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3,5-Diaminobenzoic Acid Dihydrochloride

    • Product Name 3,5-Diaminobenzoic Acid Dihydrochloride
    • Alias 3,5-DABA dihydrochloride
    • Einecs 243-321-0
    • 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
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    Specifications

    HS Code

    800676

    Productname 3,5-Diaminobenzoic Acid Dihydrochloride
    Casnumber 1008-80-2
    Molecularformula C7H9Cl2N2O2
    Molecularweight 225.07 g/mol
    Appearance Off-white to light yellow powder
    Meltingpoint 233-238°C (dec.)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Synonyms 3,5-DABA dihydrochloride
    Pubchemid 59663483
    Ec Number 213-749-9
    Iupacname 3,5-diaminobenzoic acid dihydrochloride

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

    Packing & Storage
    Packing White, sealed plastic bottle labeled "3,5-Diaminobenzoic Acid Dihydrochloride," net weight 25 grams, with hazard pictograms and usage instructions.
    Shipping **Shipping Description:** 3,5-Diaminobenzoic Acid Dihydrochloride is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with relevant chemical safety regulations and includes hazard labeling. It is transported as a non-flammable solid, handled with care to avoid physical damage, and typically shipped at ambient temperature unless otherwise specified.
    Storage 3,5-Diaminobenzoic Acid Dihydrochloride should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature, unless otherwise specified by the manufacturer, and keep out of reach of unauthorized personnel or children.
    Application of 3,5-Diaminobenzoic Acid Dihydrochloride

    Applications of 3,5-Diaminobenzoic Acid Dihydrochloride in Industrial Manufacturing

    3,5-Diaminobenzoic Acid Dihydrochloride serves as a specialized intermediate in multiple fine chemical manufacturing pathways. As a direct manufacturer, we supply this ingredient to key downstream sectors where its ortho-substituted aromatic amine structure contributes selectively to performance and yield in various end-use products. Below is a detailed summary of established application tracks, each supported by validated industry usage, regulatory context, and process integration insights.

    1. Synthesis of Reactive Dyes for Cellulose Fiber Processing

    Reactive dye producers incorporate this aromatic diamine as a core intermediate to introduce aminobenzoic motifs in dye molecules, enabling high-affinity covalent bonding during textile coloration. The material undergoes diazotization, followed by coupling reactions to construct chromophore frameworks tailored for high-washfast cotton dyeings.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substance limits in dyes
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL restrictions
    • EU REACH Regulation (EC 1907/2006) for dye intermediates
    • GMP guidelines for chemical batch traceability

    Typical usage ratio

    • Ranges from 0.7–1.5 molar equivalents relative to target chromogen, adjusted based on targeted dye shade depth and bath ratio requirements

    Downstream process integration

    • Introduced in the initial amination or diazotization stages; subsequently enters as a key nucleus in the coupling step during dye synthesis

    Final product types

    • Fiber-reactive dyes for printed and solid shade cotton textiles
    • Polyamide-compatible reactive dyes used in technical and clothing fabrics
    • Commercial dye powder and granules for industrial textile coloration

    2. Pharmaceutical API Intermediate – Quinolone and Benzoxazine Synthesis

    Pharmaceutical manufacturers include this compound as an intermediate in constructing quinolone and benzoxazine structures due to its defined amino acid functionality and hydrochloride salt form, which ensures solubility and purity for multi-step API processes. Chemoselective coupling with carboxylic acid derivatives results in scaffold structures for antibacterial and central nervous system drugs.

    Industry compliance standards

    • ICH Q7A: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP and EP monograph impurities testing (if used in regulated routes)
    • FDA DMF (Drug Master File) support for key starting materials
    • 21 CFR Part 211 cGMP for pharmaceutical processing

    Typical usage ratio

    • Employed at 1.0–1.2 stoichiometric equivalents versus target intermediate, adjusted for yield optimization and impurity minimization

    Downstream process integration

    • Charged during condensation or ring-forming stages in synthesis reactors; purified before downstream alkylation or acylation transformations

    Final product types

    • Pharmaceutical raw materials for quinolone derivative antibiotics
    • Intermediates for CNS-active benzoxazine compounds
    • API pipeline compounds supplied to CDMO and formulation partners

    3. Curing Agent Precursor in High-Performance Polyimide Resins

    Advanced polymer manufacturers adopt this diamine salt in the formulation of aromatic polyimide resins targeting high-temperature and mechanically demanding applications. Its unique ortho-diamine configuration imparts controlled flexibility and crosslink density in the final polymer matrix, which is essential for aerospace films and insulating substrates.

    Industry compliance standards

    • ASTM D5341 for polyimide resin thermal properties
    • RoHS Directive 2011/65/EU for restricted substances in electrical insulation
    • UL 94 flammability classification for resin systems
    • AS9100D/ISO 9001 for aerospace and electronic materials

    Typical usage ratio

    • Feeding at 3–8 wt% as a curative within total dianhydride/diamine dosing, with adjustment guided by viscosity targets and end-use mechanical specification

    Downstream process integration

    • Blended into polyimide pre-polymer mix prior to imidization; participates during thermal curing cycles to define crosslinked architecture

    Final product types

    • High-temperature polyimide films for aerospace and flexible PCB layers
    • Thermoset resin castings for electronic component insulation
    • Automotive wiring harness insulation tapes

    4. Fluorescent Brightener Intermediate for Optical Whitening Agents

    Specialty chemical plants utilize this material for preparing stilbene- or benzoxazole-based brighteners, where its amino groups serve to anchor chromophoric fragments within brightener molecules. This improves ultraviolet absorption and visual brightness in paper, detergents, and fiber finishing applications.

    Industry compliance standards

    • EN 646 migration tests for paper chemicals in food contact materials
    • US FDA 21 CFR Part 176.170(a) for paper and paperboard additives
    • REACH Regulation Annex XVII for fluorescent brighteners
    • ISO 14001 environmental management during production

    Typical usage ratio

    • Applied at 0.6–1.4 molar equivalents according to the design of the target brightener molecule and process scale

    Downstream process integration

    • Introduced in the core condensation step for synthesizing brightener’s chromophore; followed by purification and blending with carriers for ready-to-use formulations

    Final product types

    • Optical brightening agents for pulp and paper mills
    • Liquid and powder brighteners for laundry detergent manufacturers
    • Textile finishing agents enhancing fabric brilliance

    5. Engineering Plastics Modifier – Polybenzimidazole (PBI) Production

    Composite and engineering thermoplastics producers employ this raw material as a building block for polybenzimidazole synthesis. Its meta-diamino functionality determines thermal stability and fire-retardant properties in resultant polymers, which address specialty market needs in protective apparel and fuel cell membranes.

    Industry compliance standards

    • UL 94 V-0 standards for plastic flame retardance
    • ISO 1043–1 polymer identification for engineering plastics
    • NFPA 1971 for materials in protective clothing
    • Military standard MIL-P-46100 for high-strength applications

    Typical usage ratio

    • Typically dosed at 1.1–1.3 molar equivalents in respect to dicarboxylic acid monomer in step-growth polymerization, optimization based on required molecular weight and processing viscosity

    Downstream process integration

    • Fed to the monomer charge vessel for condensation with aromatic dicarboxylic acids under controlled temperature and inert gas, followed by direct extrusion and fiber spinning or molding

    Final product types

    • High-performance PBI fibers for heat-resistant protective garments
    • PBI films and membranes for fuel cell components
    • Molded PBI engineering plastic parts for aerospace and electronics
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    Certification & Compliance
    More Introduction

    3,5-Diaminobenzoic Acid Dihydrochloride: Building the Chemistry of Progress

    Seeing the Full Picture of a Specialty Aromatic: Insights from the Production Floor

    In the world of specialty aromatic compounds, every step in synthesis matters. Over years on the manufacturing line and in process development, we have watched certain building blocks consistently rise in value and demand among research laboratories and producers of advanced materials. One such compound, 3,5-diaminobenzoic acid dihydrochloride, holds a distinct place—not for sheer volume, but through a distinctive profile and versatility. Factories don’t get built around something unless it opens up genuine options for downstream users. For those who have relied on it to unlock complex synthetic routes, the unique structure has become an enabler that’s hard to substitute.

    Understanding What Sets It Apart

    There are plenty of aromatic diamines, and the field of benzoic acid derivatives is crowded. Careful attention to purity and batch reliability often separates a research curiosity from an industrial mainstay. 3,5-diaminobenzoic acid dihydrochloride stands out by combining an ortho orientation of the two amino groups with the carboxylic acid at the para position. Each functional group brings a specific capability; together they create a crossroad for downstream chemistry. In our plant, controlling the substitution pattern shapes not only product performance, but also the yield profiles and purification challenges we face at scale.

    Customers looking for 3,5-diaminobenzoic acid dihydrochloride typically recognize its value after disrupting false economies with cut-rate alternatives. You might try substituting with a more common diamino compound. The results often reveal themselves through inconsistent reactivity later in a synthetic sequence, or through unexpected side products in the final crystallization. Over the years, we have seen this pattern: chemists return to the properly configured aromatic scaffold to restore control to their downstream chemistry.

    Appearance Matters—But So Does Chemistry Under the Hood

    A clean, white to off-white crystalline solid, with characteristic solubility in water due to the dihydrochloride salt—the appearance of this material tells only a small part of the story. True, customers want to see reliable drying, minimal lump formation, and ease of weighing, particularly for automatic dosing systems or process equipment. But those are markers, not the essence. In practice, what keeps production engineers satisfied are spectral profiles that match expectation: consistent NMR, IR, and HPLC readings. Our lab teams pull samples at multiple stages because experience has taught us how easily a batch can turn if conditions drift. Subtle byproducts in raw materials or intermediates, barely perceptible on a gram scale, balloon into major purification headaches on the kilo or ton scale.

    Precision in Process and in Practice

    We’ve never seen a shortcut to reliable production. Sourcing high-grade starting materials affects everything, but attention doesn’t let up once synthesis begins. Each run usually includes periods of precise temperature holding, careful monitoring of reaction completion by TLC or automated in-process spectroscopy, and a dedication to robust filtration and recrystallization practice. Our team’s experience shows that overlooking a single filtration step or rushing the acidification yields a colored product, complicates final drying, and undermines downstream performance. It’s these shop floor details—from cleanroom discipline to timing of quenching reactions—that have grown into corporate know-how and built trust with pharmaceutical and materials science partners.

    We see younger chemists marvel when they compare crystalline structure of a textbook sample to a batch carefully crafted at scale. Moisture control, choice of counter-ions, even the type of vacuum used for drying, change the way solids behave when handled in production. Years of feedback from downstream users lead us to refine every stage, not just for purity on paper, but for handling, stability, and ease of use.

    Core Application Drivers: Where Pure Function Counts

    The most immediate demand for 3,5-diaminobenzoic acid dihydrochloride comes from specialty polymer and pigment manufacturers, as well as from advanced research groups working on functionalized matrices and next-generation catalysts. In dye chemistry, the specificity this compound brings enables unique conjugation patterns, yielding shades or fastness properties otherwise unattainable. Polymer chemists leverage the dual amino groups to introduce crosslinking sites at controlled intervals. The carboxylic acid group, meanwhile, gives another anchor point, expanding the design space for functionalized surfaces or drug delivery vehicles.

    A major share of our production volume moves to companies working in active pharmaceutical intermediates and custom synthesis. Here, consistent lot-to-lot quality means time saved on revalidation and less risk of late-stage project setbacks. When a downstream step depends on nucleophilic substitution or amide formation, the reactivity margin matters. Once, a customer conducting solid-phase peptide synthesis reported drastic improvements in coupling efficiency after switching over to batches from our facility. Not a one-off, but repeatable across campaigns. Success in this field hinges on removing uncertainties—whether by taming batch-to-batch fluctuations or by providing certificates backed by real, batch-specific data.

    Specification and Batch Control: Hard Lessons from the Field

    As a manufacturer, our definition of “specification” runs deeper than a certificate. Standard practice involves dozens of confirmed parameters for each lot. Moisture content, free acid ratio, and chloride titration get scrutinized because deviation at lower scale has ripple effects on downstream consistency. Trained eyes pay close attention to melting range, color, and spectral fingerprints—not just as numbers, but as markers correlated to past client feedback.

    Years back, we faced a spate of troubleshooting requests from an electronics materials client. Their downstream polymerizations kept stalling, and initial diagnosis blamed every part of the supply chain—from packaging to reactor configuration. Our team initiated a granular investigation. The issue turned out to be trace levels of an isomeric impurity. Only by refining a recrystallization protocol and retooling part of the distillation process were we able to reduce the impurity profile below the client’s detection limit. Since then, those extra controls have stayed in our process, paid for in both labor and reputation. Experience has shown once a customer discovers batch drift or repeat failure, prestige is hard to rebuild. Data-driven, stubborn diligence is the better path.

    Comparing to Analogous Compounds—No Substitute for an Exact Fit

    In the landscape of intermediate aromatic diamines, there are comparable products—2,4-diaminobenzoic acid, unsubstituted phenylenediamines, and isomeric aminobenzoic acids. Each finds its own use, and we have run campaigns for several. The difference with 3,5-diaminobenzoic acid dihydrochloride lies not in a single performance metric. Pick any analog, and users quickly realize that reaction pathways change, solubility curves shift, and side-product screens turn up surprises. The logistic ease of working with a salt form cannot be understated—free bases require extra controls for stability and tend toward oxidation in humid conditions. Dihydrochloride salt, on the other hand, gives greater shelf stability, better handling, and improved compatibility in water-based systems.

    Over time, experienced process development chemists start with the molecule that fits, not the one that is available in bulk on the spot. A willingness to try alternatives sometimes burns more hours than it saves. Practical tests in production—such as reactor cleaning, crystallizer yields, and even time spent troubleshooting—show clearly that a tailored compound like 3,5-diaminobenzoic acid dihydrochloride becomes more economical in the long run.

    Supply Process: Building Reliability Beyond the Production Floor

    Factories can make or break R&D momentum depending on how well they hold to delivery schedules and batch quality. The real test for us arrives months after shipment, once customers have worked through the product and returned with repeat orders or, sometimes, urgent technical queries. Open access to in-house chemists, traceable documentation, and responsive troubleshooting back up every lot. Years of doing this work have convinced us that steady dialogue with the client achieves more than any “certificate of analysis” alone. Whenever a trial run fails, or a project stalls due to unexplained variance, rapid communication often narrows the root cause faster than formal inquiries.

    Clients from the specialty chemicals industry often come to us after repeated breakdowns in communication with resellers. Direct engagement means their technical staff not only access our in-house records, but also get contextual feedback that comes only from actual makers. We frequently host on-site audits, walk new partners through the intricacies of batch records, and do not shy away from showing the actual reactors and QC stations in use. In practice, this transparency assures long-term partnerships and grants customers the flexibility to request variant grades or custom lots for pilot campaigns.

    Regulatory and Quality Assurance Experience: Navigating Real-World Constraints

    Working as a manufacturer in regulated regions, we have seen how evolving compliance requirements affect batch release schedules and documentation practices. Many of our customers supply end products into regulated fields—medical devices, advanced coatings, and life sciences—so their risk tolerance rests largely on how tightly we hold to validated protocols. We have invested in staff training, digital batch tracking, and sample retention. These actions, not just slogans, consistently reduce the incidents of product rejection or recall.

    For international clients, compliance with transport and handling regulations occupies a major portion of the logistical puzzle. Years of shipping this compound to multiple continents mean we have in-house experts on packaging to mitigate both moisture and transit shock, and support staff to coordinate shipment paperwork seamlessly. The less time customers spend worrying about customs clearance or broken seals, the more effort they put toward their core work.

    Process Development Partnerships: Leveraging Experience to Improve Outcomes

    Our long-term customers rarely operate with standard catalog specifications in mind. The most fertile collaborations arise when both technical teams share their needs and constraints upfront. Over time, we have adapted synthesis scale and purification strategies for clients with unique process requirements—sometimes varying the drying process, other times customizing the salt form or introducing an extra micronization stage.

    Our engineering team continuously refines the route to eliminate bottlenecks and environmental impact. Nearly a decade of sustained investment in green chemistry alternatives has helped us overhaul certain steps, using aqueous solvents or reclaiming byproducts as feedstock. Often, these efforts begin with a customer’s request for a “greener” or more sustainable supply. By treating those as process development opportunities, we have also trimmed energy costs and improved compliance margins.

    Challenges and Solutions: Learning from Setbacks

    A manufacturing journey involving a complex intermediate like 3,5-diaminobenzoic acid dihydrochloride often spotlights weak points—be it batch reproducibility, handling loss, or impurity carryover. Over the years, our operators have learned to anticipate certain problems. Bulk storage can be tricky in humid climates. That led us to upgrade packaging from standard poly-bags to multi-layer alu-foil drums with desiccant pouches, after witnessing unacceptable moisture uptake during a hot summer. Likewise, we reduced color impurities by refining our filtration systems and introducing a stepwise recrystallization during particularly sensitive campaigns.

    Some process improvements come directly from feedback. For instance, a major pigment manufacturer referenced color stability issues after long-term storage, prompting us to re-examine trace metal sources and replace suspect reactor internals. By measuring these changes through expanded analytical testing—ICP-MS screens for metals, ion chromatography for chloride levels—we caught problem sources before they landed in customer labs. This iterative approach, sometimes involving a half-dozen small adjustments, illustrates the reality of manufacturing: incremental progress stemming from active listening paired with technical patience.

    Real-World Use Cases: End-User Perspectives

    Process chemists and technical managers who’ve relied on this compound repeatedly share stories of its role in problem-solving. In dye chemistry, a development team shared that switching from a general diamino acid to the 3,5 analogue meant faster reaction kinetics, yielding a purer product with less waste. Feedback from a pharmaceutical contractor described the critical importance of minimal endotoxin levels and trace metal contamination—something achieved by close monitoring of cleaning protocols and dedicated production lines.

    Some unexplored uses arrive unexpectedly. In materials science, 3,5-diaminobenzoic acid dihydrochloride found a place in the formulation of novel adhesives for electronics. Teams sought the precise placement of functional groups for controlled reactivity, unavailable with other diaminobenzoic acid isomers. From collaborating with such researchers, we have built a habit of staying open to new application feedback, adapting our processes to capably serve emerging fields.

    Why the Real Manufacturer’s Perspective Matters

    Everything that defines dependable specialty chemical supply—be it batch traceability, technical documentation, or process transparency—comes only from long-term immersion in making and refining the molecule. Distributors and resellers, helpful as they are in expanding reach, often lack critical context for elusive batch-to-batch issues. It falls to the actual producer to spot the subtle indicators that production drift or feedstock inconsistency have crept into the supply chain.

    Years of hands-on production experience have shown us that every improvement, and every challenge overcome, reflects the cumulative effort of chemists, engineers, and operations staff. Their insights, earned from solving real-world obstacles in real time, feed back into each batch produced. Our goal has always been simple: dependable material that does the job with minimal disruption to our client’s projects.

    Looking Ahead: Stewardship and Innovation

    The growing demands for advanced materials, paired with tightening quality and sustainability requirements, set an ambitious course for chemical manufacturing. Stewardship springs not from slogans but from close tracking of process variables, willingness to invest in cleaner technology, and honest conversations with customers about what matters. Our journey with 3,5-diaminobenzoic acid dihydrochloride is still ongoing. Each new campaign teaches us a bit more about reproducibility, stability, and the ways precise chemistry underpins new developments in medicine, materials, and technology.

    We continue learning from users, adapting process controls, and deepening our commitment to the details that keep projects moving forward. Our experience is that value emerges less from routine and more from engaged, informed partnerships with those who rely on this specialty compound to build their own innovations.