle form impacts feed rates in extruders and mixers. Tight feedback from operators allows rapid tweaks to upstream crystallization settings, securing not only technical specs but also tangible throughput improvements.

    Purity Checks and Analytical Realities

    Consistently passing HPLC, GC-MS, and Karl Fischer titration accumulate to more than just regulatory tick boxes. Staff on spectroscopic analysis lines see how a cleaner spectrum line-up saves time and cost by reducing secondary purification runs and boosting overall yield. Detection limits for related aromatic amines and trace metals pose ongoing challenges; hands-on improvements in our in-line filtration and drying setups keep the numbers headed in the right direction.

    Compared to related compounds, the challenge in 3,5-diaminobenzoic acid always comes down to isolating exactly the desired isomer and keeping residual solvents in check. Our practical adjustments, say to vacuum levels or tray stacking in drying ovens, target these pain points directly.

    Safety from Production to Packing

    From reaction startup to finished drum, worker safety shapes every SOP at our plant. 3,5-diaminobenzoic acid in free acid form does not tend toward acute volatility or rapid oxidation, but dust exposure, potential for skin and respiratory sensitization, and long-term residue build-up drive our PPE and ventilation protocols. Training staff to recognize early signs of exposure helps avoid near misses and keeps our operation on track for zero recordable incidents.

    We baton responsibility right to the packing room, where keeping clumping and static at bay means workers avoid unnecessary physical exposure. Automated weighing, dust-extracting hoods, and the right bin liners pay dividends in both health and final product quality.

    Difference from Other Diaminobenzoic Acids: Direct Plant Observations

    Much discussion in the industry compares the performance and application differences among diaminobenzoic acids. From our vantage point as primary producers, the chief distinction emerges in both reactivity and downstream compatibility. The 3,5- isomer gives better results where steric effects tune selectivity in catalyzed reactions or minimize side-product formation. Working side by side with the 2,4- and 2,5- variants, technicians note that meta positions in 3,5-diaminobenzoic acid drive unique behaviors in dye and peptide synthesis—differences that make or break a new process scale-up.

    In pigment manufacture, 3,5-diaminobenzoic acid's unique geometry leads to increased dispersibility and shade reproducibility in waterborne applications. We have tracked significantly reduced batch rejection rates where this product replaces ortho- or para-isomers. End-users often report smoother processing and fewer color-matching headaches, translating to lower rework costs and customer returns on their finished goods.

    Sustainable Practices and Environmental Commitment

    A commitment to sustainable production goes beyond regulatory compliance. In the trenches, our investments lean heavily into reducing solvent waste and capturing amine-laden emissions before they reach air or water. Years of experience troubleshooting wash protocols have led us to refine filtration and solvent recycling circuits, keeping operational footprints minimized.

    Residual handling—never an afterthought—gets plenty of attention. Used filter cake and off-spec fractions go straight into a planned recovery circuit, with trained staff regularly auditing waste flows. We’ve seen real reductions in disposal volume and cost through vigilant attention to raw material recycling. This focus not only benefits the environment but also tightens cost control, a win-win visible across quarterly reports.

    We see more customers pressing for green chemistry improvements, echoing our own push for safer and more resource-efficient chemistries. Regular feedback loops with researchers and purchasing agents help pinpoint where new solventless routes or alternative catalysts fit best with our product lineup, showing clearly that environmental leadership comes straight from practical plant know-how.

    Traceability and Transparency Up Close

    Maintaining a clear chain of custody for all material shipments builds trust, not just with auditors but with every formulator and operator along the value chain. Our in-house systems gather batch data, retention samples, and processing logs. From raw material input to finished shipment, transparent documentation proves its worth when customers want to trace a single drum’s provenance.

    We have learned that traceability is not just about ticking regulatory boxes. It allows for rapid root-cause analysis when something doesn’t meet expectations, and it cuts through guesswork in multi-party supply chains. Years of real experience reinforce that good data collection makes continuous improvement more than a talking point.

    Packaging, Logistics, and Customer-Facing Realities

    Fielding feedback from logistics partners and purchasing agents, practical experience has taught us how details like drum lining materials and moisture barrier selection deter product degradation. Tight seals, rapid loading, and minimized transit times all play into final usability for our customers.

    We avoid using bulk handling shortcuts that can lead to compaction or agglomeration, preferring scheduled small-lot shipments to keep every user closer to freshly-prepared, free-flowing material. This becomes especially clear in hot, humid climates, where so many specialty acids can cake quickly or develop undesired hydration.

    Long-term partners regularly bring up how straightforward it becomes to dispatch further blending or compounding when supply is predictable in both quantity and behavior. Strong logistics feedback loops save time for both users and handlers up and down the chain.

    Supporting New Entrants and Small-Lot Buyers

    Lab scale and early-stage R&D buyers need extra support. We do not treat small-lot users as afterthoughts. Dedicated production campaigns ensure laboratory and pilot quantities receive the same purity checks and handling attention as metric-ton shipments.

    Technical questions that come back from these partners—on dissolution profiles or impurities—drive ongoing process tweaks and sometimes inspire new production innovations. Regular interaction with emerging companies and academic labs supports our own learning, keeping procedures up to date and strengthening the wider network of formulation chemists and plant managers.

    We see first-hand how solid relationships built on responsiveness and direct support add value not just for customers, but for our own staff, giving everyone a front-row seat to challenges and victories across the field.

    Challenges and Improvements—Daily Realities at the Coalface

    In the trenches, troubleshooting batch reactions or shipping hiccups shows where continuous improvement finds its real home. Temperature sensitivities, moisture pickup, and risks of cross-contamination with similar benzoic acids sit on the daily checklist. Our team revises drying cycles, adjusts climate control in storage rooms, and monitors transport humidity to minimize the frequency of off-spec returns.

    Feedback from pumps and line meters helps us prevent bridging or jamming in feed hoppers—a practical fix that means less downtime and better batch yields. We take a direct approach: plant-floor observations and routine staff debriefs drive technical changes in how we store, package, and deliver this vital intermediate.

    Cost management, especially as raw material prices shift, also stays front and center. We've piloted raw material pre-processing on-site to shield against market disruptions, which gives operators more flexibility and helps customers benefit from greater consistency over time.

    Final Thoughts from the Manufacturer’s Perspective

    Years spent up close with 3,5-diaminobenzoic acid continually prove that the details matter—subtle structural features, batch-to-batch purity, reliable documentation, and the right handling all play straight into user success. We listen hard not only to the chemists at the bench but also to the operators and handlers who spot material shifts first.

    The impact of careful production and hands-on experience flows through every downstream process—pharmaceutical innovation, specialty dye creation, high-performance materials, and more. This approach does not spring from spreadsheets or sales decks. It grows from the daily reality of producing, testing, and shipping a compound that helps drive progress in so many fields.

    Direct, honest feedback and a commitment to tangible, on-the-floor improvement keep both our operations and our customers on track for better results with every lot of 3,5-diaminobenzoic acid produced.