|
HS Code |
938613 |
| Cas Number | 90-41-5 |
| Iupac Name | 2-Aminobiphenyl |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.23 g/mol |
| Appearance | Off-white to light brown crystalline solid |
| Melting Point | 54-56 °C |
| Boiling Point | 305 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.18 g/cm³ |
| Flash Point | 174 °C |
| Pubchem Cid | 7512 |
| Un Number | UN 2671 |
| Synonyms | o-Aminobiphenyl, 2-Phenylaniline |
As an accredited 2-Aminobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Aminobiphenyl, 25g, is supplied in a sealed amber glass bottle with a secure screw cap and safety labeling. |
| Shipping | 2-Aminobiphenyl should be shipped in tightly sealed containers, clearly labeled, and packaged according to hazardous chemical transport regulations. It must be kept away from ignition sources and incompatible materials. Handling should comply with UN 2671 and relevant local, national, and international transport guidelines, specifying its classification as a toxic substance. |
| Storage | 2-Aminobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. It should be clearly labeled and kept in a designated poison or hazardous materials cabinet, with access limited to trained personnel due to its toxic and potentially carcinogenic properties. |
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Purity 99%: 2-Aminobiphenyl with 99% purity is used in pharmaceutical intermediate synthesis, where high purity ensures reduced by-product formation. Melting Point 50°C: 2-Aminobiphenyl with a melting point of 50°C is used in dye formulation, where controlled melting behavior enables precise processing. Particle Size <10 µm: 2-Aminobiphenyl with particle size under 10 µm is used in specialty pigment production, where fine particle size improves color uniformity. Stability Temperature up to 120°C: 2-Aminobiphenyl stable to 120°C is used in polymer modification, where heat resistance maintains chemical integrity. Molecular Weight 169.22 g/mol: 2-Aminobiphenyl with a molecular weight of 169.22 g/mol is used in organic synthesis, where accurate molecular composition aids in reproducible reactions. Viscosity Grade Low: 2-Aminobiphenyl with low viscosity grade is used in coating manufacturing, where improved flow characteristics enhance application consistency. Solubility in Ethanol: 2-Aminobiphenyl soluble in ethanol is used in analytical reagent preparation, where solubility facilitates homogenous mixing. Assay ≥98%: 2-Aminobiphenyl with assay ≥98% is used in research laboratories, where reliable concentration guarantees experiment accuracy. |
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Our journey with 2-Aminobiphenyl began at a time when aromatic amines were seeing a shift in industrial roles. This compound, known by chemists for its role in advanced synthesis work, presents a daily reminder of the responsibilities and technical demands of chemical manufacturing. Many see it on a spreadsheet as a CAS number—133-06-2—yet in our facility, it’s a product shaped by decades of hands-on practice.
We take the solid crystalline form and maintain rigorous controls over its consistency—off-white to pale yellow, crystalline with a faint odor. Production runs have shown that even slight impurities greatly alter downstream application. Every batch goes through central analytical checks for melting point, purity above 99%, and moisture by Karl Fischer titration. No step occurs without direct supervision. Each phase, from solution mixing to crystallization, is handled by experienced staff, not a generic automation sequence. We monitor for byproduct formation, odor contaminants, and oxidation traces, especially since 2-Aminobiphenyl handles sensitive applications. Consistency is not achieved by accident—it’s the outcome of constant adjustment, process optimization, and real-time problem-solving.
Many view 2-Aminobiphenyl within the framework of specialty chemicals. Its structure, with two fused benzene rings split by a single amine group at the 2-position, offers unique reactivity pathways. In the hands of an experienced synthesis chemist, this compound forms building blocks for anti-inflammatory drugs, agricultural protection agents, advanced dyes, and materials for electronics.
Most demand comes from laboratories working at pilot or scale-up levels. Still, the chemical remains important for core research into aromatic amine substitution, cross-coupling reactions, and N-arylation chemistry. We have supported teams developing new OLED materials, where electronic structure tuning relies on biphenyl scaffolds. Our technical staff often assists process engineers in optimizing yields for diazotization or electrophilic substitution on the amino group—these steps require direct interaction with the material, not just theoretical calculations.
Historically, 2-Aminobiphenyl drew attention for other reasons—a handful of early studies cited health risks after improper handling. That record guides modern safety infrastructure. We’ve installed advanced fume extraction, touchless transfer systems, and full-body PPE requirements. These measures did not come from checklists but from lessons learned through regular training and persistent feedback from the shop floor.
Comparisons with other biphenyl derivatives raise an important point: no two batches, even of widely produced compounds, behave exactly alike. 2-Aminobiphenyl distinguishes itself from 4-Aminobiphenyl and substituted biphenyls in several ways. The 2-amino group is ortho to the biphenyl bond, increasing reactivity for directed ortho-metalation and classic Fischer indole synthesis. Substitution at this site matters—certain applications, especially in pharmaceutical intermediates, only accept the 2-isomer because of downstream reactivity or pharmacological pathways. In custom synthesis, positional isomers like 3-aminobiphenyl give different yields, stereochemistry, and side product profiles. Procurement officers from global pharma understand the need for these precise details—downstream synthetic failures often trace to minor impurities or incorrect isomer selection.
4-Aminobiphenyl, for comparison, tends to be less sterically hindered but also offers different electronic properties. Our team has measured differences in nucleophilicity, reaction rate in Buchwald–Hartwig aminations, and side-product distribution. Physical handling is another area. 2-Aminobiphenyl requires careful storage under inert gas to prevent slow discoloration or oxidation, especially in humidity above 60%. By contrast, substituted biphenyls with bulky alkyl or halogen groups often resist oxidation and are less prone to cake in bins—a detail much appreciated by operators during winter humidity changes.
Production-wise, the synthesis demands tight temperature control at each stage. The route starts from biphenyl, proceeds through nitration, then selective reduction. One challenge lies in minimizing over-reduction or ring amination, both of which create hard-to-remove impurities. The sequence has become more efficient with modern catalysts and monitoring by in-process HPLC, yet even now, certain side reactions need manual intervention. Unlike commodity benzene derivatives banked in multi-ton tanks, 2-Aminobiphenyl batches are comparatively short, often micro-managed at every step to minimize waste. Regular checks for iron, copper, and other trace elements remain essential because these catalyze unwanted degradation—lessons learned from early trial errors.
Public and regulatory pressures have narrowed the margin for error. Our facility has responded by introducing closed transfer systems, solvent recycling, and rigorous emission controls. These practices go beyond compliance—they arise from hard experience with volatile organic emissions and the cost of post-production clean-up. Chemical workers taking direct readings and troubleshooting carbon filters have shaped these protocols.
2-Aminobiphenyl’s history gives every operator a personal stake in safety and environmental stewardship. Sensors track amine vapor above workstations, and shift leads monitor the efficacy of containment. Our company has worked with university partners to test less hazardous reduction agents and novel solvent systems. Implementing aqueous phase transfer catalysis, for instance, cut down hazardous waste without impacting final purity—a solution discovered after months of direct comparison with traditional organic reduction runs.
Clients rarely request large-scale volumes of 2-Aminobiphenyl; projects typically need on-demand batches from half a kilo up to tens of kilos. We learned early that strict adherence to schedule and flexible response trump mere bulk availability. Research teams often require customized handling—sometimes they ask for pre-weighed portions in glass bottles under nitrogen, sometimes for syn-proven documentation of isomeric purity. These experiences guide how we pack, label, and ship every lot, according to the real needs in pharmaceutical or material labs working under regulatory scrutiny.
Issues arise frequently from storage—humidity infiltration, temperature excursions, or shelf-life considerations. We offer extended stability data where possible, backing our claims with accelerated aging tests. Some customers request recent COAs promptly for method validation. We address these requests directly, relying on our in-house analytical data rather than third-party assurances. Trust builds over repeated performance, not declarations.
Intellectual property issues sometimes crop up around custom derivatives or application-specific lots. As manufacturers, we focus on the technical feasibility and consistent quality attributes, but we’ve built confidentiality and chain-of-custody practices to match stricter supply-chain transparency demands from international buyers—especially those working with regulated markets.
Challenges multiply as batch sizes move from pilot reactors to mini-plants. Heat management, mixing efficiency, filtration rates—details overlooked in small vessels become major operational bottlenecks. In the last major process overhaul, our team spent months charting yield loss and impurity drift during scaling trials. These efforts prevented latent process safety risks and cut cycle times by hours. Scale-up remains a technical craft, not a copy-paste from engineering handbooks.
Feedback from formulation chemists, especially those working with new drug candidates, led us to fine-tune particle size distributions and residual impurity profiles. Some end-uses, such as in OLEDs and polymer additives, demanded adjusted drying protocols and packaging to limit environmental exposure during the critical transition from storage to final use. Any lapse in handling introduced out-of-spec batches, traceable by UV-Vis or HPLC fingerprinting. Processes now include stepwise verification at critical stages, with manufacturing team leads documenting actions and decisions—a practice grown from real, not theoretical, quality assurance.
Years working with 2-Aminobiphenyl shaped a practical understanding of the intersection between lab-scale innovation and industrial reality. Trends point toward highly customized chemicals—with a focus on trace impurity control, supply chain transparency, and product-specific documentation. From the manufacturer’s side, the story is less about chasing volume and more about adapting to evolving customer science.
Our team watches regulatory shifts, from revised REACH protocols to international transport standards. Adjusting to these changes means more than documentation—it requires tweaking processes, staff retraining, and regular internal audits. Facing new realities, such as requests for extended analytical dossiers or digital chain-of-custody, we invest directly in analytical infrastructure and staff development.
Every kilo of 2-Aminobiphenyl shipped from our facility carries the cumulative lessons of real people—operators who handle the compound, chemists who problem-solve process issues, and technical support addressing customer constraints. Beyond spec sheets, our manufacturing knowledge rests in making demanding chemistry work at scale, while anticipating and solving the inevitable bumps along the way.
Those who work with 2-Aminobiphenyl, whether as chemists, product managers, or regulatory reviewers, share a tacit understanding: successful production hinges on a combination of technical skill, vigilance, and ongoing adaptation. This deep experience is what defines our approach, guiding how we continue to manufacture a product that stands up to the scrutiny and challenges of advanced industrial chemistry.