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N,N-Dimethyl-M-Phenylenediamine Dihydrochloride

    • Product Name N,N-Dimethyl-M-Phenylenediamine Dihydrochloride
    • Alias DMPD
    • Einecs 219-601-3
    • 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

    165417

    Product Name N,N-Dimethyl-m-Phenylenediamine Dihydrochloride
    Synonyms 1,3-Benzenediamine, N,N-dimethyl-, dihydrochloride
    Cas Number 536-46-9
    Molecular Formula C8H14Cl2N2
    Molecular Weight 209.12 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 144-147 °C
    Solubility Soluble in water
    Storage Temperature Room temperature
    Pubchem Cid 61163

    As an accredited N,N-Dimethyl-M-Phenylenediamine Dihydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of N,N-Dimethyl-m-Phenylenediamine Dihydrochloride is packed in a sealed amber glass bottle with hazard and handling labels.
    Shipping N,N-Dimethyl-m-Phenylenediamine Dihydrochloride is shipped in tightly sealed containers to protect from moisture and light. It is classified as a laboratory chemical and should be handled according to standard hazardous material protocols. Ensure shipping complies with local regulations and uses proper labeling, cushioning, and secondary containment to prevent leaks or contamination.
    Storage N,N-Dimethyl-m-phenylenediamine dihydrochloride should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature (15–25°C) and avoid exposure to heat. Ensure proper labeling and restrict access to trained personnel only.
    Application of N,N-Dimethyl-M-Phenylenediamine Dihydrochloride

    Applications of N,N-Dimethyl-M-Phenylenediamine Dihydrochloride in Industrial Manufacturing

    As a direct manufacturer, we supply N,N-Dimethyl-M-Phenylenediamine Dihydrochloride to global B2B customers whose production relies on highly specified raw materials. The following scenarios detail the material’s established roles in chemical processing, underscoring real-world standards, formulation specifics, integration routes, and end products backed by industrial adoption.

    1. Diagnostic Reagent Production for Clinical Chemistry

    In clinical diagnostics, labs rely on high-purity N,N-Dimethyl-M-Phenylenediamine Dihydrochloride as a chromogenic agent for the colorimetric quantification of hydrogen peroxide and peroxidase activity. This material plays a core role in enzymatic assay formulation, where batch consistency, sensitivity, and regulatory standards are critical to ensuring valid patient results and traceable performance. Our vertical integration maintains full traceability from synthesis through final packaging, supporting IVD kit manufacturers that demand both REACH conformity and EN ISO 13485-compliant supply chains.

    Industry compliance standards

    • EN ISO 13485 (Medical Devices–Quality Management Systems)
    • IVD Directive 98/79/EC (Europe)
    • 21 CFR Part 820 (FDA QSR)
    • REACH (EC No. 1907/2006) Registration

    Typical usage ratio

    • Assay formulation: 0.02–0.2 mg/mL in final reaction mixture. Adjustment depends on targeted enzyme activity, detection limits, and sample matrix interferences.

    Downstream process integration

    • Added to buffered assay reagents during final liquid kit compounding or dry reagent functionalization; filtered and aliquoted under cleanroom conditions; included in single-use IVD test cartridges or multi-analyte panel reagent bottles.

    Final product types

    • Clinical chemistry reagent kits (H2O2 detection)
    • Automated IVD system cartridges
    • Point-of-care diagnostic strips
    • High-throughput screening microplate-based reagents

    2. Polymerization Chain Transfer Agent Manufacturing

    Polymer producers employ N,N-Dimethyl-M-Phenylenediamine Dihydrochloride as a chain transfer additive in the controlled synthesis of specialty polyamides and conductive polymers, tuned for electrical and mechanical performance. This compound precisely moderates molecular weight distribution during condensation or oxidative polymerization stages, facilitating reproducible polymer structures and low residual monomer content, a necessary condition for electronic and automotive supply chains governed by detailed technical standards.

    Industry compliance standards

    • ISO 9001:2015 (Polymer Manufacturing Quality)
    • RoHS 3 (Restriction of Hazardous Substances for electronics)
    • IEC 60216-1 (Thermal endurance of insulation materials)
    • Applicable client-specific automotive material specs (e.g. VW TL501.11, GM GMW16157)

    Typical usage ratio

    • 0.05–0.25% w/w of total monomer feed; precise level determined after pilot batch evaluation of chain length and electronic conductivity targets.

    Downstream process integration

    • Introduced to the polymerization reactor together with monomers; dissolved for uniform mixing, then copolymerized under inert atmosphere; monitored via in-line analytics for degree of polymerization and chain end-group analysis.

    Final product types

    • Conductive polyamides (used in antistatic packaging)
    • Polyaniline-based films
    • Electronic encapsulating polymers
    • Precision-molded polymer composites for automotive harnesses

    3. Boiler and Cooling Water Oxygen Scavenger Formulation

    Steam generation and recirculating cooling systems in power plants and heavy manufacturing facilities require efficient oxygen scavengers to limit corrosion and scale. N,N-Dimethyl-M-Phenylenediamine Dihydrochloride serves as a benchmark active ingredient in proprietary oxygen scavenging blends, ensuring rapid reaction kinetics and stable performance in both high- and low-pressure operational contexts. Its use aligns with industry maintenance protocols and environmental discharge regulations, supporting system integrity and process uptime.

    Industry compliance standards

    • ASME Consensus on Operating Practices for Control of Feedwater and Boiler Water Chemistry
    • EN 12952-12:2003 (Water-tube boilers–Requirements for boiler feedwater and boiler water quality)
    • EPA Guidelines for Effluent Limitations (US NPDES)
    • ISO 14001 (Environmental Management Systems, applicable to chemical water treatment plants)

    Typical usage ratio

    • 5–50 ppm of active ingredient relative to total water volume, depending on dissolved oxygen load, water temperature, and cycle time.

    Downstream process integration

    • Blended into oxygen scavenger liquid concentrates; dosed into feedwater streams before deaeration phase or directly into main water loop; residual levels monitored via online chemical dosing and titration.

    Final product types

    • Industrial water treatment chemical blends
    • Boiler feedwater conditioners
    • Cooling system corrosion inhibitor packets
    • Pre-mixed oxygen scavenger dosing solutions

    4. Dyes and Colorant Intermediate Synthesis

    The dye and pigment sector uses N,N-Dimethyl-M-Phenylenediamine Dihydrochloride as a key intermediate in manufacturing triarylmethane and azo dyes for high-performance textile, paper, and ink coloration. Its substitution pattern enables targeted electrophilic aromatic coupling to generate vivid and consistent dye structures, with batch-to-batch color fastness confirmed by industry QC protocols.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Chemical Safety)
    • ISO 105-B02 (Textiles—Tests for color fastness: Xenon arc fading)
    • ZDH/Chemie–Sicherheit und Umwelt (European Dyes Compliance)
    • REACH Annex XVII (Restrictions on certain hazardous substances)

    Typical usage ratio

    • Employed at 0.5–3.5 mol% relative to total coupling component, with exact charge optimized per dye structure, final shade intensity, and process yield.

    Downstream process integration

    • Charged into reactors during initial condensation or secondary diazotization steps; pH and temperature tightly controlled to regulate coupling; intermediate isolated by crystallization prior to further derivatization.

    Final product types

    • Triarylmethane dyes for textile manufacture
    • Azo colorants for non-impact printing inks
    • Paper coloring agents
    • Specialty laboratory indicator dyes

    5. Pharmaceutical API Impurity Testing and Identification

    Pharmaceutical quality control laboratories apply N,N-Dimethyl-M-Phenylenediamine Dihydrochloride as a derivatization agent for trace-level detection of carbonyl compounds and related impurities in active pharmaceutical ingredients (APIs). The material’s specificity enables sensitive post-column derivatization in HPLC and LC-MS workflows, fulfilling compendial method requirements for impurity profiling in regulated drug release environments.

    Industry compliance standards

    • USP <823> (Chromatographic Purity)
    • European Pharmacopoeia 2.2.46 (Chromatographic Separation Techniques)
    • ICH Q3A/B (Impurities in new drug substances/products)
    • cGMP (Current Good Manufacturing Practices, 21 CFR Parts 210/211)

    Typical usage ratio

    • Derivatization reagent prepared at 0.1–1 mg/mL in chromatographic mobile phase, fine-tuned for sensitivity and linear response based on target impurity range and matrix complexity.

    Downstream process integration

    • Added on-line or post-column during routine and batch-release analyses; utilized in QC and R&D laboratory environments; incorporated into method-validated analytical kits.

    Final product types

    • Pharmaceutical impurity detection kits
    • APIs with fully characterized impurity spectra
    • High-purity pharmaceutical preparation batches
    • Validated QC documentation for regulatory submissions

    6. Photographic Chemical Manufacture

    In the photographic industry, N,N-Dimethyl-M-Phenylenediamine Dihydrochloride is utilized in processing formulations as a color developer, particularly within chromogenic films and photographic paper. Controlled addition stabilizes image tone and sharpness by facilitating the reduction of exposed silver halide crystals, a step governed by precise ISO performance and composition requirements for imaging chemicals.

    Industry compliance standards

    • ISO 18902 (Imaging materials—Processed safety-film—Storage)
    • ANSI/NAPM IT2.17 (Photographic Processing Chemistry Standards)
    • REACH compliance for photographic chemical supply
    • Environmental Health & Safety guidelines (local and regional)

    Typical usage ratio

    • Color developer concentrate: 1–5 g/L in working solution; dose adjusted via sensitometric calibration for film or paper format and intended color balance.

    Downstream process integration

    • Incorporated into developer composition during liquid blending; applied in film processing tanks during color development step, under light-controlled conditions and with automated replenishment systems.

    Final product types

    • Photographic developer concentrates and working solutions
    • Chromogenic films and papers with enhanced color stability
    • Imaging laboratory chemical processing kits
    • Archival-grade photographic prints
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    Certification & Compliance
    More Introduction

    N,N-Dimethyl-M-Phenylenediamine Dihydrochloride: Hands-On Insights from Chemical Manufacturing

    Introduction to Our Experience

    Few specialty chemicals draw more attention from oxidative dye synthesis, color development in analytical chemistry, and detection reagents than N,N-Dimethyl-m-phenylenediamine dihydrochloride. As a manufacturer directly involved in both the scale-up and bulk preparation of this aromatic diamine salt, we’ve had years to witness its value and the fine details that make it distinct. Chemical research has opened many applications for this compound, yet we find that each customer, whether coming from a diagnostics lab, a water analysis facility, or a lab supply chain, cares about one thing: knowing they can trust the real story behind what’s in their shipment.

    Model and Specifications: Considerations Built From Production

    Our plant’s most frequently produced batch involves the prima facie variant, typically in the form of a white to yellow crystal powder. As for purity, rigorous distillation and multiple recrystallizations make sure that the defined product grade exceeds 99% when tested by HPLC or standard gravimetric analysis. While minimal impurities such as N-mono-methyl aniline or other amines can appear as by-products, field experience tells us they seldom cross measurable thresholds set by major pharmaceutical and research standards. Each production run includes titration-based chloride content confirmation and melting point analysis, which typically records values between 170 and 175°C for the dihydrochloride salt, giving preparative chemists and analysts a consistent physical reference.

    Handling this compound on the manufacturing floor doesn’t present issues common with hygroscopic salts, but staff work in climate-controlled rooms to prevent any risk of clumping or breakdown during packaging. The powder dissolves well in water and alcohols, thanks to the dual hydrochloride groups, which is a notable improvement compared to the base free diamine. Not all end users require the same mesh size or particle distribution, but the drying and winnowing stage gives us flexibility to customize for spectrophotometric work or large-scale chemical synthesis.

    Understanding the Chemistry: Functional Differences from Similar Products

    We have noticed a lot of confusion among new buyers over the differences between N,N-Dimethyl-m-phenylenediamine and its closely related analogs, especially the o- and p- isomers. The meta position of the methyl groups on the aromatic ring in our product sets it apart. The electron distribution and steric demand introduced by this configuration changes its reactivity with oxidants, especially in colorimetric assays or as a coupling agent in pigment formation.

    Across manufacturing and downstream applications, the main competitor has usually been N,N-Dimethyl-p-phenylenediamine. Though the para isomer performs similarly as a redox agent, it’s not as reliable for certain kinetic analyses requiring controlled rates of dye formation, and the color stability can drop under prolonged exposure to light or heat. Comparative trials with the ortho isomer point toward more rapid degradation in environmental testing scenarios, where trace amines reduce analytical longevity. Over many years, we have supplied all three products on request and have tracked feedback closely. The meta form consistently draws repeat buyers from academic groups investigating electron transfer and companies involved with colorimetric detection of industrial pollutants such as nitrites and ozone.

    Using N,N-Dimethyl-M-Phenylenediamine Dihydrochloride Well: Practical Lessons from the Production Line

    Manufacturing at volume means dealing head on with operational safety and batch-to-batch reproducibility. While the compound presents less inhalation risk compared to volatile amines, technicians still use proper PPE, and use of explosion-proof mixers prevents accidents during large-scale dissolution. Overheating the compound will not just threaten classification purity; it can trigger a slow decomposition, yielding sticky residues that complicate clean-up—no substitute exists for measured temperature control during drying and crystallization.

    Our in-house chemists often work directly with formulators who optimize this compound as a color developer in the Griess reaction and a chromogenic substrate in peroxidase assays. Insights gleaned from their results frequently feed back to fine-tuning our in-process controls. Even a single degree lost in drying can affect spectral absorption, so we calibrate our vacuum ovens several times per day. Laboratories depending on this product for trace detection—water quality testing for nitrites, smoke gas analysis, or aldehyde determination—rely on this kind of rigorous approach.

    We have handled customer requests for pre-measured vials, dust-suppressed grades, and even granulated forms, for those needing ease of handling on automated lines. Most requests come from end users who have wrestled with competing products that either degrade before arrival or don’t dissolve as expected. Shipping at the peak of summer or through long customs holds can be challenging, yet the double-sealed, nitrogen-purged drums minimize moisture pickup. No amount of theoretical shelf-life matters if years of experience haven't taught a supplier how to get the real material to the customer’s doorstep looking as fresh as the day it left the plant.

    Field Application: How Real-World Usage Sets This Product Apart

    First-hand reports from national environmental laboratories say the detection limits achieved using our m-phenylenediamine compound often edge out alternative substrates by several micrograms per liter for nitrite colorimetry. In clinical laboratories, rapid dye formation and the predictable red-violet color in peroxidase catalysis bring much-needed repeatability. Analytical chemists wanting clear end points during redox titrations and chloroform colorations appreciate that no lingering background persists—physical cleanliness courtesy of the crystal structure itself.

    Applications extend to organic synthesis as well, where several groups exploring new medicine precursors report fewer by-products relative to the p- and o- derivatives. This results from lower rates of undesired side reactions during condensation and oxidative coupling, which matter greatly when one’s final product must meet regulatory scrutiny. Even in pigment chemistry, manufacturers prefer our product for certain quinone-producing reactions, since color yield and lightfastness rates beat those achieved with the p-isomer, especially in high-throughput, high-volume settings.

    Experience shows that switching to this compound can reduce both solvents and reagents used for purification downstream. In-house trials have shown up to 12% shorter synthesis cycles for some dye intermediates and reduced energy use during drying, facts that matter both to the bottom line and those aiming for leaner environmental operations.

    Quality Control and Consistency: Challenges and Advances

    Producing this compound to a consistent standard took several years of experience, not just in reaction engineering, but also in monitoring raw material trends worldwide. Over time, even the best aniline suppliers change their processing methods, affecting downstream purity and yield. We test every lot of inbound feedstock for color, specific gravity, and contamination before approval. Far fewer headaches arise later if we reject materials that don’t hit our exacting standards.

    Once synthesis begins, real challenges crop up: amine oxidation, pH shifts, and moisture ingress during acid addition. We never rely on a single analytical method—HPLC, GC, NMR, and wet chemistry all serve a role in confirming identity, purity, and residual solvents in each batch. Instead of waiting until something goes wrong, our operators pull samples at multiple intervals, making corrections on the fly. This proactive approach means fewer out-of-spec batches, and explains why returns or complaints remain rare year after year.

    We also tailor our batch records and COAs to reflect customer requirements. Pharmaceutical partners want to see impurity profiles, not just simple purity lines. Environmental labs care about heavy metal content and photostability over time. We developed separate protocols for each case. Documenting it all is a tedious task, but after years of tracking quality metrics, we know no shortcut beats hard-won process understanding.

    Meeting New Demands: Rethinking Packaging and Delivery

    Our experience shows that packaging frequently makes or breaks a product’s reputation. Low-volume orders for research rarely bring complaints, but commercial-scale contracts put every bag and drum under the microscope. Sealed mylar liners inside UN-approved drums extended shelf life dramatically, especially for warm, humid regions. Adding tamper-evident closures and robust labeling cut down on warehouse confusion and cross-contamination. Over the years, users have asked for smaller aliquots or pre-weighed kits. Fulfilling those requests taught our team to invest in precision filling robots and build out cleanrooms, further driving down particulate and cross-contaminant risks.

    Delivering this compound by air or sea reveals further challenges. Dihydrochloride forms resist temperature swings far better than free bases, yet a few weeks in unregulated freight conditions can still create minor caking or darkening. Coordinating with reliable couriers and using insulated secondary containers pays off. Direct feedback loops with logistics partners taught us how to handle customs paperwork, route planning, and on-ice shipments for customers in the harshest climates. Developing those skills did not arrive overnight, but the reduced risk of lost or spoiled lots makes up for every extra logistical effort put in.

    Environmental and Regulatory Considerations

    Long before sustainability became a public watchword, our facility was cutting solvent losses through closed-loop recovery, drawing inspiration from a time when solvent prices were far more volatile. We limited effluent and minimized energy demand with smarter reactor design and batch scheduling. Our in-house waste treatment system neutralizes all mother liquors before discharge, and captured amine vapors see catalytic destruction.

    Regulatory compliance travels with every shipment. For pharmaceuticals, the route to registration depends on tight documentation, traceability, and third-party validation—three things only a committed chemical manufacturer provides. Internal audits cover everything from safety data sheets to hazard labeling and transportation documentation. Reach and TSCA status change as jurisdictions update their rules; we keep data current so that no import or export headaches fall on our customers. In a world where substances cross borders and regulatory scrutiny only grows, being a producer fully familiar with both the chemistry and the paperwork prevents expensive delays and costly missteps.

    Challenges and Ongoing Solutions

    Manufacturing is never problem-free. Impurity management poses one hurdle—trace levels of mono-methyl derivatives require both fine-tuned reaction conditions and novel extraction protocols. Repeated investment in analytical hardware helped us catch even tiny contaminants promptly.

    Employee safety marks another challenge. Training staff for safe handling, equipping with top-standard PPE, and backing that up with air monitoring and spill drills took several years to refine. After hearing stories from users who struggled with off-spec deliveries or problematic batches, we raised our own expectations. Every error becomes a lesson, and sharing those stories internally builds a safer, smarter team.

    On the user side, requests for higher purity or unique packaging formats sometimes test equipment limits. We listen, adapt, and invest accordingly—whether in technology, training, or supply chain partnerships. This spirit of continuous improvement is as much a manufacturing issue as an end-user need.

    Looking to the Future: Innovation and Responsiveness

    This aromatic diamine will remain a staple in diverse analytical and industrial circles. Increasing demand for trace analysis in water, more sophisticated diagnostics, and next-generation dye chemistry drive our own R&D. We’ve participated in collaborative projects with both universities and industrial partners, working on custom modifications, labeled isotopes, and fresh applications. Every new request brings not just challenges, but openings to support innovation from the heart of manufacturing know-how.

    Sustainable production, compliance, and application-focused customization now drive our operations as much as price and quality once did. The shift isn’t just about marketing; it’s driven by the people who work here, solve process issues, and answer the anxious calls when a shipment faces Customs holdups. Honest, experienced manufacturing remains the foundation for everything.

    Conclusion: Why Manufacturing Matters

    Trust in specialty chemicals like N,N-Dimethyl-m-phenylenediamine dihydrochloride depends as much on consistency, transparency, and real-world feedback as it does on raw purity or technical specifications. End users from research, industry, and analysis all depend on more than a spec sheet—they need insight, support, and accountability from those at every link in the chain. Decades of experience manufacturing this compound show nothing replaces hands-on familiarity, not just in what fills the drum, but in the knowledge shared across applications and challenges. Listening to user experience, innovating in packaging or analysis, and owning every step from sourcing to shipment: that’s the only way to deliver the trustworthy product the market really needs.