Products

Ethyl 4-Chlorobutyrate

    • Product Name: Ethyl 4-Chlorobutyrate
    • Alias: Ethyl 4-chlorobutanoate
    • Einecs: 206-334-7
    • 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

    884336

    Chemical Name Ethyl 4-Chlorobutyrate
    Cas Number 623-03-0
    Molecular Formula C6H11ClO2
    Molecular Weight 150.6 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 195-197°C
    Density 1.08 g/mL at 25°C
    Refractive Index 1.427-1.431
    Flash Point 92°C
    Solubility In Water Slightly soluble
    Smell Fruity odor
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Ethyl 4-Chlorobutyrate is supplied in a 250 mL amber glass bottle, securely sealed, with a chemical-resistant screw cap and labeling.
    Shipping Ethyl 4-Chlorobutyrate is shipped in tightly sealed containers to prevent leaks and contamination. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition and incompatible substances. Shipping must comply with local, national, and international regulations for hazardous materials due to its flammable and irritant nature.
    Storage **Ethyl 4-Chlorobutyrate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, open flames, and incompatible substances like strong oxidizers or acids. Protect from moisture and direct sunlight. Use secondary containment if possible, and keep the storage area clearly labeled. Handle under a chemical fume hood if transferred frequently.
    Application of Ethyl 4-Chlorobutyrate

    Applications of Ethyl 4-Chlorobutyrate in Industrial Manufacturing

    Ethyl 4-Chlorobutyrate supports multiple value-added chemical syntheses across regulated industrial sectors. As a primary manufacturer, we provide this intermediate to downstream processors with demanding formulation, compliance, and integration requirements. Below are the main application tracks, with details based on real industry practices.

    1. Pharmaceutical Intermediate Synthesis

    This material enables core steps in active pharmaceutical ingredient (API) and advanced intermediate production, specifically for anticonvulsant, antihypertensive, and central nervous system drug molecules. Users employ it for constructing heterocyclic moieties and as an alkylating intermediate in multi-step syntheses. Process consistency and impurity control are critical to support cGMP compliance and regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Parts 210/211 (FDA cGMP regulations)
    • Ph. Eur., USP, JP (Pharmacopoeial monographs related to intermediates and APIs)
    • EDQM CEP certification requirements

    Typical usage ratio

    • Mol-to-mol substitution based on target API synthesis route; typically 0.8–1.2 equivalents relative to the nucleophilic reactant
    • Adjusted for impurity profile and downstream yield targets as per validated process batch records

    Downstream process integration

    • Feedstock to alkylation, esterification, and cyclization steps in the batch reactor train
    • Introduced under controlled pH and temperature in stepwise syntheses for API-building blocks
    • Subject to in-process QC before work-up and downstream reactions

    Final product types

    • Bulk generic APIs such as levetiracetam intermediates
    • Custom small-molecule drugs based on proprietary syntheses
    • GMP-certified advanced intermediates
    • Regulated API starting materials for global and regional drug markets

    2. Agrochemical Intermediate Manufacturing

    Downstream manufacturers apply this compound in producing selective herbicide and insecticide active ingredients. The material serves as a chain-elongation building block, especially in preparing butyric acid-derived agrochemical cores. Formulators focus on purity control to prevent residual organochloride contamination in the finished actives.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 quality management in agrochemical manufacturing
    • REACH registration for European distribution
    • China ICAMA regulatory dossier for pesticide intermediates

    Typical usage ratio

    • Usually 0.9–1.5 molar equivalents relative to main active ingredient precursor
    • Optimized according to kinetic models and conversion efficiency for target actives

    Downstream process integration

    • Added as a chain-extending intermediate in block synthesis reactors
    • Merged in condensation or alkyl-chlorination sequences under controlled agitation
    • Purification, neutralization, and off-gassing managed to meet residue controls

    Final product types

    • Technical-grade herbicides (e.g., chloroacetanilide and butyric acid derivatives)
    • Insecticidal actives with chlorinated terminal groups
    • Intermediate stock for specialty crop protection chemicals
    • Bulk pesticide precursors certified for export formulation

    3. Flavors and Fragrance Synthesis

    Flavor and fragrance manufacturers use this ester as a synthetic precursor for developing fruit and berry aroma notes. It enters critical esterification or chain-extension reactions to build complex flavor molecules for food and personal care. Compliance with food safety and allergen management remains a top priority in this segment.

    Industry compliance standards

    • FCC (Food Chemicals Codex) guidelines for ingredient purity
    • IFRA Standards for fragrance materials
    • 21 CFR §182 (FDA GRAS for direct food additives, where applicable)
    • ISO 22000 food safety management

    Typical usage ratio

    • Generally 2–5% in synthesis blends for top note formulation batches
    • Final inclusion in compounded flavor/fragrance—typically below 10 ppm in end-use products

    Downstream process integration

    • Charged to flavor/fragrance intermediate reactors during esterification or amidation reactions
    • Processed under vacuum distillation and flavor compounding protocols
    • Batchwise conformational analysis to ensure odor profile

    Final product types

    • Berry, grape, and tropical fruit flavor bases for beverages and confectioneries
    • Functional fragrance bases for personal care products
    • Concentrated flavor compounds for worldwide export to food producers
    • Perfume raw materials for fine fragrance blending

    4. Specialty Polymer and Resin Modifier

    Producers utilize this chemical as a monomer or functional group modifier during the synthesis of specialty polyesters and resin systems, particularly for performance coatings and automotive materials. Precision in process addition and residual removal ensures system integrity and end-use safety, especially where high resistance or flexibility is needed.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical manufacturing
    • RoHS & REACH compliance in finished materials used in electronics and automotive sectors
    • ASTM D256 (Polymer impact testing) for downstream mechanical performance validation
    • OEM resin technical and eco-tox requirements

    Typical usage ratio

    • Typically 0.5–2% by weight in polyester resin formulations
    • Adjusted for molecular weight tuning and targeted polymer branching

    Downstream process integration

    • Added at the oligomerization or pre-polymerization stage in closed-vessel systems
    • Combined with co-monomers and chain regulators under temperature-controlled conditions
    • Ensured complete consumption or post-polymerization removal for compliance

    Final product types

    • High-performance automotive coatings and plastics
    • Engineering polymer intermediates for electronics insulation
    • Functionalized resins for specialty adhesives and sealants
    • Custom polyesters for medical device encapsulation (non-implantable)

    5. Chemical Reference Standards and Analytical Reagents

    Accredited laboratories and synthesis firms use this compound as a calibration standard or reaction reference in analytical protocols, including GC and HPLC method development. The compound’s assignments necessitate batch traceability, documented impurity profiles, and certificate of analysis support for each delivery.

    Industry compliance standards

    • ISO/IEC 17025 accreditation (General requirements for the competence of testing and calibration laboratories)
    • USP Reference Standard guidelines for laboratory reagents
    • OECD GLP (Good Laboratory Practice) for regulatory submissions
    • ISO Guide 34 for reference material production

    Typical usage ratio

    • Prepared in solution at 1–500 ppm concentration depending on analytical method sensitivity
    • Solid standard aliquots weighed precisely based on required response calibration

    Downstream process integration

    • Used for validating analytical equipment response in quality control and research labs
    • Added to test matrices for method development and inter-lab proficiency studies
    • Supports secondary working standard preparation for routine batch release analysis

    Final product types

    • Certified reference standards for chemical analysis
    • Calibration solutions for HPLC, GC, and related spectroscopy techniques
    • Quality control working standards for regulated manufacturing labs
    • Analytical kits for process validation studies

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    Certification & Compliance
    More Introduction

    Ethyl 4-Chlorobutyrate: A Reliable Building Block for Chemical Synthesis

    Introduction

    For years, our work in chemical synthesis puts us in direct contact with demand for precise, consistent halo-ester compounds. Ethyl 4-chlorobutyrate has quietly become an essential tool for many of our customers working on agrochemicals, pharmaceuticals, and advanced organic synthesis. In our facility, we see its versatility every day, as it streamlines specific reactions, enables certain targeted molecular transformations, and provides a practical approach for introducing butyryl and chlorine functionalities into more complex molecules.

    Product Profile and Specifications

    Our ethyl 4-chlorobutyrate meets purity expectations for demanding laboratory and industrial processes. Consistently, we achieve a minimum assay of 99% purity (by GC), with moisture content maintained below 0.2%. Each batch undergoes GC-MS and NMR confirmation before reaching our shipping area, and transparency on impurity profiles is a point of pride for our team. The product appears as a colorless to light yellow liquid, with a characteristic faint ester odor, and a boiling point typically near 201-203°C. We maintain standard packaging in 200-kilogram drums for commercial-scale use and also offer smaller containers on request, always meeting the strict requirements for safe handling of chlorinated esters.

    Application in Synthesis

    Years of ongoing partnerships have shown us how widely ethyl 4-chlorobutyrate travels through the fine chemical industry. Its chlorinated position at the terminal carbon enables straightforward nucleophilic substitution, broadening the set of downstream products that formulators and researchers can achieve compared to other esters. We receive constant feedback from teams in pharmaceutical labs who rely on its predictable reactivity to produce intermediates for novel APIs. Cropscience companies frequently build herbicides and insecticides on this base structure, appreciating its effective role in constructing specific side chains that aren’t so easily formed through other pathways.

    Taking one example, it converts easily into 4-substituted butyrate esters using amines or thiols, shortening the route for producing β-amino acid derivatives or thiol-functionalized molecules. In another application, we’ve noticed that fragrance chemists prefer this compound over similar butyrates, since the chlorine atom allows access to unique musky notes after further transformations. Even for polymer research, the introduction of a single chloro group on a four-carbon spacer gives end products with distinct physical or chemical performance, without introducing complications from unwanted branching or over-chlorination.

    Distinguishing Features and Comparison

    Over the years, we’ve experimented with various chlorinated and non-chlorinated butyrate esters in our R&D and contract manufacturing divisions. Ethyl 4-chlorobutyrate stands apart from other halo- and alkoxybutyrates in several useful ways. The chlorine atom sits away from the ester moiety, which minimizes unwanted side reactions, such as elimination or hydrolysis, during sequential steps. For researchers scaling up from milligrams to kilograms, this structural reliability helps avoid variability or batch-to-batch changes, which sometimes arise with less well-defined ester products.

    It’s worth noting the differences from ethyl 2-chlorobutyrate: with the chlorine at the gamma (4-) position, the reactivity profile is less inclined toward α-elimination or side addition products. Chemists chasing mono-functionalized precursors tell us that reaction control tends to be much more straightforward, and the yield for intended substitution is consistently higher. Compared to methyl or propyl analogues, the ethyl group offers a more balanced boiling point for distillation, improved solubility in a variety of solvents, and easier recovery after reaction.

    There are options—such as 4-bromobutyrates or 4-iodobutyrates—when enhanced leaving group ability is needed, but these come with higher costs, more challenging logistics, and less shelf stability for most applications. We’ve chosen to focus on chlorinated derivatives because they hit a practical middle ground between reactivity, handling safety, and production cost.

    Production Experience and Process Control

    Our long-term experience manufacturing ethyl 4-chlorobutyrate draws from process design knowledge rooted in continuous chlorination technologies. Over the last decade, we have refined reaction conditions to maintain high selectivity for the 4-chloro position, eliminating problematic side products like di-chlorinated or over-chlorinated esters. Unlike batch production often seen in older facilities, our approach involves tight monitoring of temperature, feed rates, and residence time through the reactor, which helps us minimize waste and keep yields high.

    The starting material—the corresponding butyric acid ester—undergoes direct chlorination using a carefully controlled flow of chlorine gas under UV or catalytic conditions, depending on application. Volatile by-products are stripped early to prevent cross-contamination, and final product passes through distillation under vacuum, which preserves thermal purity and keeps batch-to-batch color and odor differences to a minimum. For customers in regulated markets, we welcome audits of our traceability and quality documentation, and supply full regulatory support for specifications like REACH or region-specific requirements.

    Several customers have remarked on the low residual acid content and minimal halide impurities, and we’ve pursued incremental process improvements to keep both well below industry-acceptable thresholds. Downtime for cleaning and maintenance is scheduled after reviewing batch analytics rather than arbitrary time intervals—another lesson learned from responding personally to customer complaints in the early years. Feedback directly led us to invest in in-line monitoring tools, which detect off-spec production in real time rather than after the fact.

    End-Use Stories and Technical Insights

    Collaboration with downstream processors often brings new perspectives on how ethyl 4-chlorobutyrate functions in specialized applications. For example, in synthesizing intermediates for anticonvulsant drugs, the precise carbon backbone and terminal chlorine position matter more than theoretical reactivity. A misplaced halogen or an over-chlorinated by-product can compromise not just yield, but the viability of final pharmacopoeial approval. We have learned—sometimes the hard way—that even a 0.1% impurity can introduce completely unexpected color changes or slow down hydrogenation in subsequent steps, so we run additional analytical checks before shipping lots headed to pharmaceutical customers.

    In the fine fragrance industry, smaller-scale batches are the norm, but demands for sensory purity and absence of trace organochlorines remain strict. We’ve tailored our production timing, minimizing hold time before packaging, to avoid development of off-odors and to preserve the volatile characteristics essential for perfumery building blocks. Many fragrance houses trust our supply to deliver better blending properties, resisting unwanted hydrolysis or foaming during headspace analysis.

    Agricultural projects using ethyl 4-chlorobutyrate often involve pre-plant seed treatments or custom molecule development, where the balance of cost and reactivity is crucial. Our customers rely on our consistency so they can focus on fine-tuning the molecular features which influence crop safety or pest control efficacy, without wasting time troubleshooting raw material variation. The uniform performance in nucleophilic substitution procedures makes new trial batches more predictable, helping bring new actives to field testing sooner.

    Addressing Technical and Environmental Challenges

    Manufacturing chlorinated esters requires addressing environmental responsibility at every stage. Chlorination can generate waste streams containing residual halides, trace organics, and acidic by-products. From our own journey, reducing our environmental footprint started with installation of on-site scrubbing systems to neutralize off-gas and wastewater, paired with solvent recovery infrastructure to reclaim and reuse process solvents. Our team routinely runs environmental audits and invests in training our operators, thinking ahead to probable tightening of chemical regulatory standards.

    Product stewardship matters—customers not only ask after yield and purity, but often want to know how disposal and recovery options might affect their operation’s licensing or compliance audits. This has driven us to offer returnable containers, product take-back programs for large users, and dedicated support for lifecycle planning. We are continually rationalizing our supply of raw materials, favoring lower-impact routes and suppliers with documented improvement in sustainability or worker safety standards. Each small step forward—from scrubber upgrades to reusing secondary containers—strengthens our relationship with companies committed to sustainable growth.

    Risk management is never theoretical in our industry. Years ago, a supplier’s minor shift in reagent purity led to a week-long production stop for us, and forced us to dig deeper into analytical traceability systems. Today, each lot receives traceable barcodes from incoming raw acids to finished drums, making it possible for both us and our customers to pull archived data at a moment’s notice, should any quality or safety concern emerge.

    User Handling and Storage Insights

    People sometimes underestimate the volatility of ethyl 4-chlorobutyrate, especially in open vessels or during scaling stages. Vapor can cause irritation, so we have developed in-house training for all operators, with reinforced protocols for closed system transfer and emergency eye-wash availability. Storage on-site takes place under nitrogen or tightly sealed, moisture-free conditions to prevent slow hydrolysis to butyric acid, which would otherwise impact downstream product quality.

    Transport reliability comes from bulk packaging that balances mechanical safety with chemical compatibility. Polyethylene-lined steel or fluoropolymer drums have proven themselves robust enough for long-distance shipments. We learned through customer feedback that reducing headspace in drums prevents unnecessary vapor losses and keeps product odor consistent, making handling simpler for both our team and the end user upon receipt.

    For research users with bench-scale needs, we offer decanted, sealed bottles packed under inert atmosphere, with accompanying spectral data from our analytical team. These practices might seem meticulous, but they have paid off by drastically reducing returned product and supporting customer traceability when unexpected results occur in sensitive analytical applications.

    Ongoing Improvements and Customer Collaboration

    Continuous improvement doesn’t stop at making the same product over and over. We have learned from both mistakes and successes to keep refining our offering. Customers who encounter solubility or yield problems have direct lines into our technical support team, and we regularly visit user sites—sometimes traipsing through muddy pilot plant setups or peering into analytical benches cluttered with glassware—to gather feedback firsthand.

    In one instance, a pharma client noted an unexplained fragment in their mass spec results. Instead of defending our batch, we dug through archived process logs, repeated distillation under alternative conditions, and ultimately tweaked our drying protocol. The result: fewer by-products and a cleaner, more reliable supply chain for both parties. Exchanges like these build the give-and-take that technical innovation demands in a rapidly evolving market.

    We also regularly update our technical literature based on trial and error, pilot experiences, and customer-driven process tweaks. Our chemists contribute real data from their own lab books—not just generic summaries—so colleagues at our customer companies benefit from the insight earned in hands-on production.

    The Value of Expertise and Authenticity

    Having manufactured ethyl 4-chlorobutyrate for many years, we have witnessed its rise from a niche intermediate to a staple in the toolkit for chemical innovation. We handle every batch knowing that end users depend on us for more than just a commodity. Those who have been on the receiving end of poorly manufactured halo-esters understand the headaches that come from mystery impurities, inconsistent reactivity, or challenging handling properties. Consistency, transparency, technical backing, and a willingness to collaborate set expert manufacturers apart from traders and resellers.

    We believe this substance deserves a place in every advanced synthesis division tasked with building the next breakthrough molecule—be it a lifesaving medicine, a new fragrance, or an agricultural solution fit for modern sustainability needs. Our commitment goes beyond the chemistry; it extends to stewardship, support, and continuous improvement, made possible only by working with and listening to those who use our products every day.

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