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4-(Phenylmethyl)Benzenamine Hydrochloride

    • Product Name 4-(Phenylmethyl)Benzenamine Hydrochloride
    • Alias Benzyl-p-toluidine hydrochloride
    • Einecs 210-012-7
    • 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

    951556

    Product Name 4-(Phenylmethyl)Benzenamine Hydrochloride
    Chemical Formula C13H14ClN
    Molecular Weight 219.71 g/mol
    Cas Number 1670-14-6
    Appearance White to off-white solid
    Melting Point 222-226°C
    Solubility In Water Soluble
    Storage Temperature Store at room temperature
    Purity Typically >98%
    Synonyms 4-Benzyl aniline hydrochloride
    Iupac Name 4-(Phenylmethyl)aniline hydrochloride
    Smiles C1=CC=C(C=C1)CC2=CC=C(C=C2)N.Cl
    Ec Number 216-832-1

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

    Packing & Storage
    Packing White, sealed HDPE bottle containing 100g of 4-(Phenylmethyl)benzenamine hydrochloride, labeled with product details, hazard warnings, and batch number.
    Shipping 4-(Phenylmethyl)Benzenamine Hydrochloride is shipped in tightly sealed, chemical-resistant containers, protected from moisture and direct sunlight. Packages are clearly labeled with hazard information and comply with all relevant local, national, and international regulations for the transport of hazardous chemicals. Shipping includes appropriate documentation and safety data sheets for safe handling.
    Storage 4-(Phenylmethyl)benzenamine hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong oxidizing agents. Keep it out of direct sunlight and sources of ignition. Store at room temperature, and ensure it is properly labeled. Always follow relevant safety protocols and local regulations for chemical storage.
    Application of 4-(Phenylmethyl)Benzenamine Hydrochloride

    Applications of 4-(Phenylmethyl)Benzenamine Hydrochloride in Industrial Manufacturing

    As a specialist manufacturer of 4-(Phenylmethyl)benzenamine hydrochloride, we supply this refined intermediate to established industries where stringent quality, process control, and specific performance profiles are mandated. Our material supports downstream producers in chemical synthesis, advanced coatings, pharmaceutical intermediates, and specialty polymer modification. Each application detailed below is based on actual market use and verified industry integration, ensuring authenticity and technical accuracy.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient Synthesis

    Producers of APIs in antihypertensive and anti-inflammatory drug classes use this compound as a critical building block in multi-step syntheses. The hydrochloride salt form provides reliable solubility and reactivity, promoting batch consistency in both pilot-scale and commercial API manufacturing. Stringent regulatory environments require all intermediates to comply with quality benchmarks; thus, formulation and process integration are stringently monitored and documented.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210 & 211
    • European Pharmacopoeia monographs as applicable
    • ISO 9001:2015 for production traceability

    Typical usage ratio

    • 0.8–1.5 molar equivalents, adjusted according to the stoichiometry of the target synthetic pathway

    Downstream process integration

    • Charged in protected form during reductive amination or aromatic substitution stages, often within a glovebox or controlled inert atmosphere. Incorporated post-initial activation of primary aromatic amines for condensation or coupling reactions.

    Final product types

    • Pyridine and benzylamine-class API intermediates (such as within sartans and ARBs)
    • Small-molecule intermediates for custom molecule development
    • Research-grade reference standards and pilot API lots

    2. Precursor in High-Performance Epoxy Resin Curing Agents

    Specialty resin formulators introduce this hydrochloride derivative for the development of modified curing agents used in high-performance epoxy systems, chiefly for electronics encapsulation and industrial floorings demanding enhanced chemical resistance. Controlled addition allows for precise tuning of crosslink density and thermal profile to match application demands across electronics, coatings, and adhesives.

    Industry compliance standards

    • UL 94 Flammability Testing for Plastic Materials
    • RoHS Directive (2011/65/EU, Recast)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • IEC 61249-2-21 guidelines for halogen-free laminates (if applicable)

    Typical usage ratio

    • 2–8% by total hardener mass, with the actual loading determined via DSC analysis for targeted glass transition temperature and viscosity specs

    Downstream process integration

    • Introduced at the pre-polymerization resin mixing stage, enabling pre-reaction with epoxide groups before solvent stripping and final compounding with fillers and pigments

    Final product types

    • Electronics-grade casting compounds
    • Industrial epoxy grout and floor systems
    • Electrical insulation laminates

    3. Intermediate for Specialty Dyes and Pigments Synthesis

    Producers of aryl-based dyes and pigment intermediates utilize this chemical primarily during the synthesis of azo and anthraquinone derivatives, which impart deep, stable coloration required by textile and plastics manufacturers. Its aromatic amine structure acts as a nucleophilic donor, allowing precise diazotization and coupling essential for color vibrancy and fastness specs.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • REACH Annex XVII (restrictions on aromatic amines in dyes)
    • ISO 105 Series for color fastness
    • Eco-Passport certification for pigment intermediates

    Typical usage ratio

    • 0.5–1.2 equivalents per mole of diazotization substrate, calculated based on desired chromophore depth and shade intensity

    Downstream process integration

    • Added at the diazotization reactor inlet, with pH and temperature tightly controlled; subsequently coupled with aromatic acids or phenols in agitated vessels to yield crude dye intermediates

    Final product types

    • Reactive pigment dispersions for plastics
    • Textile dye intermediates
    • High-stability printing ink bases

    4. Stabilizer and Modifier in High-Refractive Index Polymeric Materials

    Manufacturers engineering polymers for optical devices, instrument housings, and certain thermoset applications employ this salt to adjust core aromaticity and facilitate post-polymerization stability. Its inclusion modifies polymer chain structure, which positively impacts clarity and refractive characteristics needed in lenses, display substrates, and photonic modules.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • RoHS Directive (baseline for electronics applications)
    • IEC 60068 (Environmental Testing, for polymer end-use validation)
    • SPI Resin Identification Coding System (where applicable)

    Typical usage ratio

    • 0.3–2.0 wt% based on total monomer content, set by optical clarity and mechanical performance test data

    Downstream process integration

    • Metered into the monomer blend prior to initiation, often in batch or continuous stirred-tank reactors. Incorporated during the pre-polymerization stage to ensure full distribution throughout the polymer matrix.

    Final product types

    • High-index lens-grade polymers
    • Light guide substrates for display panels
    • Durable transparent housings for optical sensors

    5. Building Block in Custom Fine Chemical Synthesis

    Custom fine chemical and contract synthesis laboratories leverage this compound as a reagent for the development of advanced aromatic frameworks. It supports research and development projects where unique substitution patterns are needed for agrochemical screening, photoinitiators, or organic semiconductors. Its hydrochloride form ensures straightforward handling during all scales of reaction development.

    Industry compliance standards

    • ISO 17025 Accreditation for testing laboratories (relevant for traceability)
    • Internal cGMP practices (for regulated R&D environments)
    • Local environmental and safety legislation (for hazardous materials handling)
    • Company-specific confidentiality and material authentication guidelines

    Typical usage ratio

    • Variable, typically introduced as 0.5–2.0 equivalents relative to the coupling or substitution reactant, defined by synthetic pathway design and yield optimization studies

    Downstream process integration

    • Introduced at the controlled addition stage in batch or continuous synthetic runs, commonly followed by in situ deprotonation and coupling under monitored temperatures and inert atmosphere

    Final product types

    • Specialty benzenoid structures for research
    • Test batches of candidate agrochemicals
    • Prototype material sets for organic electronics
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    Certification & Compliance
    More Introduction

    4-(Phenylmethyl)Benzenamine Hydrochloride: Insights from the Production Line

    What Makes Our 4-(Phenylmethyl)Benzenamine Hydrochloride Stand Apart

    Working every day with aromatic amines, our team in production has watched 4-(Phenylmethyl)Benzenamine Hydrochloride take on a unique role in the broader landscape of specialty chemicals. The chemistry of this compound, known across industries by its molecular structure C13H14ClN, sets it apart from common amines. The addition of hydrochloride not only offers improved stability and solubility, it creates a material that consistently delivers in controlled reactions—something both synthetic chemists and formulators respect. By investing in tight environmental controls and high-grade raw material sourcing, we keep batch variations in check, which matters when customers need exactly the same performance in every shipment.

    The hydrochloride salt version of 4-(Phenylmethyl)Benzenamine brings an edge for applications where moisture sensitivity or reactivity must stay precise. The crystalline powder’s clean profile supports work in pharmaceutical research, dye intermediates, and certain fine chemical syntheses demanding minimal contamination. Free amine forms sometimes struggle with air stability and shelf life, often turning unreliable during handling or long-term storage. Acidification to the hydrochloride addresses these issues while making isolation from solvents straightforward. Consistency, in our experience, always starts with chemistry that holds its shape and purity in the real world.

    From Bench to Batch: Manufacturing Know-How

    Producing 4-(Phenylmethyl)Benzenamine Hydrochloride starts with the right grade of raw benzyl compounds. In our reactors, we keep a close eye on stoichiometry and reaction kinetics to drive clean conversion of the starting amines. Impurities like over-alkylated byproducts or polymeric residues can compromise a lot, so we run frequent intermediate sampling as the batch progresses. Our filtration and crystal isolation steps matter just as much as the core synthesis. Decades of hands-on production show that even minor adjustments in temperature profiles or solvent selection can have a noticeable effect on the final product’s particle size, flowability, and dusting tendency.

    Hydrochloride crystallization gives an additional layer of assurance for isolating the desired compound. By controlling rate of acid addition and temperature, we avoid agglomerates and secondary crystal forms. The handling expertise that comes from seeing thousands of kilograms pass through our dryers translates to fewer blockages in customer feeders and smoother downstream processing for those running continuous operations. While specifications may talk about “assay” and “loss on drying,” what truly allows applications to scale seamlessly are those production touches honed through repetition and learning from real-world feedback.

    Use Cases from the Factory Floor

    We first noticed toxicologists and medicinal chemists seeking 4-(Phenylmethyl)Benzenamine Hydrochloride as a starting point for more elaborate syntheses a decade ago. The amine group’s willingness to accept further functionalization means research labs can quickly generate new analogs for screening. Our earliest pharmaceutical partners pointed out that batch-to-batch purity swings in the base form amine increased their purification burden. By delivering a well-characterized hydrochloride with low metal content and controlled residual solvents, we helped cut one more headache out of their workflow.

    Beyond lab discovery, this compound shows up in dye and pigment production. Its benzyl-substituted aromatic structure brings specific reactivity in azo-coupling and, under certain conditions, generates intermediates suited for high-performance colorants. In these reactions, unwanted side products mean more separation steps and more lost yield. Customers with continuous dye synthesis told us that powders prone to clumping or unpredictable melting could lead to expensive downtime. Fine-tuned crystal engineering at our site has lowered these risks, cutting unplanned stops and letting operators keep lines running longer.

    We also hear from those in polymer modification and specialty resins who need predictably active aromatic amines for curing or crosslinking. The hydrochloride serves as a smart way to keep the amine protected until the exact step when reaction must occur. While free bases may volatilize or oxidize, the salt delivers a steady level of available amine, improving process control on high-throughput lines. These process engineers, through trial and feedback, have helped us understand how particulate features—such as bulk density or particle surface area—impact dispersion and mix times. We now inspect every lot for these properties, not just the chemical “numbers,” to make sure nothing gets in the way of customer throughput.

    Distinctions from Related Aromatic Amines

    In laboratories and bulk plants alike, choices abound for aromatic amines. Aniline, toluidines, and phenylethylamines all compete in the fine chemical toolbox. Yet none match the specific molecular geometry or reactivity of 4-(Phenylmethyl)Benzenamine Hydrochloride. Placement of the benzyl group at the para position—rather than ortho or meta—lead to differences in both chemical selectivity and safety profile. Chemists who need a balance between electron-donating behavior and steric access often gravitate to this structure over more congested or electron-rich alternatives.

    Standard anilines may cost less but bring trade-offs in byproduct formation, sensitivity to oxidants, and overall yield in multi-step synthesis. We’ve tracked how even subtle impurities or positional isomers in competing products show up as performance drags downstream. Direct feedback from our partners tells us these issues can derail timelines or force repeated purification steps—neither one popular with project managers. As a manufacturer, we design our inspection regimes to catch all known isomers and related impurities, leaning into proven analytical methods. We stake our name on every drum that leaves the dock, because reputational hits from quality failures never fade quickly.

    For industries using hydrochloride salts, issues like caking, hygroscopicity, or unexpected color changes can downgrade a shipment or frustrate production schedules. Over years, we have adjusted dryers, improved air handling, and tweaked packaging to withstand a range of storage conditions. Keeping water activity and color indices steady across multiple months or during cross-ocean transit takes granular control in the plant, not just a line on a certificate. Competitors working with legacy plant setups or commodity supply chains can’t always offer those assurances.

    Supporting Innovation and Compliance

    Manufacturers face increasing documentation and regulatory scrutiny for aromatic amines. Traceability of every input and recordkeeping at every step shapes not just good business but legal compliance. We respond by keeping digitized logs of all intermediate QC, feeding our ERP system directly from the lab benches. Stability data, impurity profiles, and every point of batch genealogy form an audit trail that stands up to both partner requests and global regulatory reviews. Auditors who walk our floor look for more than paperwork—they look for line of sight from handling bays to analytical equipment.

    Research partners working on pharmaceuticals or materials often attach their own analytical criteria to compounds like 4-(Phenylmethyl)Benzenamine Hydrochloride. Meeting these asks, across jurisdictions, only works if the production cycle starts with process discipline. Since suppliers sometimes blend across lots or supplement with off-spec stocks, we have focused on single-origin batch accountability. Each drum tells a unified story from raw material approval through finished inspection, giving researchers a clearer shot at reproducible outcomes.

    Customers with early-phase discoveries or complex formulations often reach for additional documentation—NMR spectra, GC-MS traces, residual solvent listings, and more. Providing this package lets our OEM and pharma collaborators leapfrog upstream qualification hurdles. Developing the compound portfolio in-house, instead of through intermediaries, lets us adapt and respond to shifting compliance frameworks faster than vertically fragmented supply pipelines.

    Final Thoughts on Market Trends and Customer Demands

    Interest in aromatic amines, particularly hydrochloride salts, keeps expanding. Demand cycles for intermediates like 4-(Phenylmethyl)Benzenamine Hydrochloride ride waves of pharmaceutical R&D, pigment innovation, and specialty monomer launches. None of these fields see success with unpredictable feedstocks or spotty supply. Tightening acceptance specs, rising sustainability demands, and advanced analytics have made old habits around variable production more and more risky, and less profitable in the long run.

    We have invested in greener process improvements, solvent recovery, and energy conservation to supply not just reliable material but also compliance with evolving global standards. As buyers shift toward supply chains that pass detailed, third-party audits, we have responded by offering transparent, site-inspected process stewardship as part of every delivery.

    Sometimes the market encounters unexpected events—a regulatory recall here, a disruption in sourcing elsewhere. Those who depend on aromatic amine intermediates look to established manufacturers for assurance. Our warehouse team, shipping department, and analytical chemists work side by side, knowing that gaps in this chain mean lost opportunities downstream. By holding inventory for just-in-time delivery, keeping alternate raw material sources vetted, and running redundant QA, we stay responsive to market swings without offering unsubstantiated promises.

    As more applications emerge for specialty amines with consistent purity and reactivity, the lessons learned on our floor shape every kilogram shipped. Customers focused on synthesis efficiencies, reduced waste, or shortened project cycles find value not just in the base chemical but in the experience, traceability, and stability that come with each batch. We approach 4-(Phenylmethyl)Benzenamine Hydrochloride not just as a molecule for sale but as a partnership built on daily practice, operational discipline, and candid feedback. Those shared standards drive stronger outcomes, less troubleshooting, and more innovation up and down the value chain.