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2-Chloroveratraldehyde

    • Product Name 2-Chloroveratraldehyde
    • Alias 2-Chloro-3,4-dimethoxybenzaldehyde
    • Einecs 219-964-7
    • 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

    389858

    Chemical Name 2-Chloroveratraldehyde
    Cas Number 4548-71-2
    Molecular Formula C9H9ClO3
    Molecular Weight 200.62
    Appearance Yellow to brown crystalline solid
    Melting Point 50-54°C
    Density 1.28 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles COC1=CC(Cl)=C(C=O)C=C1OC
    Iupac Name 2-chloro-3,4-dimethoxybenzaldehyde
    Storage Conditions Store in a cool, dry, well-ventilated place
    Synonyms 2-Chloro-3,4-dimethoxybenzaldehyde

    As an accredited 2-Chloroveratraldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Chloroveratraldehyde, 25g, is securely packaged in an amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping 2-Chloroveratraldehyde is shipped in tightly sealed containers, protected from light and moisture to prevent degradation. It is packed according to relevant chemical safety and transportation regulations. Proper labeling and documentation, including hazard identification, are ensured for safe handling during transit. Avoid exposure to heat or incompatible substances during shipping.
    Storage 2-Chloroveratraldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Ensure that the storage area is equipped with appropriate spill containment and properly labeled according to chemical safety regulations to prevent accidental exposure or leaks.
    Application of 2-Chloroveratraldehyde

    Applications of 2-Chloroveratraldehyde in Industrial Manufacturing

    2-Chloroveratraldehyde is an essential aromatics intermediate extensively used in production processes across several industrial sectors. As a direct manufacturer, we supply this raw material in compliance with prevailing international regulations to support targeted customer applications.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    Leading pharmaceutical companies utilize 2-Chloroveratraldehyde for the synthesis of specific active pharmaceutical ingredients, including custom small molecules and advanced intermediates. It is routinely involved in stepwise condensation and reduction reactions to introduce protected aldehyde functionalities in drug scaffolds. Manufacturers must adhere to pharma-grade quality control while managing process traceability and batch containment under validated conditions.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as per 21 CFR Parts 210/211
    • ICH Q7 for Active Pharmaceutical Ingredients
    • Relevant pharmacopoeia (USP, EP, ChP) monographs for intermediates
    • REACH regulation for chemical safety and documentation

    Typical usage ratio

    • Ranges from 0.5 to 3.0 molar equivalents per synthetic batch, depending on target API route and protection requirements
    • Adjusted for final molar yield and specific step selectivity in multi-stage syntheses

    Downstream process integration

    • Entry in early- to mid-stage fragment coupling or as a capping agent in building core structures
    • Subjected to reductive amination, nucleophilic addition, or cyclization processes
    • Integrated with QC checkpoints for residual solvent and impurity analysis before subsequent conversion steps

    Final product types

    • Small molecule APIs for central nervous system therapeutics
    • Precursors and intermediates for cardiovascular drugs
    • Synthetic building blocks for anti-infective compounds
    • Fine chemical intermediates for custom API projects

    2. Fragrance and Aroma Compound Manufacturing

    The aromatic aldehyde structure of 2-Chloroveratraldehyde lends itself to use in synthetic fragrance formulation, particularly in the production of musky and woody note compounds by the perfumery sector. Synthesis of high-value aroma chemicals often exploits the compound's reactivity and ortho-substituted pattern as a precursor for both macrocyclic and linear aldehydic fragrances. Producers implement strict identity, purity, and trace screening according to global standards for perfumery feedstocks.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • Regulation (EC) No 1223/2009 for cosmetic ingredients, including annex standards
    • IFRA Analytical Methods for Quantitative and Qualitative Identity
    • Safety Data communication per GHS (Globally Harmonized System of Classification and Labelling of Chemicals)

    Typical usage ratio

    • Between 0.2%–2.5% of total mass in base aldehyde blends, depending on olfactory intensity and target composition
    • Final ratio established by aroma threshold studies and compliance with finished product safety limits

    Downstream process integration

    • Entry as a key aldehyde precursor in condensation with aroma alcohols, or through Wittig-type reactions for musk synthesis
    • Modified via controlled hydrogenation or acetalization during batch synthesis of aroma components
    • Processed with batch-specific odor panel and chromatographic identity confirmation

    Final product types

    • Synthetic musks for fine fragrance
    • Woody base note chemicals for high-end perfumes
    • Functional fragrances for detergents and cosmetics
    • Aroma ingredients for food flavor blends (subject to regional approvals)

    3. Agrochemical Synthesis

    Downstream agrochemical producers deploy 2-Chloroveratraldehyde as a versatile key starting material for synthesizing selective herbicides, fungicides, and crop protection agents. The specific electron distribution in its molecular structure supports the creation of heterocyclic scaffolds applied in modern agrochemistry. Formulators maintain production in accordance with strict active ingredient regulations, minimizing cross-contamination and environmental release.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH registration for plant protection intermediates
    • ISO 9001:2015 for quality management during process scale-up

    Typical usage ratio

    • From 1.0%–8.0% w/w relative to main active moiety synthesis kits; varies per specific active ingredient structure
    • Accurate ratio determined by targeted crop selectivity and efficiency trials

    Downstream process integration

    • Utilized for input into Grignard reactions or as an electrophile for Suzuki couplings during heterocycle formation
    • Chemoselective transformation under controlled temperature and catalyst loads
    • Integration monitored via in-line chromatographic process controls and impurity profiling

    Final product types

    • Broad-spectrum pre-emergent and post-emergent herbicides
    • Azole-based fungicides for cereals and fruits
    • Specialty crop protectants for integrated pest management systems
    • Finished technical grade agrochemicals for formulation

    4. Dye and Pigment Intermediate Production

    Industrial dye manufacturers source 2-Chloroveratraldehyde as an intermediate in the synthesis of complex aromatic dyes and pigments, targeting textile, paper, and plastic coloration. The chlorinated aromatic backbone serves as an anchoring point for sequential condensation with amines or coupling with diazonium salts, ensuring color strength and stability. Adherence to product purity and environmental regulations is fundamental throughout the dye preparation process.

    Industry compliance standards

    • OEKO-TEX Standard 100 for hazardous substances in textile dye intermediates
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) dye registration
    • Zero Discharge of Hazardous Chemicals (ZDHC) guidelines for dye production emissions
    • ISO 14001:2015 Environmental Management for chemical handling

    Typical usage ratio

    • 0.8%–5% of total intermediate mass, depending on target chromophore and dye application substrate
    • Adjusted according to required color intensity and performance under end-use conditions

    Downstream process integration

    • Undergoes condensation with specific amines in high-temperature batch reactors
    • Participates in diazo coupling as a precursor for azo dye classes
    • Incorporated in continuous or semi-batch pigment production with strict impurity controls

    Final product types

    • Reactive dyes for cotton and cellulosic fibers
    • Sulfonated pigments for paper and inks
    • Color-fast direct dyes for plastics and synthetic leathers
    • High-performance pigment intermediates for specialty finishes
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    Certification & Compliance
    More Introduction

    2-Chloroveratraldehyde: Practical Experience and Key Distinctions

    Understanding 2-Chloroveratraldehyde from a Manufacturer’s Perspective

    Long years spent on the factory floor and in the development lab have given us more familiarity with 2-Chloroveratraldehyde than almost any molecule in our aldehyde line. The process begins with fine control over chlorination, as 2-Chloroveratraldehyde sits in a family of aromatic aldehydes with significant application in the synthesis of specialty intermediates. This particular compound carries the CAS number 4548-04-3 and is recognized for its structural formula, where a chlorine atom attaches at the second position of the veratraldehyde ring. The resulting chemistry delivers selectivity that few other derivatives can equal.

    Our Production Commitment: Consistency and Purity Standards

    We focus heavily on stability in process operations because trace impurities in aromatic aldehydes can impact downstream performance, especially in custom synthesis or the manufacture of advanced active pharmaceutical ingredients. Before filling any order, our QC team relies on chromatographic purity thresholds and residue-on-ignition tests that exceed industry norms. Material leaves our facility as white to slightly yellow crystalline solid—free-flowing, without visible contaminants. All batches carry a minimum purity of 98%, which helps support reproducibility in customer applications, particularly in those where batch-to-batch variation could set projects back by weeks or months.

    What Sets 2-Chloroveratraldehyde Apart?

    Many chemists ask for veratraldehyde derivatives without a strong sense of the impact that different substituents bring. For those not so familiar, the chlorine atom at the ortho position significantly shifts both the physical properties and reactivity compared to unsubstituted or para-substituted veratraldehydes. Using methyl or ethoxy substitutions does not achieve the same electronic effect: chlorination enhances certain pathways, especially in heterocycle construction and pharmaceutical exploration, where regioselectivity and reactivity under mild conditions save both time and reagents.

    The major distinction versus standard veratraldehyde emerges during condensation or cyclization steps, for example, when synthesizing complex heterocycles. Chlorine withdrawal increases the aldehyde’s susceptibility to nucleophilic attack, providing higher yields for some intermediate targets while reducing the formation of byproducts. Over the years, we have seen many R&D groups shift to 2-Chloroveratraldehyde when others failed to deliver consistent reactivity.

    Preferred Specifications: Designed with Application in Mind

    We do not chase after generic specs that simply tick off industry checkboxes. Our product consistently meets NMR and mass spectrometric confirmation for structure, and controlled particle size distribution allows for quick dissolution in most polar organic solvents. This should mean faster reaction setup and less downtime in prep. Over the past decade, several major customers have built their custom library synthesis protocols around our specifications—the consistency of melting point between 56°C and 59°C, the absence of strong odor that suggests breakdown byproducts, and the reliable color range allow for dependable workflow with minimal requalification upon arrival at the end user’s lab.

    Where 2-Chloroveratraldehyde Is Used Most Effectively

    Customers draw on this intermediate primarily for the construction of fine chemicals, especially where chlorine as a leaving group or modulator opens up new synthetic paths. The role of 2-Chloroveratraldehyde in the design of potential pharmaceutical leads is well documented. Our clients in the pharma sector rely on this product to introduce a controlled chlorine moiety into complex aromatic scaffolds, which can later serve as a handle for further functionalization. In agrochemical synthesis, introducing an ortho-chloro group supports the design of molecules displaying improved selectivity, environmental profiles, or metabolic stability. The aldehydic functionality provides sites for condensation and addition, so the molecule works well in the design of new heterocyclic compounds, ligands, and catalysts.

    Some research institutions and startups have shifted to 2-Chloroveratraldehyde due to growing pressure to find alternatives to more hazardous chlorinating conditions in late-stage modification. Beginning with a well-characterized, high-purity aldehyde cuts several reactivity steps and reduces downstream impurity burden, which often simplifies isolation and purification of target products—the time savings add up over the course of a multi-step synthesis.

    Feedback and Case Studies from the Industry

    Customers often mention that alternatives, such as 4-chloroveratraldehyde and unsubstituted veratraldehyde, led to extra reaction steps or unwanted formation of regioisomers. Before scaling up to the pilot stage, many spent months troubleshooting inconsistent conversions, only learning later that switching to our ortho-chlorinated version produced sharper separations and better reproducibility. Over a fifteen-year partnership with one specialty chemical house, their shift from the para to the ortho isomer accelerated their timeline to full registration of a new active ingredient by over eight months. In peptide and ligand synthesis, researchers highlight improved coupling yields and more robust product isolation, often noting that analytical traceability improved once procedures started with our controlled lots.

    Our product also helped several pharmaceutical development firms remove unwanted side-products from their HPLC traces, which previously caused regulatory delays. Many times, changes in regulatory climate require process-dependent documentation that pinpoints every raw material’s impurity profile—having a tight in-house manufacturing setup, as opposed to piecing together intermediates through external traders, made it possible for customers to clear audit reviews without repeating lengthy validation protocols. Day-to-day, downstream cost savings often turn up in reduced waste disposal requirements and avoidance of unnecessary solvent washes, thanks to the product’s controlled purity.

    Industry Standards and Compliance – Our Experience Matters

    Inspector visits and customer audits demand more than declarations. Our team handles every kilo from synthesis to final packing with direct oversight. As a manufacturer, not a trading agent, we have full transparency into raw material sources, in-process checks, and finished product release. Our facilities apply GMP-inspired systems along with ISO-compliant sampling and record-keeping. We archive every batch sample for traceability and support full change-control logs for our long-term customers. This hands-on experience helped us assist several multinational partners in aligning with evolving compliance requirements, such as REACH, without surprise shortages or out-of-date paperwork.

    Every packaging operation takes into account the aldehyde’s sensitivity to moisture and oxygen. We avoid overstocking to reduce the aging of material in storage, since fresh, recently packed material always outperforms older lots in key synthetic endpoints. Repeating these best practices, year after year, builds a real-world understanding of both supply chain reliability and product performance—as opposed to speculative claims from intermediaries with less at stake.

    Managing Risk and Supporting Innovation

    Over time, supply chain interruptions have challenged many chemical companies—especially those relying on spot-market sourcing for key intermediates. Owning our production line offers greater assurance against import delays and variable quality, so our customers rarely face unplanned lineup changes or yield losses due to contaminant spikes. The same applies during innovation cycles: customer pilot groups developing new flavors, fragrances, or bioactive molecules have worked with us to design short runs of customized 2-Chloroveratraldehyde with specific particle size, residual solvent cutoffs, or differentiated analytical profiles, giving them an edge in submissions and time to market.

    Our technical specialists stay engaged beyond the sale. We provide insight on optimal storage and suggested order quantities to minimize degradation, always acting as a ready support partner if a new reaction or scaleup brings unexpected outcomes. Customers benefit from our direct access to process history—troubleshooting or tweaking protocols becomes faster with someone who can explain why a particular trace contaminant appeared, or why a melting point fell outside the expected range. Years of feedback and repeat analysis guide our improvements to specification, batch release criteria, and packaging safeguards.

    What Customers Should Watch for Compared to Other Products

    Some shops attempt to substitute other chlorinated aromatic aldehydes or shift to generic sources, hoping for cost savings. What’s often overlooked is the impact of slight variations in isomer purity or trace byproducts—a minor impurity may stall a Suzuki coupling, poison a catalyst, or lead to regulatory hold-ups. Our batches always meet a strict GC purity cutoff, verified by both independent laboratory and in-house chemical analysis. We avoid outsourced blending or repackaging, problems common with brokered material.

    Another frequent issue arises from storage or handling conditions: too many suppliers disregard exposure to moisture or air, causing unwanted oxidation, affecting both appearance and subsequent reactivity. We use airtight, protective packaging—interior liners and nitrogen blankets where needed—and time each shipment to support prompt transfer into end-use processes. Users notice improved performance and fewer delays due to failed incoming inspections.

    Technical Support and Collaboration—Lessons Learned

    We have learned that technical questions go beyond COAs and spec sheets. Project leads occasionally need real answers about scaleup feasibility, reaction workup, or impurity management. Our technical team collaborates directly with user groups—academic labs, commercial synthesis firms, pharmaceutical pilot sites. Case examples include troubleshooting pale yellowing that indicated marginal hydrolysis, offering advice on best solvents for solid-state storage, and helping groups track down the origin of trace fines that interfered with analysis. Our documentation includes real-world experience, from optimal reaction temperatures to recommended workup solvents, backed by continuous testing in our own R&D lines.

    Sometimes, academic groups use 2-Chloroveratraldehyde in proof-of-concept or medicinal chemistry campaigns, exploring new substitution patterns on aromatic rings. These teams often work with small budgets and aggressive timelines. Our experience cataloging and analyzing prior production lots means we can flag potential interaction issues or performance risks early, so collaborators cut down experimental cycles and optimize their experimental plans.

    Why Direct Manufacturing Makes a Difference

    Over the years, customers shared stories about how direct sourcing from a manufacturer beats layered supply chains. Many colleagues found that reagents coming through brokers arrived repackaged with incomplete documentation, sometimes ending up with off-grade product and delayed reaction windows. We mitigate those headaches by holding full responsibility for both material quality and delivery schedule. This approach encourages us to refine process yields, improve process safety, and keep technical support close at hand. It also means every complaint or support call returns directly to the team who produced the material, prompting rapid root cause investigations and faster long-term fixes.

    Our teams were among the first to move toward digital monitoring for batch records and sampling schedules—this now forms the backbone of credible, traceable documentation, helping R&D and regulatory groups run smoother filings. Ensuring transparency throughout every step helps end users avoid regulatory or audit-related setbacks. With reliable records and direct communication, our customers frequently compress timelines to new product registration and achieve more predictable manufacturing schedules.

    Improvements and Next Steps for the Industry

    Remaining at the front of the pack requires continuous review—of in-house procedures, raw material sources, purification technologies, and analytical methods. Our production staff spends time refining isolation and finishing techniques, reducing byproduct carryover, and improving batch-to-batch uniformity. This attention shows up at customer sites, where less time is needed in analytical review, and lab cleanup is simpler due to lower impurity profiles. Investments in process intensification set the groundwork for handling specialized orders where unique derivatives or alternative packaging is essential.

    We keep talking to project managers, chemists, and supply chain coordinators—listening to real challenges in their projects is often the most direct way to guide improvement. Their practical insights point to new testing parameters or user-friendly packaging that further cut down conversion overheads and re-inspection steps. We know every hour saved at the bench or pilot stage counts, and we push those time savings back through our process lines to bring sharper efficiency to the market.

    Supporting Sustainable Progress

    No responsible manufacturer ignores sustainability. Chlorinated intermediates require diligence—on effluent management, air quality controls, energy efficiency, and worker safety. We invest in closed processing and state-of-the-art air handling, and we treat all waste to prevent environmental exposure. Our yearly reviews aim for process changes that lower input waste, raise output purity, and cut overall environmental footprint. Direct production control allows us to integrate these changes quickly, as opposed to waiting out approval cycles of off-site partners. Many customers, including those under pressure from new environmental directives, are looking for this level of serious environmental management—it saves money, avoids fines, and upholds public trust in the specialty chemical sector.

    With every iteration of our process, we balance the need for creativity in application with responsibility for safe, low-impact operations. By keeping manufacturing in-house and maintaining open customer communication, we keep improving our standard for quality and reliability—not just for 2-Chloroveratraldehyde as a molecule, but for the evolving landscape of specialty organic synthesis. Customers choose us not by accident, but for the certainty that every batch performs as expected and supports real-world innovation at the bench, in the plant, and in the global market.