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4-(Methylthio)Benzyl Alcohol

    • Product Name 4-(Methylthio)Benzyl Alcohol
    • Alias 4-(Methylthio)phenylmethanol
    • Einecs 261-594-7
    • 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

    631582

    Chemicalname 4-(Methylthio)Benzyl Alcohol
    Casnumber 3446-89-7
    Molecularformula C8H10OS
    Molecularweight 154.23
    Appearance White to pale yellow solid
    Meltingpoint 45-48°C
    Boilingpoint 290°C
    Density 1.18 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CCSC1=CC=C(C=C1)CO
    Inchikey LMJVYGUCGPDHLL-UHFFFAOYSA-N
    Flashpoint 131°C

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

    Packing & Storage
    Packing The 25g of 4-(Methylthio)Benzyl Alcohol is supplied in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping **Shipping of 4-(Methylthio)Benzyl Alcohol:** This chemical is shipped in secure, airtight containers to prevent leakage and contamination. It should be handled according to standard hazardous material protocols—protected from moisture, heat, and direct sunlight. Proper labeling and documentation are required to ensure safe transportation and regulatory compliance. Use appropriate personal protective equipment during handling.
    Storage 4-(Methylthio)benzyl alcohol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. Protect the chemical from direct sunlight and moisture. Ensure the storage area is clearly labeled and has proper spill containment measures. Use only with appropriate chemical safety precautions and personal protective equipment.
    Application of 4-(Methylthio)Benzyl Alcohol

    Applications of 4-(Methylthio)Benzyl Alcohol in Industrial Manufacturing

    4-(Methylthio)Benzyl Alcohol serves as a valuable intermediate in several specialized industrial sectors, connecting upstream synthesis to the production of high-value finished goods. Our expertise as a primary manufacturer ensures precise material performance for each downstream process, enabling efficient integration in demanding applications. See below for key application segments and critical data for B2B industrial users.

    1. Pharmaceutical Intermediate Synthesis

    This compound plays a targeted role as an intermediate in the synthesis of specific active pharmaceutical ingredients (APIs), particularly for products containing methylthioaromatic moieties. It contributes to the construction of molecular frameworks required in anti-inflammatory and antineoplastic agents. Its aromatic alcohol group provides functional versatility during multi-step organic synthesis routes, allowing controlled transformation during high-purity manufacturing under validated cGMP conditions.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 8: Sampling of starting and packaging materials
    • United States Pharmacopeia (USP) General Chapters on Bulk Compound Quality
    • China Pharmacopoeia (current edition) for intermediate inputs

    Typical usage ratio

    • 0.3%–1.8% (w/w) relative to total API batch mass; adjusted according to target synthesis route, desired yield, and purity requirements

    Downstream process integration

    • Used during key condensation or substitution reactions in multi-stage API synthesis; typically introduced after initial building blocks to form core pharmacophores

    Final product types

    • Oral solid dose tablets and capsules containing advanced small molecule drugs
    • Parenteral formulations for oncology applications
    • Bulk pharmaceutical chemicals registered as intermediates

    2. Agrochemical Synthesis (Herbicide & Fungicide Intermediate)

    In agrochemical manufacturing, this specialty benzyl alcohol derivative is employed as a key precursor in the synthesis of active molecules, including several patented herbicidal and fungicidal formulations. Its ability to introduce methylthio functionalities empowers downstream reactions to achieve selective target-site binding, critical in modern crop protection chemistry.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB 20810 (General Rules for Agrochemical Technical Material)
    • ISO 17034 (Reference Material Producers—Agrochemicals)
    • REACH (EC) No. 1907/2006 for raw material authorization in the EU

    Typical usage ratio

    • 2–7% (w/w) of total mass in the targeted agroactive intermediate batch; specific ratio set by end-use molecule structure and crop-specific efficacy studies

    Downstream process integration

    • Introduced during heterocycle formation or coupling reactions, often as the final aromatic modification prior to formulation

    Final product types

    • Technical grade herbicides (active ingredient intermediates)
    • Fungicidal concentrate bases for crop protection
    • Granular and EC (emulsifiable concentrate) agrochemical formulations

    3. Fragrance Ingredient (Fine Fragrance and Flavors)

    This raw material is valued in the fragrance and flavor industries as a unique modifier, imparting warm, sulfurous, and slightly green notes in high-end compositions. Its controlled addition supports the design of stable, distinctive aromatic profiles in personal care and specialty flavorings after rigorous olfactory panel approval and regulatory compliance assurance.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Amendments
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • US Food and Drug Administration (FDA) Flavor and Extract Manufacturers Association (FEMA) GRAS regulations
    • ISO 9235:2013 (Aromatic raw materials—Definitions)

    Typical usage ratio

    • 0.01%–0.15% in fine fragrance concentrate or flavor base; dosage set below IFRA safety limits and fine-tuned based on target accord intensity

    Downstream process integration

    • Added during perfumer’s final blending process or pre-mixing for flavor compounding; always under batch QC and sensory panel guidance

    Final product types

    • Luxury perfumes (EDP/parfum bases)
    • High-value personal care scents (body wash, lotions, soaps)
    • Flavoring ingredients for specialty beverages and gourmet foods (subject to GRAS listing)

    4. Cross-Linking Agent for Specialty Polymer Synthesis

    As a functional monomer with a reactive alcohol and methylthio group, this material finds application as a cross-linking agent in the synthesis of specialty resins and engineering polymers. It imparts flexibility and chemical resistance, especially desired in coatings and molded components requiring stable, high-performance materials with custom functional profiles.

    Industry compliance standards

    • ISO 9001: Quality Management Systems for Polymer Manufacture
    • REACH Registration for Polymers and Additives
    • RoHS Directive 2011/65/EU (applicable if used in electronics-adjacent materials)
    • UL 94 Flammability Standard (for certain molded parts)

    Typical usage ratio

    • 0.5–3% (by mass) based on total monomer content; dosage flexes with polymer chain length, required cross-link density, and end-use performance

    Downstream process integration

    • Metered addition into batch reactor during co-polymerization or condensation; typically added after primary monomers for controlled chain termination or branching

    Final product types

    • Solvent-resistant specialty coatings (for electronics, automotive parts)
    • High-performance molded resins
    • Custom-engineered adhesive matrices

    5. Fine Chemical Intermediate for Photoinitiator Production

    This compound serves as a targeted building block in the manufacturing of advanced photoinitiators used in UV-curable inks, coatings, and adhesives. The methylthio group contributes to desired UV absorption and reactivity, optimizing polymerization rates and final cured coating quality for industrial applications.

    Industry compliance standards

    • ISO 17025: Testing and Calibration Laboratories (relevant to photoinitiator QC)
    • China GB/T 21810-2008 (Photoinitiator in UV-curable coatings)
    • Oeko-Tex Standard 100 (for ink and coating contact applications)
    • CFR Title 21 for indirect food contact materials (where applicable)

    Typical usage ratio

    • 0.8%–2.5% in intermediate photoinitiator synthesis batches; exact ratio varied by intended absorption spectrum and formulation curing requirements

    Downstream process integration

    • Processed through nucleophilic substitution or condensation steps, entering as a key precursor during intermediate-stage synthesis

    Final product types

    • UV-curable ink photoinitiators (for offset, flexo, and inkjet printing)
    • Initiator additives for UV-cured adhesive and coating formulations
    • Hybrid photopolymer formulations for additive manufacturing
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    Certification & Compliance
    More Introduction

    4-(Methylthio)Benzyl Alcohol: A Behind-the-Scenes Perspective from the Manufacturer

    Our Hands-On Approach to Producing 4-(Methylthio)Benzyl Alcohol

    Walking into any bustling fine chemicals workshop, you’ll notice a few compounds generating more chatter than others among the crew. 4-(Methylthio)benzyl alcohol stands as one of those substances. Over the years, as a manufacturer, we've built a direct relationship with this compound, not just in handling but in the technical journeys that take it from a paper concept into a ready-to-ship product.

    The chemical structure, a benzene ring attached to a methylthio group at the fourth position and a benzyl alcohol sidearm, gives this product more than one personality in organic syntheses. With a molecular formula of C8H10OS and a molecular weight near 154.23 g/mol, the compound finds itself in the thick of several key chemical routes. In our experience, every aspect of production from raw material sourcing, reaction kinetics, purification, and packaging requires a bespoke approach. This isn’t just lab jargon—slight variations in feedstock or temperature control can alter its appearance and, more importantly, purity, which often divides a reliable lot from one that sets projects back.

    Quality Matters: How Purity Impacts Results

    Among research chemists and process engineers, the talk inevitably turns to quality. Purity, by far, shapes the outcome of reactions involving 4-(methylthio)benzyl alcohol. That's often what separates a successful new molecule from an expensive lesson. We’re familiar with the sorts of challenges that show up in R&D labs: color changes, side reactions, mysterious yields lower than expected, all linked back to trace impurities. Years of troubleshooting taught us the importance of high vacuum distillation, carefully tuned recrystallization, and detailed batch analytics to make sure the purity consistently exceeds 99%.

    Every decision in the plant—choice of solvents, the rate of addition, termination temperatures—shows up in the final specifications. As a result, the feedback loop between our Q.C. team and the production lines stays short. Any bump in impurity fingerprint or unexpected residue triggers a review that sometimes has us revisiting the earliest steps in synthesis, even if it slows delivery. In the end, reliable product means fewer headaches downstream for formulation chemists and fewer reworks for intermediates in pharmaceutical or agrochemical synthesis.

    Use Cases: Real-World Roles and Value Creation

    We’ve watched 4-(methylthio)benzyl alcohol carve out a defined role in both academic and industrial research. Over time, the substance became indispensable for constructing building blocks in pharmaceuticals, flavor ingredients, and specialty polymers. In our own facility, customer requests range from multi-kilogram runs for small-molecule pharma to modest samples for materials science labs pushing new boundaries.

    A recurring theme among our clients: time-to-solution drives decisions. This alcohol serves as a popular starting material for sulfoxide and sulfone formation, which can atomically tune the electronic properties of biologically active compounds. It’s also popular for etherification, acylation, and oxidation experiments. One process chemist described how swapping less soluble analogs for our high-purity lots immediately eliminated months of column chromatography headaches. That alone saves both cash and morale.

    Our practical exposure extends further than textbook transformations. We've observed new demand patterns tied to custom functional group manipulation, including the use of 4-(methylthio)benzyl alcohol as a masked aldehyde or for the installation of methylthio groups in constrained molecular frameworks. Synthetic biologists use it as a probe for redox studies involving sulfur-containing side chains, while agrochemical teams ask for modifications designed for photo-stability testing.

    Handling and Storage: Why the Little Details Count

    We’ve fielded questions about the appearance and storage of 4-(methylthio)benzyl alcohol. The product forms a pale yellow to colorless liquid at room temperature and can sometimes solidify depending on ambient temperatures. Each lot responds differently to micro-impurities and storage. Over the years, we realized the importance of nitrogen purification and dark glass containers to limit oxidation and photolytic changes.

    Feedback from university labs and batch process lines revealed one thing: overlooked storage details cause headaches. Oxygen or light exposure, even briefly, causes slow darkening or formation of trace sulfur oxides. That “off” tint hints at more trouble below the surface—a shift in reactivity, increased byproducts, or a musty odor that sends syntheses sideways. This led us to invest in smaller, sealed containers that reduce user exposure to air and light. By continuously reviewing feedback and fielding complaints directly, we found that not every shipment benefits from one-size-fits-all packaging, so larger users sometimes request inert gas blankets while smaller labs need single-use options.

    Comparisons with Other Benzyl Alcohols: Where the Differences Lie

    Among related compounds, the unique feature stems from the methylthio group—a sulfur atom featuring an attached methyl group—directed at the para position of the aromatic ring. That distinguishes this product from its simple cousin, benzyl alcohol, which lacks any ring substitution, and others such as 4-methoxybenzyl alcohol or 4-chlorobenzyl alcohol. We’ve worked with each, and the methylthio group lends a noticeable edge in practical use.

    This specific substitution imparts distinct electronic effects and increases the compound’s nucleophilicity. Feedback from medicinal chemists suggests that, when compared to the more commonly used methoxy or halogen substituents, the methylthio group reliably pushes reactivity into territory amenable for challenging transformations. We’ve noticed customers working with electron-rich systems prefer our product due to this subtle, yet critical, difference.

    Handling-wise, sulfur-containing compounds can sometimes emit distinct odors or suffer from higher oxidation rates. By controlling air exposure during every step, we avoid the common fate of related benzyl alcohols turning unpleasant during storage or shipment. Thinking back to early production, we recall the frustrations of sourcing inconsistent lots from resellers who failed to control air and light exposure. So, our focus stays on consistent purity, batch testing, and stability in actual-use scenarios, not just on paper or in catalog listings.

    Conversations with formulation specialists point out another key difference: 4-(methylthio)benzyl alcohol rarely crystallizes in ambient lab conditions, giving it a liquid handling advantage over analogs prone to solidification and clumping. Fewer clogs and less heating translate to smoother operation on pilot and full-scale plants. That practical handling advantage often isn’t discovered until a researcher makes the switch and sees firsthand how improved flow properties save time and reduce waste during mixing or transfer.

    Safety and Compliance from the Production Floor

    Every chemical manufacturer faces the reality that safety isn’t just a compliance checkbox. We live it daily, checking off personal protective equipment, fume hoods, and eye-wash stations as part of our normal pre-shift routine. For 4-(methylthio)benzyl alcohol, even with its manageable hazard profile, crew members never treat it as “just another” aromatic alcohol. We document worker training, environmental containment, drum labeling, proper venting, and diligent batch record-keeping because these matter if recall or traceability is ever required.

    From our experience, the product’s moderate volatility and typical low acute toxicity ease several concerns, but we still respect its sulfur content and reactivity profile. That’s why we designed closed transfer systems and set aside designated lines for sulfur-organics, averting any chance of cross-contamination that might create hard-to-remove odors or trace impurities in other batches. Regulators and auditors commonly review our batch histories, environmental logs, and disposal records, so every step—down to spill response and secondary containment rules—remains second nature.

    Our long-term goal involves regular engagement with end users to improve communication about best practices. For research customers, transparent certificates of analysis and storage advice prove far more valuable than boilerplate recommendations, and everyone benefits when problems get flagged early instead of after a product has spent weeks in a warehouse.

    Production Challenges and Lessons Learned

    Scaling up 4-(methylthio)benzyl alcohol challenged more than a few assumptions at the outset. Reactions that looked smooth and predictable in two-liter vessels became unpredictable in plant-scale reactors. Subtle factors—mixing speed, agitation blade geometry, even clean-out sequence—affected batch yields or resulted in unwanted by-products. One batch in particular put our in-process analytics to the test, revealing a contaminant that traced back to an overlooked gasket material in a reactor. Immediate corrective action avoided further incidents, and we revised our standard operating procedures based on the lesson.

    We also discovered that heat transfer issues, often brushed aside during scale-up on other products, emerged earlier in 4-(methylthio)benzyl alcohol’s prep due to the exothermicity of thioether introduction. With time, we improved temperature monitoring, moved to higher-precision jacketed reactors, and tracked each run with more sensors and real-time chromatography. The end result pays off in peace of mind—the facility team can catch deviations before they become runaway problems.

    Waste treatment brought its own challenges, mostly because sulfur compounds can create distinctive odors if not handled properly. Upgrading scrubber capacity, adjusting waste pH, and regularly changing absorber media now keep both the shop and the surrounding community comfortable.

    Market Demand and Our Response as a Manufacturer

    Since we keep a direct line to our customers, trends in market demand become clear quickly. In cycles where pharmaceutical companies investigate new series of sulfur-containing compounds, inquiries for 4-(methylthio)benzyl alcohol surge. At other times, material scientists look for electronic modifications in polymers and coatings, again elevating requests. Sometimes, a spike arrives when a journal article puts the compound back in the spotlight, sending researchers scrambling for fresh supplies.

    To meet swings in demand, we adjust production schedules instead of pushing excess onto the market. We maintain strategic stock, keeping just enough finished product to supply new projects while keeping it fresh. Overproduction only leads to quality degradation, so team discipline keeps inventory current. If a customer faces an urgent project, we draw directly from quality-assured lots instead of old stock.

    During certain shortages, we talk directly with purchasing agents and research teams to understand their project timelines. Open lines with repeat buyers help us prioritize those urgently needing a product for discovery efforts, not just the biggest buyers. As compounders ourselves, we know the pain of project delays due to slow deliveries, so direct coordination has reduced friction for everyone involved.

    Continuous Improvement: Innovation in Manufacturing

    Years at the production line taught us that innovation doesn’t mean gutting successful systems, but making steady, practical changes. For 4-(methylthio)benzyl alcohol, several improvements resulted from user feedback and internal brainstorming. High-throughput screening asked us to tweak purification to support larger, purer fractions. Other clients requested tailored specifications, whether for water content or precise assay, pushing us to invest in new instrument calibration, improved drying, and better post-synthesis analytics.

    Our laboratory team works closely with operations, sharing data and samples regularly. Rather than relying on isolated complaints or rare events to drive change, we hold weekly meetings where operations crew, analysts, and customer support discuss recent batches and feedback. These discussions led to adopting digital batch records, routine trending of impurity profiles, and deeper integration between departments.

    Years ago, it would be unthinkable to have this level of transparency across teams or with end-users. But the process keeps problems from growing larger and ensures the fewest surprises once material leaves the factory.

    Looking Forward: The Evolving Role of 4-(Methylthio)Benzyl Alcohol

    Many chemicals pass through a production facility and fade from daily memory, but certain products become long-term companions. 4-(methylthio)benzyl alcohol holds its spot not only for its core utility but because of the real relationships developed with those who use it. Every project, every challenge regarding stability or custom packaging, and every outlier batch that sent alarms through the building shaped how we now produce and ship.

    Our hope is that this compound remains as indispensable in the coming years as it has in the past decade. To keep this status, we’re always watching both the chemistry literature and the remarks we hear at conferences or over daily emails with customers. The next breakthrough molecule or synthetic method may again pivot on 4-(methylthio)benzyl alcohol, and staying engaged means staying ready to adapt.

    So, for those seeking not just a catalog commodity, but a product with ongoing, transparent support from the people making it, our approach to manufacturing 4-(methylthio)benzyl alcohol stands ready to meet the needs of researchers, process chemists, and entrepreneurs tackling new chemical frontiers.