Products

Isobutyryl Chloride

    • Product Name: Isobutyryl Chloride
    • Alias: Isobutyryl chloride
    • Einecs: 203-548-0
    • 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

    923942

    Chemicalname Isobutyryl Chloride
    Casnumber 79-30-1
    Molecularformula C4H7ClO
    Molarmass 106.55 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Pungent, acyl chloride-like
    Boilingpoint 91-93°C
    Meltingpoint -76°C
    Density 1.017 g/cm³ at 20°C
    Solubilityinwater Reacts violently
    Vaporpressure 61 mmHg at 20°C
    Flashpoint 9°C (closed cup)
    Refractiveindex 1.406 at 20°C
    Storageconditions Store under dry, inert atmosphere, away from moisture
    Unnumber 3261

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

    Packing & Storage
    Packing Isobutyryl Chloride is packaged in a 500 mL amber glass bottle, tightly sealed, and labeled with hazard and safety information.
    Shipping Isobutyryl Chloride is shipped as a hazardous chemical, classified as a corrosive and flammable liquid. It must be securely packed in airtight, corrosion-resistant containers and clearly labeled. Transportation follows strict safety regulations, typically in accordance with UN 2396, to prevent leaks, spills, and exposure during transit.
    Storage Isobutyryl chloride should be stored in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as water, alcohols, amines, and strong bases. Keep the container tightly closed and protected from direct sunlight. Use corrosion-resistant containers, typically made of glass or specific plastics. Proper labeling and secure storage to prevent leaks or spills are essential for safety.
    Application of Isobutyryl Chloride

    Applications of Isobutyryl Chloride in Industrial Manufacturing

    Isobutyryl Chloride serves as a critical intermediate in multiple chemical synthesis processes. Our direct manufacturing capacity enables large-scale, secure, and consistent supply for diverse industrial sectors. Below we detail verified application scenarios matched to real market demand.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Isobutyryl Chloride plays a key role in the synthesis of pharmaceutical intermediates, especially during the acylation of heterocycles and amines. API producers utilize it for manufacturing antibiotics and local anesthetics. Reaction controls require precise dosing and monitored addition under regulated atmospheres. Its use must consider batch traceability and validation documentation to ensure regulatory approval for downstream actives.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • USP & EP monographs specific to intermediates
    • 21 CFR Part 211 (US FDA)
    • Chinese Pharmacopoeia standards

    Typical usage ratio

    • Generally 0.8–1.2 molar equivalents per target molecule
    • Adjustments based on the reactivity of amines or alcohols in the synthesis
    • Excess minimized to reduce by-product contamination

    Downstream process integration

    • Introduced during the acylation step in stepwise or one-pot syntheses
    • Dosed into temperature-controlled reactors with inert gas blanketing
    • Residual removal by aqueous workup and extraction

    Final product types

    • Cephalosporin antibiotic intermediates
    • Anilide-based local anesthetic active ingredients
    • Custom pharmaceutical intermediates for CDMOs

    2. Agrochemical Intermediate Manufacturing

    The acylation function of this reagent is essential in production of select herbicides, pesticides, and fungicide intermediates. Agrochemical plants rely on its strong acylating power to modify ring structures for bioactive compound development. Environmental and worker safety controls must match crop protection regulation standards, with careful storage and handling during reaction and waste management phases.

    Industry compliance standards

    • FAO/WHO JMPR pesticide standards
    • ISO 9001:2015 Quality Management System
    • REACH registration under ECHA
    • China ICAMA registration for pesticide intermediates

    Typical usage ratio

    • Normally 1.0–1.4 molar equivalents per functional group
    • Optimized based on desired acylation conversion rate

    Downstream process integration

    • Added at the acylation phase of the molecule assembly process
    • Reacted in jacketed, corrosion-resistant reactors with closed handling
    • Hydrolysis and post-treatment to minimize impurities

    Final product types

    • Pyrazole-derived herbicide intermediates
    • Proprietary insecticide components
    • Sulfonylurea pre-cursor compounds for weed control

    3. Fragrance and Flavor Ester Production

    This raw material acts as an acid chloride source for manufacturing isobutyric esters, preferred in fragrance and flavor compounds. Flavor and F&F producers carry out esterification reactions with high attention to purity and trace organochlorine control. Commercial significance arises in scale production of flavoring agents for the beverage and food industry.

    Industry compliance standards

    • IFRA Standards for fragrance materials
    • 21 CFR 172.515 (US FDA flavor ingredient regulation)
    • EU Regulation (EC) No 1334/2008 for flavorings
    • FEMA GRAS status for permitted esters

    Typical usage ratio

    • 0.9–1.1 equivalents per alcohol used in esterification
    • Ratio variance depending on feed alcohol purity and desired yield

    Downstream process integration

    • Charged into batch reactors with alcohols and acid scavengers
    • Reaction under controlled temperature and agitation, with acid acceptor
    • Crude and fractional distillation to isolate target esters

    Final product types

    • Isobutyl acetate and other isobutyric esters for fruity notes
    • Specialty fragrance blenders for perfumery compounds
    • Synthetic flavoring agents used in food and beverage formulations

    4. Custom Synthesis for Specialty Polymers

    Chemical manufacturers of advanced polymers incorporate this compound for chain-end capping and as a source of acyl functions during block structure assembly. Use in high-value specialty polymers often mandates full reaction traceability and documentation for export to regulated markets. Its reactivity profile facilitates incorporation at ambient or slightly elevated temperatures, allowing consistent molecular weight control of the final polymer product.

    Industry compliance standards

    • ISO 9001:2015 for QMS in specialty chemicals
    • REACH Annex VII for polymer intermediates
    • RoHS (for polymer electronics use)
    • Customer-specific technical agreement documentation

    Typical usage ratio

    • 0.05–0.2 molar equivalents referenced to chain ends or functional sites
    • Adjusted according to polymer molecular weight and desired end-group control

    Downstream process integration

    • Fed at terminal chain modification step
    • Reacted under controlled atmosphere to cap or derivatize polymer ends
    • Process monitored by GPC and FT-IR to verify modification

    Final product types

    • High-performance polycarbonates and polyesters with tailor-made end groups
    • Engineering resins for automotive and electronic housing manufacturing
    • Specialty block copolymers for adhesives and coatings

    5. Fine Chemical Intermediate for Veterinary Pharmaceuticals

    Veterinary drug manufacturers use this compound in the acylation of several bases to prepare building blocks for animal health active substances. Reaction control is optimized for selectivity, and full batch documentation is implemented, as materials enter regulated veterinary drug synthesis pipelines. Secure closed-system transfer mitigates the risk of operator exposure and environmental release.

    Industry compliance standards

    • VICH GL40 GMP for veterinary products
    • US FDA 21 CFR Part 225
    • European Pharmacopoeia (Ph. Eur.) specifications for veterinary active ingredients
    • Local Ministry of Agriculture standards

    Typical usage ratio

    • Usually 0.95–1.25 equivalents per reactive amine or alcohol group
    • Monitored to ensure high conversion and controlled impurity level

    Downstream process integration

    • Introduced in controlled dosing at the acylation step in multi-step syntheses
    • Secondary reaction purification to remove side products
    • Documentation supports full traceability to final drug batch

    Final product types

    • Intermediate for amide-based antiparasitic agents
    • Pre-cursors for injectable veterinary antibiotics
    • Key raw material for animal health API synthesis

    6. Photographic Chemicals and Imaging

    Specialty manufacturers use isobutyric derivatives as components in photographic processing, particularly for formulating acylated color couplers and grain control agents for film technology. Processing requires careful environmental controls to meet safety and disposal regulations. Metered addition and tailored reaction conditions ensure reproducible film performance in final application use.

    Industry compliance standards

    • ISO 18902 Imaging Material Storage
    • REACH compliance for sensitizing agents
    • US EPA hazardous waste control for spent processing chemicals
    • Company-specific QC/QA documented processes

    Typical usage ratio

    • 0.5–1.0 equivalents per target color coupler
    • Adjusted for desired activity and film sensitivity
    • Process refinement according to coupler type

    Downstream process integration

    • Fed directly into acylation stage of dye or coupler synthesis
    • Strict reaction monitoring for color purity and performance consistency
    • Waste stream neutralization prior to disposal

    Final product types

    • Color film couplers for analog photography
    • Stabilizer additives for archival imaging films
    • Special grain control agents in photographic emulsions
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    Certification & Compliance
    More Introduction

    Isobutyryl Chloride: Manufacturing Insights and Practical Applications

    Experience in Large-Scale Production

    Over more than a decade in the chemical manufacturing sector, we’ve watched the demand for acyl chlorides rise, particularly those which combine robust reactivity with dependable storage properties. Among these, Isobutyryl Chloride stands out. With a CAS number of 79-30-1 and the molecular formula C4H7ClO, this compound occupies a unique place in downstream synthesis routes. Our teams, backed by years of hands-on experience, have adopted proven reaction routes optimizing output and safety. Chlorination of isobutyric acid forms the foundation; details like controlled reflux, advanced distillation, and moisture-free handling determine yield and purity. Operators remain vigilant to manage HCl off-gassing and maintain reactor integrity. Keeping equipment corrosion-resistant cuts both downtime and maintenance, factors that matter in bulk runs.

    Quality benchmarks go beyond basic GC purity results. Customers increasingly scrutinize residual acid numbers, trace water, and halide content. We routinely produce Isobutyryl Chloride offering purity above 99.5%, tailored for both scale-up R&D and commercial supply. Our in-house labs confirm attributes relevant for sensitive synthesis: low free acid below 0.5%, water content kept below 0.1%, and chloride ion levels carefully managed to avoid interference downstream. Not every producer can consistently ensure these figures batch after batch; even small deviations trigger issues further down the value chain, especially for pharma or agrochemical intermediates.

    Physical Properties and Handling Know-How

    Isobutyryl Chloride appears as a colorless to pale yellow liquid. With a boiling point hovering near 105–107°C and a specific gravity close to 1.01, the material stores and dispenses easily with standard acid chloride-resistant lines, though we never take shortcuts. The characteristic acrid odor signals the presence of residual HCl, and so ventilation and PPE are non-negotiable. Reactions with moisture generate HCl gas; our storage zones use dry inert gas blanketing and moisture traps at every interface.

    Seasoned operators know even a minor leak can corrode fittings and overwhelm lower-grade seals, so regular inspection cycles prevent downtime. Drum and IBC design also matters—standard HDPE containers suffice for shipment, but only with seals certified against acid chlorides. With every outgoing shipment, our technical team checks drum lining integrity and confirms shipment temperature control during transit.

    Comparison With Other Acid Chlorides

    It helps to see where Isobutyryl Chloride fits among similar acid chlorides. Compared to Acetyl Chloride, Isobutyryl Chloride brings steric bulk that modulates its reactivity in acylation steps. This can reduce overreaction and side product formation, especially in more complex organic synthesis. Unlike Propionyl Chloride, whose volatility raises site safety concerns, Isobutyryl Chloride sits in a safer boiling range, allowing tighter process control and fewer incidents during handling.

    Both Acetyl and Propionyl Chlorides are notorious for their aggressive hydrolysis; Isobutyryl Chloride delivers a manageable rate, meaning downstream protection chemistry benefits from less moisture sensitivity while still offering the full acyl chloride reactivity. Some users move to Pivaloyl Chloride for even greater stability but pay premium prices and deal with difficult storage. Isobutyryl Chloride, in our experience, strikes the best cost-to-utility balance for many acylation and synthesis routines.

    Downstream Uses in Fine Chemical and Industrial Synthesis

    Few organochlorine compounds play as central a role in API and agrochemical intermediate manufacture as Isobutyryl Chloride does. As both a chlorinating agent and an acylating partner, it unlocks the synthesis of a variety of esters and amides. The extra methyl group, compared to simpler acid chlorides, brings desirable lipophilicity to target molecules, affecting both their physical behavior and biological activity. In the pharmaceutical field, it features in the preparation of APIs where branching is a key pharmacophoric motif.

    Agriculture chemists rely on it to introduce isobutyryl groups into herbicide and fungicide molecules, conferring the fine-tuned absorption and metabolic profiles that modern markets demand. In polymer chemistry, Isobutyryl Chloride enables precise end-capping or pendant group installation, allowing for custom-tailored polymer performance traits. Through repeated collaborations with clients, our technical teams have refined process conditions that maximize selectivity, simplify workup, and minimize hazardous waste—critical when adhering to ever-tightening environmental rules.

    Insights on Sourcing and Project Planning

    Over the course of supplying both specialty and high-volume acyl chlorides, we’ve learned that not all buying criteria are visible on a standard COA. Partners who involve us early spot potential bottlenecks, whether in material compatibilities, storage requirements, or regulatory documentation. While some acyl chlorides enter supply gaps from trader stocks, legitimate manufacturers ensure backward integration of starting acids, tight control over batch histories, and documented corrective action logs.

    Developers scaling bench chemistry to pilot volume rely on consistent impurity levels from one batch to the next. We collaborate closely, providing not only product but application notes and onsite troubleshooting. Isobutyryl Chloride’s hydrolytic sensitivity and hydrochloric acid byproduct mean receiving sites must manage venting and scrubbing, and our years supplying acids and acid chlorides mean we’ve gathered many practical solutions for neutralization and material compatibility. Customers don’t face surprises from undiscussed reactivity or off-spec waste.

    Regulatory and Safety Considerations

    Isobutyryl Chloride occupies a regulated position in most jurisdictions. SDS sheets outline the direct irritant and corrosive risks to skin, eyes, and respiratory systems. Having responded to more than a few near-misses in decades of handling chlorinating agents, we never skip training for both our plant staff and carrier crews. Spill drills, full-body chemical suits, fixed gas detectors and staged neutralization barrels support our facility routines. In shared supply chains, customers often bring us in for joint HAZOP reviews, looking for advice on custom scrubbing or neutralization set-ups.

    We don’t stop at site barriers. Compliance with international shipping laws—covering both hazardous materials labeling and customs categories—matters if deliveries must route through multiple ports or customs zones. Mislabeling or incomplete documentation can delay containers at border checks, with temperature and moisture shifts spelling disaster for sensitive batches. Drawing on our logistics partners and direct experience, we keep paperwork transparent, product secure, and lines of communication open up to the point of final receipt.

    Improving Environmental Footprint

    The environmental impact of acid chloride chemistry draws more scrutiny every year. Our team has overhauled vent handling, introducing closed-loop HCl recovery units which transform acid gas into commercial-grade hydrochloric acid, supplied to local buyers. We route waste chlorinated waters through dedicated treatment that scrubs and neutralizes emissions, allowing us to surpass both local and international compliance numbers by significant margins.

    Most improvement comes from close review of process step yields. Tracing loss points, shifting reaction stoichiometries, and developing less wasteful work-up routines mean less raw acid and thionyl chloride routed to waste. Where off-site destruction can’t be avoided, we provide full disposal documentation—something site auditors now expect as part of risk-assessment checklists. Newer advances, such as solid-phase scavenging or membrane-based purification, show promise for future efficiency, though deployment at scale requires steady investment and process tuning.

    Support From Direct Manufacturer Experience

    Receiving calls for advice on unexpected mix flags, cold weather gel formation, or dimerization during transit has shaped our technical support model. Drawing from direct manufacturing data, we answer with detail rather than guesswork—whether a batch failed because of incompatible pump linings or atmospheric moisture ingress. We work with end-users to develop specific drying and transfer protocols, with site visits paid upfront to avoid guessing. Our process engineers share lessons learned from our own troubleshooting, from line clogging to thermal runaway prevention.

    Feedback from end users shapes each round of improvements. Users often ask about color shifting or trace impurity drift between batches. With Isobutyryl Chloride, even trace byproducts can foul catalytic processes or shift downstream selectivity. We control raw feedstock origins and incorporate adapted distillation, always keeping analytical labs informed. For longer shipping routes, we equip shipments with environmental loggers, building batch data that correlates any downstream flag back to specific transit or storage events. Open loops between manufacturer and end-user cut troubleshooting time and wasted inventory.

    Industry Trends and New Directions

    Demand for Isobutyryl Chloride shows no sign of slowing, being driven both by renewed pharma activity and expansions in advanced materials. Patents and generic drug registrations routinely cite this acid chloride in both core builds and late-stage transformations. Newer applications keep emerging: recent battery electrolyte systems and specialized photoinitiators incorporate it to balance performance, processability, and regulatory acceptance.

    The ongoing push for greener chemistry models also reshapes production and use expectations. Clients, pressed for certificate-of-analysis depth and regulatory traceability, now expect supply chain transparency from origin to final use. We’ve opened up our digital documentation systems for select customers, offering real-time site release data and live process audit options. This takes work—training staff, certifying IT systems—but delivers trust in regulated sectors. Investing sweat and capital in better process control, cradle-to-gate traceability, and downstream problem-solving offers more to the chemical supply chain than price competition ever can.

    Challenges Unique to Isobutyryl Chloride

    Isobutyryl Chloride carries specific handling and process risks. Unlike less hindered acid chlorides, its reactivity profile gives narrower process windows for many reactions, so end users must tune reaction conditions accordingly. Elevated batch temperatures can increase hydrolysis and decompose sensitive substrates. Our technical resource sheets detail safe temperature and pressure boundaries because lessons learned the hard way stick best.

    Contact with sodium hydroxide or amines yields rapid, exothermic reactions, making scale up more hazardous unless dosing rates and agitation patterns match those developed in pilot runs. In production, we supply real-time monitoring standards so receiving teams can calibrate dosages at scale rather than relying only on small-lab data. Even clean transfer lines risk polymerization or plug formation during extended downtime, so purging and drying procedures form an integral part of transfer protocols. We offer remote and onsite audit support to customer plants to verify critical checks before accepting new shipments.

    Solutions for Modern Manufacturing Needs

    Modern manufacturing demands reliability above all. Isobutyryl Chloride’s niche properties align with a wide spread of creative synthesis plans, but only when both supplier and user align process expectations from quotation through delivery. We keep communications clear from the start by mapping out batch release schedules, offering contingency plans for seasonal storage, and backing shipments with direct technical advice. With growing pressure for fast response times, our plant has phased in extra shift scheduling and real-time inventory dashboards, keeping users aware of available supplies before they hit reorder points.

    By keeping deeper inventories and investing in dual-source raw feedstock agreements, we’ve kept output steady even during hiccups in global supply chains. Feedback loops with customer process teams let us adjust purification methods or blend options to fit the highest-value downstream routes. For projects scaling up from pilot chemistry, we provide not just bulk material but help with all safety and process documentation required for regulatory filings.

    Building End-User Trust Through Experience

    Success with Isobutyryl Chloride rarely comes from lowest cost alone. Users reward transparency, supply chain reliability, and expert technical backup. Through direct partnerships, we’ve seen clients maximize their own efficiency and minimize off-spec waste. Our product knowledge—gleaned from years of running plants ourselves—lets us head off complications before they arise and foster a collaborative, open-door approach to troubleshooting.

    We focus on learning with each campaign, refining internal process steps, updating risk models, and adapting technical documentation for customer-specific needs. Our commitment to both technical advancement and direct user engagement gives buyers the confidence to build new processes and scale up production without fear of unexpected hurdles or quality drifts. Isobutyryl Chloride’s role in chemical manufacturing continues to grow, and as manufacturers with hands-on expertise, we stay committed to helping customers unlock its full potential with practical, down-to-earth advice and steady operational support.

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