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3-Chloro-4-Methoxybenzaldehyde

    • Product Name 3-Chloro-4-Methoxybenzaldehyde
    • Alias 3-Chloro-p-anisaldehyde
    • Einecs 629-032-6
    • 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

    434621

    Chemicalname 3-Chloro-4-Methoxybenzaldehyde
    Casnumber 26380-45-8
    Molecularformula C8H7ClO2
    Molecularweight 170.59
    Appearance White to off-white solid
    Meltingpoint 65-70°C
    Boilingpoint 282-284°C
    Density 1.29 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC1=CC(=CC(=C1)Cl)C=O
    Inchi InChI=1S/C8H7ClO2/c1-11-8-3-2-6(5-10)4-7(8)9/h2-5H,1H3
    Refractiveindex 1.567 (predicted)
    Storageconditions Store in a cool, dry place and tightly closed container

    As an accredited 3-Chloro-4-Methoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 3-Chloro-4-Methoxybenzaldehyde is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 3-Chloro-4-Methoxybenzaldehyde is shipped in tightly sealed containers to prevent contamination and moisture exposure. The packaging complies with chemical safety regulations, and the product is labeled with hazard information. It is transported under ambient conditions, away from incompatible substances, ensuring safe delivery and preservation of chemical integrity during transit.
    Storage **3-Chloro-4-methoxybenzaldehyde** should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizing agents. Protect it from light and moisture. Ensure proper labeling, and store at room temperature or as specified by the supplier. Always keep away from heat sources and ignition points, and follow standard chemical storage protocols.
    Application of 3-Chloro-4-Methoxybenzaldehyde

    Applications of 3-Chloro-4-Methoxybenzaldehyde in Industrial Manufacturing

    3-Chloro-4-methoxybenzaldehyde supports specialized synthesis processes in several targeted downstream industries. The following application cases detail real-world usage, regulatory requirements, formulation ratios, process integration points, and end-use product categories as practiced within advanced manufacturing environments.

    1. Pharmaceutical Intermediate for Anti-diabetic Drug Synthesis

    This compound acts as a core building block in the formation of intermediate molecules for the preparation of certain classes of anti-diabetic agents, notably within thiazolidinedione and related structures. Chemists select this aldehyde for its site-specific reactivity, which allows for the precise installation of functional groups needed for active pharmaceutical ingredient (API) assembly. During controlled batch synthesis, careful monitoring of stoichiometry and impurity profiles is required to achieve finished intermediates that fit international drug submission specifications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP)
    • Ph. Eur. 10.0 (European Pharmacopoeia, Monographs applicable for intermediates)
    • China Pharmacopoeia (2020 Edition, Volume IV, chemical raw material controls)

    Typical usage ratio

    • 0.85–1.15 equivalents relative to primary amine or other condensation partner, based on optimized route design and desired yield; adjustment determined by target conversion rates.

    Downstream process integration

    • Forms key intermediate via condensation or cyclization steps in active ingredient synthesis line; usually introduced during initial coupling phase following solvent exchange or extraction from precursor stage.

    Final product types

    • Pioglitazone and rosiglitazone intermediates
    • Other synthetic anti-hyperglycemic drug precursors
    • Advanced intermediates for small molecule APIs
    • Fine chemical compounds for pharmaceutical R&D

    2. Agrochemical Active Ingredient Synthesis (Herbicides)

    Manufacturers in the agrochemical sector utilize this molecule to construct specific aromatic scaffolds in selective herbicide synthesis. The aldehyde group serves as a handle for subsequent functionalization, enabling regioselective transformations that are critical for producing high-purity crop protection agents. Strict process controls govern the use of chlorinated aromatic raw materials owing to regulatory oversight on both environmental impact and worker safety during multi-step synthesis campaigns.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration of Pesticides
    • ISO 9001:2015 Quality Management Systems for chemical blending
    • REACH (EC 1907/2006) Substances of Very High Concern (SVHC) assessment
    • GB 20784-2006 (China National Standards—Safety of Pesticide Formulations)

    Typical usage ratio

    • 15%–30% by weight in multi-component synthesis; precise ratio varies according to the molecular design of the intended herbicide and degree of substitution in final structure.

    Downstream process integration

    • Introduced during the first or second synthetic transformation as a precursor for functionalized benzene rings; serves as an electrophilic agent in key carbon-carbon bond-forming steps in pilot and full-scale reactors.

    Final product types

    • Selective herbicide actives (e.g., substituted benzaldehyde-derived herbicides)
    • Intermediates used in the synthesis of insecticides and fungicides
    • Synthetic plant protection research compounds
    • Technical grade crop science product lines

    3. Fragrance Chemical Synthesis for Specialty Aromatics

    Fine fragrance producers apply this compound to create methoxy- and chloro-substituted aromatic aldehydes for use in luxury perfume bases and aroma ingredient compositions. The compound serves as a key reactant in the construction of high-value aromatic cores that impart unique olfactory notes, especially in the development of aldehydic and spicy fragrance accords. Strict quality assurance protocols address trace contamination and sensory profile integrity from raw material onward.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and QRA Guidelines
    • ISO 9235:2013 (Aromatic Natural Raw Materials—Terminology)
    • 21 CFR 172.515 (US FDA—Food Additive Permitted for Direct Addition to Food for Human Consumption, for flavor and fragrance chemicals)
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products (for fragrance safety)

    Typical usage ratio

    • 0.5%–5% in fragrance concentrate synthesis; scale adjusted according to desired olfactory impact and target intensity in finished formulation.

    Downstream process integration

    • Employed at the initial step of aromatic aldehyde formation; enters subsequent acylation, etherification, or cross-coupling sequences in the core aroma molecule manufacturing process.

    Final product types

    • Luxury perfume and Eau de Parfum bases
    • Specialty aroma chemicals for household and fine fragrance applications
    • Flavor and fragrance additive blends for personal care goods
    • Formulated scents for home and air care markets

    4. Fine Chemical Intermediate in Liquid Crystal Material Synthesis

    Producers of advanced materials incorporate this benzaldehyde derivative into synthetic pathways for liquid crystal intermediates, supporting the fabrication of high-performance display technologies. Its structural attributes facilitate precise alignment and functionalization in the synthesis of mesogenic compounds, required for consistent optical characteristics. Tight batch control, trace impurity management, and adherence to electronic-grade material standards are central to quality assurance.

    Industry compliance standards

    • IEC 61249-2-7 (Materials for printed boards and other interconnection structures for electronics)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances for electronic components)
    • ISO 9001:2015, specialized for electronic-grade chemicals
    • JIS C5016 (Japan Industrial Standards for liquid crystal display materials)

    Typical usage ratio

    • 5%–15% molar equivalent in multi-step synthesis of mesogenic core units; adjusted according to target molecular orientation and phase transition properties desired in LCD applications.

    Downstream process integration

    • Integrated at the aromatic aldehyde formation stage; further converted via Wittig or Schiff-base reactions to build mesogenic backbones; subsequently processed in purity refinement phases prior to device assembly.

    Final product types

    • Liquid crystal intermediates for TFT displays
    • Specialty monomers for OLED and advanced photonic devices
    • Precursors for display panel material innovation
    • High-purity aromatic compounds for electronic-grade technologies

    5. Dye and Pigment Synthesis for Specialty Colorants

    Advanced pigment and dye manufacturers employ this benzaldehyde derivative to create functional chromophores and colorant intermediates. The methoxy-chloro substitution pattern provides both reactive versatility and color modulation capability, serving as a precursor in synthesis of azo and anthraquinone-based dyes. Formulators carefully control input ratios and reaction parameters to meet fastness and shade standards relevant to technical and specialty textile markets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile and leather chemicals
    • ZDHC Manufacturing Restricted Substances List (MRSL) for dye and pigment components
    • EN 71-3:2019 (Safety of Toys—Migration of certain elements, for colorants)
    • ISO 1833 Series (Textiles—Quantitative chemical analysis, relevant to dyestuffs)

    Typical usage ratio

    • 3%–12% by mole in batch or continuous dye synthesis, adjusted for chromophore density and compatibility with auxiliary components in downstream formulations.

    Downstream process integration

    • Added to diazotization, coupling, or cyclization stages in dye molecule construction; subsequent purification and blending prior to scale-up batch processing.

    Final product types

    • Technical and textile-grade organic pigments
    • Specialty colorants for inks and coatings
    • High-performance synthetic dyes for industrial applications
    • Color filter materials for electronics and printing
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Methoxybenzaldehyde: Insights from the Chemical Manufacturer's Viewpoint

    At our facility, chemists spend years perfecting the synthesis of 3-Chloro-4-Methoxybenzaldehyde. We recognize this benzaldehyde derivative for its versatility in fine chemical manufacturing, especially because its chloro and methoxy substituents set it apart from other aromatic aldehydes. Running reactions at scale brings challenges—not just in terms of yield optimization, but also in creating material that behaves consistently in downstream applications. When we pour resources into process development, the focus centers on purity, reproducibility, and safety, qualities that matter most to end users in pharmaceutical intermediates, agrochemicals, and sophisticated flavor and fragrance work.

    Understanding the Chemistry: Molecular Structure Drives Performance

    3-Chloro-4-Methoxybenzaldehyde (CAS 836-86-0) features a carefully arranged chloro group at the meta-position and a methoxy at the para-position of the benzaldehyde core. This combination of electron-withdrawing and electron-donating substituents shapes the molecule’s reactivity, changing how it contributes to condensation reactions, nucleophilic substitutions, or other complex modifications. Unlike basic benzaldehyde, which many chemists find too reactive for specialized coupling, this molecule offers both selectivity and stability. Labs rely on these predictable features, especially when precision determines yield.

    Commoditized benzaldehydes often face broad tolerances and variable impurity profiles. Over years of process improvement, we have learned to avoid the trace byproducts—like isomers, chlorinated or methylated tars, or residual solvents—that can turn a simple reaction into a purification headache downstream. Preparing this product to exacting specs under rigorous QC doesn’t only reflect pride in our work; it directly affects how easily our customers take the molecule into the next synthesis step. In medicinal chemistry, one missed impurity can cascade into high development costs or, worse, latent product failures.

    Specifications and What They Mean for Users

    We manufacture 3-Chloro-4-Methoxybenzaldehyde as a pale yellow solid at room temperature. Typical assay exceeds 98% by GC or HPLC, and the melting point typically sits between 53 and 56°C—markers that veteran chemists use as quick confirmation of identity and purity. Low residual moisture, controlled under 0.5%, makes this compound fit for moisture-sensitive transformations. Even trace water can derail reactions with Grignard reagents or boronates. Recent years have also seen rising demand for ultra-low heavy metals, especially from pharmaceutical partners whose regulatory submissions depend on tight impurity checks.

    From shipment to storage, we prepare and pack with stability in mind. Our bulk lots ship in lined fiber drums to guard against light and oxygen, which can trigger slow oxidation of the aldehyde functionality. Anyone in the business knows how stored aldehydes can discolor or polymerize, destroying both value and reactivity. We tailor quantities from a few kilograms for pilot runs up to multi-ton campaigns, drawing on decades of logistics experience in moving sensitive chemicals.

    The Role of 3-Chloro-4-Methoxybenzaldehyde in Industrial Synthesis

    Downstream users employ this aromatic intermediate across several sectors. Pharmaceutical chemists synthesize intermediates for antihypertensive agents, anti-inflammatory scaffolds, or CNS-active molecules using the unique reactivity of our product. The methoxy group makes it a more efficient coupling partner, and the chloro group offers a convenient handle for palladium-catalyzed cross-coupling (such as Suzuki or Buchwald–Hartwig reactions).

    In the agrochemical industry, this material contributes to fungicide or herbicide active core construction. A reliable supply with controlled isomer content avoids costly batch failures during scale-up. Scent formulators and flavor houses explore its utility as an intermediate for aldehydic or anisic notes, occasionally seeking custom derivatives if requested. Chemists building new ligands or heterocyclic frameworks use it for its specific leaving group chemistry and electrophilic control.

    Working directly with end users, we hear feedback on how small changes in the manufacturing process impact application. For example, in pharmaceutical research, downstream hydrogenation of the chloro group to the corresponding hydroxy often faces trouble if impurities creeping in from the oxidation of our material accumulate. Years of collaboration mean our analytical team screens specifically for these problematic byproducts, troubleshooting in parallel with our customers’ R&D teams. They benefit from our transparency, knowing we disclose exactly how the material is made and tested.

    Comparing 3-Chloro-4-Methoxybenzaldehyde to Related Benzaldehydes

    Many buyers initially view aromatic aldehydes as interchangeable. Experience shows the differences drive results. Changing the substitution pattern, such as using 2-chloro or 2-methoxy isomers instead of 3-chloro-4-methoxy, shifts both reactivity and safety profiles. Ortho substituents crowd key reaction sides and hamper selectivity, an effect evident during scale-up of condensation or arylations. Our product sits in a sweet spot, balancing reactivity due to the electron-donating methoxy and electron-withdrawing chloro, allowing both controlled nucleophilic substitutions and efficient protection in complex syntheses.

    Some projects tried cheap alternatives, like plain 4-methoxybenzaldehyde. The missing halide group turns out to be a liability for further modifications—chloride activation under mild conditions cannot be substituted by more drastic halogenation after the fact. With generic benzaldehydes, downstream chemistries often involve extra steps, harsher reagents, and longer workups, raising both total input cost and environmental impact. This direct experience, from lab bench to pilot reactor, teaches us that choice of intermediate shapes the long-term viability of synthetic routes.

    Impurity content deserves special mention. Through years of feedback, we have seen knock-on effects of low-level polar or non-polar contaminants. Even under strong purification, impurities sometimes slip into active pharmaceutical ingredients or plant protection chemicals. Our insistence on batch testing—covering GC-MS, residual solvent analysis, and water content measurement—reflects a commitment to accountable manufacturing. Competing materials from small, unverified plants often look clean on a basic assay but reveal problems under advanced chromatographic scrutiny.

    Manufacturing Realities: What It Takes to Get the Product Right

    On the shop floor, the process begins with strict control of raw materials. High-purity 4-methoxybenzaldehyde and carefully titrated chlorinating agents lay the foundation for a consistent run. Any compromise here leads to side reactions that are almost impossible to clean up at large scale. We run continuous batch monitoring using in-line spectroscopy, not just spot checks at the end, minimizing batch-to-batch variation.

    Worker safety drives every protocol—chlorinating agents can be hazardous, and venting protocols require both robust equipment and well-drilled personnel. We keep batch sizes manageable, preferring pairwise monitoring to catch excursions before a full tank run needs costly reprocessing or, worse, landfill disposal. Listening to our engineers, we have learned the balance between throughput and diligence—a small, focused upgrade in monitoring tightens specifications more than endless retesting after the fact.

    After reaction, meticulous distillation and crystallization follow. This phase determines the difference between product suited for high-performance industries and commodity-grade chemicals. The purification process targets removal of trace isomers and residual reactants, with multiple passes when necessary. We undertake this process with the awareness that, for some customers, a single contaminant can mean failed regulatory submissions. Our investments in analytical equipment—NMR, GC-MS, HPLC—keep us proactive, not merely reactive, to emerging customer standards.

    Quality Control, Compliance, and Traceability

    Quality means more to us than numbers keyed into a certificate of analysis. Our plant’s QA team works with full traceability from raw material entry to finished product shipping. Electronic batch records, retained samples, and regular reference runs allow us to support backward investigation if any client flags a problem. We rigorously adopt protocols aligned with ISO standards for chemical manufacturing.

    Regulators demand, and rightfully so, full transparency around residual solvents and potential genotoxic impurities. Each production campaign generates logs accessible to our partners and subject to regulatory review, if needed. While we serve diverse markets, we never dilute standards based on an order’s size or perceived end use. Each lot receives the same level of oversight and documentation.

    Investments in environmental monitoring and waste minimization mean neighboring communities trust our operation. Local authorities inspect our plant and audit waste handling. Our team treats these audits as an extension of the commitment made to our employees and customers; if a chemist downstream worries about residual solvent, we can point to the processes and controls we follow on a daily basis.

    Troubleshooting: Solutions Rooted in Experience

    Problems happen in chemical manufacturing, and our ability to anticipate and correct them sets our material apart in the market. In one case, a customer running a large-scale Friedel–Crafts acylation flagged a drop in conversion rate. By sharing our internal GC traces and walking through their workup, we identified a minor impurity that migrated in the cold storage phase. Adjusting the cooling rate and batch age at shipment, we solved the issue for both parties. This kind of proactive approach is only possible by holding technical conversations directly between maker and user, not broker and buyer.

    Our technical support extends into R&D partnerships. For a biotech partner struggling with site-selective modifications, we provided not only the current product but also small custom lots with altered granularity and packing gas, letting their process chemists compare effectiveness side-by-side. As a result, their yields jumped, and their lab manager could cut batch times. These collaborations deepen our understanding, feed into future process improvements, and help us spot new application trends early.

    Developing for a Changing Market

    Over the years, demand for benzaldehyde derivatives has moved beyond commodity pricing. Research-driven buyers evaluate suppliers on reputation, not just cost per kilo. Regulatory demands—especially in pharmaceuticals—push every manufacturer to invest in data integrity, continuous training, and cross-functional quality teams. We have responded by embedding advanced informatics, reinforcing safe storage protocols, and expanding our analytical team.

    Sustainability matters, too. Our R&D division assesses new chlorination techniques and explores greener oxidation systems. Investment in solvent recovery has reduced process emissions. When regulations shift, as they did with the restriction of certain chlorinated solvents in the European market, fast adaptation becomes the only way forward. Rather than lag behind, we share notes with regulatory experts and formulation scientists, aiming for both compliance and performance with every ton shipped.

    What Sets Us Apart: The Manufacturer’s Difference

    Working as a direct producer shapes our perspective in ways third-party suppliers cannot match. Real consequences follow if we cut corners or misrepresent product specs. Customers contact us with technical queries, often in urgent project cycles. We answer based on firsthand data, not what’s relayed from a far-off supplier. In one instance, a customer needed precise UV absorption data for an analytical column clean-up. Our team pulled reference spectra from production-grade material, enabling their team to optimize their workflow within hours.

    Long-term relationships matter. Some buyers have sourced from our plant for over a decade. They value our willingness to share process details, involve them in spec upgrades, and address root causes quickly when challenges appear. This level of transparency builds trust, and ultimately, sustains both our businesses in an industry notorious for its volatility. By connecting chemical expertise to real-world manufacturing outcomes, we position ourselves both as a reliable supplier and a partner in the innovation pipeline.

    Meeting Tomorrow’s Challenges with Today’s Know-how

    The chemical industry constantly evolves. Downstream applications demand ever-stricter purity, better documentation, and shorter lead times. By investing in both technology and people, we stay close to the needs of those who rely on our 3-Chloro-4-Methoxybenzaldehyde. Forward-thinking companies seek out proven, trustworthy partners for their supply chains, especially when compounds like ours play critical roles in high-value syntheses.

    Our technical depth lets us troubleshoot uncommon issues and adapt to shifting regulations. Customers developing novel pharmaceuticals or advanced crop-protection agents count on us to deliver not just product, but support—from early-stage sampling through to full-scale supply. By fostering direct conversations, tailoring innovation to specific needs, and keeping a close eye on production realities, we build resilience into both our own operations and those of our clients. From improvements in impurity tracking to the introduction of greener technology, our goal remains providing a foundation for safe, reliable, innovative chemistry.

    Final Thoughts: Why Quality and Partnership Define Value

    Every container of 3-Chloro-4-Methoxybenzaldehyde tells a story about dedication to craft. Our customers depend on products that perform well in real-world syntheses, not just on paper. Over decades in the trade, we've found that reliability means more than just fast delivery or high assay; it takes unbroken traceability, candid communication, and a drive to improve. Supplying this product from our own hands means taking pride not just in the chemistry, but in the relationships that make complex manufacturing work. The lessons learned—both from triumphs and missteps—fuel a cycle of continuous improvement, ensuring we supply more than just chemicals; we provide practical expertise to address emerging needs, regulatory shifts, and technical hurdles our customers face.