|
HS Code |
621161 |
| ChemicalName | 4-Aminobiphenyl |
| CASNumber | 92-67-1 |
| MolecularFormula | C12H11N |
| MolecularWeight | 169.23 g/mol |
| Appearance | Pale yellow crystals or flakes |
| MeltingPoint | 53-55 °C |
| BoilingPoint | 302 °C |
| Density | 1.18 g/cm³ |
| SolubilityInWater | Insoluble |
| FlashPoint | 170 °C |
| VaporPressure | 0.00008 mmHg (25 °C) |
| Odor | Amine-like |
| PubChemCID | 5800 |
As an accredited 4-Aminobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled "4-Aminobiphenyl," featuring hazard symbols, batch number, CAS 92-67-1, and safety precautions. |
| Shipping | **4-Aminobiphenyl** is shipped as a hazardous chemical under strict regulations. It must be packaged in sealed, labeled containers resistant to leaks, with secondary containment to prevent spills. Shipping follows UN 1549 guidelines for toxic solids, with clear hazard labeling and documentation. Only authorized carriers and handlers are permitted. |
| Storage | 4-Aminobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. It must be kept away from direct sunlight and protected from moisture. Use appropriate safety containment (e.g., chemical fume hood) due to its toxic and carcinogenic nature. |
Applications of 4-Aminobiphenyl in Industrial Manufacturing4-Aminobiphenyl is used in several highly controlled industrial settings as an intermediate for specialty synthesis. The following established downstream sectors employ this material in distinct formulations and production environments, each operating under strict technical and regulatory controls. 1. Industrial Dye and Pigment SynthesisThis compound serves as a critical intermediate for manufacturing certain azo dyes and pigments with high thermal stability and specific colorfastness attributes. Producers incorporate it through a diazotization or coupling stage to generate colorants for plastics, fiber, and specialty coatings where alternative aromatic amines do not meet required chromatism or performance benchmarks. Its use remains subject to restricted approvals in developed markets, often limited to legacy processes for industrial-grade products requiring technical color standards beyond mainstream alternatives. Industry compliance standards
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2. Specialty Polymer Additive ManufacturingChemical processors utilize this material for tailored synthesis of specific polyamides and functionalized copolymers where controlled aromatic amine incorporation improves UV resistance, melting point, or mechanical integrity. These niche polymers service select engineering applications, particularly where downstream use benefits from the biphenyl motif for performance in demanding thermal or chemical environments. All usage operates under stringent toxicological control, limited to regulated workplace settings. Industry compliance standards
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3. Research & Development of Carcinogenicity Test StandardsRegulatory laboratories and contract research organizations apply this compound as a controlled positive control in long-term animal carcinogenicity testing and standardization of laboratory detection procedures. Only licensed facilities with robust safety infrastructure can handle the material; worker exposure, waste management, and analytical protocols comply with advanced chemical safety requirements. The primary purpose is calibration, method validation, and protocol harmonization for occupational health and environmental analysis. Industry compliance standards
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4. Analytical Reagent Synthesis for Environmental MonitoringThis compound is required for the preparation of certified reference materials used in calibration of GC-MS and HPLC methods for trace aromatic amine detection in environmental, occupational, and public health surveillance. Government and industrial laboratories need traceable, high-purity batches to guarantee method consistency and regulatory compliance. Handling, storage, and waste protocols require full traceability and are subject to national poison control standards. Industry compliance standards
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Years on the plant floor and working through countless reaction batches give a different perspective compared to catalog descriptions. 4-Aminobiphenyl, with its molecular structure C12H11N, remains one of the more challenging aromatic amines to produce and handle. The backbone combines two phenyl rings, joined by a single bond, and introduces an amino group at the 4-position. It’s that slight shift of the amino group that changes both reactivity and industrial utility compared to its more benign relatives.
The chemical structure alone tells only part of the story. In the plant, purity, particle size, and free-flowing character all matter for downstream applications. In reality, preparing material within tight specification bands involves close attention to reactor temperature, stirring rates, and vigilant purification. Straight from the reaction kettle, crude product never meets the mark. Over years, we’ve worked up purification pathways that consistently deliver a product with assay levels above 98%. Moisture is a sensitive issue; too much and you see caking, too little and static can cause dust hazards. Controls on residual solvents have to be strict – both for downstream process compatibility and regulatory compliance. Lot-to-lot reproducibility never happens by accident; it’s earned by monitoring every batch parameter, even when data loggers suggest conditions look “routine.”
Aromatic amines as a family show up across many sectors, but 4-aminobiphenyl holds a specific niche. Research labs, especially in toxicology and carcinogenesis studies, have long relied on the compound as a reference. Regulatory agencies have flagged it as a marker for workplace exposure. Nobody in manufacturing can ignore its historical ties to dye production, especially before the rise of alternatives with improved safety margins. There is still occasional demand in specialty synthesis, from authenticating analytical standards to preparing complex organic molecules for reference collections.
Chemical manufacturers see first-hand why 4-aminobiphenyl stands apart from relatives like aniline or o-toluidine. Structurally similar amines might serve as intermediates for agricultural products, rubber chemicals, or pharmaceuticals — but 4-aminobiphenyl draws demand where specific aromatic positioning matters. Its selectivity for coupling reactions stems from the backbone: the two phenyl rings provide a rigid, planar core, while the para-amino group imparts predictable reactivity with diazonium compounds and acyl chlorides. Such features can’t be swapped out by simpler or smaller analogues without changing the outcome.
Users sometimes forget that subtle tweaks in structure mean large shifts in application. For example, 2-aminobiphenyl or 2-naphthylamine often seem interchangeable in written procedures, but the kinetic profiles for diazotization or electrophilic aromatic substitution diverge significantly. Only 4-aminobiphenyl’s configuration yields certain azo dye colors or particular metabolic intermediates in biological systems. Those reactions — whether they happen in a beaker or inside a liver cell — depend on the arrangement of atoms, not just the presence of an amino group.
Few substances highlight the importance of proper safety and stewardship quite like 4-aminobiphenyl. While its uses sometimes live in the shadow of past industrial incidents, today’s manufacturing site takes every step to minimize risks. Production takes place in closed systems fitted with scrubbers and redundant containment barriers. Direct handling uses gloveboxes or sealed transfer lines. Staff receive up-to-date safety training every year, and real-time air monitoring tracks fugitive emissions near workstations. We also maintain strict documentation of all shipments and waste movements, not only to satisfy regulatory bodies but to support traceability from raw input to final container label.
Shipping regulations treat 4-aminobiphenyl as a high-concern material, so shipments move under dedicated hazmat protocols. Secure packaging, tamper-proof drums, and pre-arranged delivery routes form the backbone of our logistics. Clients sometimes ask whether these controls add unnecessary overhead, and from the manufacturing perspective, the additional effort pays for itself through avoided incidents and continued license to operate. Documentation and compliance never become afterthoughts; they shape operations from the reactor design up to the outgoing pallet.
Customers expect clear, reproducible specifications. We produce 4-aminobiphenyl with a minimum assay of 98%, routinely confirming absence of key impurities by HPLC and GC-MS. Each lot comes with a certificate analytics panel showing water content, residue on ignition, and spectrophotometric analysis. During production, we monitor intermediate quality at every stage: crude melt point, color before granulation, rate of filtration, and even the odor profile. Attention to these details means our product avoids issues like off-standard color or persistent background fluorescence, problems that often emerge in competitors’ lots made through shortcut processes.
Grain size can influence performance during blending or further derivatization. We use proprietary sieving and drying controls to keep the mean particle diameter in a tight window, making for predictable dissolution or reactivity in large-scale downstream syntheses. For customers in organic pigment research or toxicological assay, uniformity in physical properties enables more reliable validation data. Our experience shows that cuts in process control quickly lead to irregular behavior during end-use, so we allocate extra time and resources to get consistency right from the outset.
Market newcomers sometimes lump 4-aminobiphenyl with other primary amines, assuming interchangeability based on broad chemical classification. Real-world processes prove the opposite. The molecular rigidity of the biphenyl core makes 4-aminobiphenyl less prone to oxidation than aniline or p-phenylenediamine under comparable conditions. That decreased reactivity can benefit manufacturers seeking shelf-stable intermediates for carefully timed coupling reactions, especially in anhydrous environments.
In analytical chemistry, the spectral fingerprint of 4-aminobiphenyl offers advantages for trace analysis. Its UV-visible absorption peaks and mass spectral fragmentation pattern deliver clearer signal separation from background impurities compared to mono-cyclic or alkyl-substituted analogues. End-users report improved sensitivity in methods designed for biomonitoring or environmental sample validation. As a manufacturer, tracking how our customers implement the product feeds back into refining our process, whether that means improving batch reproducibility or designing better packaging to minimize contamination.
Some clients evaluate alternatives such as 2-aminobiphenyl or benzanilide, hoping to address safety considerations. Our experience reveals that downstream reactions often sacrifice yield or generate harder-to-purify mixtures by substituting even a single atom in the aromatic framework. Consistency arises not just from high assay, but from repeating the precise context that chemists and toxicologists expect. Robust control of isomeric purity, and accurate analytical data supporting it, has become non-negotiable for rigorous applications.
Producing 4-aminobiphenyl safely at scale requires respect for both chemistry and practical hazards. The reduction of 4-nitrobiphenyl to the target amine involves exothermic steps, and the risk of over-reduction or side reactions rises sharply without temperature discipline. Operators work with double-walled reactors and continuous monitoring, because letting a batch overheat leads to degraded product and cleanup headaches. After reaction, filtration, drying, and purification take place in inerted atmospheres to cut down airborne dispersal – not just for occupational safety, but to avoid product loss and preserve quality.
Waste management also draws attention. A big push came in the past decade to lower total waste volume and improve catalyst recovery, which feeds back into both environmental responsibility and bottom-line economics. Workers here study the effluent stream just as closely as they monitor process yields, since small tweaks in neutralization protocols often yield big gains in regulatory compliance and cost control. For shipments outside our region, coordinating properly vetted disposal partners proves just as important as the chemistry itself.
We collaborate directly with our up- and downstream neighbors in the value chain — whether that means waste processors, safety consultants, or application scientists. This connection allows us to anticipate regulatory trends and adoption of safer or greener alternatives. For those building new workflows with 4-aminobiphenyl, consulting with the manufacturer from the outset trims many hidden risks.
The last twenty years brought sweeping changes to both the regulatory landscape and the market perception of 4-aminobiphenyl. Once a staple feedstock for a range of dyes and pigments, its use in bulk production dropped as substitutes with lower toxicological profiles gained market share. More recently, we’ve seen an uptick in small but specialized demand: reference standard supply, analytical calibrators for workplace monitoring, and biochemical assay development.
From a manufacturing standpoint, serving these evolving uses requires adaptability. Instead of vast runs feeding multi-ton dye production, current operations focus on smaller, more controlled campaign batches. This creates supply chains where traceability matters as much as cost per kilogram. Clients increasingly value supplier transparency and environmental compliance as part of their sourcing decisions, and supplier audits reflect this. In our operation, we welcome these visits, since direct engagement often uncovers new opportunities for process improvement or safer work practices.
Markets may shift, but the technical demands never fade. Producers who prioritize consistency and visibility remain best placed to supply end-users who must meet strict regulatory and documentary standards. Rather than framing compliance as a burden, integrating safety, documentation, and customer communication directly into every batch cycle boosts both quality and long-term business stability.
As a regulated substance, 4-aminobiphenyl falls under various international frameworks, including workplace exposure limits, transportation codes, and chemical registration schemes. Over the years, participating in cross-jurisdictional compliance has meant harmonizing internal procedures with REACH, TSCA, and analogous regulations elsewhere. Regular updates in guidance — such as stricter permissible exposure limits or new labeling requirements — push the manufacturing side to invest in better monitoring and upgraded documentation tools.
On the factory floor, this translates into concrete changes: retrofitting ventilation, instituting badge monitoring for all personnel near open processing steps, and investing in real-time environmental detection equipment. These choices reduce risk not only for our staff, but for the communities near our operations and downstream users. Document retention and immediate access to batch-specific metadata ensure that any question posed by auditors or end users receives evidence-based answers.
Our policy steers clear of greenwashing. Instead, we work to provide full disclosure of OELs, waste management metrics, and incident response plans when customers make inquiries. Over time, such transparency builds trust — and that trust in turn supports our continued license to operate in tightly regulated sectors.
In the modern landscape, responsibility does not end at the factory gate. We trace each batch of 4-aminobiphenyl produced, recording inputs, process deviations, and chain-of-custody records from raw material supplier through to final dispatch. Third-party auditors and certification programs add another layer of verification, supplementing our own monitoring.
Occasionally, concerns arise over cross-contamination with other aromatic amines or nitro compounds, especially where multistep syntheses run side-by-side. We respond with validated cleaning protocols, separated production lines, and periodic environmental swabbing, ensuring our materials live up to analytical scrutiny. For sensitive clients – especially those in the forensic or environmental monitoring sectors – we provide detailed chain-of-custody dossiers and supplier affidavits on request.
Direct dialogue drives process improvement. By listening to researchers, formulators, and QA leads from client organizations, we adapt packaging sizes, refine drying procedures, and adjust campaign scheduling to support just-in-time manufacturing practices. No third-party distributor filters this feedback: as a producer, we get the best learning by talking straight to the people who rely on our 4-aminobiphenyl every day.
Innovation in this sector finds its pace not in radical changes but in incremental improvements. We monitor developments in catalysis, new purification media, and advanced analytical instrumentation, taking lessons from the broader field and folding them back into the 4-aminobiphenyl process. For instance, recent advances in solvent swap-out and energy recovery lowered our carbon footprint per kilogram supplied, while updated containment technology further reduced direct worker exposure risk.
On the research side, demand remains from labs developing new analytical methods. Each tweak in the regulatory framework drives analytical labs to demand tighter-purity standards, more reliable reference data, or completely traceable lot documentation. The role of the manufacturer in this context is more than passive supplier — we partner with method developers, offering material that meets their growing exactness requirements.
Many industries move toward “greener” chemistries and safer alternatives, but the need for authentic reference compounds in toxicological and environmental research still drives demand for classic 4-aminobiphenyl, particularly in the context of legacy pollutant monitoring. Our plant invests the necessary care to supply both the product and the associated compliance supports.
4-Aminobiphenyl, with all its handling challenges and historical footprint, remains a compound that demands respect across its lifecycle. No shortcuts exist, whether producing, testing, packaging, or delivering this chemical. Consistent quality, direct dialogue with end users, and a willingness to meet evolving standards form the basis of responsible manufacturing in this sector. The lessons learned from years of hands-on production guide us not just to meet specifications, but to anticipate how the product and its management can best serve those who require certainty in every vial and drum they open.