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(4-Carboxyphenyl)Thiourea

    • Product Name (4-Carboxyphenyl)Thiourea
    • Alias 4-(Thioureido)benzoic acid
    • Einecs 221-679-8
    • 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
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    Specifications

    HS Code

    532184

    Chemical Name (4-Carboxyphenyl)thiourea
    Synonyms 4-(Thioureido)benzoic acid
    Molecular Formula C8H8N2O2S
    Molecular Weight 196.23 g/mol
    Cas Number 4318-56-3
    Appearance White to off-white solid
    Melting Point Approx. 240°C (decomposition)
    Solubility Slightly soluble in water and organic solvents
    Smiles C1=CC(=CC=C1C(=O)O)NC(=S)N
    Inchi InChI=1S/C8H8N2O2S/c9-8(13)10-6-3-1-5(2-4-6)7(11)12/h1-4H,(H3,9,10,11,12,13)

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

    Packing & Storage
    Packing White HDPE bottle, 25 grams, amber safety seal, clear chemical label with name, CAS number, hazard symbols, and lot number.
    Shipping (4-Carboxyphenyl)Thiourea is shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a non-hazardous laboratory chemical, with appropriate labeling and documentation. During shipping, the chemical is kept in a cool, dry place and protected from direct sunlight, following standard safety and regulatory guidelines.
    Storage (4-Carboxyphenyl)thiourea should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. It should be kept away from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental spillage or contamination. Always follow appropriate chemical storage guidelines and safety regulations.
    Application of (4-Carboxyphenyl)Thiourea

    Applications of (4-Carboxyphenyl)Thiourea in Industrial Manufacturing

    (4-Carboxyphenyl)Thiourea supports a range of industrial synthesis and functional applications in specialized chemical manufacturing settings. Below, we detail key downstream sectors where this molecule directly advances process efficiency, product quality, and targeted material properties.

    1. Pharmaceutical Intermediate Production

    In pharmaceutical synthesis, (4-Carboxyphenyl)Thiourea serves as a versatile intermediate for the construction of heterocyclic scaffolds and bioactive ingredients. Medicinal chemistry teams employ it for controlled introduction of the thiourea and carboxylic acid groups to build targeted drug candidate structures. Process chemists focus closely on reaction parameters to preserve functional group integrity and achieve regulatory-compliant purity, as final actives must pass stringent impurity and residual solvent tests. The compound remains prevalent in the downstream formation of sulfonylurea antidiabetic agents and select anti-tumor compound families where its functionality is irreplaceable.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Residual Solvents Guideline Chapter <823>
    • European Pharmacopoeia General Monograph 2034
    • GMP site audit requirements (FDA/EMA/CFDA-specific as applicable)

    Typical usage ratio

    • 0.5–3.5 weight % in stage-specific active synthesis routes, adjusted to product molecular weight and downstream coupling efficiency; ratio can be adjusted based on required yield and byproduct suppression.

    Downstream process integration

    • Integrated at the primary condensation or cyclization step for building heterocyclic core structures
    • Co-charged with other aromatic amines in pre-API step
    • Purified via recrystallization or column chromatography before formulation

    Final product types

    • Oral antidiabetic agents (e.g., sulfonylurea derivatives)
    • API intermediates for anticancer compounds
    • Advanced building blocks for combinatorial chemistry platforms
    • Bulk intermediates supplied to multinational API manufacturers

    2. Agricultural Chemical Synthesis (Herbicide & Pesticide Intermediates)

    Crop protection manufacturers use (4-Carboxyphenyl)Thiourea to introduce selectivity and stability in new-generation herbicides and pesticides, especially where sulfur-containing linkers or acid groups enhance bioactivity or soil mobility. Downstream plants integrate this input at the early condensation or esterification stage, enabling tailored modifications before product formulation. Product stewardship and operator safety teams emphasize adherence to agrochemical-specific standards throughout the process, given the strict residue and environmental requirements set by national agencies.

    Industry compliance standards

    • ISO 9001:2015 for agrochemical manufacturing
    • FAO/WHO JMPR technical specification limits
    • REACH Regulation (EC) No 1907/2006 Substances of Very High Concern evaluation
    • OECD Guideline 509: Residues in Plants

    Typical usage ratio

    • 1–6 weight % based on the specific synthetic pathway, adjusted for active loading and target molecule mass; modification possible for different crop spectra and environmental fate profiles.

    Downstream process integration

    • Introduced in the initial amide or ester bond-forming stages for core pesticide construction
    • Reacted under controlled pH to ensure correct group orientation
    • Undergoes in-situ monitoring for unreacted precursor removal

    Final product types

    • Systemic herbicide intermediates
    • Pre-emergent weed control agents
    • Insecticide precursor compounds
    • Bulk actives for post-patent crop protection solutions

    3. Dye and Pigment Intermediate Manufacturing

    (4-Carboxyphenyl)Thiourea functions as a key linker and modifier in the production of certain azo and reactive dye classes. Dyes requiring improved fiber binding and color fastness incorporate this molecule for its dual functionality, granting the operator process flexibility when adjusting batch coloration profiles. Quality assurance teams ensure the absence of regulated aromatic amine byproducts during scale-up. Environmental and occupational health protocols are enforced due to direct worker contact and effluent treatment requirements in the downstream operations.

    Industry compliance standards

    • ZDHC MRSL V3.1 (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • OEKO-TEX® Standard 100 (relevant for dyes in textile applications)
    • China GB 19601-2005 (Textile Dye Manufacturing Standards)
    • ISO 14001:2015 Environmental Management for chemical processing

    Typical usage ratio

    • 0.7–2.2 moles per mole target dye structure; optimized for color intensity and washfastness according to fiber class and application end-use.

    Downstream process integration

    • Fed into the diazotization or coupling stage for the generation of color bodies
    • Used as a functionalized aromatic unit in the dye backbone assembly
    • Processed via continuous or batch mode, followed by pH-neutralization and salt removal

    Final product types

    • Reactive dyes for cotton and cellulosic fibers
    • Azo pigment intermediates for plastics coloration
    • Dye precursors for high-performance printing inks
    • Specialty formulations for technical textiles

    4. Polymer Additive and Functional Monomer Synthesis

    Leading polymer manufacturers use (4-Carboxyphenyl)Thiourea as a comonomer and reactive additive for performance engineering plastics. Its integration provides increased compatibility, adhesion, and selective crosslinking in specialty resin systems. Production lines utilize the compound during melt blending or solution polymerization steps, and downstream QC focuses on confirming additive uniformity and residual content in the finished matrix. Final applications range from films with tailored permeability to engineered adhesives that require specific acid or sulfur functionalities within their crosslinked frameworks.

    Industry compliance standards

    • ISO 9001 Quality Management (polymer compounding and formulation plants)
    • FDA 21 CFR 177.1520 (when used in polymers for food-contact applications)
    • EN 71-3:2019 (relevant for toys and consumer goods polymer items)
    • RoHS Directive 2011/65/EU for electronics-related polymers

    Typical usage ratio

    • 0.3–2.0 weight % in resin blends; dose determined by desired adhesion, surface energy, or barrier property adjustments in end-use component.

    Downstream process integration

    • Charged as comonomer during initial resin solution-up or melt blend
    • Dispersed in masterbatch or additive concentrate preparation
    • Process monitoring includes melt-flow index and thermal stability testing

    Final product types

    • Functionalized polyethylene films for packaging
    • Polymer coatings for automotive/industrial substrates
    • Sealant and adhesive formulations with engineered reactivity
    • Specialty engineered plastics for electronics assembly

    5. Corrosion Inhibitor Formulation for Industrial Water Treatment

    Chemical formulators rely on (4-Carboxyphenyl)Thiourea as an active agent in high-performance corrosion inhibitor packages, particularly for steel and brine system applications. It imparts both film-forming protection and targeted adsorption on metal surfaces under diverse temperature and pH conditions. Plant engineers incorporate the compound during concentrated batch make-up, and water treatment operators must document compliance with regulatory discharge standards due to the presence of sulfur-containing moieties in downstream effluent.

    Industry compliance standards

    • ASTM G170–06 Standard Guide for Evaluating Inhibitors in Industrial Systems
    • ISO 8044:2020 Corrosion of metals and alloys
    • European Biocidal Products Regulation (BPR, Regulation (EU) No 528/2012)
    • Local regulatory effluent discharge limits (e.g., China GB 8978-1996, US EPA 40 CFR 136)

    Typical usage ratio

    • 60–250 ppm in final industrial water and cooling circuit formulations; adjusted based on alloy composition, water hardness, and system flow conditions.

    Downstream process integration

    • Predissolved into corrosion inhibitor concentrates at operator works
    • Dosed online via automated injection into water loop or steam circuit
    • Process monitored by iron release rate and surface film characterization

    Final product types

    • Corrosion inhibitor concentrate blends for industrial water systems
    • Ready-to-use water treatment agents for closed and open-loop circuits
    • Specialized anti-fouling formulations for oilfield brine treatment
    • Additive packages for boiler and heat exchanger maintenance kits
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    Certification & Compliance
    More Introduction

    (4-Carboxyphenyl)Thiourea: Performance, Purity, and Practical Advantages

    A Deeper Look at (4-Carboxyphenyl)Thiourea from the Manufacturer’s Bench

    Every day in the lab, the discovery of fine-tuned molecules like (4-Carboxyphenyl)thiourea, also known as 1-(4-Carboxyphenyl)-2-thiourea or PCTU, opens doors to new possibilities in research and production. With nearly twenty years of hands-on experience handling thioureas, the journey from small-scale syntheses to routine, large-batch production has taught practical lessons about quality, reproducibility, and user needs. Consistent control over raw materials and meticulous reaction monitoring allow us to ensure product consistency.

    We produce (4-Carboxyphenyl)thiourea with an eye for both purity and versatility. Most lots reach purity levels above 99% by HPLC analysis. Typical batch sizes range from a few kilograms for pilot work to several hundred kilograms for regular industrial clients, with each lot carrying a certificate of analysis matching the data our own R&D chemists expect. Granular, off-white to slightly yellow powder is a common appearance, reflecting minor variations during crystallization, but never impacting usability.

    Reliable Handling and Practical Performance

    A careful, reproducible drying procedure keeps residual moisture well below 0.5%. We store and pack (4-carboxyphenyl)thiourea in sealed containers under nitrogen. This prevents slow oxidation, especially if storage exceeds six months or in regions with high humidity. End-users in pharmaceuticals, dye intermediates, polymer research, or specialty chemicals comment on the product’s flowability and solubility. Dissolution in water, DMF, or DMSO runs smoothly, usually without requiring extra filtration steps. As manufacturers, we keep a close watch on physical properties like particle size to keep the process simple for downstream users.

    Handling thioureas for so long uncovers subtle patterns: products with broader particle size distributions often clump in automated dispensers. We monitor our granulation repeatedly and adjust dryer temperatures and sieving steps to ensure uniform handling during dissolution and weighing. These details, though minor on paper, save time and budget for our customers’ chemists.

    Applications: Real Results on the Lab Bench and Beyond

    (4-Carboxyphenyl)thiourea’s unique structure provides both a urea-like unit for hydrogen bonding and a carboxy group for further reaction or salt formation. Academic collaborators in medicinal chemistry pursue new bioactive libraries using our material as a key building block. Its N–C(=S)–N linkage brings reactivity not seen in most simple thioureas—giving it value in everything from pharmaceutical screening to custom ligand development. Polymer engineers request the carboxy aryl thiourea motif for new conductive materials and responsive polymer chains, leveraging its specific coupling potential.

    Large-scale formulators use (4-carboxyphenyl)thiourea as a functional monomer for specialized resins and adhesives. Its reactivity fits well in cross-linking schemes, especially where sulfur-containing linkages enhance resistance or promote conductivity. Textile dye chemists appreciate the product’s role in mordanting or as a precursor for developing chromophores with unique bathochromic shifts. All of these uses depend on keeping trace impurities—like oxidized forms or unreacted aniline—under strict limits. Our analytical protocols routinely screen for contaminants down to below 100 ppm, confirming each lot’s readiness for demanding syntheses.

    Comparing with Other Thioureas and Functionalized Aromatics

    Our team often fields technical questions on why chemists select this particular carboxy-substituted thiourea over, say, a simple unsubstituted thiourea or a 4-carboxyaniline. Feedback shows that the carboxyphenyl group unlocks reactions not possible with smaller or less functionalized aromatic rings. It offers easy coupling for peptide and amide bond formation and can be activated for further elaboration, which comes in handy during multi-step syntheses.

    Comparing (4-Carboxyphenyl)thiourea with p-tolylthiourea or unsubstituted thiourea, the major difference lies in its dual functionality: the carboxylic acid group provides a reactive site for additional chemistry—amidation, esterification, or salt formation—while the thiourea core maintains classical hydrogen bonding and nucleophilic properties. In pharmaceutical contexts, it enables library growth in combinatorial chemistry or SAR studies by providing a handle for straightforward derivatization. Regular thiourea, while versatile, cannot couple as easily to biomolecules or surfaces, and derivatives lacking the acid group miss out on key reactivities for crosslinked systems.

    Key Observations from Scale-Up and Routine Manufacturing

    Experience shows that (4-Carboxyphenyl)thiourea’s synthesis hinges on high-quality starting materials and real-time pH management. We employ direct condensation of 4-carboxyaniline with thiocyanate sources, followed by careful crystallization—no shortcuts, because rushed cooling steps lead to occluded solvents, reduced shelf stability, and batch inconsistency. Extended experience with this route yields high reproducibility, typically above 90% isolated yield. We fine-tune solvent ratios and filtration speeds to minimize inclusion of micron-sized impurities.

    Packaging and shipment receive attention, as even small dampness can shift physical properties. Storing at room temperature out of sunlight usually keeps the product stable for years if the seal remains intact. Internal stability trials include temperature cycling and humidity testing, simulating transport across continents. These data often convince our customers to replace unreliable suppliers: repeat shipments behave the same way and show no loss of performance even after prolonged voyages.

    Supporting Research and Process Development

    Over many projects, researchers tell us their biggest headaches involve inconsistent product lots. In-house QC labs, coupled with regular communication between production and R&D, allow us to offer consistency exceeding most traders and third-party resellers. This lowers the risk of batch-to-batch surprises and avoids expensive rework. Our lead chemists frequently visit customer sites to troubleshoot unexpected results, bringing direct manufacturer insights to process refinement.

    Documentation comes from the same hands formulating, synthesizing, and packaging each lot, so discrepancies and paperwork errors remain minimal. Should a customer need a nonstandard mesh size or special drying protocol, we transfer lab findings to plant scale without delays. Such adjustments—not just theoretical purity—keep real-world projects on track.

    Minimizing Impurities and Maximizing Reproducibility

    Every batch’s success hinges on impurity control. A low content of inorganic salts from side reactions, absence of colored by-products, and minimal decomposition byproducts make (4-carboxyphenyl)thiourea trusted for high-sensitivity applications. We’ve learned that high-performance liquid chromatography, NMR, and mass spectrometry together catch almost every trace impurity, including those only appearing after stress testing.

    From experience, skipping confirmatory analyses might save time, but even minute impurities can ruin lability tests or cause undesired side reactions downstream. Rigorous analytics, supported by an on-site technical team, mean more reliable results with every batch. When a client’s own in-house data conflicts with ours, we dive into root-cause analysis—checking their solvent quality, reviewing sample handling, and repeating critical tests until we agree on the outcome.

    Sustainable Manufacturing Practices

    Modern production must respect both environmental limits and operator safety. Our facilities invest in automated solvent recovery, on-site neutralization of acidic waste, and rigorous PPE protocols. Every kilogram of product comes with minimized waste and documented batch-level carbon impact. Lessons learned over the years mean more efficient solvent loops, less off-gas, and cleaner effluent. Our R&D chemists share their best practices at industry forums, supporting green chemistry initiatives that benefit the broader field.

    Real-World Case Studies: Feedback Directly from the Field

    In one project, a customer’s high-throughput screening campaign flagged unexpected crystallization problems with a competitor’s material. Sourcing our in-house (4-carboxyphenyl)thiourea resolved the solubility anomalies, returning their hit rates to normal. In another case, a European adhesive manufacturer required ultra-low chloride content to avoid downstream polymer discoloration: adjustments to our filtration protocol reduced residual salts by a further 40%, delivering clear, color-stable end products.

    These collaborations make our plant teams proud and build trust within our client base. Regular site audits ensure our claims match what customers witness during their own quality reviews.

    Future Outlook: Continuous Improvement, Open Doors

    Looking forward, we aim to combine careful process control with flexibility. At least twice a year, customer feedback sessions inform our investments in plant upgrades and QC instrumentation. The target never stands still, as emerging applications—especially in biomedicine and electronics—demand even higher purity or special modification of existing molecules. Our task as manufacturers remains to listen, adapt, and supply (4-carboxyphenyl)thiourea that meets the very latest standards without undue additives, shortcuts, or hidden variables.

    We encourage technical partners, research groups, and scaled-up end users to visit our facility, witness the process, and shape future spec adjustments together. Building on a foundation of chemistry, transparent partnership, and hard-won lessons ensures that each delivery reflects more than just a catalog entry—it reflects years of practical know-how and a commitment to advancing the chemistry field as a whole.