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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 | 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. |
Applications of 3,5-Diaminobenzoic Acid in Industrial ManufacturingOur 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 PlasticsIn 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
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2. Reactive Dye Intermediates for Synthetic Textile FibersReactive 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
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3. Specialty Polybenzoxazole (PBO) Fiber ManufacturingPBO 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
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4. Pharmaceutical Impurity Standards and Process IntermediatesPharmaceutical 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
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5. Advanced Epoxy Curing AgentsEpoxy 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
Typical usage ratio
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.