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(2-Aminophenyl)(Phenyl)Methanone Oxime

    • Product Name (2-Aminophenyl)(Phenyl)Methanone Oxime
    • Einecs 629-624-5
    • 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
    VTB
    Specifications

    HS Code

    172384

    Iupac Name (2-aminophenyl)(phenyl)methanone oxime
    Molecular Formula C13H12N2O
    Molecular Weight 212.25 g/mol
    Cas Number 765932-89-8
    Appearance White to off-white solid
    Melting Point 132-135 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=C(C=C1)C(=N/O)C2=CC=CC=C2N
    Inchi InChI=1S/C13H12N2O/c14-12-8-4-6-11(9-12)13(15-16)10-2-1-3-7-10/h1-9,16H,14H2
    Storage Conditions Store at 2-8°C, keep container tightly closed

    As an accredited (2-Aminophenyl)(Phenyl)Methanone Oxime factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1 gram of (2-Aminophenyl)(Phenyl)Methanone Oxime supplied in a sealed amber glass vial with tamper-evident cap and labeling.
    Shipping (2-Aminophenyl)(Phenyl)Methanone oxime should be shipped in tightly sealed containers, under dry and cool conditions, protected from light. It must comply with all applicable regulations for chemical transport. Packaging should prevent leaks or contamination, and include appropriate hazard labeling, documentation, and safety data sheets for safe handling during transit.
    Storage (2-Aminophenyl)(phenyl)methanone oxime should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances, such as strong oxidizers and acids. Avoid humidity and temperature extremes. Always label the container clearly and keep it in a designated chemical storage cabinet, preferably with secondary containment to prevent spills.
    Application of (2-Aminophenyl)(Phenyl)Methanone Oxime

    Applications of (2-Aminophenyl)(Phenyl)Methanone Oxime in Industrial Manufacturing

    As a direct manufacturer specializing in (2-aminophenyl)(phenyl)methanone oxime production, we supply this advanced intermediate to technically demanding sectors. Our material consistently supports precision downstream synthesis, backed by documented application evidence across key industries. Below, we outline specialized use cases, each structured to address compliance, formulation, integration in production, and final goods delivery as encountered by industrial customers.

    1. Pharmaceutical Synthesis – Active Intermediate for Cephalosporin Antibiotics

    This oxime serves as a strategically selected building block in the multistep synthesis route of advanced cephalosporin APIs to achieve high regioselectivity and minimized impurities. Its functional groups facilitate crucial N-alkylation and subsequent protective strategies under controlled pharma manufacturing environments, where batch consistency and traceability directly affect released product quality.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • EU GMP Part II (Basic Requirements for Active Substances)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia chp 2020, Cephalosporin-related monographs

    Typical usage ratio

    • Applied in 0.85–1.2 molar equivalents relative to the key cephalosporin nucleus, adjusted per specific route requirements and downstream impurity profile control.

    Downstream process integration

    • Introduced after β-lactam ring formation for selective oximation, acting as a protected intermediate in vacuum reflux reactors with in-process HPLC monitoring.

    Final product types

    • Third-generation cephalosporin bulk APIs (e.g., cefotaxime sodium, ceftriaxone sodium)
    • Lyophilized cephalosporin injectable formulations
    • Oral tablet and capsule finished dosage forms
    • Sterile solution preparations for parenteral use

    2. Agrochemical Manufacturing – Precursor for Aryloxime Ether Herbicides

    Downstream agrochemical synthesis operations select this compound as a precursor when engineering aryloxime ethers. Its aromatic amine and oxime functionalities provide unique substitution patterns necessary for herbicide activity against broadleaf weeds, and reduce byproduct formation through predictable condensation behavior in high-throughput crop protection plants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 1750 (International Standard for Common Names of Pesticides)
    • China GB 2763—National Food Safety Standard For Maximum Residue Limits for Pesticides
    • REACH (EC) No. 1907/2006

    Typical usage ratio

    • Added at 0.5–0.9 mole ratio based on the core halogenated benzene or pyridine in the batch process, with adjustments for desired selectivity and downstream coupling efficiency.

    Downstream process integration

    • Employed in the stages following halogenation, entering Williamson ether or Mitsunobu reactions for O–aryl oxime ether formation prior to formulation into technical concentrate.

    Final product types

    • Technical grade aryloxyphenoxypropionate herbicidal actives
    • Formulated EC (emulsifiable concentrates) and SC (suspension concentrate) crop protection products
    • Granular, wettable powder herbicides for direct field application
    • Water-dispersible tablet herbicide products

    3. Dye and Pigment Synthesis – Intermediary for Azo and Anthraquinone Chromophores

    This intermediate is valued in colorant industries to control electron-donating capacity during the key coupling steps that determine dye chromophore structure and shade. By inserting the oxime at a strategic point, pigment manufacturers reduce side-reaction tints and improve batch reproducibility in large-scale dye houses dealing with strict customer quality metrics for textile and polymer applications.

    Industry compliance standards

    • Oeko-Tex® Standard 100 (product class-specific requirements for dyestuffs)
    • ETAD Code of Ethics for colorant manufacturers
    • EU REACH Annex XVII regulation (restrictions on certain azo compounds)
    • ISO 9001 (Quality Management certified industrial blending)

    Typical usage ratio

    • Charged at 1.0 mol equivalent per target diazonium salt, adjusted by color strength requirements and chromatic stability targets specific to textile grades.

    Downstream process integration

    • Introduced during the azo coupling phase or pre-condensation of anthraquinone ring systems, utilizing controlled pH and temperature regimes to maximize dye purity and lightfastness.

    Final product types

    • Reactive and disperse dyestuffs for cotton, polyester, and blends
    • Semi-pigmented printing inks for packaging and plastics
    • High-color-strength pigment pastes
    • Specialty textile auxiliaries for technical fabrics

    4. Specialty Chemical Synthesis – Starting Material for Benzanilide Derivatives

    Chemical processing companies utilize the oxime as a key input to produce substituted benzanilide derivatives, often adopted in high-value fluid formulations, polymer additives, or advanced material science. The molecular design ensures clean amidation steps with reduced over-oxidation byproducts and offers downstream developers the flexibility to fine-tune molecular architecture for new functional materials under controlled lab and pilot-scale trials.

    Industry compliance standards

    • ISO 14001 (Environmental Management for chemical synthesis)
    • Responsible Care® Management Systems
    • GHS/CLP hazard communication compliance
    • Chinese GB 30000.2—2013 for chemical safety and labeling

    Typical usage ratio

    • Typically 0.95–1.1 equivalents per carboxylic acid derivative in amidation, with adjustment for scale-up or pilot studies based on molecular yield targeting.

    Downstream process integration

    • Charged during the first-stage condensation, prior to cyclization or further modification, in reactor vessels equipped for high-purity, low-contamination synthetic routes.

    Final product types

    • Benzanilide-based heat stabilizers for polymer processing
    • Custom lubricant additive packages
    • Functional material intermediates for electronic chemical production
    • Specialty performance coatings and films
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    Certification & Compliance
    More Introduction

    Insight Into (2-Aminophenyl)(Phenyl)Methanone Oxime Production and Application

    Understanding (2-Aminophenyl)(Phenyl)Methanone Oxime from a Manufacturer’s Perspective

    Working directly in the synthesis and supply of specialty chemicals, we have seen how subtle changes in molecular structure alter both the performance and the demand for a compound. (2-Aminophenyl)(Phenyl)Methanone Oxime is a prime example. The manufacturing process for this oxime remains intricate, requiring clear attention to temperature control, purity monitoring, and precise formulation at each stage. This hands-on approach influences not only the quality but also the potential versatility of what reaches our customers.

    The product commonly emerges as an off-white to faint beige crystalline powder, with a purity that, through our standard processes, exceeds 98% by HPLC. This tight control on analytical values comes from repeated investment in both raw material quality and monitoring at several checkpoints. Over years of manufacturing, we have improved the reproducibility of this oxime batch-to-batch through incremental changes in reaction stirring, collection methods, and solvent recovery. Oximes, by their nature, are sensitive to both pH and ambient humidity during crystallization, so our technicians document each batch’s parameters. What that means for the end user is reliability in downstream reactions and less need to second-guess test results.

    What Makes This Oxime Distinctive?

    The core difference between (2-Aminophenyl)(Phenyl)Methanone Oxime and other benzylic or aromatic oximes centers on the arrangement of the amino functionality in the ortho position of the phenyl ring. From years of laboratory and pilot plant observation, this design often offers superior reactivity in transformations such as Beckmann rearrangement or specific condensation routes. In targets where substituent position affects yield, this compound often delivers higher selectivity. Chemists we supply in both applied pharmaceutical research and material sciences have noted that ortho-amino substitution increases the lability of the oxime group, especially compared with the para or meta positions. This translates to modifications in melting point, solubility, and reaction rates.

    Manufacturing at scale allows us to be certain about the physical properties delivered: melting points typically fall just above 130°C, confirming the purity of each batch and helping our buyers sidestep wasted time on chromatographic purification. Moisture content stays below 0.5% thanks to controlled drying protocols, which matters in applications where even a trace of water can spoil subsequent processes. Side-by-side trials with regular benzophenone oximes and their substituted cousins reveal that few offer the same chemical flexibility. The amino group at ortho not only directs reactivity but also opens the option for further customized derivatization—a fact that customers in small-molecule screening and pigment research often report as critical.

    Direct Usage Experience and Functional Benefits

    We have serviced researchers using (2-Aminophenyl)(Phenyl)Methanone Oxime for over a decade, watching their work in hydrazone synthesis, ligand discovery, and as intermediates in specialty polymer projects. In one notable case, an R&D team from a medical device manufacturer highlighted how our oxime outperformed generic alternatives in a photoinitiator application, leading to greater process consistency and fewer side reactions. In another example, API developers selected this oxime precursor because it made their scale-up phase more predictable, enabling them to replicate laboratory successes at pilot plant scale.

    In combinatorial chemistry, where large libraries of compounds get screened for activity, speed and reproducibility hinge on reagents with proven batch consitency. By tightening every batch’s homogeneity, we minimized the risk of outlier results or failed syntheses. This reliability means customers face fewer unexpected process interruptions, spend less time troubleshooting, and progress to next stages of their research sooner.

    Some customers prefer to avoid excessive handling of specialized chemicals. Our experience shows that producing large, free-flowing crystals not only simplifies sample preparation but reduces the likelihood of dust contamination and loss, which become significant in high-throughput laboratories. We train our production staff to focus on not just yield but also granule shape, filterability, and ease of weighing, all of which speed up laboratory and manufacturing operations. These small adjustments, often missed by outsourcers or low-tier suppliers, save hours and keep research lines and production floors moving.

    Real-World Applications and Market Needs

    In the pharmaceutical sector, (2-Aminophenyl)(Phenyl)Methanone Oxime finds repeated use as a building block in heterocycle synthesis and as a precursor to various active pharmaceutical ingredients. The ortho-amino function allows for unique cyclization and annulation reactions not accessible with para- or meta- analogues. Our clients in agrochemical R&D seek out this molecule to tap into newer classes of biocidal and crop-protection agents, given its facilitation of tailored substitution patterns. We have observed growing demand among colorant and dye researchers, who value precise oxime compounds to fine-tune dye precursors for improved lightfastness, color saturation, and environmental stability.

    Within materials science, this compound shows promise as a customizable anchor in the construction of chelating agents or coordination polymers. Over the past five years, several collaborations with university research groups have shown it acting as a core scaffold, linking additional functional groups via the amino site, thus expanding polymer architectures for both electronic and structural applications. Experts in fine chemicals point out that the exact placement of functional groups in these molecules often means the difference between a viable process and a wasted effort. Feedback from customers consistently aligns with our internal test records—orthogonality in reactivity makes this compound hard to substitute.

    Quality Focus: Challenges and Solutions in Manufacturing

    Maintaining a high and consistent purity in (2-Aminophenyl)(Phenyl)Methanone Oxime does not happen by accident. Too many operators overlook cleaning protocols or allow cross-contamination from similar intermediates. In our experience, the presence of minor side products or incomplete conversions affects not just appearance, but can drive up downstream rejection rates. We solved this through regular revalidation of our purification steps. Frequent in-process checks, not just on finished goods, have reduced off-spec batches. Where necessary, our team adopts double recrystallization or column purification, followed by targeted drying under vacuum, to match the precise needs of each customer order.

    Years ago, trace metals or unreacted starting materials occasionally led to product cloudiness or diminished reactivity. By partnering with analytical laboratories and investing in updated GC-MS, NMR, and ICP-MS capability, we pinpointed and eliminated several sources of contamination. On the shop floor, we introduced real-time feedback systems for key process parameters such as pH and material feed rates, which has translated to less variability from shift to shift. The result is better crystal size distribution, easier dissolution during customer use, and a more stable shelf life in warehouse conditions.

    Our logistics team takes lessons from the lab and applies them to packaging and shipping. We use multi-layer moisture-resistant bags and rigid outer drums to keep each shipment safe in transit. Humidity, static, and vibration during transit can impact crystalline quality, so we continuously refine our packaging to keep integrity high from our door to the user’s bench. Customers rarely report issues with caking or degradation, and repeat orders have grown as a direct result.

    Comparative Analysis with Other Oximes

    Chemists often ask why this particular oxime should be picked over simpler ones such as benzophenone oxime or acetophenone oxime. Having studied reaction outcomes across dozens of projects, our chemists can confirm that the ortho-amino group introduces new reactivity patterns. In nucleophilic substitution reactions, this oxime displays enhanced activity. Under acidic conditions, it offers improved cyclization yields, attributed to the activating effect of the amino group. Some competing alternatives fall short during oxidative transformation or require harsher conditions, which can degrade sensitive substituents. With our product, milder reaction parameters suffice, which shortens reaction time and reduces risk of unwanted byproducts.

    The difference in melting point and solubility also matters outside the laboratory. Storage experiences show (2-Aminophenyl)(Phenyl)Methanone Oxime resists moisture pick-up and degradation, compared with less substituted analogues. Storage in standard warehouse conditions meets both shelf-life and regulatory requirements, without frequent loss from degradation or need for specialized climate control. Purity and physical stability help minimize hazardous waste, which translates to both cost savings and a smaller environmental footprint.

    Environmental, Regulatory, and Safety Considerations

    We produce our oxime with a focus on both laboratory utility and downstream safety. Over time, environmental regulations have changed how chemicals like this are handled, labeled, and shipped. Our facilities adhere to industry best practices for emissions, waste minimization, and worker protection, applying closed-system handling and proper effluent treatment. This focus on responsible production does more than satisfy compliance; it protects both our workforce and our neighbors in the community. Feedback from audits and third-party inspectors confirms the effectiveness of our protocols, reinforcing commitment to continuous improvement.

    End users continue to appreciate transparency in sourcing and traceability. For each lot shipped, we link analytical certificates and detailed production notes, reducing uncertainty in research and industrial documentation. Compliance across regions, especially where REACH and other safety regulations apply, remains a priority, and adjustments to process chemistry reflect these evolving standards. Over the past few years, we’ve integrated more environmentally benign solvents and recycled process water to reduce the unit environmental impact of each kilogram produced.

    Supporting Innovation through Collaboration

    As a manufacturer rather than an intermediary, we see beyond the catalog page. Our technical support draws on the day-to-day knowledge of chemists and technicians who run these reactions every shift. We answer customer queries based on actual experience—how particle size can affect suspension stability, which solvents bring out the best yields, and what analytical methods work quickest for lot verification. We provide not just material, but context and evidence for optimal use. Whether it’s a minor tweak in synthesis or an entirely new downstream target, open exchange with users informs our own process refinement. Future shifts in end-user needs, from tighter impurity thresholds to greener synthesis steps, push us to upgrade equipment, improve analytics, and test new purification schemes.

    In research-driven fields, small differences between oximes can lead to big wins or big losses. Only by producing at scale, handling numerous feedback loops, and tracking lots across years can these subtleties turn into consistent advantages for our customers. By focusing not just on certificates of analysis but also on real-world outcomes, we guide project managers and bench chemists toward more successful synthesis campaigns and faster time to application.

    Anticipating Future Demands and Process Improvements

    The market for (2-Aminophenyl)(Phenyl)Methanone Oxime has widened to encompass both established applications and new innovations. Chemical R&D faces pressure to move faster and embrace safer, cleaner processes, and both of these trends highlight the need for precisely prepared intermediates. We continue to monitor emerging synthetic routes that further reduce side product formation and dependence on hazardous reagents. Internal process improvement groups focus on maximizing atom economy and reducing total solvent input, both for cost and environmental goals.

    Digital batch records, automation in reactor control, and in-line analytical monitoring keep our own operations accountable. These measures deliver direct benefits to customers—not just lower defect rates, but a documented trail that makes upward or downward scaling less risky. New requests for custom derivatives based on this oxime compound push us to collaborate with university labs and contract research organizations on process tweaks, new salt forms, and post-derivatized variants tailored for expanding application space.

    Other research teams find value working directly with the producer, rather than negotiating through several links in the chain. From firsthand experience, scientists want more than just purity figures; they seek insight on thermal stability, interaction with other popular reagents, and guidance on protocol optimization. By working side by side with users, we continue to adapt our offering to match not just current, but anticipated industry requirements.

    Conclusion: Value in Experience and Focus

    Every year brings fresh analytical tools and new synthetic challenges, but some fundamentals remain unchanged. Direct control of production, real-world feedback, and constant refinement of our procedures have shaped the consistency and performance of (2-Aminophenyl)(Phenyl)Methanone Oxime produced at our facility. Whether destined for pharmaceutical development, new materials research, or advanced chemical intermediates, this compound responds best to a manufacturing approach that prizes detail, traceability, and informed experience.

    In summary, (2-Aminophenyl)(Phenyl)Methanone Oxime stands out for its purity, reproducibility, and versatility, underpinned by direct feedback from those who use it. Reliable results in high-stakes settings do not happen by chance—they follow from generations of technical mastery and an ongoing commitment to serving the needs of chemists, engineers, and innovators worldwide.