Products

3-Chloro-4-Methoxyaniline

    • Product Name: 3-Chloro-4-Methoxyaniline
    • Alias: 3-Chloro-4-methoxybenzenamine
    • Einecs: 220-976-8
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    407725

    Chemicalname 3-Chloro-4-Methoxyaniline
    Casnumber 6237-06-3
    Molecularformula C7H8ClNO
    Molecularweight 157.60
    Appearance Light brown to beige solid
    Meltingpoint 63-67°C
    Boilingpoint 285°C
    Density 1.26 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles COC1=CC(=CC(=C1)Cl)N
    Inchi InChI=1S/C7H8ClNO/c1-10-7-3-5(8)2-6(9)4-7/h2-4H,9H2,1H3
    Refractiveindex 1.615

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

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled "3-Chloro-4-Methoxyaniline," sealed with a screw cap, features hazard warnings and batch information.
    Shipping 3-Chloro-4-Methoxyaniline is typically shipped in tightly sealed containers, protected from light and moisture. It should be handled according to safety regulations, labeled as a potentially hazardous material. Transport must comply with local, national, and international regulations, ensuring the chemical’s integrity and minimizing risk of exposure or environmental contamination.
    Storage 3-Chloro-4-Methoxyaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from light and moisture. Ensure proper chemical labeling and access is restricted to trained personnel. Store at room temperature and use secondary containment to prevent spills or leaks.
    Application of 3-Chloro-4-Methoxyaniline

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

    3-Chloro-4-Methoxyaniline serves as a key intermediate in the synthesis of specialty chemicals, where its distinct reactivity supports controlled substitutions and elaborate molecular frameworks. Our production integrates this material for advanced applications where regulatory compliance, precise dosing, and process compatibility are critical to the development of high-value end products. Below, we outline the primary industrial scenarios where downstream manufacturers depend on our quality-controlled supply to achieve targeted performance and regulatory benchmarks.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Downstream pharmaceutical producers incorporate this compound as a crucial building block in multi-step syntheses for certain APIs, leveraging its selective amine and halide reactivity. Its performance influences not only the reaction yield in the initial stage but also the impurity profile of later intermediates, making it integral to route selection and regulatory audits in small molecule drug manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP and EP monographs relevant to process validation
    • U.S. FDA DMF registration practices
    • EU EudraLex Volume 4 GMP guidelines

    Typical usage ratio

    • Functioning as a starting arylamine, the material typically constitutes 15–28% w/w of the first condensation or coupling stage reactants. The ratio is defined by process stoichiometry and target molecular yield per batch.

    Downstream process integration

    • Introduced during the initial amination or acylation reaction under inert atmosphere, often in a closed continuous reactor or multi-kilogram batch reactor, followed by purification steps such as crystallization or preparative chromatography.

    Final product types

    • Small molecule APIs including custom kinase inhibitors, analgesic precursors, and select anti-infective agents dependent on an aniline substructure.

    2. Synthesis of Agrochemical Actives and Intermediates

    Agrochemical formulators utilize the precise reactivity of this aniline derivative to introduce controlled heteroatom substitution on aromatic rings, which is essential in the production of particular herbicides and insecticide active ingredients. Its batch-to-batch consistency directly affects the downstream purity and regulatory acceptance of technical grade actives.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • EPA 40 CFR Part 158 (U.S. pesticide registration guidelines)
    • REACH Annex VI for chemical registration and safe handling
    • ISO 9001:2015 quality management for agrochemical synthesis

    Typical usage ratio

    • Commonly incorporated at 10–19% w/w of the reaction charge during key substituted aniline condensation steps. The ratio may be adapted to the specific ring substitution patterns targeted by the downstream synthetic route.

    Downstream process integration

    • Charged directly into the coupling or cyclization vessel following in situ pH adjustment; monitored by in-process HPLC for conversion and unreacted starting material. Post-reaction, the crude product undergoes vacuum distillation or solvent extraction before being advanced to the next synthetic stage.

    Final product types

    • Technical grade herbicide actives, selective insecticides, and fungicidal intermediates featuring methoxy- and chloro-modified aromatic moieties.

    3. Production of Specialty Dyes and Pigments

    Producers in the specialty dyes sector employ this compound to control chromophore arrangement during diazo-coupling and condensation processes, achieving fine-tuned color performance and lightfastness for industrial and textile dye applications. Consistency in substitution pattern is critical for repeatable hue and shade strength in large-scale colorant manufacturing.

    Industry compliance standards

    • Oeko-Tex Standard 100 Annex 6 for restricted substances
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL compliance for textile auxiliaries
    • ISO 105-X12:2016 for dye fastness testing
    • EU REACH SVHC monitoring for aromatic amines

    Typical usage ratio

    • Integrated at 6–12% w/w in primary azo-coupling, with the specific level varying for direct vs. disperse dye types and the shade depth specified by the customer’s formulation team.

    Downstream process integration

    • Reacted in diazotization stage using controlled low-temperature addition, followed by immediate coupling with a specific coupling component in aqueous or organic media; finished dye paste is typically filtered, milled, and spray dried prior to blending for customer-specific formulations.

    Final product types

    • Aromatic azo and anthraquinone dyes for textile fibers, high-stability pigments for coatings, and intermediate compounds for permanent marker and ink manufacturers.

    4. Precursor for Electronic Chemical Materials

    Manufacturers of electronic grade chemicals rely on this intermediate for the preparation of functionalized aromatic compounds used in photoresist resins and conductive polymer additives. Purity and trace impurity control of the starting aniline directly affect the dielectric properties and batch reproducibility demanded in semiconductor fabrication and display manufacturing.

    Industry compliance standards

    • SEMI C93 for electronic chemical purity
    • IEC 62474 for material declaration (RoHS, REACH substances)
    • ISO 14644-1 cleanroom processing requirements (for ultrapure intermediates)
    • Customer-specific TOC/anion/cation limits for photoresist raw material suppliers

    Typical usage ratio

    • Employs 3–8% w/w in initial condensation or cross-linking stages, the ratio set according to polymer backbone design and desired electrical or photoactive properties of the finished functional additive.

    Downstream process integration

    • Dispensed into closed-system reactors equipped with solvent recovery and advanced filtration; undergoes further purification by distillation or preparative HPLC to meet electronic chemical grade specifications before conversion into specialty aryl ether or heterocyclic derivatives.

    Final product types

    • Photoresist intermediates for microelectronics lithography, charge-transport layer additives, and customized precursors for OLED and flat panel display production.

    Free Quote

    Competitive 3-Chloro-4-Methoxyaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    3-Chloro-4-Methoxyaniline: Reliable Performance from Trusted Chemical Production

    Direct from the Source: Our Experience with 3-Chloro-4-Methoxyaniline

    We have spent years tailoring the synthesis of 3-Chloro-4-Methoxyaniline to deliver results our customers can count on. In our industry, precision sometimes makes the difference between a successful project and costly delays. Having walked the production floor, we recognize that the devil lives in the details: every shift, our staff consistently monitors quality from the raw material stage right up through final packaging. Integrity isn’t just about marketing a product—it's about supplying chemists and technicians with a material that meets their exact standards when they take that bottle off the shelf.

    Chemical Profile and Model Overview

    3-Chloro-4-Methoxyaniline falls among halogenated aniline derivatives and carries the CAS number 695-34-1. Its molecular formula, C7H8ClNO, reflects its structure—a benzene ring substituted at the 3-position with chlorination and at the 4-position with a methoxy group, plus an amine at position 1. In our line, this compound retains consistently high purity, with lot assays routinely reading above 99%. Our technicians analyze each batch by HPLC, and we keep GC-MS records on hand for any customer inquiry.

    From discussions in the lab to troubleshooting on the production line, the melting point remains a key indicator of purity for specialty amines like this one. You can expect a melting range centered around 71–75°C, and this consistency takes careful control of crystallization conditions and solvent recovery. The molecular weight checks in at 157.6 g/mol—a factor relevant for large-batch calculi and downstream synthesis design. Samples show off-white to pale brown crystalline appearance, a shade easily spotted by eye, which reveals any major contamination at once. Each container passes a manual visual inspection by trained eyes before sealing. In our experience, chemical color is often the quickest early warning signal, long before a QC instrument picks up drift.

    Key Applications in Fine Chemical Synthesis

    As an intermediate, 3-Chloro-4-Methoxyaniline occupies a unique niche. We have watched pharmas, agrochemical formulators, and pigment houses incorporate it into syntheses where both functional group compatibility and regioselectivity matter. On the pharma side, our partners apply it in constructing cores for kinase inhibitors and beta-lactam analogues where the positioning of a chloro and a methoxy next to an amine provides both the electronic profile and reactivity needed for downstream coupling steps. In pigments, customers tell us that the combination of chloro and methoxy substitution aids the development of tone and fastness properties in specialty azo dyes and imaging compounds.

    Based on years of feedback, we see demand coming strongest from companies focused on creating value-add benzene derivatives, rather than simple commodities. Recurring purchase orders often cite the role of 3-Chloro-4-Methoxyaniline in Suzuki and Buchwald–Hartwig cross-couplings, where robust halogen stability is required. We've also supported academic groups working on heterocyclic scaffolds that leverage the ortho-chlorination for specific hydrogen-bonding patterns. In the world of custom chemical synthesis, small changes at the molecular level frequently determine the difference between a dead end and a scalable process.

    Within dye and pigment manufacturing, the regulated aromatic amine substitutions have real-world consequences for lightfastness and shade performance. Some newer ink systems bank on this compound to balance sublimation and heat resistance in high-spec imaging applications, as heard from process engineers troubleshooting faulty batches where the wrong isomer made its way into the supply chain.

    What Sets This Compound Apart: Practical Differences in Use

    Some may ask what makes 3-Chloro-4-Methoxyaniline specifically valuable compared to other chloro or methoxyanilines. Direct conversations with our R&D clients highlight that most competing isomers either lack the desired reactivity at crucial positions or bring in unwelcome side products during key reactions. For example, 4-chloro-3-methoxyaniline, an isomeric alternative, often delivers a different substitution pattern, leading to entirely different coupling profiles or unwanted byproduct distributions.

    Productivity on the customer’s end improves not just because of chemical structure but also from high batch-to-batch reproducibility. Our production protocols have been honed to minimize trace contaminants—recent analytical checks show less than 0.5% impurities in final product lots, translating into fewer purification headaches in customer synthesis. Unlike broader-spectrum technical grades, we tune our process to control dimer and over-chlorination content, which frequently causes issues downstream for sensitive pharmaceutical projects.

    Safety and handling requirements mirror those for other aromatic amines, though the specific combination of chloro and methoxy groups means that material management teams see lower volatility and reduced skin sensitization issues compared to lighter, more volatile anilines. Our facility invests in proper containment and air filtration at every stage—less about compliance, more about keeping both teams and partners protected from occupational hazards.

    Several partners have told us they’ve switched from generic overseas suppliers because of cost-in-production savings realized once they receive consistently pure product from us. Less time spent filtering or repurifying translates to fewer wasted labor hours and, as some purchasing managers note, greater confidence with regulators inspecting their own process documentation. For end-users in regulated markets, that kind of real assurance often matters as much as any price point.

    Control and Traceability—The Reality of Modern Chemical Production

    Every successful batch tells a story written in high-purity inputs, disciplined equipment maintenance, and real-time feedback from experienced technicians. Small measures in the setup stages prevent headaches downstream; data logging every filtration and reactor load means traceability is built in, not something patched on later. Certificates of analysis back every outgoing shipment, and we archive supporting data for years, in line with both internal policies and customer requirements.

    Our QA team, brought up through both hands-on roles in plant operations and formal analytical backgrounds, finds it pays off to run checks above the minimum spec. Sometimes, what matters isn’t just the numerical purity, but fine details—trace elemental content, water content within hundreds of ppm, residual solvents, or isomeric drift. These issues can mean the difference between first-pass success and last-minute process delays. Our plant modifies incoming material checks for bulk intermediates based on downstream partner requirements; sometimes customers need tighter specs than the standard catalogue states, and we accommodate.

    From the vantage point of daily operations, people count on their suppliers to behave less like vendors and more like fellow problem-solvers. Our own team answers technical questions directly—not through call centers, but by drawing on personal bench and pilot plant work. Regular customer site visits and audits are both welcome and routine; we treat transparency not as a buzzword, but as an ordinary part of business.

    Environmental Responsibility at Every Stage

    Any discussion about aromatic amines brings up environmental responsibility and waste management. Our sector has seen enough headlines about soil and groundwater issues to understand the importance of containment, recycling, and responsible air handling—not from public relations, but because we live in these communities too. Waste streams arising from 3-Chloro-4-Methoxyaniline production can include spent acids, residual solvents, and fine particulates.

    We have built our plant with closed-loop solvent recovery systems, so emissions and liquid discharge reach well below mandated limits. We developed purification protocols to permit recycling wash solvents back into the process, slashing not just direct costs but environmental footprint. Staff undergo regular safety and environmental training, and liquid and solid waste all pass through in-house neutralization and filtration facilities. We work with outside auditors for periodic review, not to chase certifications, but to get an extra set of eyes looking for improvement.

    Our product managers field questions every quarter about compliance with REACH and other international frameworks. We maintain documentation to cover the demands of European, North American, and East Asian regulatory clients, and provide all available toxicological and ecological risk data with each lot upon request. For downstream users focused on “greener” synthesis, we work directly to formulate lower-toxicity or solvent-optimized versions, reducing the need for chlorinated solvent extraction or hard-to-vent downstream processes.

    Supporting Growth and Innovation

    By keeping the process in-house, from raw inputs to final kilo or multi-ton outputs, we ensure both supply reliability and consistency. In fast-evolving application spaces such as specialty pharmaceuticals, new polymer systems, and next-generation dyes, this matters greatly. It isn’t just about selling a product; collaboration drives our own process refinement too.

    We have assisted numerous small and mid-sized enterprises scaling up bench processes to full plant runs. Sometimes the challenge involves adjusting crystallization conditions for new downstream impurity limits; in other cases, customers need real-time troubleshooting when unexpected color or flow properties present during compounding. Experience has taught us that even minor deviations in raw material purity or process temperature can lead to major changes in the outcome, particularly for intermediates with multiple reactive handles like 3-Chloro-4-Methoxyaniline.

    Regular technical exchanges and lab-to-plant visits foster problem-solving. Our chemists often work jointly with customer R&D, especially when adapting 3-Chloro-4-Methoxyaniline for novel coupling strategies or entirely new material systems. We listen not only for product demands, but for emergent needs—whether in polymer additives, colorants, or field-applied agro formulations.

    Feedback shapes our process controls and product improvements. It is not uncommon for us to customize particle size distribution or supply a custom packaging format to fit a partner’s handling setup. Our QC managers coordinate directly with client analytical teams when deeper trace impurity data is requested—sharing not just the summary but the raw chromatograms and underlying lab notes.

    Addressing Challenges and Providing Solutions

    The majority of challenges in working with 3-Chloro-4-Methoxyaniline arise from sensitive downstream chemistries and increased regulatory scrutiny. Production teams from customers have flagged issues tied to variable isomeric purity, packaging stability during intercontinental transport, or limits placed on aromatic amine content in final products intended for strictly regulated markets.

    Our company responds by controlling isomeric content at the synthesis source, not relying on after-the-fact purification or blending. We use process analytics to monitor each stage and catch inconsistencies immediately. For packaging stability—especially during extended shipments or in regions with wide temperature swings—we have shifted to multi-barrier foil and HDPE drums with vapor seals, preventing both temperature excursions and ingress of atmospheric moisture which can degrade material over time.

    Regulatory documentation support runs from initial SDS sheets through to custom data sets for end users. We field technical requests about batch histories and impurity profiles daily, and no lot leaves the site without a dataset ready to satisfy due diligence from even the strictest agencies. Our philosophy remains simple: the more upfront data we provide, the more efficiently our partners can run compliance and get through due diligence with their own customers.

    Many chemists value direct conversation over scripts. Our technical group remains accessible for practical troubleshooting, whether the issue is crystallization speed, filterability, or downstream reaction compatibility. With years in both production and research, our staff often predicts pain points and preps contingency solutions—be it modified drying protocols for tropical climates, or analytical grade product for highly sensitive pharma scale-ups.

    Lessons Learned: Reliable Partnership and Continual Evolution

    This compound represents just one node in the web of modern synthetic chemistry, but the lessons apply broadly: real value comes from tangible evidence of quality, practical technical support, and ongoing responsiveness to shifting industry standards. Partners tell us they return not only because our 3-Chloro-4-Methoxyaniline meets their process needs, but because the reliability transcends paperwork. When scale-ups run smoothly and new projects launch with confidence in material quality, the impact shows on both production floors and bottom lines.

    Every season brings new expectations—whether tighter impurity specs, new market regulations, or unanticipated supply chain challenges. Instead of resisting change, we invest in process upgrades and encourage staff to adopt new analytical techniques or automation methods. A past changeover to automated in-line purification reduced not only error risk but environmental impact, and enabled us to share more robust impurity data with customers. Partnerships with analytical labs and direct-user feedback accelerate this cycle of improvement; even a small process tweak at our end often spares hours of troubleshooting for plant and bench scientists downstream.

    We recognize that great chemical manufacturing is a team effort—from raw material procurement through synthesis to technical support long after delivery. We keep the line open not just to fulfill requirements, but to advance progress in every industry that depends on our products. 3-Chloro-4-Methoxyaniline is just one example of what it looks like to pair chemical mastery with a real commitment to customer partnership and safe, responsible production.

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