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2-Methylvaleryl Chloride

    • Product Name 2-Methylvaleryl Chloride
    • Alias Isovaleryl chloride
    • Einecs 211-852-5
    • 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

    756434

    Cas Number 4563-36-8
    Molecular Formula C6H11ClO
    Molecular Weight 134.61
    Iupac Name 2-methylpentanoyl chloride
    Synonyms 2-Methylpentanoyl chloride, α-Methylvaleryl chloride
    Appearance Colorless to pale yellow liquid
    Boiling Point 143-145°C
    Density 0.978 g/mL at 25°C
    Melting Point -60°C (approximate)
    Refractive Index n20/D 1.418
    Flash Point 48°C
    Solubility Reacts with water

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

    Packing & Storage
    Packing 2-Methylvaleryl Chloride is packaged in a 500 mL amber glass bottle with a secure screw cap and proper hazard labeling.
    Shipping 2-Methylvaleryl Chloride is shipped in tightly sealed containers made of materials compatible with corrosive and moisture-sensitive chemicals, typically under inert gas. It must be labeled as a hazardous material, transported in compliance with regulations for corrosive and toxic substances, and kept away from heat, water, and incompatible materials during transit.
    Storage 2-Methylvaleryl chloride should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen. Keep it in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible materials like strong bases, oxidizers, and alcohols. Protect from direct sunlight and avoid prolonged exposure to air to prevent hydrolysis and decomposition. Handle in a chemical fume hood.
    Application of 2-Methylvaleryl Chloride

    Applications of 2-Methylvaleryl Chloride in Industrial Manufacturing

    As a dedicated manufacturer, we supply high-purity 2-Methylvaleryl Chloride for specialized industrial uses that require traceable quality and consistency. Below, we detail the primary application scenarios implemented by leading chemical, pharmaceutical, and flavor sector producers worldwide.

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

    2-Methylvaleryl Chloride is a preferred acylation agent for the synthesis of certain pharmaceutical intermediates, where precise introduction of the 2-methylvaleryl group is required for molecular modification. Our direct customer base leverages its reactivity during critical steps in the preparation of antiepileptic and central nervous system (CNS) active compounds. The exact addition is determined by the stoichiometric needs of the drug synthesis pathway, which is strictly monitored to maintain batch-to-batch consistency for GMP compliance. Downstream manufacturers typically utilize this chloride for the formation of amide, ester, or ketone linkages specific to their patented pharmaceuticals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US FDA cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) residual solvent and impurity controls
    • China Pharmacopoeia (ChP) analytical methods when used in APIs registered in China

    Typical usage ratio

    • Stoichiometric to slight excess (1.05:1 to 1.2:1 molar ratio to the amine/alcohol substrate), based on process route and impurity profile targets

    Downstream process integration

    • Charged in the acylation or esterification reactor, typically at the intermediate synthesis stage following core scaffold preparation

    Final product types

    • Antiepileptic drug APIs (e.g., derivatives related to valproic acid)
    • CNS modulator intermediates
    • Other regulated small-molecule pharmaceutical actives

    2. Synthesis of Specialty Aroma and Flavor Esters

    Flavors and fragrance formulators employ 2-Methylvaleryl Chloride for the manufacture of esters imparting unique branched aliphatic notes that enhance fruity, green, or complex nutty aromas. Its dosing requires careful calibration, as esterification yields and residual acid chlorides directly influence the sensory profile, with traceability supported by batch-wise quality transparency. Downstream use involves direct preparation of flavor-active esters, often as part of manufacturing accords for use in both fine fragrances and food-grade blends.

    Industry compliance standards

    • IFRA (International Fragrance Association) use restrictions and purity requirements for raw materials
    • US FDA 21 CFR 172.515 for flavoring substances in food
    • EU Regulation (EC) No 1334/2008 for flavoring substances
    • FEMA GRAS status for resulting esters (where applicable)

    Typical usage ratio

    • 0.8:1 to 1.2:1 molar ratio relative to the alcohol substrate, adjusted to drive complete conversion and minimize unreacted acid chloride depending on target ester purity

    Downstream process integration

    • Acid chloride is dosed into batch or continuous reactors for direct esterification with specific polyalcohols or monoalcohols under controlled pH and temperature; neutralization and purification steps follow to ensure product is free of chlorinated byproducts

    Final product types

    • Food-grade fruit, creamy, and nutty aroma esters for beverage and confectionery flavoring
    • Fine fragrance ingredients for perfumery
    • Complex aroma bases used in flavor houses

    3. Agrochemical Intermediate Manufacturing

    Multinational crop protection companies utilize 2-Methylvaleryl Chloride as a building block for the acylation of amines or alcohols to construct novel herbicide and fungicide intermediates. Its role is critical in the formation of bioactive branched-chain structures which demonstrate selectivity and efficacy against resistant weed populations. Production is controlled under detailed process hazard analysis to ensure yield optimization and environmental safety within regulatory limits set by agrochemical frameworks.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for active ingredient synthesis
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • US EPA Pesticide Registration (PR) Notice 98-9 for impurity control and identity
    • China GB2763 for maximum residue limits in agricultural products (for downstream assessment)

    Typical usage ratio

    • 1.0:1 to 1.3:1 molar ratio to the reacting amine or alcohol, fine-tuned based on individual molecule requirements and impurity control

    Downstream process integration

    • Integrated in multi-step batch synthesis following precursor amine or polyol protection; reactive step-utilized in controlled acylation and then passed to further derivatization or formulation for final technical concentrate

    Final product types

    • Technical grade herbicide intermediates
    • Fungicide precursor compounds for in-field application products
    • Post-application safener intermediates

    4. Fine Chemicals Synthesis – Custom Aliphatic Acid Derivatives

    Chemical custom synthesis producers employ 2-Methylvaleryl Chloride in the tailored production of specialty aliphatic acid derivatives, particularly in contract research and advanced material supply. Its reactivity profile supports the stepwise manufacture of unique acid anhydrides, activated esters, and modified acids for use in specialty plasticizers, lubricants, or surfactants, especially where molecular branching imparts distinctive physicochemical properties to end materials. Our traceable supply chain and batch-specific analytics facilitate stringent control of impurities critical for high-value specialty uses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for specialty chemical production
    • REACH Regulation (EC) No 1907/2006 for pre-registration and safety data support
    • Specific customer-driven QC and impurity profile specifications for fine/advanced materials
    • GHS-compliant labeling and transport for laboratory or pilot-scale supplies

    Typical usage ratio

    • From 1.0:1 up to 2.0:1 molar ratio depending on desired conversion degree and downstream purification recovery targets; adjustments depend on reaction scale and end-use purity cut-off

    Downstream process integration

    • Loaded at the stage where acyl functionalization is required, frequently following substrate dehydration or base-catalyzed activation; excess scavenged and recovered as part of closed-loop operations to minimize organochloride emissions

    Final product types

    • Specialty esters and anhydrides for advanced textile auxiliaries
    • Branched-chain lubricating additives
    • Alkylated surfactants and emulsifiers with controlled hydrophobicity
    • Custom intermediates for material R&D contracts
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    Certification & Compliance
    More Introduction

    2-Methylvaleryl Chloride: Reliable Performance from the Manufacturer’s Bench

    Meet 2-Methylvaleryl Chloride: A Crucial Intermediate Shaping Modern Synthesis

    From inside the walls of a chemical manufacturing site, nothing replaces the direct experience of working day in and day out with specialty acid chlorides. Over the years, tight controls and patient testing have taught us what makes each compound stand apart. 2-Methylvaleryl Chloride—sometimes called 2-methylpentanoyl chloride—serves as an excellent illustration of the advantages a well-developed production process brings to customers demanding real dependability and purity.

    The molecule carries the formula C6H11ClO and registers a clear, colorless to pale straw liquid at room temperature. An unmistakable, sharp acyl odor greets anyone opening a fresh drum. This chemical serves as a reactive acyl chloride, favored by manufacturers in pharmaceuticals, agrochemicals, and specialty chemical synthesis. High-purity lots often tilt key reaction yields in the right direction. Skipping corners on water content or controlling for side-reaction byproducts means wasted solvent, fouled reactors, and downstream headaches. No pilot plant or kilo-lab forgets this lesson for long.

    Understanding the Process from Raw Material to Finished Acid Chloride

    Every drum, can, or flask that leaves our site started with select raw 2-methylvaleric acid. Whenever the supply chain gets rocky or global shortages weigh on timing, those choices in sourcing ripple all the way through the value stream. We have seen how upsets in raw acid content, trace impurity levels, or unexpected bycatch from feedstock affect acid chloride output and application downstream. Over the years, by sticking with fixed suppliers vetted for tight control, we have avoided batches haunted by nagging traces of tars, residual water, or unwanted halides.

    Chlorination uses classic thionyl chloride and anhydrous conditions. Early on, inadequate drying or poorly controlled reflux temperatures left a mark: color drift, trace SO2 contamination, and—you guessed it—the sort of residual acid chlorides that turn scale-up trials into guesswork. Improvements in our reaction control, in-line monitoring, and aggressive post-process stripping allowed us to deliver a material trusted for bench and production use. We routinely test for free acid, water, residual SO2, and unwanted isomers. The sharp chemical odor and stable color indicate a product kept far from contact with metal surfaces or atmospheric moisture.

    Specifications from Those Doing the Work

    We do not talk about minimum standards or compliance checkboxes in the abstract here. Every lot sent to valued partners clears a transparent water-content threshold, with Karl Fischer titration guiding each batch release. Chloride purity, typically above 98%, comes not from arbitrary labeling but from real-world product runs demanding consistent, predictable reaction profiles. Residual acid, if present, is flagged immediately and never leaves the site.

    The liquid form makes dosing by weight or volumetric addition straightforward, though our in-plant crews always vent setups well and stage secondary containment. Volatility and reactivity require glass, PTFE, or stainless steel in transfer lines and valves. In our labs, each new drum runs through a small test batch to confirm acylation reactivity before further downstream use.

    Application: Preferred Pathways in Fine Chemical and Pharmaceutical Synthesis

    Acylation Reactions: The biggest call for 2-methylvaleryl chloride comes from chemists building up complex molecules with branched side chains, masking groups, or advanced intermediates for pharmaceuticals and crop protection agents. These days, active ingredient synthesis in both research and commercial settings still relies on straightforward acid chloride chemistry rather than futuristic alternatives, since they give consistently high yields, easy removal of byproducts, and little need for additives.

    Agrochemical Building Blocks: Our partners in crop science routinely turn to this molecule when constructing new herbicides, plant growth regulators, and pesticide active ingredients. The branched C6 skeleton offers a great handle for unique structure–activity explorations, and its reactivity under controlled temperature conditions keeps eliminations or rearrangement to a minimum. Direct feedback from our friends at formulation labs has repeatedly circled back to the advantage of matching the acid chloride quality to reaction stage—one batch of subpar material can stall optimization by weeks.

    Flavor, Fragrance, and Specialty Markets: In smaller but innovative directions, 2-methylvaleryl chloride stands out in flavor and fragrance chemistry. Its reactivity allows creation of esters and amides with unique fruity or herbal characteristics. Unlike unbranched analogs, these substituted derivatives often survive process scale-up while holding onto their desired volatiles, a fact that only gets proven after multiple pilot runs.

    How this Compound Differs from Other Acid Chlorides

    Comparing straight-chain vs. branched-chain acid chlorides, the difference in downstream product properties is frequently obvious to users. 2-Methylvaleryl chloride, with its branching at the alpha carbon, delivers steric hindrance that changes reactivity, affecting selectivity and product outcome in multi-step organic synthesis. Contrast that with n-valeryl chloride—customers tuning amide, ester, or acylated pharmaceutical intermediates notice the difference in yields right away. The methyl branch noticeably improves regioselectivity, which often means less need for post-reaction purification.

    Those who have only worked with more basic acid chlorides such as acetyl or propionyl chloride miss the opportunity 2-methylvaleryl chloride gives for creating more complex molecules: pharmaceutical active ingredients or specialty polymers that demand molecular complexity for both function and regulatory compliance. While production costs run higher, the yield gains, streamlined purifications, and reduced generation of hazardous byproducts provide value back to research and manufacturing partners.

    Moisture sensitivity sets this molecule apart from more forgiving acyl chlorides; even a few parts per thousand water content can destroy reactivity or lead to quick hydrolysis, which is why in-plant checks on drum seals, warehouse air controls, and pack-off logistics deserve extra attention. The scent test, color check, and careful titration at unloading deliver real confidence to downstream users who do not want to risk losing days of batch time or generate corrosive HCl spikes mid-process.

    Lessons Learned in Scale-Up and Long-Term Supply

    Our years in the business have taught us not to underestimate the knock-on effects of minor improvements to the production process. Investments in better moisture controls, faster analysis turnaround, and direct line sampling did more to erase batch-to-batch headaches than any fancy marketing. Small changes on our end—better glass lining, filtered gas supplies, automated data capture—bring real benefit to those trusting us for a reliable supply chain.

    Some customers who started with lab-scale purchases switched to higher-volume contracts after seeing reduced off-spec batches and easier process validation in their own plants. Keeping formulation drift under control also helps keep hazardous waste to a minimum, which benefits both environmental performance and operating budgets. Improved batch tracking records, easy access to certificates of analysis, and histories of each lot build trust over the long haul.

    From the production floor, no one wants returns for broken seals or isolated complaints that a batch “smelled off” or lost its activity in storage. Every shipment of 2-methylvaleryl chloride gets a close look before release. Storing containers in dry, shaded, and cool storage stretches shelf life and maintains the physical properties that give this compound a good name in specialized synthesis. Regular reviews with customers—including follow-up on new downstream regulatory tests—keep our process honest and flexible.

    Handling Challenges and Safety at the Source

    In real plants, every acid chloride brings risks. Fumes from 2-methylvaleryl chloride cause real trouble if not handled with proper systems. Operators at our facility rely on local exhaust, reinforced PPE, standard glove protocols, and emergency shutoffs. Each incident and near-miss, even minor ones, drive constant improvement: better drum designs, quicker venting, and staff training updates. We do not wait for slow-moving regulatory guidance—peer warnings and lessons from chemical forums prompt faster upgrades.

    Customers consistently ask about the interaction between our synthesis and environmental stewardship. Any waste generated—either unreacted residuals, rinse streams, or spent absorbents—is segregated and treated according to current best practice. Analytical chemists at the site test exit streams well beyond the mandated levels, driven by internal standards and audit history, since nobody wants surprises months or years after shipment. These added steps reflect learning from decades of environmental audits, insurance-driven reviews, and plenty of sleepless nights responding to earlier near-misses.

    Consistency, Communication, and Partnership in 2-Methylvaleryl Chloride Supply

    Our customers—from small startups chasing a novel insecticide to established pharma players fine-tuning blockbuster intermediates—teach us daily about the real demands of chemical sourcing. Predictable product performance and the elimination of costly surprises are worth more than short-term price incentives or vague promises of “top quality.” We worked through winter storms, new regulatory patches, and pandemic logistics crunches. Along the way, we learned the value of giving full batch traceability and maintaining open channels for questions or feedback. Changes in regulatory requirements or regional import hurdles rarely catch us sleeping, and we routinely help partners through changing paperwork, test tolerances, and new data requests.

    Some partners care less about price per drum than batch uniformity. These users—especially in pharmaceuticals and advanced materials—regularly request custom labeling, lot history files, and in-person audits. We welcome this scrutiny, because it circles back to our commitment to real-world quality. Any batch that hiccupped in transport or ran into technical issues gets flagged and held for review; truthfully, we would rather run thin on shelf than push out anything short of our benchmark. No fancy label or sales pitch replaces the confidence born from years of direct supply without failures.

    Supporting Partners with Real-World Advice and Technical Back-Up

    Those who buy 2-methylvaleryl chloride for the first time often have formula-specific questions or need guidance on process integration. We remember the steep learning curve on acid chloride handling and do not hesitate to share application notes, troubleshooting passed down from shift leads, or tricks for safe storage and use in high-humidity locations. Our technical staff invests a good deal of time demystifying bottlenecks on scale-up, foiling issues with glass-lined reaction vessels, or advising on purification steps for unique chemical targets. This back-and-forth runs deeper than just filling orders—it’s a matter of professional courtesy and pride to keep users safe, successful, and fully informed.

    From advancing pharmaceutical research to enabling the next wave of crop protection innovation, 2-methylvaleryl chloride stands for more than a reagent grade—it delivers the flexibility, safety, and predictability built from years of manufacturing discipline. Current partners count on us for strict controls, complete batch histories, and day-by-day responsiveness borne of firsthand experience, not distant trading desks or intermediaries. If your applications demand tough sourcing, regulatory assurance, and application support, we invite continued conversation and technical collaboration.