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1,2,4-Benzenetriamine Dihydrochloride

    • Product Name 1,2,4-Benzenetriamine Dihydrochloride
    • Alias triaminobenzene dihydrochloride
    • Einecs 209-451-2
    • 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

    165636

    Chemical Name 1,2,4-Benzenetriamine Dihydrochloride
    Synonyms Benzene-1,2,4-triamine dihydrochloride
    Molecular Formula C6H9Cl2N3
    Molar Mass 194.07 g/mol
    Appearance Light brown to beige crystalline powder
    Cas Number 585-98-4
    Solubility In Water Soluble
    Melting Point 233-236 °C (decomposes)
    Storage Conditions Store at 2-8°C, protected from light
    Pubchem Cid 10899

    As an accredited 1,2,4-Benzenetriamine Dihydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with a red screw cap, labeled "1,2,4-Benzenetriamine Dihydrochloride, 25g", featuring hazard warnings and lot number.
    Shipping 1,2,4-Benzenetriamine Dihydrochloride should be shipped in tightly sealed containers, protected from moisture and incompatible materials. Handle as a hazardous material, following all applicable regulations for storage and transport. Appropriate labeling, documentation, and use of secondary containment are essential to ensure safety during shipping. Avoid exposure to extreme temperatures and direct sunlight.
    Storage 1,2,4-Benzenetriamine dihydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of moisture, heat, and incompatible substances such as strong oxidizing agents. Protect it from light and store it in a corrosion-resistant area, ideally a dedicated chemical storage cabinet. Clearly label the container and restrict access to trained personnel only.
    Application of 1,2,4-Benzenetriamine Dihydrochloride

    Applications of 1,2,4-Benzenetriamine Dihydrochloride in Industrial Manufacturing

    As a specialized manufacturer, we supply 1,2,4-Benzenetriamine Dihydrochloride to downstream partners utilizing this intermediate in rigorously regulated chemical sectors. The material’s unique triamine structure positions it as an essential compound in synthetic pathways for various advanced applications, where precise formulation and compliance are non-negotiable. Below we detail principal industrial segments utilizing this intermediate, highlighting regulatory adherence, typical formulation ratios, integration stages, and representative downstream outputs.

    1. High-Performance Polymer Synthesis (Specialty Polyamides and Polyimides)

    Producers of advanced engineering polymers deploy this triamine as a vital monomer when constructing heat-resistant polyimides and specialty polyamides, lending the finished polymers superior mechanical stability and thermal tolerance for demanding environments such as aerospace, electrical insulation, and automotive components. Compliance and high-purity standards dictate not only the monomer purity but also precise blending ratios to ensure repeatable polymer architecture and dependable in-service properties.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • UL 94 Flammability Standards (for finished polymers)
    • REACH Annex XVII Restrictions (monomer use and processing safety)

    Typical usage ratio

    • 5–15 mol% relative to total diamine/diacid monomers; adjustment based on target glass transition temperature and desired aromaticity in polymer backbone

    Downstream process integration

    • Material introduced in initial polycondensation stage, dissolved into high-purity solvents with anhydrous conditions before controlled polymerization and subsequent imidization or solid-state curing

    Final product types

    • High-temperature polyimide films
    • Polyamide-imide (PAI) resins for insulation enamels
    • Thermoplastic polyimide pellets for precision molded electrical parts

    2. Dyes and Pigments Manufacturing (Triazine and Azo Dyes)

    Established dye formulators incorporate this triamine as a key aromatic amino precursor enabling construction of vibrant triazine and azo dye molecules. It supports the tuning of chromophore intensity and solubility profiles in pigment formulations used in inks, plastics coloring, and fiber dyeing. Formulation precision and regulatory control of aromatic amines are strictly enforced due to downstream consumer and environmental safety requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (restriction on aromatic amines in textile dyes)
    • DIN EN ISO 105-X12 (colorfastness to rubbing)
    • ECHA REACH SVHC (screening for carcinogenic aromatic amines)

    Typical usage ratio

    • Typically 1–8 wt% of total amine input, depending on required dye chromophore complexity and solubility margin

    Downstream process integration

    • Introduced in initial diazotization or triazine-ring closure step, facilitating subsequent coupling or condensation with halogenated or nitroaromatic compounds to yield the targeted high-intensity colorant structure

    Final product types

    • Reactive dyes for cotton and cellulose blends
    • High-strength azo pigments for plastics and coatings
    • Printing ink colorants with improved wash/light stability

    3. Pharmaceutical Intermediate Synthesis (Heterocycle APIs)

    Pharmaceutical API manufacturers deploy this polyamine in tightly controlled synthesis routes for select heterocyclic drugs, using it as a building block for triazine and benzimidazole-based molecules known for applications in antiviral, anti-cancer, and enzyme inhibitor therapeutics. Manufacturing requires adherence to stringent cGMP systems, minimizing impurity carryover and confirming traceability from raw material through to isolation of the active intermediate.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF <467> Residual Solvents Limits
    • 21 CFR Part 211 Finished Pharmaceuticals

    Typical usage ratio

    • Stoichiometric input per synthetic step, often 0.9–1.2 eq relative to limiting substrate, subject to yield and byproduct optimization

    Downstream process integration

    • Charged during initial condensation with activated carboxyl or halogenated intermediates, followed by cyclization or functional group elaboration under monitored temperature and pH conditions

    Final product types

    • Pharmaceutical intermediates for anti-infective APIs
    • Precursors for cancer therapeutic scaffolds
    • Key intermediates for benzimidazole and triazine-based drug candidates

    4. Corrosion Inhibitor Synthesis for Metalworking Fluids

    Metalworking fluid additive producers integrate 1,2,4-benzenetriamine dihydrochloride into multi-functional corrosion inhibitor packages for high-humidity or high-acidity environments, where its multiple amine functionalities enhance film-forming protection on ferrous and non-ferrous surfaces. The finished additive must comply with occupational health restrictions and meet multi-country quality assurance schemes for industrial lubricants.

    Industry compliance standards

    • ASTM D4627-16 (standard method for corrosion inhibitors efficacy in water-reducible metalworking fluids)
    • ISO 14001 Environmental Management (for end-use applications)
    • OSHA 29 CFR 1910.1200 (Hazard Communication Standard)

    Typical usage ratio

    • 0.05–0.3% by weight of finished fluid formulation; precise ratio tailored based on metal type, desired inhibitor film thickness, and fluid service interval

    Downstream process integration

    • Combined with secondary alkanolamines or carboxylates in finishing blend, heat-mixed before dispersing into base oil or aqueous phase depending on formulated fluid

    Final product types

    • Water-based metalworking coolants
    • Cutting and grinding fluids with enhanced rust prevention
    • Storage and transport corrosion inhibitor packages

    5. Specialty Chemical Catalysts (Reductive Amination and Coupling Agents)

    Catalyst system manufacturers employ this amine as a nucleophilic or chelating ligand within specialty catalyst preps, especially for promoting selective hydrogenation, reductive amination, or coupling reactions under mild-to-moderate temperature regimes. Systematic performance benchmarking and safety qualification are essential, with the final catalyst’s identity and trace amine content strictly controlled under chemical process regulations.

    Industry compliance standards

    • ISO 17025 Analytical Testing Laboratories (QC of catalyst intermediates)
    • EU Regulation No 1907/2006 (REACH – registration for specialty catalysts)
    • Responsible Care® Global Charter (chemical process safety)

    Typical usage ratio

    • 0.1–5 mol% relative to central metal content or limiting substrate in catalytic batch; fine-tuned during scale-up based on conversion and selectivity data

    Downstream process integration

    • Introduced either as free amine during catalyst pre-synthesis or post-metallation modifier adjustment; subjected to in-situ activation, then charged into batch or continuous reactors according to catalyst system design

    Final product types

    • Catalytic reductive amination agents for fine chemicals
    • Selective hydrogenation catalyst precursors
    • Niche coupling catalysts for agrochemical intermediates
    Free Quote

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    Certification & Compliance
    More Introduction

    1,2,4-Benzenetriamine Dihydrochloride: Building Blocks for Trusted Synthesis

    Why This Chemical Earns Attention in Serious Manufacturing

    In our chemical production lines, a good intermediate does more than sit quietly in a barrel. 1,2,4-Benzenetriamine dihydrochloride, sometimes called triaminobenzene dihydrochloride, steps up in applications that ask for both dependability and high reactivity. We deal with plenty of amine compounds in the lab—few compare to this one in terms of clean reaction rates and the way it supports complex molecular builds, especially in specialty dyes and advanced pharmaceutical research.

    Our batches of 1,2,4-benzenetriamine dihydrochloride go through rigorous quality controls—years of process fine-tuning let us pull off minimal batch-to-batch deviation and a consistent granule texture. What this means for a formulator or synthesist isn’t just theoretical. A steady supply lowers the chance of troubleshooting unexpected reactivity shifts, saving hours on correcting a process that drifted off track.

    Common Usage: Tangible Solutions in the Lab and Factory

    Direct experience in the plant shows that this triamine’s value really lies in its capability as a nucleophile in complex syntheses. It’s trusted for building core structures in azo and quinoxaline dye chemistry. Laboratories engaged in pharmaceutical intermediate development and fine chemical synthesis pick our 1,2,4-benzenetriamine dihydrochloride when constructing heterocyclic scaffolds. Over the years, we have observed that it produces robust yields in condensation reactions due to its three amine groups positioned on the benzene ring, providing multiple reactive sites and supporting powerful functionalization strategies.

    We see this compound show up as a starting material in new active molecules for diagnostic reagents. Dye manufacturers highlight its coloring properties and the way it binds with metal ions. It usually appears as a pale to light brown crystalline powder and dissolves easily in water and alcohol, making it practical for in-lab adjustments and scalable industrial recipes. Unlike some related triamines, 1,2,4-benzenetriamine dihydrochloride keeps solubility high without leaving behind cloudy suspensions within typical working concentrations. Downtime tied to filter clogging or rework from incomplete dissolving drops to a minimum.

    Relevant Specifications That Chemists Trust

    Over a decade of custom manufacturing provides us with direct feedback on the actual priorities of our end-users—purity and consistency top the list. Our 1,2,4-benzenetriamine dihydrochloride commonly ships at a purity higher than 98 percent by HPLC analysis, with controlled moisture and chloride levels. It has a molecular formula C6H9N3·2HCl and typical batch sizes range from a few kilograms in pilot lots to drum-scale in established syntheses.

    Particle size also comes up in conversations with users who pursue fine chemical synthesis or scale-up. Overly large crystals often slow down dissolution, so we keep the granule size tight to speed up reaction charge-ins and avoid the bottlenecks that can crop up downstream. No added stabilizers or inert fillers are mixed in, because these have led to interference in downstream reactions in the past—a problem we solved by adjusting our post-synthesis drying and purification windows.

    How 1,2,4-Benzenetriamine Dihydrochloride Stands Out

    Benzene triamines form a family, but positioning of the amines on the ring makes a major impact. Compared to 1,2,3-benzenetriamine or 1,3,5-benzenetriamine, the 1,2,4-isomer introduces a different pattern for cross-linking and side-chain addition reactions. This has fundamental consequences in dye synthesis, where color shade and fastness can shift noticeably between isomers. Our clients in textile and pigment sectors who have trialed alternative isomers often discover that only the 1,2,4-arrangement delivers the shades and stability they require.

    We’ve processed requests for substitute products, including other triamine or diamine hydrochloride salts, yet the yields and color properties don’t line up. The hydrochloride version has significant handling advantages compared with its free base form. Free base triaminobenzene can oxidize quickly, giving darkened, tarry product and tough-to-handle residues; converting to the dihydrochloride salt helps keep the compound stable and easier to weigh and manage in humid environments. Shipping teams and warehouse operators appreciate the lower volatility and reduced hazard during transfers.

    Commitment to Safety and Reliability

    No matter how useful a product proves, operators don’t cut corners with safety or documentation. Our facility, certified for best practices, runs syntheses in isolated vessels and constantly monitors for temperature and pressure changes. All employees undergo regular training to minimize risk, especially during charging or product filtration phases, where exposure to concentrated amines can irritate the skin or eyes. While we monitor every lot for off-spec odors or unexpected color, we also maintain continual reviews of literature updates and new regulatory requirements.

    Customer support lines don’t limit themselves to logistics. Inquiries often cover recommended storage practices or reaction optimization, since small tweaks upstream in your process sometimes yield savings much further down. Our experience shows that cool, dry storage delays degradation, and sealed containers guard against moisture intrusion—small but direct factors that keep the product at specification, whether it sits for a week or several months.

    Supporting Innovation in End-Use Applications

    1,2,4-Benzenetriamine dihydrochloride may not win headlines, but it quietly powers innovation throughout specialty chemicals. As a direct supplier, we receive product feedback that ranges from requests for smaller, custom lots for R&D up to multi-ton batch manufacturing to support a new dye or active ingredient launch. Our technical teams respond to these diverse needs, adapting production parameters and shipment scheduling while always prioritizing product quality.

    Development scientists rely on the clean conversion and low side-product rates achieved with this triamine. In practice, this means less time spent scrubbing up reaction mixtures or characterizing mystery peaks on an HPLC. Especially when scaling from the bench to a plant production run, reducing unknowns in a multi-step synthesis translates directly to fewer failures and greater confidence in transferring technology from pilot to commercial stages.

    Real Manufacturing Experience: Overcoming Production Hurdles

    Manufacturing never runs solely on textbook procedures. We have faced and solved challenges, from managing exothermic reaction spikes to troubleshooting unexpected coloration in the final product. The trickiest issues tend to arise during purification or drying, where the delicate triamine structure can break down in too much heat. Our team responds by integrating lower-temperature vacuum distillation and gentle crystallization techniques. Over time, we refined the workup to eliminate unwanted by-products that risk impacting subsequent reactions for end users.

    One major improvement came after early batches showed mild pinkish discoloration, traced back to trace metal contamination. Collaboration with specialty filter suppliers led to a switch to all-plastic filtration assemblies, successfully dropping metal content below detection levels. Since then, our production line hasn't faced additional discoloration issues and downstream users report fewer chromatographic artifacts.

    Another common challenge arrives during packaging and shipment of hygroscopic materials. To counter this, we invested in improved container sealing technology using multi-layered moisture barriers. Not only did this reduce product loss in humid seasons, customer feedback highlighted easier material transfers and fewer caking issues after long storage times.

    Listening to Users: Adaptation and Responsiveness

    Our product’s reputation in the market owes a lot to real-world partnerships. We regularly take calls from chemists and plant engineers reporting novel bottlenecks or asking about practical ways to integrate this triamine into their synthesis schemes. Years ago, one pharmaceutical customer outlined a bottleneck in their procedure caused by slow solubility in alcohol-based media. Our process team switched up drying methods, landing on a balance between particle size and residual chloride content. Their next lot ran without stoppages, saving both time and ingredient cost.

    Stories like these shape our approach to continuous improvement. Unlike handling set-and-forget products, we treat each batch as a step forward—incorporating notes from end users, logging minor tweaks, and sharing real-world adjustments back through our technical support staff. Working with specialty dye makers helped us pinpoint a blend of batch purity and grain size that gives optimal conversion with their unique catalysts—something no third-party formulation could deliver consistently.

    Bench to Plant: How Our Approach Helps Transition

    It’s easy to overlook the jump from benchtop to pilot-scale chemistry. In practice, variations in triamine grain size, dust content, and even packaging shape can disrupt automated feed systems and spillage controls. On-site visits to partner plants taught us the critical role packaging and flowability play in a plant’s reliability statistics. Altering the compaction step in the final stage of production now lets us offer material that feeds smoothly through most common powder hoppers—an overlooked but crucial win that isn’t visible in a lab scale-up brochure.

    Moving further, repeatability isn’t just a comfort for quality managers. For the production chemist working through long, multi-step syntheses, every failed run translates to urgent questions on material sourcing. That’s why we provide data packets with each consignment, outlining exact batch history from raw material intake to packing time. These records form a backbone for troubleshooting and allow users to pinpoint sources of change, delivering more uptime for everyone handling the product.

    Comparing Industry Standards and Clear Improvements

    While many suppliers list 1,2,4-benzenetriamine dihydrochloride among their catalogs, we have noticed several differences after benchmarking competitor samples. Higher impurity profiles and inconsistent wetness levels showed up repeatedly in third-party analyses. These details matter little in a general catalog, but in a regulated production environment, out-of-spec profiles quickly translate to lost lots or even regulatory action. After working closely with international partners, we set a strict maximum for total related impurities and perform additional checks for residual solvents.

    Similarly, documentation standards mark a point of difference. Alongside certificates of analysis, we provide a complete analytical report with retention times, peak area integration, and moisture analysis for every shipment. Our clients point out that, compared to competitors shipping “off-the-shelf” grades, this level of transparency lets them integrate our product seamlessly into their internal compliance systems.

    Tackling Environmental Responsibility in Manufacturing

    Manufacturing specialty amines traditionally relies on aromatic nitration and reduction routes, which generate waste streams containing inorganic salts and excess solvents. Awareness of environmental impact has led us to invest in recovery and treatment systems. By switching to closed-loop solvent recycling and improved aqueous waste handling, we have cut effluent loads per unit output year over year. Our next initiative seeks to lower the overall use of water through more selective crystallization and filtration upgrades.

    Waste minimization isn’t just about compliance—it protects workers and the surrounding community as well. Each improvement in waste routing and air handling not only ensures regulatory clearance but also reduces downtime, incidents, and product yield loss. We share these results with our customers, many of whom audit our facilities as part of their sustainability initiatives. These audits hold us to continually higher standards—both in the process room and at the shipping dock.

    Direct Engagement: Supporting Technical Questions and New Ideas

    Our technical support team fields practical inquiries every week, ranging from solvent compatibility to analytical troubleshooting. Exposure to such a variety of requests tunes our production methods and documentation. For those developing analytical methods, we supply reference spectra and additional standards for method validation. If a novel application arises—from a new diagnostic dye to an unexpected agricultural intermediate—we are ready to collaborate on small-lot prototypes or modified purity grades.

    On more than one occasion, a customer’s request for a tighter specification or custom packaging configuration has prompted internal innovation. Years ago, a research group working on metal-chelate dye systems asked for the lowest possible iron and copper levels in their material. Our lab adjusted the filtration and resin purification sequence, and the result satisfied both their application and became a new offering for other customers.

    Moving Forward: A Foundation for New Chemistry

    Every product batch we ship carries the weight of what our users build next. We engage with advanced developers in pharmaceuticals, specialty textile, and electronic materials as they break new ground—using 1,2,4-benzenetriamine dihydrochloride in syntheses that call for structural precision and strict reproducibility. Process feedback, be it positive or constructive, shapes how our materials and documentation evolve.

    Through all these efforts, our position remains clear: manufacturers choosing their triamine intermediates aren’t just looking for another commodity. They want an ingredient with a proven track record, a transparent supply chain, and direct technical support that keeps pace with cutting-edge research and production goals. That’s the standard we set for every shipment of 1,2,4-benzenetriamine dihydrochloride leaving our facility.