4-Thiopentanal

    • Product Name: 4-Thiopentanal
    • Alias: 4-Mercaptobutanal
    • Einecs: 211-566-5
    • 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

    580228

    Cas Number 4396-90-1
    Molecular Formula C5H10OS
    Molecular Weight 118.2 g/mol
    Iupac Name 4-sulfanylpentanal
    Synonyms 4-Thiopentanal, Pentanal-4-thiol
    Appearance Colorless to yellow liquid
    Density 1.016 g/cm3 (approximate)
    Smiles CCCC(S)=O
    Inchi InChI=1S/C5H10OS/c1-2-3-5(6)7/h5H,2-4,7H2,1H3

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

    Packing & Storage
    Packing 4-Thiopentanal is supplied in a 25g amber glass bottle with a secure screw cap, labeled with hazard warnings and chemical details.
    Shipping 4-Thiopentanal should be shipped in tightly sealed containers, protected from light and moisture. It must be transported according to local, national, and international chemical transport regulations. The chemical should be clearly labeled as hazardous and handled by trained personnel, ensuring spill containment measures and safety documentation accompany the shipment.
    Storage 4-Thiopentanal should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation and degradation. Keep it in a cool, dry, well-ventilated area away from heat sources, sparks, and incompatible substances (e.g., strong oxidizers). Refrigeration may prolong stability, and the container should be clearly labeled and protected from direct sunlight.
    Application of 4-Thiopentanal

    Applications of 4-Thiopentanal in Industrial Manufacturing

    4-Thiopentanal serves as a specialized intermediate in multiple industrial sectors. Its reactivity and sulfur-containing structure make it valuable for controlled synthesis, particularly in systems requiring selective functionality introduction. Our manufacturing expertise ensures consistent purity to meet stringent industrial demands.

    1. Pharmaceutical Synthesis: Thiazole Derivative Building Blocks

    Pharma manufacturers use 4-thiopentanal as a key precursor for thiazole-ring formation, which is essential in the synthesis of antimicrobial agents and enzyme inhibitors. The aldehyde and thiol functionalities allow precise cyclization reactions, supporting custom process optimization to yield intermediates for small molecule drugs. Our process allows direct integration into multistep synthesis under monitored conditions to maintain target impurity profiles.

    Industry compliance standards

    • Complies with ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • Supports production under US FDA 21 CFR Part 210/211 conditions for pharmaceutical ingredients
    • References to European Pharmacopoeia monographs relating to thiazole derivatives
    • Follows cGMP standards with batch traceability

    Typical usage ratio

    • Acts as 0.2–0.6 molar equivalent in thiazole ring-forming step depending on stoichiometry of coupled reactants
    • Adjusted for product yield optimization and impurity control

    Downstream process integration

    • Direct addition to the batch reactor in stepwise condensation cycles
    • In-line monitoring to ensure full consumption and to limit side-product formation
    • Scaling compatible with kilo lab and pilot plant equipment

    Final product types

    • Thiazole-based APIs for antimicrobial therapies
    • Enzyme inhibitor intermediates
    • Building blocks for custom drug discovery pipelines

    2. Agrochemical Intermediate for Fungicide Synthesis

    Agrochemical companies incorporate 4-thiopentanal during the formation of sulfur-heterocycle moieties within fungicide actives. Its aldehyde group reacts specifically to fuse sulfur-preserving chains in a controlled environment, yielding high-purity intermediates crucial for downstream efficacy in crop protection agents. Accurate dosing and quality checks safeguard against off-target reactivity.

    Industry compliance standards

    • Production aligned with ISO 9001:2015 certified quality management systems
    • Ensures compliance with EU Regulation (EC) No 1107/2009 for active substances
    • Records supporting crop protection product registration requirements

    Typical usage ratio

    • Integrates at 0.15–0.4 equivalent based on the fungicide active synthesis protocol
    • Ratio tuned according to batch scale and substrate reactivity

    Downstream process integration

    • Added to closed reactors post-activation of cyclic precursors
    • Used in sequential functionalization and purification steps
    • Downstream compatibility with solvent extraction and crystallization units

    Final product types

    • Thiazole-based fungicide intermediates
    • Precursor compounds for triazole and strobilurin synthesis
    • Sulfur-enriched crop protection agents

    3. Odorant and Flavor Synthesis for Fine Chemical Markets

    In the fragrance and flavor industry, 4-thiopentanal is utilized for the selective synthesis of sulfurous notes in perfumery and savory formulations. Its aldehyde and sulfur group enable focused creation of character impact compounds such as thiophenes and thioesters. Controlled reaction environments, with tailored solvent systems, achieve high selectivity and minimal by-product formation, supporting downstream blending and compliance with safety legislation.

    Industry compliance standards

    • Adheres to IFRA (International Fragrance Association) guidelines for restricted substances
    • Complies with FEMA and JECFA safety evaluations for food flavor ingredients
    • Production documentation aligned to ISO 22000 food safety standards for odorant and flavor chemicals

    Typical usage ratio

    • Utilized at 0.1–1.5% weight in reaction mass depending on flavor strength targets and regulatory thresholds
    • Fine-tuned according to desired olfactory impact and downstream blend concentration

    Downstream process integration

    • Reacted under inert atmosphere to limit oxidation
    • Batch feeding into esterification or cyclization processes for thiol-derived flavor precursors
    • Subjected to GC analysis for purity and target compound confirmation

    Final product types

    • Sulfur-derived flavor base chemicals
    • Trace-level natural and synthetic odorants
    • Intermediate for functionalized aroma compound design

    4. Specialized Polymer Modifier for Electronic Materials

    Manufacturers of electronics-grade polymers introduce 4-thiopentanal during the functionalization of polymer backbones to impart sulfur-based conductivity or chemical resistance. Its reactivity supports incorporation into side-chain modified polyacrylates and polyurethanes, improving final material stability against oxidative degradation. Rigorous process control at the addition stage enables homogeneous integration without color contamination.

    Industry compliance standards

    • Quality management according to ISO 9001:2015 for electronic and specialty polymer production
    • Meets RoHS (Restriction of Hazardous Substances) Directive 2011/65/EU for polymer additives
    • Supports processes following IPC-4101 standards (laminate and prepreg material specifications)

    Typical usage ratio

    • Blended in at 0.4–1.2% by polymerizable mass
    • Optimization according to polymer chain length and desired electrical properties

    Downstream process integration

    • Fed in continuous or batch reactors at pre-polymerization or post-polymerization stages
    • In-line monitoring to maintain dispersion and control molecular weight distribution
    • Processed with inert gas blanketing where required to prevent sulfur oxidation

    Final product types

    • ESD (electrostatic dissipative) coatings
    • Conductive polymer films for flexible electronics
    • Oxidation-resistant encapsulant systems

    5. Custom Synthesis Intermediate for Organic Laboratory Reagents

    Specialty chemical and research laboratories leverage 4-thiopentanal for target synthesis of thiol and thioether-functionalized organic reagents. Its controlled introduction into condensation and cyclization reactions produces compounds used in analytical testing, catalyst development, and material science research. Manufacturing batches supply precise stoichiometric units, supporting downstream scaling and reproducibility of laboratory protocols.

    Industry compliance standards

    • Supplied under ISO 9001:2015 documented quality systems for laboratory chemicals
    • Material safety data sheets and REACH registration support for EU R&D laboratories
    • Analytical certificate availability for regulatory and quality traceability

    Typical usage ratio

    • Applied at 0.25–1.0 mole equivalent based on desired reagent output and process optimization
    • Adjusted per synthetic route and purity requirements

    Downstream process integration

    • Charged directly to reaction vessels for nucleophilic addition or cyclization steps
    • QC sampling at critical points for NMR and HPLC validation
    • Packed for direct laboratory or pilot plant use

    Final product types

    • Thiol-functionalized organic linkers
    • Analytical reference reagents
    • Building blocks for small-scale catalyst and ligand screening

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    Certification & Compliance
    More Introduction

    4-Thiopentanal: From Manufacturer’s Bench to Your Application

    For the past decade, I’ve worked in sourcing and specialty synthesis, overseeing the production of organosulfur compounds. Among them, 4-Thiopentanal has proved to be one of the most reliable intermediates, delivering value for chemists searching for performance and process consistency. This compound earns a place in many laboratories and process lines because it bridges the gap few other aldehydes can: it introduces a thioether group at the fourth carbon of pentanal, offering a distinct nucleophilicity and reactivity that turns into an asset in downstream applications.

    What 4-Thiopentanal Brings to the Table

    Our main lot, 4-Thiopentanal 98% GC, arrives as a pale yellow liquid—one sign of its stability, even under storage in glass or Teflon containers. It serves as an excellent aldehyde partner for condensation reactions where the sulfur atom’s influence draws out novel activity in product formation. A good aldehyde like this doesn’t just add carbon atoms; it imparts controllable reactivity. For researchers in flavors, fragrance intermediates, and sulfur-based heterocyclic synthesis, this molecule adapts and performs in challenging conditions where pure pentanal or other aliphatic aldehydes fall short.

    Through years of synthesis work, our teams have shaped a protocol that uses purified starting materials and stainless steel autoclaves. This practice ensures a clean product and eliminates stray sulfur compounds that would otherwise show up as unpleasant off-notes or color changes over time. Sulfur management is something you can’t ignore with organosulfur chemistry, and the data from long-term stability studies show that unwanted degradation products stay below detectable limits for twelve months in standard container warehousing. That’s peace of mind for purchasers running just-in-time operations.

    The Application Story: Where 4-Thiopentanal Fits

    Unlike short-chain aldehydes that volatilize quickly and lack backbone flexibility, 4-Thiopentanal offers both a manageable boiling point and a functional group arrangement that attracts synthetic chemists focusing on multi-step syntheses. The sulfur atom on the terminal carbon makes this molecule not just an electrophile but a potential nucleophile after transformation. If you’re pursuing thiazole rings or sulfur-linked analogs, it can handle the pressure of sustained heating and acidic or basic conditions where less robust aldehydes would polymerize or decompose.

    In our own experience, major fragrance companies rely on this molecule as a pivotal raw material. It allows for the introduction of persistent, earthy-sulfur notes to fragrance bases, standing up through distillation and shelf life testing. Pharmaceutical researchers also use it as a starting point for custom intermediates, where the thioether group becomes a handle in cross-coupling or alkylation. This isn’t a generic aldehyde—it opens routes that would demand protective-group gymnastics if you started elsewhere. These route simplifications translate to saved time, fewer chromatography steps, and lower solvent costs over the course of scale-up.

    Quality Control: From Pilot Batch to Bulk Manufacturing

    Manufacturing organosulfur compounds comes with its own set of obstacles—chief among them, controlling byproduct formation. Our reactors are calibrated and logged for temperature and pressure deviations that can spike impurity content, especially as scale increases and mixing rates slow. I recall several years back, an early pilot batch produced a disulfide impurity that masked the desired aldehyde peak on the GC-FID trace. We made a swift change to nitrogen blanketing and tweaked agitation speeds, which cut the unwanted reaction pathway and locked in the right isomer. This attention to detail isn’t a luxury—it’s essential when supplying academic and commercial clients who track performance to three decimal places.

    The analytical data on each lot includes not just area percent by gas chromatography but also infrared and NMR verification of the absence of higher sulfur homologues, which would confound downstream reactivity. Our SOPs require walk-away documentation: no container leaves our dock without a digital certificate. Customers in regulated synthetic pathways can then be assured that their own regulatory filings won’t hit a snag.

    Where the Competition Fails—and Why We Excel

    There are other aldehydes in the C5 range, some of which tout a similar performance envelope, but few offer the specific thioether arrangement at the fourth carbon. Many competitors offer bulk pentanal or 4-pentenal, yet these lack sulfur’s soft nucleophilicity, which in turn restricts the versatility in synthesizing sulfur-containing heterocycles or flavor compounds with depth. I often see batches from lesser suppliers where the presence of aldehyde polymers or sodium thiosulfate byproducts sour the material and trigger mid-process failures.

    Because of in-process controls and the avoidance of open-flame distillation setups, our 4-Thiopentanal contains less than 0.05 percent by mass of secondary sulfur species. Even after six months at room temperature, customers have reported conversion rates into target molecules that match the initial pilot data. To a synthetic chemist, batch-to-batch predictability removes one variable from projects that already work on narrow deadlines and tighter budgets.

    Innovation in Storage and Transport: Protecting the Value

    By investing in corrosion-resistant containers and desiccant protection, we catch routine issues before they reach the formulation stage. During a recent bulk shipment, a temperature excursion threatened to increase color formation and spike the acid number. Careful tracking and spot checks with benchtop titration kits stopped the problem before any material left the facility. Several of our largest clients have told us repeat deliveries match spec without surprises—something less tangible than a COA but just as real in the trenches of chemical manufacturing.

    The odor profile of 4-Thiopentanal also differentiates it from other aldehydes. For those unfamiliar, the compound presents a mild, somewhat burnt-sulfur top note intermixed with a faint grassiness that fades after air exposure—worlds apart from the sharp, suffocating odor of lower molecular weight thioaldehydes. This subtlety in aroma means handlers deal with fewer workplace complaints and the storage area never triggers ventilation alarms unless there’s a real problem.

    Sustainability and Responsible Manufacturing

    Making organosulfur chemicals comes with environmental responsibilities. Unlike smaller operators, we reuse all reaction wash waters after careful neutralization, minimizing impact on effluent streams. All spent solvents are processed through a local waste-to-energy facility, turning old mother liquors into raw process heat. Regulatory inspectors recognize the difference, and it’s not about ticking boxes but about building trust in supply chain resilience.

    Our team spent two years finding a catalyst system that cut hazardous byproduct formation during the key acetylation step. Side streams once measured in kilograms per batch now show up only as detector blips—this is real progress and ends up reflected in the cleaner fingerprint of the finished product. This change decreased chemical accidents and made for an easier time with local compliance authorities, which keeps the tap on for uninterrupted supply.

    Supporting the Scientific Community

    We work with postdocs and scaleup teams in both academia and industry. Many have approached us asking about potential expansions using 4-Thiopentanal, especially as design elements for sulfur-rich ligands or next-generation cyclic compounds. In several published reports over the last five years, our material acted as the building block in patentable synthetic strategies that unlock new therapeutic scaffolds.

    During a pilot project with a pharma research group, we supported a gram- to kilogram- scale conversion using 4-Thiopentanal as an intermediate in target-oriented synthesis. Through collaborative troubleshooting, we were able to help improve yield by 13 percent and bring cycle times down, saving that team both budget and research hours. Our in-house expertise feeds back into our own QC benchmarks, creating a virtuous circle with end users and driving future innovation.

    Differences from Other Chemical Offerings

    Plenty of aldehydes are on the market and some larger corporations offer custom chain-lengths or mixtures. What they don’t provide is the thioether functionalization at this specific chain point or the guarantee that only the correct positional isomer is present. We have handled competitive samples that, due to synthetic shortcuts taken, arrive with a smattering of C4 or C6 analogs, creating analytical headaches and requiring unnecessary reprocessing.

    Beyond simple composition, 4-Thiopentanal affords a diagnostic sulfur atom for selective metal binding. Research groups working on metal-chelation agents or molecular sensors often report superior performance over analogs lacking a terminal sulfur function. In practice, customers have used it to develop sensors for food spoilage detection, capitalizing on the reactivity and odor profile unique to this compound.

    The Real-World Experience of Handling and Use

    Working daily with specialty aldehydes means staying alert to their quirks. 4-Thiopentanal stores long-term under nitrogen, but real-world operators know to monitor for moisture ingress. Even so, under dry atmosphere, material holds its quality through extended warehouse cycles and is ready for direct transfer into reactor charge tanks with minimal preparation. Over many years, our technician teams find this molecule less volatile than more basic aldehydes, leading to fewer leaks and minimized respirator use during handling. This fosters a safer, more efficient worksite and less material waste.

    Several of our longstanding customers operate in flavor ingredient synthesis, where repeat delivery and predictability are more important than price. One flavor chemist, based in Japan, shared that after switching to our 4-Thiopentanal, off-batch blending nearly disappeared and product shelf life was boosted by fifteen percent due to the minimization of off-notes. While price pressures remain a fact of life, few quality-focused suppliers keep up with the rigorous test regimens we subject each batch to—ensuring every drum matches spec before it leaves our floor.

    Industry Challenges and Problem Solving

    Chemical manufacturing isn’t about pushing ever greater volumes. It is about reliable outcomes: keeping material consistent so process engineers and synthesis teams avoid lost time. Sourcing specialty starting materials means taking procurement risk seriously—both for us and for our clients. There’s no appetite for guessing games with intermediate composition, and so we offer detailed batch profiles and open lines to our production chemists, not just sales reps.

    In the years since we started building up aldehyde production lines, we’ve seen ingredient cost swings, regulatory hurdles, and logistic bottlenecks. Making sure each kilogram of 4-Thiopentanal lands on the bench with the same reactivity and color as the last lot closes these potential gaps, and we take customer feedback seriously. If an off-spec shipment rare as it may be does show, our QC and technical leads trace raw material lots back to the source. Our supply model lets us swap in backup lots of certified reagents in days, not weeks. This flexibility has rescued several client deadlines and won us long-term partnerships with both pharma and flavor houses.

    Why Direct Manufacturing Matters

    The advantage of working directly with a manufacturer shows up in technical troubleshooting and process optimization. Traders and brokers offer access, but rarely do they supply answers to process-specific questions. We’ve logged hundreds of client calls over the years—from mitigation of mixing vessel corrosion to quick turnaround on small-lot orders or tweaking solution concentrations for analytical calibration. Customers with far-flung operations need partners who answer the phone and can send next-day shipments with the same guarantee of purity and performance as main lots. We provide that, and it’s what most end-users cite as their reason for sticking with us project after project.

    Looking Ahead: Evolving Needs and Continuous Improvement

    With regulation tightening and demands for cleaner processes growing industry-wide, 4-Thiopentanal stands as a ready-to-use solution for sulfur-modified chemistry. Partnering with brands aiming for novel food-safe flavors or new heterocyclic scaffolds in pharma, we adapt process and purification methods ahead of the curve. As climate-smart sourcing comes into focus, our operations team continues to minimize carbon footprint and waste generation, feeding back the savings in energy and compliance costs into product reliability.

    Recent improvements to our automated distillation loops trimmed waste solvent generation and increased throughput. Lessons from the shop floor drive us to keep tweaking every step, right down to operator training modules for safer handling and faster startup times. This “change-by-doing” ethos keeps us in tune with client challenges, whether they stem from regulation changes in the EU or customized batch requirements for new applications. Every customer brings us closer to the next iteration of process excellence and gives 4-Thiopentanal a reputation as a reliable, highly adaptable intermediate.

    In Closing: Experience Sets the Standard

    The day-to-day of producing 4-Thiopentanal never stands still, because chemical markets don’t pause. The process starts well before an order is placed, running through empty drum checks, raw material evaluations, and pilot-batch verification. On the production floor, minor parameters make major differences: a slight overheat here causes discoloration, too little nitrogen blanketing there sets off trace oxidation. Behind each lot stands a team who treat this product not as a commodity but as an enabling tool for serious science.

    Suppliers with experience and vigilance maintain client trust and smoothen operations for every downstream partner. As a manufacturer, we keep our processes transparent and focused on delivering 4-Thiopentanal that lives up to expectations—because we know the difference a single molecule can make, and we take pride in getting it right, batch after batch.

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