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(S)-4-Chloro-3-Hydroxybutyronitrile

    • Product Name (S)-4-Chloro-3-Hydroxybutyronitrile
    • Alias (S)-3-Hydroxy-4-chlorobutyronitrile
    • Einecs (EINECS) 411-020-1
    • 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

    336036

    Chemicalname (S)-4-Chloro-3-Hydroxybutyronitrile
    Molecularformula C4H6ClNO
    Molarmass 119.55 g/mol
    Casnumber 111205-01-3
    Appearance Colorless to pale yellow liquid
    Density 1.23 g/cm³ (approximate)
    Opticalrotation [α]D20 = +15° to +25° (c=1, CHCl3)
    Smiles C(C[C@H](C#N)O)Cl
    Inchi InChI=1S/C4H6ClNO/c5-2-1-4(7)3-6/h4,7H,1-2H2/t4-/m0/s1
    Chirality S-enantiomer
    Solubility Soluble in water and polar organic solvents
    Refractiveindex 1.452 (approximate, 20°C)
    Storagetemperature 2-8°C (refrigerated)

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

    Packing & Storage
    Packing (S)-4-Chloro-3-Hydroxybutyronitrile is supplied in a 25g amber glass bottle with tamper-evident seal and chemical hazard labeling.
    Shipping (S)-4-Chloro-3-Hydroxybutyronitrile is shipped in tightly sealed containers to prevent moisture and contamination, following all applicable hazardous material regulations. Transport is conducted at ambient temperature, with proper labeling for corrosive and toxic substances. Handling and shipping procedures comply with international standards to ensure safety and product integrity during transit.
    Storage (S)-4-Chloro-3-hydroxybutyronitrile should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Store at recommended temperatures, typically between 2–8°C, and ensure proper labeling to prevent accidental misuse or exposure. Handle with suitable personal protective equipment.
    Application of (S)-4-Chloro-3-Hydroxybutyronitrile

    Applications of (S)-4-Chloro-3-Hydroxybutyronitrile in Industrial Manufacturing

    As the original manufacturer, we supply (S)-4-Chloro-3-Hydroxybutyronitrile to leading industries focusing on advanced intermediates. Below, we present key application scenarios where our raw material contributes to high-value downstream synthesis, supported by detailed production, compliance, and process information.

    1. Pharmaceutical Chiral Intermediate for Antiepileptic Drugs

    (S)-4-Chloro-3-Hydroxybutyronitrile serves as a chiral building block in the synthesis of moderately complex antiepileptic drug molecules. Its stereoselectivity enables downstream manufacturers to achieve precise configuration, crucial for regulatory approval and bioactivity. Processing involves enantioselective transformation, followed by direct coupling with active moieties during multi-step API synthesis. Precise monitoring is mandatory for compliance with pharmaceutical standards, and the intermediate supports bulk and specialty drug production for neurology portfolios.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs for chiral intermediates
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practices for Finished Pharmaceuticals)
    • Relevant DMF (Drug Master File) requirements for supply chain transparency

    Typical usage ratio

    • Utilization rate typically 0.9–1.1 molar equivalents per API batch, adjusted based on enantiopurity control and targeted yield efficiency

    Downstream process integration

    • Introduced at the enantioselective alkylation or nucleophilic substitution stage before key ring-closure or side chain extension in API synthesis

    Final product types

    • Levetiracetam intermediates
    • Brivaracetam intermediates
    • Other chiral pyrrolidone-based CNS-active APIs

    2. Advanced Intermediate for β-Amino Acid Derivatives

    Downstream producers use the material as a precursor in β-amino acid synthesis designed for peptide therapeutics and research chemicals. Its functional groups react selectively in reductive amination or cyanohydrin conversion steps, allowing for scalable production with controlled optical purity. Manufacturers integrate tightly controlled process controls to limit racemization, aligning final intermediates with industry QC benchmarks.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals for European supply
    • Japan Pharmaceutical and Medical Device Act for API Intermediate Imports

    Typical usage ratio

    • Applied at 1.0 molar equivalent per amino acid side chain unit; higher equivalents (up to 1.2) used for double coupling strategies

    Downstream process integration

    • Added during the initial nucleophilic addition phase or reductive amination, preceding esterification or Fmoc/Boc protection in peptide synthesis

    Final product types

    • β-amino acid derivatives for peptide drugs
    • Building blocks for synthetic peptides
    • Custom amino alcohol intermediates

    3. Intermediate for Agrochemical Active Substance Synthesis

    Producers utilize this compound to introduce chiral centers in the synthesis of specific fungicide and herbicide molecules. The hydrogenation and halogen handling compatibility supports efficient downstream coupling and enables flexible scale-up. At this stage, operators stress strict traceability and contaminant control, particularly for export markets requiring documented environmental and residue profiles.

    Industry compliance standards

    • FAO/WHO Specifications for agricultural active substances
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • China GB 2763: Maximum residue limits for pesticides in food

    Typical usage ratio

    • Application rates between 0.85–1.05 mol equivalent per target molecule depending on desired crop protection class and purity goals

    Downstream process integration

    • Employed at the intermediate addition stage during heterocycle or aliphatic ring functionalization prior to final chlorination or methylation

    Final product types

    • Chiral fungicide intermediates
    • Precursor for phenoxyalkanoic acid herbicides
    • Synthetic building blocks for novel agrochemical actives

    4. Fine Chemical Intermediate for Specialty Polymer Additives

    This nitrile is a favored intermediate by manufacturers customizing specialty polymer additives, such as chiral chain extenders and UV stabilizer precursors. The molecule enters production lines where precise configuration control supports polymer property modification. Operators commonly focus on low-residual solvent and impurity content due to high-performance end use in electronics and advanced coatings, necessitating detailed batch documentation.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical processes
    • EN 71-3:2019 Safety specifications (for polymers in technical toys, applicable to final coatings)
    • RoHS Directive 2011/65/EU if used in electronics-related polymers

    Typical usage ratio

    • Used at 0.5–2.0 weight percent within additive blends; dosage adjusted to match intended polymer properties and matrix compatibility

    Downstream process integration

    • Charged during additive compounding or polymer back-integration stage prior to extrusion or molding

    Final product types

    • Chain extender intermediates for thermoplastics
    • Chiral auxiliaries in high-performance resins
    • Precursor units for UV stabilizers in coatings
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    Certification & Compliance
    More Introduction

    (S)-4-Chloro-3-Hydroxybutyronitrile: Manufacturing Insights and Real-World Application

    Introduction

    On a busy production line where quality and reliability decide tomorrow’s success, (S)-4-Chloro-3-Hydroxybutyronitrile often stands out as a trusted building block for modern synthesis. Years of refining our proprietary process at scale have given us a deep understanding of both the technical details and the day-to-day demands surrounding this product. Every batch leaves our facility reflecting the tight-knit link between method and material. As the direct manufacturer, we stay involved from raw feedstock procurement to the final packaging step. This direct oversight gives us the ability to observe, correct, and re-align in real time for every order.

    What We Produce – A Closer Look at (S)-4-Chloro-3-Hydroxybutyronitrile

    Every synthetic chemist eyeing the design of chiral intermediates eventually weighs the merits of (S)-4-Chloro-3-Hydroxybutyronitrile. For us, the details are practical and tangible. The stereochemistry matters, especially for chiral pharmaceutical ingredients, which is why we prioritize stereoselective routes during our synthesis. Unseen micro-variance in production can deeply influence downstream performance and purity, especially for customers exploring scale-up or strict impurity profiles.

    Our material supports strict chiral purity, keeping the unwanted (R)-enantiomer at very low levels. In hands-on terms, this care smooths the path for customers who rely on downstream enantiomer-specific reactions—no extra purification, less waste, and more reliable yield. A customer running a kilo-scale process targeting an (S)-configured active pharmaceutical ingredient once shared that our batch consistency took unpredictable obstacles out of their process development, letting them move straight to plant trials without rework. Results like these underscore why the way we produce matters.

    Model, Specifications, and Consistent Experience

    We intentionally produce (S)-4-Chloro-3-Hydroxybutyronitrile using established yet continuously monitored asymmetric hydroxylation techniques. We calibrate reaction temperatures, time, and flow rates to safeguard every physical property that our end-users care about—color, solubility, density, and purity above all. Our model does not change with every lot; it comes from repeatability, verified through in-house and independent analytical checkpoints. Customers see chromatograms and certificate-of-analysis sheets, not just promises. Internal samples undergo periodic NMR and HPLC checks to guard against isomeric drift, which can escape routine TLC or melting point tests.

    In our own experience, transparency speeds up troubleshooting. A scale-up customer once called about a minor yield drop, and our ability to point to archived batch characteristics cut the diagnostic time in half. Steady feedback between production staff and the analytical team builds this track record and helps us flag rare anomalies before they reach a client’s door.

    What Sets (S)-4-Chloro-3-Hydroxybutyronitrile Apart

    Similar sounding intermediates crowd the catalog lists, but minor atom placements drive major changes in downstream application. The (S)-configuration, the presence of both chloro and hydroxy sites, and the terminal nitrile handle make this compound particularly well-used in the pharmaceutical and agrochemical industries. We have witnessed projects where a less-pure racemic mixture introduced extra separation steps, drying up both time and resources.

    Technical discussions with research teams explain the differences best. While the hydroxy group boosts solubility in certain organic solvents, the chloro substituent grants reactivity at a position easily functionalized under mild conditions. Customers working on routes toward beta-blockers and antiviral agents have found this to be more of a starting point than a final goal. The performance characteristics—such as reactivity rate, minimal byproduct formation, and ease of purification after subsequent transitions—can differ substantially from closely related analogs lacking either the (S)-chirality or the chloro handle. These distinctions only become clear through direct experience with material sourced at scale, not just in a test tube.

    Everyday Value: From Synthetic Planning to Final Delivery

    Once the right intermediate is chosen, the conversation shifts to predictability and logistics. Customers tell us that minor shifts in batch consistency or delays force a hard reset on tight project timelines. Having run our own manufacturing schedules for years, we relate. Our own craftspeople coordinate production flows and blending times so that each kilogram mirrors the next. This consistency affects more than just HPLC graphs. It leads to real cost and time savings for midstream and downstream processes such as chiral resolution or catalytic hydrogenation.

    On the ground, you won’t find surprises from hidden byproducts or unexpected side reactions. We manage upstream purity from the raw starting halides and monitored solvent systems to the point of final isolation. Our technical staff sometimes get directly involved with customer troubleshooting, such as when a research group in process development faces unwanted impurities or lower yields. It means tracking the issue back through synthesis, packing, and even logistics. The transparency and fast communication arising from first-hand production involvement bring real benefit to customers—solving problems not just with talking points, but with firsthand evidence and experience.

    Use Cases: More Than a Raw Material

    Many of our collaborators pursue new pharmaceutical active ingredients or advanced agrochemicals. (S)-4-Chloro-3-Hydroxybutyronitrile frequently forms a pivotal link in multi-step syntheses. At one manufacturer, its chiral center fueled the core of a new antiviral candidate. In that project, the demands for consistency across pilot-plant and larger-scale operations highlighted the weakness of off-the-shelf or racemic analogs. Achieving high enantiomeric purity at quantity made further downstream steps—such as selective protection or nucleophilic substitution—run more smoothly and with fewer intermediates. Cost and wasted time dropped, not by a percentage point, but by half in one year.

    Not every user needs such a specialized application. Academic and CRO researchers also rely on this compound to explore new catalytic methods, such as asymmetric hydrogenations. Our facility provides tailored lot sizes that meet R&D needs while maintaining quality. We’ve had collaborative discussions with university teams about resin compatibility and solvent choices for this intermediate, often adapting our own isolation procedures to provide a better fit.

    Why Consistency Changes Outcomes in Discovery and Production

    Chiral building blocks demand more than textbook purity. In synthetic pharmaceutical work, even micro-impurities drive up the regulatory burden and can lead to lost batches or failed scale-up attempts. Our own staff experienced this dilemma not just as producers, but as partners walking our customers through their own validation hurdles. Sourcing directly from a manufacturer with demonstrated control over each production step matters. When a client’s validation chemist asks for detailed impurity profiles, original batch data, or process deviation logs, we know exactly what they mean—we go through the same procedures ourselves.

    Direct interaction with end-users lets us gather feedback and refine methods over time. One project post-mortem revealed that trace metal residues from early catalyst generations had hampered a team’s downstream palladium coupling. After joint analysis and root-cause review, we retrofitted our post-reaction purification so future lots landed well below detection limits. Production details like this don’t surface on a product sheet. They flow from hand-on work, open dialogue, and evolutionary improvement.

    Comparing to Analogues: Lessons from Experience

    It’s tempting to swap in a structurally similar compound, such as (R)-4-Chloro-3-Hydroxybutyronitrile or the racemic mixture, early on in R&D to cut costs or simplify sourcing. Our experience keeps us cautious. The (S)-enantiomer supplies specific activity in chiral catalyst systems and delivers the right configuration to match downstream biological targets. These enantiomeric differences show up in optical rotation, selectivity in further modifications, and even solubility during chromatographic steps.

    We have guided teams who switched from racemic intermediate suppliers to our high-purity (S)-variant mid-project. In several cases, the change eliminated an entire chiral separation step and reduced overall impurity carryover, translating directly to bottom-line improvements. Syntheses based on the non-chiral or wrong-handed analogs risk greater waste streams and less reliable yield. Both new and established customers value that our product arrives not just as a bottle but as an extension of chiral discipline at every stage.

    Environmental and Safety Considerations from the Floor

    Long hours at the plant floor remind us that responsible chemistry goes beyond yield and cost. (S)-4-Chloro-3-Hydroxybutyronitrile requires careful handling due to its functional groups—particularly the nitrile and chloro sites, which can present issues if not managed with correct containment and ventilation. We factor this into our production design, updating fume and waste capture systems as knowledge grows.

    A few years back, our team noticed halogen traces appearing in effluent after a higher-throughput batch run, prompting a re-evaluation of scrubber efficiency. Small incidents like this led to broader changes throughout the line, improving our internal monitoring and reducing both risk and environmental footprint. We carry forward that knowledge, advising customers on best practices in their own setups. Some have adapted pieces of our containment philosophy when scaling up; others draw on our disposal procedures for their own compliance work.

    Packaging Rooted in Practice

    Package failure causes frustration and sometimes ruins valuable material. We test our packaging with trial shipments across seasonally variable routes, not merely simulated stress models. High chiral purity (S)-4-Chloro-3-Hydroxybutyronitrile demands low-permeability containers to prevent moisture intrusion and light-driven degradation. Every lot is double-checked for seal performance and container integrity before shipping. We have replaced and upgraded packaging profiles before after customer advice or following an internal review of transit damage rates. This down-to-earth approach minimizes waste and protects our work as well as the customer’s research investment.

    Quality Drives Long-Term Partnerships

    A product story doesn’t end at the loading dock. The most rewarding relationships grow from ongoing technical support, direct troubleshooting, and honest conversation about limitations as well as possibilities. We log lessons learned into each production cycle, share process notes, and remain open to client visits at our facility. Customers see real-time process data, walk the floor with our production managers, and gain insight into every phase from synthesis to packaging.

    This mentality—fusing ongoing learning with rigorous production oversight—makes a difference for long-term collaboration. Achieving consistency with (S)-4-Chloro-3-Hydroxybutyronitrile means knowing that someone stands behind every bottle and every specification, not by repetition but by shared experience and demonstrated commitment.

    Collaborative Problem-Solving: On the Ground Experience

    Real-world chemistry rarely matches a textbook scenario. Complications develop at scale, and the unexpected appears in the form of minor side products or effects not seen at bench scale. Our involvement doesn’t finish at the shipping stage. We regularly field calls about solubility quirks, unexpected crystal forms, or downstream incompatibilities. In several instances, comprehensive production transparency and a willingness to revisit our own protocols helped pinpoint issues much faster than might be possible through third parties or distributors.

    We encourage open information flow and invite honest feedback, even when it means digging into our own procedures to find incremental refinements. One scale-up customer flagged a spectral irregularity that ultimately traced back to a rare impurity from an upstream step. We not only replaced the batch but shared a breakdown of our investigation—a level of follow-through only possible by working directly with our own process data and production specialists.

    From Lab Bench to Commercial Flow: Step-by-Step Adaptation

    No two production challenges look the same from the manufacturer’s view. Academic users may need smaller tailored lots with tighter batch data and fresh COA documentation, while large commercial plants rely on reproducibility at hundreds-of-kilos scale and just-in-time delivery. Our own facilities adapted over time, starting from kilo-scale glassware to full reactor-scale campaigns. Each expansion forced deeper attention to scale effects: not just temperature and mixing, but solvent recycling and reactor material compatibility.

    We’ve adjusted operating procedures and equipment based on both in-house pilot batches and customer site visits. A simple insight about improved mixing rates changed our agitation protocols, after reviewing problems with phase separation at large scale. Open doors between production, analytical, and logistics teams keep the links tight and response times short—qualities that benefit both sides over the project’s life.

    Future Directions: Improving Every Step

    Continuous improvement never stops. Though our process for (S)-4-Chloro-3-Hydroxybutyronitrile delivers reliable results now, we invest in greener chemistry, novel catalyst testing, and enhanced waste minimization year by year. Our R&D teams test alternative oxidants and recyclable catalysts when developing new chiral intermediates. Some of these improvements have already made it into the standard process, documented by lower waste output and better atom economy.

    We also listen when clients describe upcoming requirements—such as stricter impurity limits or more detailed documentation for regulatory filings. This ongoing exchange shapes the way we look at each run and each customer interaction, anchoring every improvement in practicality and shared goals. Years spent optimizing, troubleshooting, and collaborating ensure (S)-4-Chloro-3-Hydroxybutyronitrile keeps pace with the evolving landscape of advanced synthesis.

    Summary: Real-World Value, Not Just a Catalog Entry

    The journey from feedstock to finished product creates value measured not only in kilograms, but also in technical confidence and shared insight. Direct manufacturing experience with (S)-4-Chloro-3-Hydroxybutyronitrile reveals differences invisible from a catalog line or a distributor’s datasheet. Our position allows us to control every parameter, learn directly from each lot, and evolve with our customer base. True to our ethos, we remain tireless in our push for better quality, stronger partnerships, and practical solutions at every step—from the batch reactor to the loading dock and beyond.