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3-Chlorocinnamic Acid

    • Product Name 3-Chlorocinnamic Acid
    • Alias 3-Chloro-cinnamic acid
    • Einecs 208-950-5
    • 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

    366435

    Product Name 3-Chlorocinnamic Acid
    Cas Number 2142-68-9
    Molecular Formula C9H7ClO2
    Molecular Weight 182.61 g/mol
    Appearance White to off-white solid
    Melting Point 201-204 °C
    Boiling Point 352.1 °C at 760 mmHg
    Density 1.336 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 3-Chloro-β-phenylacrylic acid
    Smiles C1=CC(=CC(=C1)Cl)C=CC(=O)O
    Inchi InChI=1S/C9H7ClO2/c10-8-4-1-3-7(5-8)2-6-9(11)12/h1,3-6H,2H2,(H,11,12)
    Ec Number 218-403-7
    Pka 4.13

    As an accredited 3-Chlorocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Chlorocinnamic Acid, 25g, packaged in a sealed amber glass bottle with a screw cap, labeled with hazard and product information.
    Shipping 3-Chlorocinnamic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is classified as a non-hazardous material for transport but should be handled with care. Store and ship at room temperature, away from incompatible substances. Appropriate labeling and documentation are included to ensure safe and compliant delivery.
    Storage 3-Chlorocinnamic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Ensure proper labeling and keep away from food and drink. Follow standard chemical storage protocols to prevent contamination or accidental exposure.
    Application of 3-Chlorocinnamic Acid

    Applications of 3-Chlorocinnamic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Chlorocinnamic Acid to leading companies across several chemical-based sectors. Recognized for its precision as an intermediate, this material drives efficient, compliant advancements in high-value downstream production. Below we outline its established roles in industrial markets, with detailed application profiles and specification guidance.

    1. Pharmaceutical Intermediates for Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

    3-Chlorocinnamic Acid serves as a key intermediate in the custom synthesis of specific NSAIDs, where its halogenated aromatic structure enables targeted modifications during active pharmaceutical ingredient (API) assembly. Pharmaceutical formulation teams select it for its reactivity in amide coupling and cyclization steps, supporting molecules like mefenamic acid derivatives in scale-up under GMP conditions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211, US FDA)
    • EU GMP Guidelines (EudraLex Volume 4)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monograph references for intermediates according to pathway

    Typical usage ratio

    • 0.5–2.5 molar equivalents in coupling and condensation reactions; actual amount depends on API reaction pathway and yield optimization studies

    Downstream process integration

    • Introduced at the initial building block stage in multi-step synthesis; undergoes amidation, chlorination, or cyclization in glass-lined or stainless steel reactors, then purified before subsequent reactions

    Final product types

    • Active pharmaceutical ingredients for prescription NSAIDs
    • Generic bulk drugs supplied to formulation facilities
    • Key intermediates for analgesic molecule development

    2. Agrochemical Synthesis: Selective Herbicide Intermediates

    In agrochemical plants, 3-Chlorocinnamic Acid acts as a carbon skeleton donor for the synthesis of cinnamate-based herbicide molecules. Process chemists favor this compound for its stable chloro-aryl structure, which allows efficient side chain modification during oxidative coupling, contributing to the production of targeted broadleaf herbicides with selectivity in cereal crops.

    Industry compliance standards

    • FAO/WHO: International Code of Conduct on Pesticide Management
    • ISO 9001:2015 for agrochemical production management
    • OECD Guidelines for the Testing of Chemicals
    • REACH regulation (EC 1907/2006) for registration of intermediates

    Typical usage ratio

    • 1.0–3.0% w/w as precursor loading in batch or continuous-flow synthesis; adjusted based on catalyst system and desired conversion

    Downstream process integration

    • Charged at the primary synthesis stage; enters Friedel-Crafts or oxidative catalyst reactions to yield substituted cinnamic acid derivatives, then processed through crystallization and formulation blending

    Final product types

    • Technical-grade herbicide actives for post-emergence formulations
    • Emulsifiable concentrate and wettable powder herbicide products
    • Precursor blends for custom agrochemical synthesis

    3. Liquid Crystal Monomer Preparation for Display Manufacturing

    Manufacturers of advanced liquid crystal (LC) materials utilize 3-Chlorocinnamic Acid as a monomeric precursor for the synthesis of nematic and smectic phase molecules. Its conjugated structure facilitates high-order molecular alignment after esterification or etherification, crucial for the optical clarity and electro-optic response required in large-area display panels and precision instrument optics.

    Industry compliance standards

    • ISO 9001:2015 certified quality management for specialty chemicals
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances in electronics
    • IEC 62321 for LC panel environmental compliance
    • Corporate proprietary QC protocols for electronics-grade raw materials

    Typical usage ratio

    • 7–18 mol% as a backbone component depending on the specific LC blend and index targets; content adjusted based on birefringence, dielectric anisotropy, and stability parameters of the final mix

    Downstream process integration

    • Supplied as a purified intermediate for direct monomer synthesis; processed by acylation or etherification combined with alkyl/aryl tails to improve LC phase behavior, followed by vacuum distillation and blending under nitrogen

    Final product types

    • Nematic and smectic liquid crystal mixtures for TFT-LCD manufacturing
    • Specialty LC compounds for optical compensators and imaging displays
    • Test cell batches for new panel prototypes

    4. Fragrance Intermediate for Fine Chemical Aroma Ingredients

    Fine chemical fragrance formulators select 3-Chlorocinnamic Acid for synthesizing chiral esters and alcohols with nuanced green and spicy notes. Its aromatic backbone is preferred in the esterification and reduction steps essential to create signature ingredients for designer perfumes and high-end personal care applications, where traceability and purity meet IFRA requirements for safety and performance.

    Industry compliance standards

    • IFRA Code of Practice for ingredient safety and quality
    • ISO 9235:2013 for terminology and criteria in aroma chemicals
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • Good Manufacturing Practice (ISO 22716)

    Typical usage ratio

    • 2–9% by weight in initial formulation batches; scaled depending on target ester/alcohol structure and yield after distillation

    Downstream process integration

    • Introduced as a feedstock in batch reactors for Fischer esterification or catalytic hydrogenation; followed by fractional distillation and GC-based purity analysis before use in fragrance blending labs

    Final product types

    • Aroma intermediates for fine fragrances
    • Specialty alcohols for luxury cosmetic formulations
    • Signature notes for personal care and home scent products
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    Certification & Compliance
    More Introduction

    3-Chlorocinnamic Acid From The Chemist’s Bench

    Meeting The Needs Of Modern Synthesis

    At our factory, chemists and engineers rely on tried and true bench experience to turn the blueprint of 3-Chlorocinnamic Acid, also called trans-3-chloro-3-phenylacrylic acid, into a consistent product. The interest in this specialty chemical comes from both its unique structure and the reactions it enables. Our process focuses on producing the trans isomer, recognized by its practical profile and better handling in a variety of organic transformations. We always work to keep specifications clear and purposeful—so our 3-Chlorocinnamic Acid batch typically offers an assay above 98%. Moisture and impurity levels hold close to the detection limits achievable by current GMP laboratory practice, keeping the product free from side-process residues and problematic aromatic byproducts.

    As a manufacturer, we see demand for this acid from laboratories large and small. Universities, pharmaceutical developers, dye makers, and specialty polymer research teams all send inquiries at some point. We don’t see this as a commoditized chemical. Every pathway and process tends to require specific parameters: some users need finer crystals or certain solubility, others ask for larger one-time volumes or regular scheduled shipments. In every case, the request reflects the downstream chemistry, so we respond by tuning drying conditions, filtration methods, and packaging integrity. Whether it’s a kilogram clamshell or a full drum, we prepare batches with clear purpose and real-world lab use in mind.

    What Sets 3-Chlorocinnamic Acid Apart?

    Aromatic cinnamic acids offer broad value, but the 3-chloro version stands out for how it helps bridge classic and modern synthetic steps. The molecule anchors a conjugated system that can undergo many types of typical organic transformations—amidation, esterification, hydrogenation, and various coupling reactions. The chlorine substitution at the 3-position opens further functionalization routes and increases stability under many lab conditions. When researchers want to build up molecules with organochlorine signatures, or shift the reactivity patterns compared to unsubstituted cinnamic acid, this one chemical makes a real difference.

    Each year we get requests comparing 3-chloro to its siblings—plain cinnamic acid, methoxy, methyl, or para-chloro substituted versions. The 3-chloro group changes more than just reactivity. It raises melting points modestly, provides new leverage for cross-coupling, and shifts absorption properties enough that some dye and pigment manufacturers use it over alternatives. In pharmaceuticals, subtle steric and electronic effects play a role: some bioactive compounds trace their improved profile back to a strategic chlorine atom introduced on the aromatic ring at this location.

    Manufacturing Insights And Quality Considerations

    Having a hands-on role in production means understanding which parameters make the biggest difference at each step. In our workshop, we monitor the condensation process that forms the base trans-cinnamic acid and apply careful temperature and reagent controls to introduce the chlorine at the third position. Early on, we learned that leaving even small amounts of the cis isomer or di-chlorinated byproducts during workup led to headaches for downstream customers. Quality analysis reaches into every drum and jar—a blend of classic titration and NMR runs for identity and purity, with HPLC and GC methods for residual solvents and side materials. We’ve seen projects fail at bigger companies because a supplier underestimated the significance of a consistent UV profile or dry weight. That’s a lesson we keep front-of-mind.

    We take pride in documenting real-world lot data. Our 3-Chlorocinnamic Acid never hides behind vague numbers. Lot-by-lot, we record melting points, visual appearance, and even minor sensory characteristics. Some labs use our material for optical clarity tests, so we track particle shape and size distribution regularly. Those aren’t just numbers on a spec sheet—they’re outcomes of hands-on work, monitored by people who value getting things right for the next person down the chain.

    Why This Product Still Draws Research Interest

    Each month brings different project leads. Sometimes it’s an academic researcher scaling organometallic couplings with this acid as a precursor; sometimes a medicinal chemist working on a lead compound for oncology or anti-viral research. In those cases, the need for pure material at larger scales pushes us to evaluate every step of our workflow. Over time, the market has shown that 3-Chlorocinnamic Acid forms a niche without being exotic. It isn’t a commodity like acetic acid, but neither is it so rare that replacement options look more attractive in routine R&D. Its role is often as a scaffold, an intermediate for new ring systems, or as a labeled standard for chromatography. Each use case brings different purity requirements or documentation expectations.

    Pharmaceutical and agrochemical researchers frequently compare our 3-chloro product directly to the unsubstituted cinnamic acid when searching for selective biological effects. That extra chlorine atom, especially in the meta-position, can alter everything from solubility in formulation to cell-line uptake in tests. Researchers see, sometimes, a jump in efficacy or a change in toxicity profile. In synthetic pathways involving palladium or nickel-catalyzed chemistry, the 3-chloro group can serve as a launching point for Suzuki, Heck, or Stille couplings. The region-selective reactivity simplifies later transformations and avoids unwanted side reactions. This capability encourages manufacturers, including us, to keep refining cost, scale, and purity.

    Safety, Handling, And Real-Life Observations

    From the factory floor to the shipping room, we see the importance of clear labeling and smart handling of aromatic acids. 3-Chlorocinnamic Acid deserves respect in open-bench chemistry for its mild irritant nature. Unlike some halogenated aromatics, it doesn’t generate acute hazards with standard lab gloves and goggles, but dust control and careful packaging play a role in real-world safety. Staff preparing weight-outs in our facility use particulate hoods and wear dust masks when measuring large volumes. On rare occasions, static or humidity can complicate powder handling; we counter this with anti-static liners and humidity controls in our packing rooms.

    We regularly advise clients to reseal containers promptly to avoid moisture uptake. The trans-crystalline form can clump if exposed to wet air for too long, which impacts not only dosing but also solubility in some solvents. These are little things that add up in efficiency—especially when downstream teams depend on accurate weighing and dissolution for their next reaction, scale-up, or biological assay. Our own shipping staff have developed tricks for keeping containers tight without adhesives that might off-gas or contaminate the material, and we choose packaging compatible with both chemical resistance and ease of opening in a busy lab.

    Environmental And Regulatory Perspectives

    Working as a manufacturer with firsthand sights on regulatory developments means staying nimble when standards shift. For 3-Chlorocinnamic Acid, the major focus areas are waste minimization and traceability of halogen-containing aromatic waste streams. Our operation puts energy into solvent recycling systems and batch documentation capable of passing scrutiny from local and international oversight. There’s no substitute for detailed batch records—it comes down to trust and verified control, not just internal pride. Our team has seen audits move faster when paperwork is transparent and every lot can be traced back through every lab log and storage cycle.

    We observe increased attention to halogen-containing fine chemicals from authorities in both chemical production and transport. As more countries implement reporting requirements around aromatic chlorine derivatives, adaptability and honest communication come to matter more than ever. In our business, knowledge transfer between generations of chemists keeps everyone sharp about safe handling, legal requirements, and up-to-date disposal strategies.

    Comparing 3-Chlorocinnamic Acid With Related Products

    With years in the business, we’ve fielded technical comparisons from customers—how does the 3-chloro version measure up against 4-chloro, 2-chloro, or plain cinnamic acid in practice? The differences go beyond what’s written on a reaction scheme. The 3-chloro group’s position can improve yields in catalyzed reactions where ortho- or para- isomers would generate byproducts. The electron-withdrawing effect fine-tunes biological target affinity in exploratory agrochemical work. In dye chemistry, the color shift and stability under various processing steps can lead a formulator to select our 3-chloro acid over more common variants or mixtures.

    In our own experience, solvent selection often changes when working with the 3-chloro compound. Whereas plain cinnamic acid dissolves more easily in less polar solvents, the substituted versions sometimes demand extra heat or substitution with chlorinated or polar aprotic solvents to obtain fast dissolution at higher scales. For teams scaling up reactions for pilot plant runs, these solubility and crystallization quirks affect everything from batching speed to filtration equipment. We record and share real-world notes with long-standing clients looking to optimize for specific protocols—sometimes an extra note from a past batch can save hours of repeat trials in a separate lab.

    Addressing Production And Market Challenges

    Making and marketing 3-Chlorocinnamic Acid rarely runs on autopilot. Supply chain shifts, spec changes, or regulatory updates always bring new wrinkles. Occasionally, upstream shortages of chlorinated precursors or market swings in aromatic feedstocks force us to switch suppliers, screen new lots, or redesign purification systems. Transparency about what’s in, and not in, the product keeps our users in the loop on any potential shifts. Some applications, especially in pharma or analytical standards, demand strict consistency: one misplaced contaminant can invalidate months of research. With that in mind, our batch records, sample archiving, and customer communication loops run deep.

    New requests keep us on our toes. Researchers sometimes want minor modifications—slightly adjusted particle sizes, reduced residual solvents, or documentation on batch-specific spectral features. That’s more than a paperwork exercise. In several cases, we’ve rebuilt part of a purification train to squeeze out an unwanted trace impurity, even when that meant adjusting batch scale or running extra analytical controls. It’s not just about “meeting a spec”—it’s about real chemistry and open feedback. That approach has earned loyal customers who keep returning with fresh problems for us to solve.

    Storage and transit create their own daily challenges. International shipping of fine chemicals can attract scrutiny, especially with halogenated organics. We learned early to work directly with customs brokers and offer alternative documentation based on shipment destination. Stable packaging in airtight, chemical-resistant containers allows product to survive long journeys with reliable purity. That stage comes after dozens of hands-on checks, but it’s no less important than any lab step before it. Our best customers know they can trust the product to arrive in working shape because they see it firsthand, not just on a certificate.

    Research, Innovation, And Looking Ahead

    From drug screening projects to organic electronics, the space for novel halogenated aromatic acids continues to expand. We exchange ideas with academic collaborators and industrial users, passing hard-won knowledge up and down the lab chain. Some clients push beyond current boundaries—attaching labels, generating isotopically marked molecules, or testing new coupling catalysts built around the robust trans-3-chloro skeleton. In that sense, 3-Chlorocinnamic Acid acts as both a classic building block and a starting point for creative synthetic plans.

    Our crew tries to keep ears open to the needs of frontline researchers. Sometimes that means running a smaller batch just to test an unusual purification method; other times it’s about repeated short-run lots to match a development timeline. Timelines and budgets rarely stretch far in research, so our feedback loops and in-process documentation keep everyone agile and avoid delays.

    From real-world use, we know that even a reliable reagent can surprise—unexpected polymorphs, minor color variations, or subtle shifts in IR signatures can crop up with scale or process tweaks. Not all of these bumps prove critical, but rigor, honesty, and open dialogue help keep research on track. Over time, it’s these relationships and the flow of technical know-how, not just paperwork, that set good manufacturers apart.

    Conclusion: Genuine Craftsmanship In Chemical Supply

    To us, 3-Chlorocinnamic Acid isn’t just another molecule. The journey from raw material, through synthesis and purification, to a shelf-ready product reflects years of collective learning. Our process runs on both experience and listening—watching for shifting needs, capturing user feedback, and sharing practical know-how. This acid continues to find new roles as researchers chart the boundaries of chemistry and industry. Our commitment remains hands-on and real-world: no shortcuts, no guesswork, and a dedication to making sure the next batch lives up to both expectation and imagination.