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4-Aminobenzylamine

    • Product Name 4-Aminobenzylamine
    • Alias 4-(Aminomethyl)aniline
    • Einecs 214-456-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    886281

    Chemical Name 4-Aminobenzylamine
    Synonyms p-Aminobenzylamine
    Molecular Formula C7H10N2
    Molar Mass 122.17 g/mol
    Cas Number 4403-71-4
    Appearance White to off-white crystalline solid
    Melting Point 65-68°C
    Boiling Point 272°C
    Solubility In Water Soluble
    Density 1.15 g/cm3
    Smiles CC1=CC=C(C=C1)N
    Pubchem Cid 14239

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

    Packing & Storage
    Packing The packaging for 4-Aminobenzylamine (25g) is a sealed amber glass bottle with a tamper-evident cap and labeled safety information.
    Shipping 4-Aminobenzylamine should be shipped in tightly sealed containers, protected from moisture and light. Ensure the packaging is compliant with relevant regulations, such as DOT and IATA guidelines. Ship via a recognized carrier experienced in handling chemicals. Proper labeling, documentation, and safety data sheets (SDS) must accompany the shipment to ensure safe transport and handling.
    Storage 4-Aminobenzylamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Careful labeling and secure storage help prevent contamination and degradation. Personal protective equipment should be used when handling and transferring the chemical to ensure safety.
    Application of 4-Aminobenzylamine

    Applications of 4-Aminobenzylamine in Industrial Manufacturing

    4-Aminobenzylamine finds use in several specialized chemical manufacturing sectors due to its primary amine and aromatic functionality. As a manufacturer, we supply this intermediate to downstream producers who rely on consistent quality for demanding synthesis and formulation environments. Below we detail authentic downstream application scenarios based on practical integration of 4-Aminobenzylamine into commercial production lines, with a focus on compliance, usage parameters, process steps, and resulting finished products.

    1. Pharmaceutical Intermediate Synthesis: Active Pharmaceutical Ingredient (API) Building Blocks

    Pharmaceutical companies use 4-Aminobenzylamine for nucleophilic substitution and reductive amination steps when building diverse heterocyclic structures for APIs targeting antihypertensives, antipsychotics, and anti-inflammatory agents. Its high purity and batch stability support strict production regimes where consistent reactivity is critical to meet downstream regulatory filing and global submission requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EP, USP, JP monograph compliance for trace impurity control
    • Global Drug Master File (DMF) documentation
    • 21 CFR Part 211 U.S. FDA cGMP requirements

    Typical usage ratio

    • 0.5–3.0 molar equivalents relative to the core intermediate; the exact ratio depends on the desired substitution pattern and scale of synthesis

    Downstream process integration

    • Introduced during early-stage condensation, reductive amination, or ring closure steps prior to functional group protection and purification cycles in multi-step API processes

    Final product types

    • Bulk drug substances and API intermediates for solid oral, injectable, and topical dosage forms

    2. Specialty Dye and Pigment Synthesis

    Producers of high-performance azo and diazo dyes incorporate 4-Aminobenzylamine as a diazotizable aromatic amine, serving as a key coupling partner to develop colorfast chromophores for textile, printing ink, and plastic coloration. Its reactivity allows for selective substitution, enabling upstream chemists to achieve precise tone control and batch consistency essential for global textile quality assurance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dyes
    • REACH (EC) No 1907/2006 registration for chemical safety
    • EN 71-3:2019 for toy safety (migration of colorants)
    • ISO 9001:2015 quality management for dye manufacturers

    Typical usage ratio

    • 0.8–1.2 molar equivalents as a diazo component, adjusted for chromophore length and application (textile or ink systems)

    Downstream process integration

    • Added during diazotization and coupling stage, preceding salting out, filtration, and milling of pigment dispersion

    Final product types

    • Azo dyes for synthetic fibers, acid dyes for nylon, specialty pigments for plastics, and stable colorants for water-based inkjet printing

    3. Epoxy Resin Curing Agent Formulation

    Manufacturers of electrical encapsulation materials and structural adhesives use 4-Aminobenzylamine as a hardener or cross-linking agent in epoxy systems. Its bifunctional amine structure influences cure kinetics, glass transition temperature, and mechanical performance, which proves critical for applications requiring long-term thermal stability and insulation integrity, such as printed circuit boards and automotive electronics potting.

    Industry compliance standards

    • UL 94 flammability testing (insulating materials)
    • IEC 61249-2-7 for base materials for PCBs
    • RoHS Directive 2011/65/EU compliance (electrical/electronic equipment)
    • ISO 9001:2015 for manufacturing process control

    Typical usage ratio

    • 2–8 parts per hundred resin (phr) in multifunctional epoxy systems; adjusted for target mechanical properties and working time

    Downstream process integration

    • Dispersed into epoxy pre-mix under vacuum with controlled heating, facilitating nucleophilic ring opening during ambient or thermal cure cycles

    Final product types

    • Encapsulated modules, high-performance epoxy adhesives, and PCB substrates for consumer electronics and industrial automation

    4. Polymer Modification: Polyamide Chain Extender

    Leading engineering plastics producers use 4-Aminobenzylamine as a chain extender during the polycondensation of aromatic polyamides. The amine’s molecular structure allows precise adjustment of molecular weight and end-group functionality, which increases toughness and heat resistance in high-performance polymers required for aerospace, automotive, and industrial components under demanding mechanical loads.

    Industry compliance standards

    • ISO 1874 for polyamide materials classification
    • UL Yellow Card listings for polymer flammability and performance
    • ISO 14001 for environmental management in polymer production
    • REACH (EC) No 1907/2006 for chemical registration and safety

    Typical usage ratio

    • 0.2–1.0% by weight of total polyamide monomer feed, with specific addition rate tuned to achieve target viscosity and end-use mechanical strength

    Downstream process integration

    • Metered into molten monomer blend immediately following initial chain growth, prior to final vacuum devolatilization and pelletization step

    Final product types

    • Glass fiber-reinforced polyamide pellets, engineering masterbatches, and high-performance injection molding grades for precision technical components

    5. Agrochemical Active Ingredient Precursor

    Major crop protection companies employ 4-Aminobenzylamine in the synthesis of select bactericides and herbicide actives through targeted condensation reactions. The amine group provides reactive access to bioactive heterocyclic cores, with reliable handling properties that facilitate route scouting and scale-up in pilot and full plant environments.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • ISO 9001:2015 for batch traceability and process validation
    • EU Regulation (EC) 1107/2009 on plant protection product market authorization
    • Globally Harmonized System (GHS) for chemical labeling

    Typical usage ratio

    • 0.7–2.5 molar equivalents in condensation with specific acid chlorides or isocyanates; dosage determined by targeted molecule yield and impurity profile

    Downstream process integration

    • Charged at the precondensation stage of multi-step syntheses, generally following in situ pH adjustment and monitored by HPLC for endpoint specification

    Final product types

    • Agrochemical actives formulated into emulsifiable concentrates, water-dispersible granules, and suspension concentrates for agricultural field application

    6. Analytical Reagent and Monomer Scaffold

    Producers of analytical test kits and specialty chemical libraries integrate 4-Aminobenzylamine as a derivatization reagent for aldehyde and ketone determination, as well as a monomeric scaffold for combinatorial library construction. Its reliable lot-to-lot reactivity supports critical detection sensitivity in diagnostic labs and enables precise functionalization for custom molecular screening.

    Industry compliance standards

    • ISO 17025 for laboratory measurement accuracy
    • OECD Good Laboratory Practice (GLP) Guidelines
    • CLSI EP7 for interference testing in clinical diagnostics
    • REACH compliant material safety data documentation

    Typical usage ratio

    • 10–200 μM concentration for reagent-based analytical kits; concentration range tailored to analytical method sensitivity and matrix complexity

    Downstream process integration

    • Dosed into sample derivatization step or used as a core scaffold during automated or manual combinatorial synthesis prior to purification and analytical validation

    Final product types

    • Analytical probes for HPLC/UV or fluorescence assays, molecular building blocks for lead discovery in pharmaceutical or agrochemical screening
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    Certification & Compliance
    More Introduction

    4-Aminobenzylamine: Manufacturing Perspective on a Versatile Intermediate

    Real-world Role of 4-Aminobenzylamine in Synthesis

    As a chemical manufacturer with decades rooted in aromatic amine chemistry, we have seen 4-Aminobenzylamine step into many versatile shoes. Chemists rely on its robust para-amino substitution and benzylamine backbone for crafting pharmaceutical building blocks, brightening agents, and specialty monomers. Every batch traveling through our facilities starts as pure technical-grade 4-(Aminomethyl)aniline—most often as a white to off-white crystalline powder, CAS number 2497-43-6, and processed to deliver a minimum assay of 98%.

    Our manufacturing line ensures each shipment meets controlled moisture content and a precise melting point, as stability and color purity guide consistent performance in downstream coupling, reductive amination, or diazotization processes. Many of our clients use it directly in specialty drug research where any trace of byproducts alters target yield or creates regulatory headaches. Four decades of experience taught us never to underestimate how subtle impurity profiles affect crystallization or reaction times, especially in lab-scale up to plant-scale runs.

    Why Structure Matters Beyond Commodity Aromatic Amines

    Experience separates 4-Aminobenzylamine from similar aromatic amines by its position and function of its two reactive groups—the para-amine and the benzylamine. Benzenoid chemistry can frustrate process chemists; a small difference, like that between a para-amine and a meta-amine, determines not just reactivity but how products behave under hydrogenation, acylation, or diazo coupling. We saw this difference most in the intermediates for certain antihypertensive agents and brightener products, where our customers reported irreversible color drift and incomplete reaction from materials supplied from poorly controlled origins.

    Years back, a customer’s pilot plant faced stoppages when they used a mixed-isomer batch from a bulk trader. They found out too late how easily a single misplaced amino group in the aromatic ring contaminated the downstream synthetic route, introducing unexpected byproducts during reductive amination. Since then, our entire process, from nitro reduction step to purification protocols, aims at eliminating cross-isomer contamination. Precision automation in the last decade helped consistently separate and monitor any ortho or meta- isomers, which never leave our plant in finished products.

    Direct Benefits to Formulators and Researchers

    4-Aminobenzylamine serves as a highly functional intermediate. Small molecule innovators count on its free amine groups for direct alkylation, sulfonation, or acylation, and its benzyl portion acts both as a spacing unit and a stabilizer for more complex molecular scaffolds. Through long relationships with dye manufacturers, we’ve seen how its particular arrangement enables vivid azo and amino-coupled colors that outperform what can be made from standard aniline or benzylamine derivatives.

    Generic pharmaceuticals makers see it as a key to flexible design. In our years serving international clients, several have optimized their synthetic yields using our high-purity 4-Aminobenzylamine, as it offers an easier workup and cleaner chromatographic separation as compared to other aminobenzyl isomers or unpurified material. We hear about a smoother route to coupling, fewer byproducts, and less need for labor-intensive recrystallization.

    Differences from Analogous Amines and Competitive Edge

    Put 4-Aminobenzylamine beside benzylamine or para-aminophenyl derivatives and differences in reactivity become clear. In process development, researchers select 4-Aminobenzylamine for its dual-amine design—rarely duplicated in other low molecular weight intermediates. While para-phenylenediamine offers two amines, it lacks the methylene bridge flexibility offered by the benzylamine moiety. That flexibility matters in sterically hindered syntheses, or in the creation of linkers and spacers for bioconjugation.

    Comparisons with ortho- and meta-aminobenzylamine underscore why positional isomerism affects synthetic selectedivity. As a manufacturer, we have invested in spectral analysis and process QA to guarantee ‘no mix-ups’ between these similar names and distinct chemicals. Para-substitution means less cross-linking and a more predictable outcome in colorant or pharmaceutical active manufacturing. Process yields and purity improve, making our partners’ scale-ups less risky.

    Challenges in Manufacturing and Quality Assurance

    We have faced our own set of issues making 4-Aminobenzylamine. Not every aromatic nitro compound hydrogenates cleanly, and precise pH and temperature curves hold the difference between a successful batch and a pile of unreacted intermediates. Early in our production, we learned that catalysts prone to minor poisoning—like nickel or palladium catalysts—call for extra monitoring when upstream raw materials fluctuate. Operations improved only when we began sourcing more rigorously tested precursors and bolstering our in-house analytical checks for every lot.

    The market has seen some low-cost alternatives enter, but industry veterans know that shortcuts bring headaches. We built our in-process controls to spot rapid shifts in color, solubility, or byproduct formation. Every step, especially the finer finishing and drying, means more than meeting specs—it means fewer surprises on the customer side. Our best feedback comes from long-term users who report greater batch consistency and lower waste factors, especially in early synthesis steps where downstream yield hinges on initial input quality.

    Regulatory and Environmental Accountability

    Today’s market landscape holds manufacturers to higher environmental and safety standards. Our decades in the industry taught us firsthand that regulatory headaches start with careless waste management and incomplete documentation. By keeping our waste stream tight and tracking every outgoing drum, not only do we stay compliant with REACH and other international frameworks, we also prevent ambiguous lot origins, which we know has caused recalls at other facilities.

    We take solvent management seriously—recycling as much as possible, and strictly controlling any vented emissions of aromatic amines. Waste from the purification stream, particularly where amine hydrochloride salts build up, gets neutralized in multi-stage, closed-loop systems. Many companies let these residues accumulate, leading to inconsistent salt forms or byproducts in shipments. Our customers know every drum from us comes with well-documented analysis, batch history, and precise COA records.

    Partnering with Formulators: Lessons from the Lab and Plant

    Our direct involvement with R&D partners shaped how we standardize 4-Aminobenzylamine offerings. Project chemists often push for specialized specs: ultra-low chloride, reduced moisture, specific crystalline forms. We learned that close attention to drying conditions and careful storage in inert atmospheres can minimize cyclization and darkening—issues that lead to bottlenecks in fine chemical synthesis where color and clarity signal quality. We offer technical discussions to help customers interpret their own analytics or troubleshoot purification steps, because we know a lot doesn’t always match a spec on paper just by checking numbers.

    From fine-tuning particle size for specific reactors to troubleshooting interactions with metal-based catalysts, our technical support stays hands-on. Once, a Japanese pigment manufacturer encountered inconsistent tints during azo coupling. Jointly, we traced it to an overlooked variation from a secondary supplier’s batch. Adjustments on our line tightened up particle size and reduced an imine impurity, fixing their color inconsistency. Experiences like these cemented our philosophy: collaboration bridges the gap between specification and real-world performance.

    Innovations in Processing and Analytical Methods

    Advancements in process analytics strengthened how we deliver reproducible batches. Years ago, classical wet chemistry sufficed for purity, but current standards rely on HPLC, NMR, and mass spectrometry every batch. These days, partners in API research want precise impurity profiles. With our proprietary process controls, we’ve managed to keep batch-to-batch variance well below industry norms, a difference that shows in downstream process yields and product profiles.

    As process research moves faster, our analytical R&D group developed in-line monitoring for faster feedback. Quick turnaround on batch release means less downtime for our customers, especially those running pilot plant campaigns on tight schedules. We share empirical data with our customers as they develop new transformations or scale up novel derivatives. Transparency, both in testing and in observed outliers, keeps surprises to a minimum when projects transition from gram scale to multi-ton lots.

    Raw Material Integrity and Supplier Relationships

    Sourcing quality nitro intermediates and reduction catalysts underpins reliable 4-Aminobenzylamine output. Inconsistent quality from upstream suppliers remains a major concern, especially as global sourcing expands. By narrowing relationships to raw material partners with traceable documentation, we prevent most supply chain disruptions. We keep a reserve stock of both raw materials and finished product, learned from early years of production, to buffer customers from spot-market spikes and shipping delays.

    A few years back, an abrupt price surge in nitroaromatic intermediates threatened to slow production for several producers. Our long-held partnerships and inventory planning ensured continuous supply to all customers, even as others faced rationing or quality drops. This level of reliability still defines our competitive stance, especially with customers in pharmaceutical R&D who build multi-year projects around assured product access and quality.

    Sustainability: Meeting New Industry Demands

    Chemicals like 4-Aminobenzylamine often challenge manufacturers to balance efficiency with sustainability. We re-engineered our processes to reduce water use and minimize hazardous byproducts. Solvent distillation and closed-loop operations feature in our commitment to greener manufacturing. As regulatory climates rapidly evolve, we adopted early documentation and reporting habits, staying ahead of global compliance laws and trade requirements.

    Customers are rightly raising demands for accountability. Certifications on environmental management and rigorous handling of process waste match their own sustainability policies. This builds trust, but also drives us to continually improve production and documentation standards, ensuring we do our part to support safer, cleaner supply chains worldwide.

    Distinct Applications: Pharmaceuticals, Dyes, and Novel Materials

    Most 4-Aminobenzylamine demand still comes from pharmaceutical research and specialty colorants. In pharma, it serves as an intermediate for drugs targeting central nervous system modulation, blood pressure control, and experimental oncology molecules. Its free para-amino group makes coupling for active moieties straightforward, while the benzylamine connection acts as a flexible linker, stabilizing desired molecular arrangements.

    Dye manufacturers value 4-Aminobenzylamine for vividness and stability. Unlike some common amines, its substitution pattern promotes strong chromophore formation and deepens shades in finished products. In the past five years, we’ve seen fast adoption in optical brighteners and advanced functional dyes—fields where only the purest intermediates avoid tint drift and shade fade. Advanced polymer developers have also picked it up, incorporating its dual functional groups into smart material and surface coating designs.

    Supporting Industry Adaptation and Custom Specification

    Not every customer wants the same standard grade. Specialty research teams demand modifications—anhydrous material, lower metals content, or a guaranteed absence of specific trace impurities. Our batch records reflect these market shifts. As the industry advances toward more precise and personalized chemistry, flexibility in manufacture and delivery means partners can scale novel synthesis from bench to plant without backtracking on compatibility or process yields.

    From our vantage, supporting this innovation means constant feedback with end-users. We set up rapid-response lines for technical questions and off-spec observation, documenting every actionable point. Comprehensive lot records support traceability, offering security to those in regulated industries and confidence to custom laboratories. Our customers help guide product evolution; in return, we make every effort to keep specifications transparent and attainable, not hidden behind ambiguous technical claims.

    Navigating Supply Chain Stability in an Uncertain World

    Since global events disrupt chemical supply chains with little warning, stability and clear communication build customer trust. We balance regular production with strategic inventory and open communication about shifts in raw material availability or transit disruptions. In a recent logistics crunch, we kept customers updated daily, providing alternatives within our range or helping them reformulate with adjusted specifications where possible—avoiding missed deadlines or shutdowns.

    We see our responsibility as more than just producing batches. Our seasoned team anticipates shifts in market pricing, changes in import regulations, and transport delays. Rather than leaving partners guessing, we take a proactive stance—informing, consulting, and solving problems side-by-side. This loyalty built year after year leads to mutual success and keeps projects on target.

    Why Experienced Manufacturing Matters in 4-Aminobenzylamine

    At the core of every chemical project is reliability. Experience has taught us that the smallest detail—a degree too high in reduction, a day too long in drying, or a misread impurity—sets off costly downstream issues. Each process upgrade and product check reflects the lessons from past missteps and successes alike. We have implemented a culture of accountability anchored in the belief that transparency and clarity from raw material to finished product protect everyone’s investment.

    Our journey with 4-Aminobenzylamine is inextricably tied to the evolution of industry expectations. Increased scrutiny, rapid synthesis cycles, and new application areas push us to keep refining both what our product is and how it is made. Our commitment stays firmly with dependable quality and open dialogue with customers, ensuring each kilogram meets more than a technical standard—it answers the real-world needs of the chemists and formulators at the frontlines of innovation.

    Looking Forward: Enabling the Next Generation of Chemical Synthesis

    As newer synthesis technologies and application fields evolve, we observe an expanding role for 4-Aminobenzylamine across disciplines. Innovations in medical diagnostics, catalysts, and biomaterials challenge us to keep improving both product purity and service reliability. We deploy our cumulative expertise, adaptive process controls, and industry partnerships to anticipate and address technical hurdles.

    Our track record shows that long-term collaboration, real accountability, and a craftsman’s attention to detail result in chemical intermediates that not only fit the required spec sheet, but also power new discoveries. Practical know-how remains our strongest asset. With each lot, we stand behind decades of hands-on experience and a philosophy of partnership with those tackling tomorrow’s chemical challenges.