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4-Methoxybenzyl Mercaptan

    • Product Name 4-Methoxybenzyl Mercaptan
    • Alias 4-Methoxybenzyl thiol
    • Einecs 218-525-1
    • 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

    305062

    Cas Number 35119-40-7
    Molecular Formula C8H10OS
    Molecular Weight 154.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 122-124°C at 15 mmHg
    Melting Point N/A
    Density 1.13 g/cm³ at 25°C
    Refractive Index n20/D 1.571
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98%

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

    Packing & Storage
    Packing 4-Methoxybenzyl Mercaptan, 25g, supplied in an amber glass bottle with a tight-sealing cap, labeled with safety information.
    Shipping 4-Methoxybenzyl Mercaptan should be shipped in tightly sealed containers under inert atmosphere, protected from light and moisture. It must comply with relevant hazardous material regulations, labeled accordingly, and packaged to prevent leaks or breakage. Transport at ambient temperature unless otherwise specified, and ensure documentation for safe and compliant handling during transit.
    Storage 4-Methoxybenzyl mercaptan should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. It should be kept away from oxidizing agents and strong acids. Proper labeling and secondary containment are recommended to prevent leaks and contamination. Use in a chemical fume hood and avoid prolonged exposure to air.
    Application of 4-Methoxybenzyl Mercaptan

    Applications of 4-Methoxybenzyl Mercaptan in Industrial Manufacturing

    As an established producer of 4-Methoxybenzyl Mercaptan, we focus on supporting precision-driven sectors that demand high-purity intermediates for specialty chemical synthesis. Our expertise in batch control, impurity traceability, and formulation guidance allows customers to integrate this key compound into advanced processes with confidence around compliance, performance, and downstream reliability. Below, we detail its real-world industrial integrations across distinct application areas, each governed by rigorous standards and precise technical requirements.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Compounds

    Oncology research and production often rely on sulfur-containing molecular fragments for targeted therapeutic activity. 4-Methoxybenzyl Mercaptan serves as a selective nucleophile and transient blocking group within multi-step syntheses of chemotherapeutic APIs, particularly in constructing thioether linkages or protecting reactive centers during functional group transformations. This material enables greater control of reaction selectivity and minimizes side reactions in high-value batch syntheses for leading pharmaceutical innovators.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs and general chapters
    • USP <795> & <797> Compounding Standards
    • FDA 21 CFR Part 211 (CGMP for finished pharmaceuticals)

    Typical usage ratio

    • Used at 0.3–2.0 mol. eq. per target functional group, fine-tuned according to reaction pathway and batch scale from milligram to kilogram levels. Higher usage may apply in routes with multiple protection–deprotection cycles.

    Downstream process integration

    • Introduced post-halogenation or alkylation step as a nucleophile or temporary protecting group reagent.
    • Employed in intermediate steps involving thioetherification, prior to final deprotection or coupling reactions for late-stage API assembly.

    Final product types

    • Small-molecule chemotherapeutic APIs (e.g., adjuvant thioether analogues or kinase inhibitor scaffolds)
    • Synthetic intermediates for clinical trial substances
    • Regulatory-submitted API manufacturing lots for oncology portfolio

    2. Advanced Agrochemical Synthesis (Herbicides & Fungicides)

    Innovative crop protection products increasingly integrate thioether and thioester functionalities to enhance molecular stability, soil persistence, and bioactivity. 4-Methoxybenzyl Mercaptan is incorporated into the synthesis of selective herbicide actives and certain systemic fungicide intermediates, leveraging its high selectivity in alkylation or arylation reactions. This enables agrochemical formulators to scale laboratory methods to full-batch industrial deployment while maintaining residue compliance and consistent active compound yields.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products (PPPs)
    • ISO 9001:2015 Quality Management System for Agrochemicals
    • Relevant local Maximum Residue Limit (MRL) regulations, such as U.S. EPA tolerances

    Typical usage ratio

    • Added at 1–5% weight of total reactants in batch synthesis for protected or functionalized thioether intermediates; proportion varies by intended conversion and reactivity of precursor substrates.

    Downstream process integration

    • Serves in the nucleophilic substitution or S-alkylation stage to introduce sulfhydryl-derived functionalities into pre-herbicide/fungicide molecules.
    • Post-reactive quenching and aqueous workup are performed before isolation of crude actives for further purification steps.

    Final product types

    • Thioether-based herbicide and fungicide technical concentrates
    • Formulated crop protection active ingredients for field application
    • Protected precursor intermediates for novel agrochemical R&D pipelines

    3. Electronic Chemicals for Photoresist Monomer Production

    The production of high-performance photoresist polymers for semiconductor fabrication frequently utilizes aromatic mercaptans as capping agents and functional building blocks. 4-Methoxybenzyl Mercaptan is incorporated into the synthesis of tailor-made monomer units where the electron-donating methoxy group imparts controlled reactivity and thermal properties, vital for EUV and i-line photoresist resins used in photolithography. This stage demands ultra-low impurity profiles and consistent batch reproducibility to meet customers’ microelectronic quality benchmarks.

    Industry compliance standards

    • SEMI C3 Specification for Electronic Grade Chemicals
    • JEITA ED-7301 (Purity requirements for chemicals in semiconductor manufacturing)
    • ISO 9001:2015 Certified Electronic Chemical Manufacturing
    • Customer-defined impurity thresholds per defectivity testing

    Typical usage ratio

    • Dosed at 0.5–3.0 mol% relative to polymer backbone precursor during step-growth or chain-growth polymerizations. Exact level is set during pilot validation based on resin architecture.

    Downstream process integration

    • Feeds into monomer synthesis as a functionalized capping agent; integrated prior to main polymerization via controlled addition protocols.
    • Unreacted material removed via vacuum stripping and in-line chromatography prior to resin isolation.

    Final product types

    • Photoresist monomers for semiconductor lithography
    • Electronic-grade specialty polymers (e.g., poly(4-methoxybenzylthio)styrene derivatives)
    • High-purity photoresist solutions

    4. Odor Masking Compound Synthesis for Gas Leak Detection

    Natural gas utilities and industrial detection systems depend on highly stable and detectable odorant blends for rapid leak identification. 4-Methoxybenzyl Mercaptan is employed by specialty odorant compounders as a precursor for tailored masking agents, adjusting olfactory profiles when formulating mercaptan blends. This integration helps manufacturers achieve specific detection thresholds required by legal mandates while minimizing background contamination or false positives in application environments.

    Industry compliance standards

    • EN 13725:2003 Air Quality – Determination of Odour Concentration by Dynamic Olfactometry
    • U.S. DOT 49 CFR Part 192.625 (Odorization of natural gas for distribution)
    • IFRA Standards for Industrial Odorants
    • ISO 14001:2015 for Environmental Management Systems

    Typical usage ratio

    • Typically blended at 0.005–0.05% by weight in finished odorant mixes; final concentration determined by detection threshold and matrix compatibility.

    Downstream process integration

    • Used as a masking component during formulation with methyl mercaptan and other sulfur odorants.
    • Dosed into the blend tank after main mercaptan addition and homogenized prior to QC gas release testing.

    Final product types

    • Custom-formulated gas odorant blends for utility networks
    • Leak detection kit refills for industrial pipeline operators
    • Calibration standards for odorant monitoring instrumentation
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    Certification & Compliance
    More Introduction

    4-Methoxybenzyl Mercaptan: A Manufacturer’s Insight

    The Essential Role of 4-Methoxybenzyl Mercaptan in Chemical Synthesis

    Experience in heavy-duty synthesis laboratories makes one appreciate molecules like 4-Methoxybenzyl Mercaptan (CAS Number 20264-98-8), sometimes called PMB-SH. Whenever we scale up thioether protecting group chemistry or look for reliable sulfur nucleophiles, reliable supply and lot-to-lot consistency become priority concerns. Having manufactured this compound ourselves on kilogram to ton scale, we’ve observed how small changes in processing can impact purity, odor, and handling properties. The controlled environment of our reactors, along with rigorous purification, gives our partners peace of mind: end products with reliable purity suitable for demanding pharmaceutical and specialty chemical applications.

    Understanding the Molecular Structure and Properties

    4-Methoxybenzyl Mercaptan features a methoxy group in the para position of a benzene ring, married to a benzyl mercaptan functionality. This marriage gives the compound a nuanced reactivity profile—useful in situations where steric and electronic factors need careful balancing. The thiol brings potent nucleophilicity, while the para-methoxy group influences electron density and, as we have noticed, can help when selectivity is crucial in alkylation, acylation, or sulfonation sequences.

    Chemists selecting a benzyl mercaptan often ask about differences in boiling point, odor, and solubility—not to mention how these influence practical handling. With 4-Methoxybenzyl Mercaptan, the methoxy functionality modestly increases the boiling point compared to unsubstituted benzyl mercaptan, without heavily affecting miscibility in standard organic solvents. Our production batches consistently demonstrate GC-assayed purity above 99%. Over years of experience, we have minimized batch odor by refining our distillation parameters, something that downstream users frequently thank us for. Nobody wants mercaptan smell lingering in the plant, and our downstream scrubbers leave the air much fresher than in the early days.

    Comparative Handling and Safety

    Working regularly with mercaptans, we cannot ignore the challenges that come with them: strong odors, toxicity concerns, and the catalytic trickiness of sulfur in multi-step reactions. The para-methoxy substitution reduces some of the volatility compared to parent benzyl mercaptan, making this product easier and less irritating to handle in ventilated hoods. Still, personal protective equipment and sensible exhaust management guide all our handling protocols.

    From a manufacturing standpoint, every drum that leaves our dock comes with documentation specifying actual lot purity. Over time, we have learned that color can tell a lot about process variation—so we don’t dismiss customer questions about appearance. Slight yellowing usually ties back to trace air ingress or overzealous heating. We track these variables tightly: for every production lot, we log reactor pressure, timeframes, and distillation cut schedules. Raw technical know-how makes the difference between reprocessing a batch and shipping on schedule.

    Primary Uses and Application Advantages

    Most buyers come to us for 4-Methoxybenzyl Mercaptan intending to use it as a sulfur-protecting group, particularly in peptide and oligonucleotide syntheses. Its selective deprotection features draw attention—acid and base stability let chemists perform multiple steps without removal, until a final gentle release under reductive or acidic conditions. This selective lability saves time and boosts overall yield, something we’ve seen first-hand in both custom peptide work and pilot-scale runs for newer drug candidates. Customers tell us that competing products, such as benzyl mercaptan or para-methylbenzyl mercaptan, do not always deliver the same balance of stability versus removability. Subtle electronic tuning means fewer side products and less cleanup during deprotection.

    Our years of supporting medicinal and process chemists have confirmed one thing: protecting group chemistry only pays off if the removal step works cleanly. With 4-Methoxybenzyl Mercaptan, clients frequently report very high conversion and fewer stubborn impurities compared with other protecting group thiols. After processing tons of product, our own analytical results mirror this trend. Compared to other sulfur-protecting agents such as trityl or methylthiol derivatives, this compound presents a moderate air sensitivity profile—manageable with nitrogen blankets and proper storage—without the need for deep-cold storage or specialty drums. Real-world practicality keeps production lines running and makes the difference between lab-scale promise and commercial delivery.

    Model and Specifications We Control

    Over decades, we have standardized our 4-Methoxybenzyl Mercaptan production on a model that matches 98–99% minimum purity on GC, less than 0.5% water by Karl Fischer, and a maximum color index matching pale straw. Containers are selected for chemical resistance, minimizing leaching and label smudging (thermal transfer labeling holds up even in harsh logistics). We offer sizes from 0.5-kg glass bottles for R&D labs up to 200-kg drums for bulk syntheses, packed under argon to fight against oxidation and odor escape.

    Customers often ask about irradiation history, residue solvents, or unwanted stabilizers. We never use unnecessary stabilizers—the product stands pure and ready. Our dryers are regularly checked for cross-contamination: no surfactants, no anti-caking agents, just pure 4-Methoxybenzyl Mercaptan. Years ago, we had issues with trace bisulfide dimer during storage; modifications to our fill-head purging and regular headspace testing have since curtailed such side reactions. These details matter. Small compositional artifacts can jeopardize downstream hydrogenation, alkylation, or oxidations, particularly at the pilot and commercial scale.

    Customer-Centric Adjustments and Solution-Finding

    It is one thing to crank out a commodity product; it is another to adjust a process in response to a unique customer requirement. Some of our clients require extra-low halide content, due to catalyst poisoning concerns. Our team responded by setting up an additional purification loop using silver-impregnated resin—no more angry calls from process engineers. Another customer requested specification changes for residual solvents, prompting a shift to low-odor, high-seal distillation glassware and in-line nitrogen stripping. The new setup cut methanol trace content by more than half. Customers pay attention to these refinements, and so do we.

    We have learned not to assume chemical compatibility or bulk handling preferences. Our technical team regularly works with clients to match container type and closure integrity with their own storage facilities. Certain production lines specified all-stainless lines for transfer, which our QA group pre-certified. All these steps avoid contamination, waste, and unnecessary returns. We welcome requests for special packaging, regulatory certificates, or analytical data, since they give us the chance to demonstrate real attention to client needs.

    Navigating Market and Supply Chain Pressure

    Making 4-Methoxybenzyl Mercaptan means staying ahead of raw material supply swings. The market for anisole (the methoxybenzene precursor) can fluctuate, thanks to demand in flavors, perfumes, and solvents. Early on, we learned that sourcing from two continents adds resilience against sudden disruptions, so our purchasing group maintains standing relationships with global supply partners. Sometimes, local logistics or seasonal price spikes hit. The benefit of running a vertical integration model means we avoid lags and keep our end users supplied even when generic traders struggle to meet demand.

    Pandemic-era supply chain disruptions taught us other lessons. Anticipating demand growth in the biotech sector, we keep extra raw materials and packaging in stock and scheduled strategic preventive maintenance. Flexibility in scheduling and batch size lets us answer with expedited production running into the hundreds of kilograms when the crunch hits. Steep demand from peptide pioneers led us to invest in faster distillation systems, improving both throughput and quality by developing real-time GC monitoring. Failures in remote process tracking used to frustrate us; improvements to in-plant QA stations mean truckloads now ship without delay or late surprises.

    Sustainability and Environmental Responsibility

    Any chemical manufacturer operating at scale faces scrutiny for environmental performance. Mercaptan processes particularly attract regulatory attention due to potential air emissions and odor impacts. Our site design uses state-of-the-art scrubbers and activated carbon beds for off-gas streams, lowering environmental impact and keeping neighborhood relations positive. As a manufacturer, we have reduced fugitive releases and routine leaks over the years by upgrading to double-seal pumps and real-time monitoring, seeing noticeable drops in ambient odor.

    Wastewater treatment remains straightforward, but we recognize that sulfur chemistry brings unique challenges. Periodic audits and close relationship with local waste handlers mean we recycle process streams and comply with even the strictest discharge requirements. We regularly share emission and waste minimization data with regulatory authorities, reinforcing our leadership in compliance and openness. Ultimately, running a clean shop also means fewer headaches for everyone who works here.

    By investing in training, spill drills, and community engagement, we build not only safer operations but also trust with local residents. It's not just regulators who notice attention to detail—employees prefer working where safety and odor control are priorities. We pass those savings and goodwill down the supply chain, making long-term relationships easier to maintain.

    Working Alongside Pharma and Fine Chemical Innovators

    Pharmaceutical customers expect more than purity—they expect understanding of their full value chain. We offer not just 4-Methoxybenzyl Mercaptan, but insights from years spent supporting process optimization for customers making APIs, intermediates, and advanced fine chemicals. Our teams have helped users develop shorter workups, improve throughput, and minimize process impurities by adapting addition rates, solvent blends, and protection-deprotection conditions.

    Most process chemists want speed without sacrifice. To answer, we've shared advice on agitation rates, nitrogen pressure application, and even post-addition hold times to prevent premature deprotection in complex synthetic sequences. Some clients have asked us to participate in risk assessments for scale-ups; we have flagged reactivity trends that arise only in 50-L or higher glass-lined reactors. This blend of technical detail and practical support remains rare among manufacturers and distinguishes true production partners from simple traders.

    Once, a customer scaling up oligonucleotide synthesis ran into issues with incomplete deprotection. After troubleshooting together, we discovered a minor impurity with a shifted retention time was the main culprit—something standard reference samples could not detect. Using more rigorous HPLC and GC-MS, we refined batch purity and the customer quickly resolved the issue. These scientific partnerships have driven us to keep our own analytical standards ahead of the curve.

    Supporting New Research and Future Trends

    The rise of nucleic acid therapies, novel peptide drugs, and DNA/RNA modifying agents has pushed demand for selective, efficient protecting groups like ours. Our technical support team stays current on protecting group trends, academic literature, and patent filings, so we contribute meaningfully when customers face new synthetic hurdles. We field questions about alternative deprotection agents or compatibility with next-generation coupling strategies, relying on hands-on studies and the shared know-how of our in-house researchers.

    Being part of innovation means enabling process simulations and technical troubleshooting. Sometimes early investigators struggle with side reactions or yield losses at bench scale, so we send out reference samples, process notes, or batch histories for closer study. We have hosted customer visits to demonstrate the equipment, methods, and safety plans behind the product, reinforcing confidence in our production standards.

    Sustainably making 4-Methoxybenzyl Mercaptan means not just satisfying today’s demand, but anticipating tomorrow’s research needs. Emerging markets in gene-editing tools, bioconjugation, and advanced polymer chemistry look to sulfur-derived intermediates. Our development pipeline includes working with academic labs and start-ups on pilot-scale safety evaluations and modified purification strategies to meet extra-tight tolerances. These efforts reinforce that chemical manufacturing stands not as commodity production, but as an active partnership driving technological progress.

    Lessons Learned and the Path Forward

    Having manufactured and handled 4-Methoxybenzyl Mercaptan for years, we’ve built up experience not just in batch production, but in the day-to-day realities of specialty chemistry. Our partners expect transparency, technical understanding, and reliability. The little details matter: controlling color, limiting odor, minimizing impurities, and delivering on time.

    There are always new issues to overcome—whether from raw material shortages, tighter end-user specs, or higher regulatory scrutiny. We see these not as obstacles, but as opportunities to refine practices and maintain trust with those counting on us for their critical synthesis steps. Chemical manufacturing, at its best, means being present from bench-top ideas to commercial production, troubleshooting side-by-side with those driving discovery and development. We look forward to supporting innovators, researchers, and manufacturers tackling the next generation of challenges with reliable, high-purity 4-Methoxybenzyl Mercaptan supplied by those who understand what’s at stake.