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4-(2-Methoxyphenyl)-3-Thiosemicarbazide

    • Product Name 4-(2-Methoxyphenyl)-3-Thiosemicarbazide
    • Alias Methoxyphenyl Thiosemicarbazide
    • Einecs 437-520-9
    • 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
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    Specifications

    HS Code

    731830

    Product Name 4-(2-Methoxyphenyl)-3-Thiosemicarbazide
    Molecular Formula C8H11N3OS
    Molecular Weight 197.26 g/mol
    Cas Number 80847-82-7
    Appearance White to off-white solid
    Melting Point 156-158 °C
    Solubility Soluble in DMSO, slightly soluble in water
    Purity Typically ≥ 98%
    Structural Formula C1=CC=CC=C1OC(NN=C(S)N)N
    Synonyms 2-Methoxyphenyl thiosemicarbazide
    Storage Conditions Store at room temperature, away from light and moisture
    Hazard Statements May cause skin and eye irritation

    As an accredited 4-(2-Methoxyphenyl)-3-Thiosemicarbazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-(2-Methoxyphenyl)-3-Thiosemicarbazide is supplied in a 25g amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping The chemical **4-(2-Methoxyphenyl)-3-Thiosemicarbazide** is shipped in a tightly sealed container, protected from light and moisture. Packaging adheres to safety regulations, including clear labeling and handling instructions. It is typically sent via ground or air transport with all relevant safety documentation, ensuring secure and compliant delivery.
    Storage Store 4-(2-Methoxyphenyl)-3-thiosemicarbazide in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, away from heat sources and incompatible substances such as strong oxidizers and acids. Label the container clearly, and ensure appropriate chemical safety measures are in place. Handle with gloves and eye protection.
    Application of 4-(2-Methoxyphenyl)-3-Thiosemicarbazide

    Applications of 4-(2-Methoxyphenyl)-3-Thiosemicarbazide in Industrial Manufacturing

    As a direct manufacturer of 4-(2-Methoxyphenyl)-3-Thiosemicarbazide, we supply high-purity material to a diverse set of industrial segments. Our focus lies on practical, validated downstream applications, each governed by recognized process, compliance, and quality expectations. The following sections detail its integration into specialized sectors.

    1. Pharmaceutical Intermediates in Antituberculosis Drug Synthesis

    This compound serves as a key intermediate for pharmaceutical active ingredient synthesis, most notably within hydrazide- and thiosemicarbazone-based antituberculosis APIs. Downstream manufacturers value its selectivity in condensation and cyclization reactions, supporting high-yield conversion with minimal side product formation. Raw material specifications must align with strict impurity limits and process critical control points dictated by regulatory submission batches.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • Ph. Eur., USP, JP monographs for related final APIs
    • 21 CFR Part 211 (US FDA CGMP for Finished Pharmaceuticals)
    • EMEA and NMPA filing requirements for intermediates

    Typical usage ratio

    • 0.93–1.06 molar equivalents per API batch, adjusted for stepwise conversion efficiency
    • Minor excess employed (≤8%) in routes mitigating downstream purification losses
    • Stringent control of residual starting material: NMT 0.2% in API

    Downstream process integration

    • Introduced during hydrazone condensation with specific carbonyl substrates
    • Reacted in solution-phase or solventless batch reactors at 40–70°C
    • Integrated into multistep synthetic protocols with in-process controls for intermediate verification
    • Subsequent purification via crystallization or preparative HPLC before API conversion

    Final product types

    • Isoniazid hydrazones (intermediates)
    • Thiosemicarbazone-based antituberculosis APIs
    • Substituted pyridines for anti-infective pharmaceuticals
    • Precursors for nitrogen-containing heterocycles in drug research

    2. Agrochemical Synthesis: Fungicide and Herbicide Intermediates

    This raw material features prominently in the synthesis of thiosemicarbazone-class agrochemicals. It provides chemoselectivity and high yield in condensation reactions for crop protection agents. Agrochemical formulators leverage precise stoichiometry to maximize reaction throughput while minimizing unreacted residues, as mandated by international product registration requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH Regulation (EC) No 1907/2006
    • Chinese GB/T standards on agrochemical intermediates
    • EPA (US) pesticide registration and tolerance requirements

    Typical usage ratio

    • 0.9–1.05 mole ratio relative to carbonyl partners in batchwise or continuous synthesis
    • ±5% excess to offset scale-up process inefficiencies
    • Strict limits: residual material below 0.1% w/w in technical-grade actives

    Downstream process integration

    • Dosed at initial condensation step for thiosemicarbazone or hydrazone formation
    • Staged addition to maintain exotherm control and consistent particle morphology
    • Finished intermediate isolated by filtration, followed by drying and particle size reduction
    • Downstream coupling or cyclization leads to active fungicide or herbicide molecules

    Final product types

    • Protective seed treatment agents
    • Broad-spectrum fungicides (e.g., thiosemicarbazone class)
    • Pre-emergence herbicidal intermediates
    • Specialty agrochemical building blocks for custom synthesis

    3. Dye and Pigment Intermediate Manufacturing

    Thiosemicarbazide derivatives perform essential functions in dye and pigment synthesis, especially where electron-withdrawing substituents are needed on azo or thiocarbonyl backbones. The compound’s methoxyphenyl group enhances chromophore stability and spectral selectivity, crucial for high-value specialty dyes. Colour strength, shade fidelity, and batch reproducibility depend heavily on the upstream raw material’s purity profile and reaction completion.

    Industry compliance standards

    • EN ISO 9001:2015 for pigment and dye QC
    • Oeko-Tex Standard 100 (relevant non-ecotoxic dye applications)
    • RoHS Directive 2011/65/EU (where applicable in electronics dyeing)
    • REACH Annex XVII compliance for hazardous substance restrictions

    Typical usage ratio

    • 1.00–1.15 molar equivalents, adjusted for electron donor/acceptor balance in condensation
    • Batches sized 20–500 kg, with in-process colorimetric and HPLC-based monitoring
    • Excess capped at 10% to minimize color contamination during workup

    Downstream process integration

    • Reacted with diazotized aromatic amines to build high-performance pigments
    • Added at controlled temperatures (45–60°C) to prevent byproduct formation
    • Intermediate subjected to sequential coupling or sulfonation for final dye profile
    • Integrated into closed-cycle powder or granular pigment production

    Final product types

    • Special effect azo dyes (for textiles and plastics)
    • High-purity pigment dispersions for inkjet or gravure inks
    • Sulfur-based vat dyes for cellulosics
    • Non-bleeding colorants for packaging films

    4. Analytical Reagents for Heavy Metal Detection

    This compound forms stable complexes with certain transition metals, making it a valuable constituent in analytical formulations for detection and quantification of metals including mercury, silver, and copper. Laboratories in the mining, environmental, and food sectors integrate the reagent into colorimetric kits where detection sensitivity and selectivity require high-purity input. Formulations must reflect batch traceability and conform to documented evidence protocols.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • GLP (Good Laboratory Practice) guidelines
    • NIST-traceable methods for reference material preparation
    • EPA SW-846 for hazardous waste analysis

    Typical usage ratio

    • 0.5–2.5 mg/mL in solution-phase test kits, optimized per specific metal ion sensitivity
    • Custom blending into multi-component detection arrays in volumes up to 50 L
    • Adjustment based on matrix interference and background levels

    Downstream process integration

    • Dissolved under rigorously controlled conditions to ensure reagent homogeneity
    • Introduced at aliquot stage for micro-scale spot and titration tests
    • Stabilized with buffers or chelating agents to extend shelf-life
    • Final reagent incorporated into single-use, standardized detection formats

    Final product types

    • Commercial heavy metal detection kits
    • Analytical reference standards for laboratories
    • Mobile field test strips for groundwater or soil assays
    • Biochemical research reagents for transition metal studies

    5. Synthesis of Specialty Heterocyclic Compounds for Materials Science

    This raw material finds targeted use in research-scale and pilot production of fused heterocyclic scaffolds, notably s-triazoles and diazines with potential optoelectronic activity or polymer-modifying properties. R&D departments and custom synthesis providers exploit its reactivity with electrophilic carbon centers to introduce thioamide functionalities, supporting subsequent transformation into advanced engineering materials or sensor substrates. Material traceability and documentation are necessary for publication and patent support.

    Industry compliance standards

    • ISO 9001:2015 for advanced chemical process management
    • Project-specific internal SOPs and traceability records
    • RoHS compliance for materials eventually targeting electronics uses
    • Patent literature and invention disclosure best practices

    Typical usage ratio

    • 1.0–1.2 mole equivalents per starting ketone or aldehyde in staged syntheses
    • Reaction scale adjustable: 5–200 g for research, up to 25 kg for pre-commercial validation
    • Dose adjusted upwards for multi-step recycling protocols

    Downstream process integration

    • Added during key ring-closure or condensation steps for backbone assembly
    • Facilitates nucleophilic attack and sulfur transfer in presence of controlled acid/base catalysts
    • Intermediate purified via column chromatography or preparative thin-layer methods
    • Support in downstream functionalization for sensor or device applications

    Final product types

    • Triazole-based ligands for metal-organic frameworks
    • Advanced monomers for specialty polymer research
    • Optical or sensor-active heterocyclic derivatives
    • Developmental building blocks for supramolecular assemblies
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    Certification & Compliance
    More Introduction

    Introducing 4-(2-Methoxyphenyl)-3-Thiosemicarbazide: Experience Through Production

    What Sets 4-(2-Methoxyphenyl)-3-Thiosemicarbazide Apart

    In chemical manufacturing, it pays to pay close attention to individual molecule behavior. 4-(2-Methoxyphenyl)-3-Thiosemicarbazide is not just another bench reagent; for us, repeated hands-on experience has shown that its molecular structure sets it apart among thiosemicarbazides. Coupling the 2-methoxyphenyl group to the thiosemicarbazide backbone creates a distinct profile distinguished by its reactivity and selectivity. These properties attract organic synthesis specialists, who value products that cut down side-product formation and drive yields up during heterocycle or intermediate synthesis.

    Batch after batch, we monitor our processes to spot trouble early and tighten every control point. The methoxy group at the ortho position plays a big role in altering solubility and influencing the orientation during condensation reactions. Customers come back to us with reports of predictable reactivity—an asset when working to scale up research or launch new targets. Over years of experience, our adjustments in crystallization protocols have led to solid, consistent product quality. Moisture sensitivity in similar compounds can make handling tedious; we've addressed this sensitivity by fine-tuning our environment and packaging, reducing the risk of clumping or degradation during storage and transit.

    Specifications and Inspection from the Manufacturer’s Bench

    We’ve spent countless days at the bench verifying purity, melting point, and moisture profiles. Most runs reach 98% or above on HPLC, with melting points matching references and a crisp, off-white crystalline appearance. Spectroscopic profile—IR, NMR, and MS—confirms product integrity for every kilogram leaving our warehouse. Our QC process involves not only final analysis, but upstream checking at each synthesis stage. We know from long experience that one misstep during coupling or recrystallization ripples through the whole batch. That’s why our team puts effort into hands-on controls, constant equipment checks, and fresh calibration standards, rather than relying strictly on automated protocols.

    Some peers chase scale by cutting corners or using recycled solvents; we have learned the hard way that shortcutting purification can lead to batch recalls, delayed customer timelines, and wasted investment. Our commitment to detail lets customers skip laborious pre-cleans and move straight to synthesis or screening. We find that chemists tell us they value a supplier who invests in methodical standardization rather than chasing record-breaking batch size.

    Application in Synthesis: Beyond Lab-Scale Curiosity

    4-(2-Methoxyphenyl)-3-Thiosemicarbazide has found a home in both small-molecule research and the expansion of medicinal chemistry libraries. It steps up as a versatile building block in the formation of thiosemicarbazones and other heterocycles. In our experience, researchers targeting new anti-infectives and bioactive assemblies value the ease with which the methoxy group enhances nucleophilicity during cyclizations, helping to drive their reactions cleaner and faster. As a company, we hear feedback from university researchers, pharmaceutical teams, and startup ventures who recognize the difference between a commodity intermediate and a precisely manufactured specialty reagent.

    This compound’s fine balance between electron donation and sulfur-based nucleophilicity gives it a starring role in condensation with carbonyl groups—particularly for scientists attempting to adjust reaction conditions to improve selectivity. We also see customers exploring routes into metal complexation for advanced material applications. From our production side, this means maintaining a purity standard that goes beyond what is sufficient for simple organic transformations. Contaminant traces such as unreacted hydrazine or phenolic solvents can poison downstream catalysts or torque bioassay profiles, so our in-house controls reflect the practical needs of real-world users, not just spreadsheet thresholds.

    Key Differentiators Compared to Generic Thiosemicarbazides

    There is a world of difference between generalized thiosemicarbazides and the 4-(2-Methoxyphenyl) variant. Our day-to-day production confirms what research literature hints at: the methoxyphenyl moiety is far from inert. Its position directly affects solubility in mixed solvent systems and boosts electron density in the aromatic system. That alters reactivity, speeds up condensation with aldehydes and ketones, and influences ligand behavior in coordination chemistry. We’ve carried out side-by-side trials with other thiosemicarbazides, and the difference in crystallization speed, yield, and unwanted byproduct level is more than subtle—it’s striking. This hands-on evidence underpins our ongoing investment in this specific line, responding directly to real results rather than simply trending demands.

    In some commercial products, customers have reported assay drift or unexplained instability. Our technical team has reviewed these reports and traced many root causes back to inconsistent raw material quality or inadequate packing techniques. Over time, we adopted moisture-proof films and vacuum-sealed containers, severing the feedback loop between humidity and product degradation. Unlike resellers or bulk traders, we can trace impurities back to their source—down to pH adjustments during neutralization or temperature fluctuations during filtration. This level of traceability becomes a serious competitive advantage, especially for those relying on product performance for new compound synthesis, bioactivity investigations, or series expansion in SAR projects.

    The Challenges and Our Approach to Continuous Improvement

    As manufacturers, we face routine and unexpected challenges. Batch consistency draws from multiple factors: real-time data from analytics, smell and appearance for early warning signs, and solid communication across production staff. We know from bitter experience that an inattentive shift or minor equipment variance ripples straight into customer labs in the form of puzzling NMR baselines or unexplained losses during purification. Through experience, we have developed a feedback-driven system: every lab, every customer, every return is investigated, and staff meetings dig into root causes, no matter how minor.

    Some difficulties are unique to this compound’s synthesis. Handling methoxyphenyl hydrazines safely and efficiently calls for custom hood modifications and upgraded filtration. The inherent reactivity drives up costs for maintenance and protective gear. We have responded with process refinement, focusing on maximizing reactant conversion while minimizing hazardous waste. With green chemistry in mind, solvent selection and waste handling are modernized continuously—our operators now use recovery and recycling systems that both protect the environment and keep costs reasonable. This kind of commitment reflects years of learning and a refusal to sacrifice quality for speed or short-term profit.

    Collaborative Development with the End User in Mind

    Over time, we’ve moved far beyond the “make and ship” mentality. Our years in the laboratory have taught us the value of two-way communication—many of our process improvements trace their origins to customer conversations. Recently, we collaborated with an academic lab developing thiosemicarbazone analogues for antiparasitic applications. Their exacting solubility requirements led us to adjust particle size control and drying regimes, improving both shelf-life and downstream function. Another group pushed for lower residual solvent limits, prompting a reevaluation of our crystallization steps and gas-phase drying parameters.

    These exchanges bridge the gap between manufacturer and bench scientist. We recognize that chemists working on grant funding, contract research, or competitive R&D projects cannot waste time troubleshooting starting material variability. From weighing to charging reactors to final dispensing and labeling, our entire approach forms a chain of trust, built through attention to detail and shared experience. Customers know their concerns will not vanish into a bureaucratic queue or generic email address; we put specific staff onto feedback, offer direct phone consultations, and document every improvement.

    Regulatory and Safety Perspectives Shaped by Manufacturing Practice

    Years in production teach valuable lessons about compliance, both for our own staff and our clients working under regulatory guidelines. Our records and batch documentation support every delivery out the door, giving transparency into origin, processing steps, and test data. In regulated industries, such as pharmaceuticals or specialty fine chemicals, this paper trail reduces both project risk and the administrative burden on downstream teams during audit season.

    We face regular inspections and adapt to shifting safety standards. For example, reviews by on-site safety teams have prompted revision in containment strategies, with continuous training refreshers for operators and routine emergency drill reviews. Waste profile monitoring matters in high-volume production—a small oversight can trigger unplanned hazard classifications or disposal headaches. Our manufacturing response centers on prevention: regular audits, attention to incident reports, and a culture of precision instead of rushed output.

    We understand that some users must meet not only material compliance standards but also document handling requirements for global shipping or import. Our operations staff take care to prepare traceable documentation, translation support, and rapid sample responses, all with a sense for the time pressures and project budgets of our clients.

    Beyond the Product: Manufacturer’s Commitment

    Manufacturing 4-(2-Methoxyphenyl)-3-Thiosemicarbazide is more than a transactional act. Behind every kilogram stands a host of process improvements, lessons learned from failures, and innovations driven by collaboration. We have seen instrument calibration drift subtly change analytical results; hand inspection offers a final line of defense. We have experienced real-world supply chain disruptions—the kind not found in textbooks—and built backup plans for raw material sourcing, packaging, and expedited testing.

    Unlike anonymous market players, manufacturers gain perspective from exposure to every step, from synthesis to end-user outcome. This informs our dedication to honesty in reporting, responsiveness to feedback, and pursuit of continuous improvement. Chemists, R&D leads, and process engineers who rely on our product get not only a reliable raw material but a partner committed to supporting their goals, understanding the real-world context, and sharing decades of cumulative lessons.

    In the landscape of specialty chemical manufacturing, real expertise means more than reading a data sheet. The outcome for our users is predictability and security: the knowledge that with each use, product behavior reflects hundreds of adjustments, close control, and a manufacturer’s personal stake in performance. We continue to refine our approach based on field experience, new literature, and the honest assessment of our own results. By keeping the dialogue open and the standards high, we work to earn trust one batch at a time.