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HS Code |
738618 |
| Chemical Name | 4-Phenylbenzylamine |
| Cas Number | 1644-98-8 |
| Molecular Formula | C13H13N |
| Molecular Weight | 183.25 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 60-62°C |
| Boiling Point | 349.3°C at 760 mmHg |
| Density | 1.09 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 4-Benzyl aniline, 4-(Phenylmethyl)aniline |
| Smiles | c1ccc(cc1)CC2=CC=C(C=C2)N |
| Inchikey | QULJYFZANNAZMJ-UHFFFAOYSA-N |
As an accredited 4-Phenylbenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 25g of 4-Phenylbenzylamine is an amber glass bottle with a secure screw cap, labeled with safety and chemical details. |
| Shipping | 4-Phenylbenzylamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with chemical safety regulations, with clear hazard labeling. Transport follows standard procedures for organic amines, typically via ground or air freight, ensuring temperature stability and minimization of physical damage or contamination during transit. |
| Storage | 4-Phenylbenzylamine should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area, separate from oxidizing agents, acids, and strong bases. Ensure the storage area is equipped to contain spills and properly labeled. Use appropriate personal protective equipment when handling the chemical. |
Applications of 4-Phenylbenzylamine in Industrial ManufacturingAs the original manufacturer of 4-Phenylbenzylamine, we supply this specialty amine to advanced sectors where high-purity aromatic amines support critical undertakings in pharmaceutical synthesis, organic pigment manufacture, crop protection chemistry, and specialty polymer production. Below, we outline the definitive downstream markets confirming sustained, regulated processing demand, focusing on exact technical requirements to guide industrial formulators and process integrators. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisOur 4-Phenylbenzylamine enables precise selective amination during the construction of complex pharmaceutical intermediates and final APIs, particularly in the synthesis of antihypertensive, antipsychotic, and anticancer drug core scaffolds. The amine’s benzylphenyl backbone takes part in directed aromatic substitutions and reductive aminations to achieve high-purity molecular targets under GMP-compliant conditions, supporting validated downstream drug manufacturing flows. Industry compliance standards
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2. Raw Material for Organic Pigment and Dye ManufactureThis aromatic amine participates directly in azo coupling and condensation reactions in the colorants sector, enabling high-tint-strength and purity in pigments used by plastics, coatings, and textile dyeing downstream partners. Carefully controlled incorporation during diazotization and subsequent pigment modifications allows for custom hue development that matches high-end industrial standards for fastness and dispersion. Industry compliance standards
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3. Precursor in Agrochemical Synthesis (Plant Protection Products)Utilized for the N-alkylation and construction of selective herbicide and fungicide active agents, our 4-Phenylbenzylamine supports the formation of aromatic-amino scaffolds that confer crop protection selectivity. Its entry at the step where nitrogen introduction determines biological activity ensures compliance with stringent residue and formulation controls, promoting downstream synthesis repeatability and targeted field performance. Industry compliance standards
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4. Chain Modifier in Specialty Polyamide and Polymer ProductionOur 4-Phenylbenzylamine introduces desired aromaticity and chain termination functionality into bespoke polyamide and epoxy resins for advanced engineering plastics. Its integration either as a co-monomer or as a chain stopper allows for deliberate modulation of molecular weight, rigidity, and thermal resistance, facilitating application-specific resin properties demanded in electrical enclosures, automotive parts, and structural composites. Industry compliance standards
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5. Chiral Ligand Synthesis for Asymmetric CatalysisWithin the field of industrial catalysis, 4-Phenylbenzylamine serves as a building block for chiral ligand production, which supports large-scale enantioselective processes—especially in fine chemicals and pharma. The orthogonally substituted amine delivers steric and electronic properties crucial for ligand-catalyst assembly, driving asymmetric hydrogenation, reduction, and carbon–nitrogen coupling in enantio-enriched downstream intermediate manufacture. Industry compliance standards
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Having manufactured aromatic amines for decades, we know the important role each building block plays on the production floor. 4-Phenylbenzylamine (CAS No. 3970-43-2) stands out for us due to its unique structure: a benzylamine backbone capped with a para-phenyl ring. This molecular arrangement delivers a thoughtful balance between reactivity and stability, which most other benzylamines don’t manage to combine in quite the same way.
Our technicians have grown accustomed to 4-Phenylbenzylamine’s pale yellow to off-white crystalline form, which consistently signals that the batch meets production targets for purity—an aspect we rigorously track because downstream chemistry depends on it. The minimum assay for our offered batches rarely drops below 99%, with moisture and impurity controls validated batch after batch using in-house HPLC and NMR facilities.
Unlike generic benzylamines, this compound’s additional aromatic ring keeps the amine group distanced from the main hydrocarbon scaffold. Through countless hours at the bench, we observe that this specific geometry reduces excessive side reactions during reductive aminations, condensing a reaction schedule that sometimes stretches across shifts using other similar amines.
On the floor, operators value the powder’s pourability and the absence of clumping or static, even after weeks in sealed drums. Such details may sound routine, but process consistency saves man-hours and keeps workspaces safer for teams handling larger cargos.
Across multiple projects, customers working in pharmaceutical discovery come to us for 4-Phenylbenzylamine when synthesizing diarylmethylamine scaffolds—common intermediates for antihistamines, antipsychotic medications, and some kinase inhibitors. Chemists find that the product’s amine reactivity lets them insert the fragment directly onto activated esters or as a nucleophile for Suzuki–Miyaura and Buchwald amination reactions.
4-Phenylbenzylamine could look similar to benzylamine or 4-methylbenzylamine on paper, but the extra ring changes how it performs. In the labs where our teams provide application assistance, medicinal chemists discover better yields when tailoring electron density of final molecules—thanks to this compound’s para-phenyl unit. This translates into fewer byproducts and less purification headaches, which is especially useful for teams with tight budgets and small-batch timelines.
Besides pharma, the material side of our business pulls 4-Phenylbenzylamine for specialty polymer synthesis. Custom polymers and resins gain rigidity when manufacturers choose this compound as a curing agent or chain extender. For example, in polyamide-imide or epoxide networks, the extra aromatic system not only boosts glass transition temperatures but also dampens unwanted chain mobility better than simpler amines do.
Clients working in coatings and adhesives bring us feedback on thermal cycling performance between aromatic diamines: 4-Phenylbenzylamine consistently outperforms benzylamines and toluidines for hardness and weather resistance. Field failures and product returns drop noticeably when we switch them to this grade, as the reinforced aromaticity fights off premature breakdown from UV and oxidation.
Repeated investment in reactor configuration and purification strategy sets our product apart. Our staff run each batch past a multi-stage recrystallization line, while washing protocols target trace isomers and byproducts from the Friedel-Crafts and reduction steps. For every hundred kilograms, we dedicate an entire shift to slow temperature ramp-down, controlling crystal morphology that regular distillation skips over.
This goes back to customer complaints from years ago, when inconsistent morphology led to charged particle buildup in equipment hoppers. Since retooling our drying and sieving, these problems dwindle, and now we supply far larger producers in pharmaceutical chemistry, electronics, and custom material synthesis.
Chemically, many lower-cost amines produce intermediate results for basic reactions, but side-by-side testing reveals limitations. For instance, classical benzylamines tend to introduce uncontrolled reaction rates in multi-step synthesis. These instabilities show up as unwanted side chains, variable coloring in final APIs or resins, and contamination that fails downstream quality checks. Reprocessing costs stack up quickly. Our teams have witnessed reduction in time spent troubleshooting unexpected UV-active impurities, and post-synthesis purification yields climb when switching to 4-Phenylbenzylamine.
This particular amine combines the amine group’s nucleophilicity with a tunable electron environment, giving formulation scientists more control. The para-phenyl group absorbs excess reactivity, acting almost like a chemical “buffer” during multi-step assembly. By extension, many of our partners now rely less on excess use of purification solvents, reducing both environmental load and material costs.
Production staff handle numerous amines side-by-side—an experience that shapes our opinions more than any data sheet. 4-Phenylbenzylamine stands out for its stability in long-term storage. Routine temperature cycling between 15–30°C doesn’t yellow the crystals or degrade odor, compared to other aromatic amines like anilines or toluidines. Batches left open too long (our internal policy frowns on that, but lapses happen) remain pourable, not forming sticky clumps as seen with more hygroscopic analogs.
Beyond storage, we see a more predictable melting point—around 70–72°C—eliminating the guesswork during phase transition calculations. Lab techs note that lower-melting competitor amines force riskier handling, with increased losses from sublimation, corrosion to stainless steel drums, or accidental spills. Over years, these seemingly small improvements prevent stock losses and chemical incompatibilities.
Factory teams appreciate that 4-Phenylbenzylamine’s vapor pressure remains low at room temperature, so health risks lessen compared to more volatile aliphatic or mono-aromatic amines. We’ve built up clear air monitoring records over time to back up this claim. Still, as a primary amine, the material carries some risk of irritation to skin and mucosa, calling for regular PPE and exhaust setups. Our training focuses on safe drum charging, accurate weighing, and high-frequency surface wipe-downs, which nearly eliminates exposure incidents.
We also run annual risk reviews on storage stability. The crystals handle heat-cycling and drum transfer with few surprises, minimizing workplace disruption and cross-contamination risks. The absence of peroxides or reactive byproducts in properly stored product means warehouse staff can trust in the stability over multiple quarters.
Having seen environmental restrictions tighten across regions, our approach to solvent recovery and waste minimization has evolved. Unlike some cheaper amines that leave behind colored tars or hard-to-treat halogenated waste, 4-Phenylbenzylamine responds well to water washing and steam stripping of off-spec material. Waste water from our lines shows much lower COD and fewer problematic extractives, supporting easier regulatory audits and smoother site licensing.
Process engineers have retooled reactor cleaning protocols, reducing aggressive mineral acid washes after campaigns involving this intermediate. The net result: less material cost for cleaning agents, fewer corrosive discharges, and simplified neutralization routines in the plant effluent system. The compound’s clean breakdown in high-temperature waste incineration matches regulatory expectations for low-chloride, low-nitrogen emissions—important for facilities operating near population centers.
Having lived through many market cycles, we know the difficulties customers face with fluctuating supply and raw material purity. Sourcing to match one-off lab use or scaling up to multi-ton annual demand both depend on a stable, responsive supply line. Our facility monitors each upstream batch of precursor benzaldehydes and aniline derivatives for trace contamination, which other chains may overlook or disregard until problems arise at scale.
Times of global shipping crisis taught us to build reserve inventories and reinforce QA procedures. 4-Phenylbenzylamine stores efficiently without refrigeration, so we maintain buffer stocks ready to ship, reducing customer wait times after spikes in demand. Contract buyers from research centers and major industry groups rely on our turnaround speed, especially during pilot-to-commercial transitions in new drug synthesis.
Following generations of technical staff through the plant, our company culture centers on practical results over mere specification compliance. The cumulative wisdom leads to choices in batch coding, traceability, cleaning step validation, and structured testing beyond industry minimums. For example, we provide user-accessible COA documentation that includes impurity profiling, ensuring transparency for chemists troubleshooting rare reactions or scale-up issues.
Our facilities maintain auditable records for every shipment of 4-Phenylbenzylamine, reflecting years of audit feedback from both international and domestic regulatory assessments. Regular staff training lets us anticipate quality bottlenecks and maintain product reliability even as plant technologies advance and regulatory targets evolve.
Many industry scientists have built new intellectual property on the back of 4-Phenylbenzylamine chemistry. From high-value intermediates in cutting-edge therapies to next-generation adhesives and dielectric coatings, the versatility of this compound enables progress that generic benzylamines struggle to match. Whether it’s scaling a novel cross-coupling route or optimizing a new polymer backbone, the combination of chemical stability, easy work-up, and reliable reaction yields reinforces its place in the synthetic toolkit.
Direct relationships with R&D groups help us refine material purity and adapt packaging—examples include dust-free, small-volume bottles for glovebox work as well as sturdy drum-liners for automated bulk transfer. Each year, feedback from working chemists pushes us to raise quality standards and expand support, because incremental gains in reliability reduce risk and open new application spaces.
The story of 4-Phenylbenzylamine in our manufacturing landscape reinforces how technical depth and continuous improvement define value. From raw material traceability to multi-step synthesis support, our commitment comes from firsthand problem-solving and listening to process chemists, operators, and industry partners. Every drum reflects years of learning and collaboration, giving real-world reliability that supports both legacy manufacturing and next-generation research.
Unlike catalogue chemicals that trade on spot price or bulk scale alone, our 4-Phenylbenzylamine stands as the outcome of practical refinement, batch-to-batch consistency, and safety experience built by people who handle these materials daily. Sourcing decisions benefit from this technical depth, whether for one-off trials or high-volume production. Each delivery reflects not just a product specification, but a promise from manufacturer to user, rooted in chemical know-how and real-world accountability.