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2-Nitrophenyl Phenyl Sulfide

    • Product Name 2-Nitrophenyl Phenyl Sulfide
    • Alias 2-nitrophenyl phenyl sulfide
    • Einecs 219-725-8
    • 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

    314313

    Cas Number 2117-03-9
    Molecular Formula C12H9NO2S
    Molecular Weight 231.27 g/mol
    Appearance Yellow to orange crystalline solid
    Melting Point 64-67°C
    Solubility In Water Insoluble
    Density 1.29 g/cm3
    Purity Typically ≥98%
    Synonyms O-Nitrophenyl Phenyl Sulfide

    As an accredited 2-Nitrophenyl Phenyl Sulfide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, 25 grams, chemical label with hazard symbols, product name, CAS number, and supplier details.
    Shipping 2-Nitrophenyl Phenyl Sulfide is shipped in secure, chemical-resistant containers, clearly labeled and compliant with regulatory standards. The packaging ensures protection from moisture and light. Shipping follows UN hazardous material guidelines, typically via ground or cargo, with appropriate documentation and safety data included. Handle with care to prevent spillage or exposure.
    Storage 2-Nitrophenyl Phenyl Sulfide should be stored in a tightly closed container within a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from light and moisture. Properly label the container and ensure storage is compliant with chemical safety regulations. Use suitable secondary containment to prevent any potential leaks or spills.
    Application of 2-Nitrophenyl Phenyl Sulfide

    Applications of 2-Nitrophenyl Phenyl Sulfide in Industrial Manufacturing

    2-Nitrophenyl Phenyl Sulfide serves as an advanced functional intermediate in specialized chemical syntheses. Its unique electron-rich aromatic structure and sulfur linkage enable targeted transformations required by downstream industrial producers. As the original manufacturer, we ensure strict quality assurance to support precise applications in multiple high-value sectors.

    1. Advanced Organic Synthesis for Pharmaceutical Intermediates

    This compound plays a critical role in the multi-step synthesis of select heterocyclic drug intermediates, particularly for active pharmaceutical ingredient (API) development where aryl sulfide motifs and ortho-nitro substitutions form essential scaffolds. Bulk processors incorporate it as a coupling component or a nucleophile in specific amination and reduction steps. The structure allows introduction of sulfur-bridged frameworks and further downstream transformation into bioactive molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Directive 2001/83/EC (as applicable to intermediates)
    • US FDA Guidance for Industry: Drug Substance
    • Enterprise-specific Standard Operating Procedures (SOP) for trace organic impurities

    Typical usage ratio

    • 0.5–2.5 molar equivalents, depending on substitution targets and yield optimization parameters; process chemists typically ascertain batch ratio following pilot trials using in-process HPLC monitoring.

    Downstream process integration

    • Charged into aromatic nucleophilic substitution or heterocyclic ring-closing steps after in-situ conditioning under nitrogen; batch addition is stage-controlled to limit undesired byproduct generation during catalyst-mediated transformations.

    Final product types

    • API building blocks such as Ar-S-aryl amine derivatives
    • Pharmaceutical lead compounds with nitroaromatic frameworks
    • Sulfur-bridged heterocycles for small molecule research
    • Specialized medicinal intermediates for CNS-targeting drug classes

    2. Custom Synthesis of Specialty Agrochemical Intermediates

    Leading agrochemical producers integrate this compound as a modular fragment for synthesizing sulfur-containing herbicide and fungicide intermediates, where the aryl-sulfide linkage provides stability against enzymatic cleavage. Process development teams utilize its predictable reactivity for constructing key bioactive moieties required in crop protection agents, leveraging directed ortho-nitro functionalization patterns for further modifications.

    Industry compliance standards

    • FAO/WHO Guidelines on Quality Control of Pesticide Ingredients
    • ISO 9001:2015 Quality Management Systems for chemical synthesis plants
    • REACH Regulation (EC) No 1907/2006 (Substance Registration and Restrictions)
    • Local authority regulations on precursor monitoring for hazardous chemicals

    Typical usage ratio

    • 0.2–1.2 weight percent in batch syntheses, adjusted according to the alkylation or cyclization endpoint; the ratio depends on the downstream chlorination or oxidation route stability required.

    Downstream process integration

    • Fed into the main reactor after completion of initial aromatic halogenation; employed as a nucleophilic substrate or sulfur linker in flow or batch reactor conditions, following solvent pre-conditioning and temperature ramp protocols.

    Final product types

    • Sulfur-linked phenyl intermediates for selective herbicides
    • Nitroaromatic fungicide precursor compounds
    • Custom-formulated agrochemical actives for rice and grain protection
    • Advanced intermediates for combination pesticide formulations

    3. High-Performance Dye and Pigment Synthesis

    In the colorant industry, formulators use this nitro-aryl sulfide as a building block for azo and sulfur dye precursors, where molecular design requires controlled introduction of sulfur bridges and activated nitro sites. Its role is indispensable during the preparation of stable colorant molecules for polyester and polyamide fibers, where fastness and chromatic performance rely on properly substituted aromatic rings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile ecology standards for dyes)
    • ETAD Guidelines for the Manufacture of Synthetic Organic Colorants
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) for dye intermediates
    • EN ISO 13321:2013 (Industrial dyestuffs)

    Typical usage ratio

    • 1.0–3.0 molar equivalents per target dye precursor, determined by stoichiometry of coupling reaction with diazonium salts or in oxidative polymerizations; actual ratio set by desired color intensity and migration resistance.

    Downstream process integration

    • Dosed into the azo coupling or oxidative condensation reactor after initial mixing of base aromatic compounds; timing coordinated to ensure controlled nucleophilic reaction with diazonium or other functionalized intermediates.

    Final product types

    • Disperse dyes for polyester yarns
    • Sulfur-based dyestuffs for polyamide and viscose textiles
    • Intermediates for high-performance pigment dispersions
    • Nonionic colorant precursors for plastics coloration

    4. Electronic Chemicals for Liquid Crystal and Polymer Synthesis

    This compound acts as a specialized intermediate in the formulation of advanced electronic materials, especially in the synthesis of mesogenic units for liquid crystal displays (LCDs) and high-refractive-index polymers. Process engineers value its rigid, planar structure and polarizable nitro groups for introducing desired optical and dielectric properties during the construction of functional materials required by device manufacturers.

    Industry compliance standards

    • IPC-4101 standards for base materials used in printed wiring boards
    • IEC 61249-2-7 for electronic industry material safety
    • RoHS Directive (Restriction of Hazardous Substances) 2011/65/EU
    • Internal quality protocols for particle size and trace impurity control in display material supply chains

    Typical usage ratio

    • 0.1–1.0 weight percent in copolymerizations or oligomeric additive syntheses; tuning based on target refractive index or liquid crystalline phase onset determined during pilot formulation runs.

    Downstream process integration

    • Introduced at the monomer synthesis stage, applied as a bridging component in Suzuki or Ullmann-type arylation, followed by integration into oligomerization or copolymerization units; precise addition timing ensures uniform distribution for device compatibility.

    Final product types

    • Mesogenic monomers for liquid crystal display applications
    • High-index oligomers for optical polymer lenses
    • Polymer intermediates for advanced printed circuit boards
    • Additives for specialty antistatic polymer films
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    Certification & Compliance
    More Introduction

    2-Nitrophenyl Phenyl Sulfide: Insight from Direct Manufacturing Experience

    A Chemical Crafted with Purpose

    In every batch of 2-Nitrophenyl Phenyl Sulfide we manufacture, years of dedicated effort stand behind the powder or crystalline flakes in the drum. Purity, reactivity, and performance do not happen by chance in this line of work, especially for intermediates like 2-Nitrophenyl Phenyl Sulfide that end up as key participants in chemical transformations well outside our plant’s walls. The compound, recognized in technical circles by CAS number 13084-81-0, emerges from process routes that demand precision, careful choice of raw materials, and an uncompromising quality control approach that we've practiced and improved year after year.

    Why Chemical Structure and Manufacturing Method Matter

    Making 2-Nitrophenyl Phenyl Sulfide requires more than following reaction equations or watching temperature gauges. Nitro and sulfide groups on the same molecule create both promise and challenge: the nitro group’s electron-withdrawing ability plays a major role in its activity in nucleophilic aromatic substitution, and the phenyl sulfide linkage opens doors in sulfur chemistry. Achieving selective synthesis without strong byproduct signals relies not just on time-honored recipes but on fine-tuned process adjustments you only find by doing. Controlling light exposure during reactions, choosing the right solvent batch, and maintaining pressure stability throughout the scale-up stage affect the color, odor, and purity of the final product.

    Unlike many simpler industrial chemicals, 2-Nitrophenyl Phenyl Sulfide does not tolerate a “good enough” mentality. Impurities and trace moisture can jeopardize downstream yields in custom syntheses—especially for pharmaceutical or advanced material intermediates. That’s why we keep rigorous control from the first drop of precursor until the final QA report clears each lot. Each kilogram packed reflects a hundred smaller checks: colorimetric analysis under daylight lamps, gas chromatography retention times stored for comparison, and periodic on-site review of every filtration step.

    From Production Floor to Lab Bench

    Our customers usually use 2-Nitrophenyl Phenyl Sulfide as a versatile intermediate. It can serve as a partner for carbon-sulfur bond formation, act as a protected phenol source after reductive cleavage, or introduce nitro groups for further chemical transformations. Its place in the development of specialty dyes, agrochemicals, and certain pharmaceutical lead compounds gets overlooked outside industry circles but not here: onsite chemists verify performance with model reactions before lots ship out.

    Different uses call for different handling techniques. Some customers need high-purity, free-flowing crystals for precise stoichiometry in research work. Others prefer a milder grind or greater bulk volumes for pilot plant syntheses. Our batch sheets show more than melting points and purity—density, flowability, even static charge characteristics get recorded and reported.

    Product Specifications that Reflect Real-World Needs

    What sets apart manufacturer-grade 2-Nitrophenyl Phenyl Sulfide from generic, repacked alternatives? It starts with traceability. We trace every precursor shipment, reactor vessel, and process operator for each run, linking batches back to their origin. Purity routinely reaches over 99.5% based on HPLC and NMR standards; water content is kept to a minimum—frequently below 0.1% as measured on a Karl Fischer apparatus—because we know moisture alters the way organosulfur compounds behave.

    Certainly, physical appearance is more than aesthetics. We see recurring patterns: a slightly yellow crystalline solid, easily recognized by experienced hands. Strong, acrid odor signals both the nitro and sulfur groups’ presence. Less experienced technicians may not give this enough attention, but we check each lot’s volatility and dust content precisely to avoid safety issues and surprises during handling. We label each drum with batch-specific storage guidance because actual stability depends on the handling environment.

    Comparison with Other Sulfide Compounds

    A common question: what makes 2-Nitrophenyl Phenyl Sulfide unique among organosulfur intermediates? Small structural choices produce large downstream effects. Compared to simple diphenyl sulfide, the presence of the ortho-nitro group changes reactivity and selectivity significantly. The nitro moiety increases the molecule’s electron-poor character, making it more suitable for certain coupling reactions, where enhanced nucleophilicity is needed. In routes where the nitro group will later serve as a leaving group or function handle, our compound often outperforms 4-nitrophenyl, 2-chlorophenyl, or 2-bromophenyl analogs because of its better balance of stability and reactivity.

    Some customers debate whether to choose 2-Nitrophenyl Phenyl Sulfide over other nitroaryl sulfides for custom synthesis. Our long-term partners trust our consistency across batches—a direct result of locking in standard process parameters and a deep understanding of how temperature ramps and solvent polarity affect side-product formation. Unlike generic catalog products that sometimes show varied melting points or yellowing from excess exposure, our lots stay within a narrow band for both color and melting point, batch after batch.

    Adaptability across Applications

    We see real diversity in how research groups and companies use this compound. In pharmaceutical preclinical chemistry, for example, 2-Nitrophenyl Phenyl Sulfide often acts as a masked phenol. Cleaving the 2-nitrophenyl group from its sulfur bridge under mild conditions releases phenol for use in constructing bioactive scaffolds. The nitro group’s electronic effects improve selectivity and minimize side reactions. Materials science groups benefit from the electron-deficient aromatic ring, using it to push substitutions that fail with less activated analogs.

    Synthetic dye manufacturers value how the nitro substituent affects color development and solubility pathways, especially in advanced pigment lines. Agrochemical developers rely on the compound’s relative hardness compared to other aryl sulfides—a feature that produces more robust pesticide intermediates or polymer-bound actives. Insights from the shop floor, such as best solvent matches for dissolution or filtration, often save clients significant time tuning their own processes.

    Attention to Quality at Every Stage

    Quality sits at the core of our work, not as a regulatory box-tick, but because everyone manufacturing specialty chemicals knows how a single off-specification drum can unravel weeks of lab work downstream. We long ago abandoned casual “spot checks” in favor of exhaustive QC protocols: visually examining every drum, running analytical tests for each sub-batch, and engaging with customer feedback even from small-scale experimental users.

    Routine internal tests include NMR, GC/MS, HPLC, moisture determination, and melting point. Each lot receives a unique identifier and comparison against a master sample. Teams keep trend records for melting point changes, color metrics, batch flow, and byproduct fingerprints. Feedback loops work both ways: we act directly on recurring customer concerns, whether about dustiness, caking, or volatility under field conditions. Our focus remains simple—ship only what we would willingly use ourselves in critical syntheses.

    Packaging and Handling—Practical Lessons from Experience

    Too many overlook packaging as a routine detail, but as direct manufacturers, we don't. Sensitive intermediates like 2-Nitrophenyl Phenyl Sulfide can degrade from air and moisture exposure, and physical damage can alter their reactivity. Over the years, we've learned which materials cause static issues, which drum liners prevent caking, and the importance of double-sealing batches for sea freight.

    We customize lot size and drum selection, considering transport duration, climate risk during shipping, and customer storage realities. On request, we share best-practice handling tips developed in our own facilities—double-glove technique for weighing, recommendations for venting after long-term storage, and step-by-step cleaning after accidental exposure. These working-level precautions help partners avoid yield drops or safety incidents that come from mishandling such reactive intermediates.

    Compliance and Environmental Commitment

    From a regulatory compliance perspective, we approach oversight as an attitude as much as a workflow requirement. Local and international standards for chemical manufacture incorporate not just product purity, but process emissions, waste minimization, and operator safety. Our facilities operate under strict internal SOPs for solvent recycling, air emissions filtration, and trace waste auditing—years of investment have dropped solvent loss and minimized unrecoverable waste per batch.

    Operators receive ongoing training on nitroaromatic and sulfur chemistries, especially as both classes pose unique handling challenges. Monitored working areas, real-time ventilation tracking, and periodic exposure checks are not afterthoughts but stitched into daily routines. We understand that responsible manufacturing decisions build reputation not overnight but across decades of safe operation.

    On the environmental front, pushback against “dirty” specialty chemical production led us to invest in catalyst recycling, off-gas scrubbing, and zero-liquid discharge targets much earlier than most in our region. Many competitors accept higher emissions or lower yields as facts of life for nitroaromatic intermediates. We’ve found well-managed recovery systems cut both costs and environmental impact, reinforcing why direct control matters at every step.

    Partnerships Built on Proven Performance

    Relationships matter in this field because many supply chain decisions ride on past performance. New partners typically arrive with detailed specification requests or batch sample comparisons from other suppliers. Few things build trust faster than direct factory visits—we open our doors for process audits, encourage on-site sampling, and participate in joint testing. Experience shows that chemists and purchasing agents who dig into the details quickly spot the advantages of direct manufacturing control: tighter spec adherence, full transparency on batch history, and flexibility to meet evolving project needs.

    Our follow-up does not stop with a shipment notice. Customer support lines connect bench chemists right to the process team—no layers of traders or vague responses. Rapid feedback channels catch storage concerns, purity questions, or application challenges before they spiral. For many R&D projects, being able to discuss specifics about raw material quality, residual solvent levels, or the impact of tiny process tweaks often unlocks both higher yields and new chemistry routes.

    Innovation and Continuous Process Improvement

    No specialty chemical production ever stands still. New synthesis demands from customers, regulatory changes, and raw material volatility keep us on our toes. Direct feedback pushed us to transition several years ago to new catalyst systems, boosting yields per batch and reducing byproducts below detection in many lots. Process chemists monitor marketplace trends and literature for upstream innovation, running small-batch experiments before full-scale implementation.

    As a manufacturer, incremental changes—re-engineering reactor paths, introducing better temperature sensors, swapping filter materials, or upgrading to advanced PLC controls—show practical returns quickly. Our teams have trimmed energy use per ton by swapping to heat-recovery lines, and solvent use fell even as capacity grew thanks to targeted recycling upgrades. Each small improvement aggregates into a plant operation that does not just chase but routinely achieves best-in-class benchmarks for output and quality.

    We participate in industry knowledge sharing, attend technical symposia, and host periodic open house events so customers and partners can witness new investments in PCR (process chemistry review) areas. Insights gained through failure—like a failed crystallization after a global solvent supplier changed their grade specs—become part of our institutional memory and drive both new SOPs and direct training for every hire.

    Looking Ahead—A Manufacturer’s Perspective

    Working at scale with complex intermediates like 2-Nitrophenyl Phenyl Sulfide brings unique responsibilities. Our experience tells us that rigorous process discipline, transparent quality management, and practical engagement with downstream users matter at least as much as technical skill. New applications will continue pushing quality requirements, pushing us to refine purification, crystallization, and packing even further.

    Global chemistry moves fast, but deliberate, well-documented changes persist longer than trend-chasing. From our vantage point inside the factory, the drive to consistently produce high-purity, reliable 2-Nitrophenyl Phenyl Sulfide in every drum comes from a simple belief: we build each lot for customers who treat their own work with the same attention to detail that we do. Years from now, that trust and shared experience will shape the routes, products, and breakthroughs that follow.