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1-Heptanethiol

    • Product Name 1-Heptanethiol
    • Alias n-Heptanethiol
    • Einecs 211-872-0
    • 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

    641266

    Cas Number 111-31-9
    Molecular Formula C7H16S
    Molecular Weight 132.27
    Iupac Name Heptane-1-thiol
    Synonyms n-Heptanethiol, 1-Mercaptoheptane
    Appearance Colorless to pale yellow liquid
    Boiling Point C 186
    Melting Point C -62
    Density G Per Cm3 0.841
    Flash Point C 66
    Solubility In Water Insoluble
    Odor Strong, unpleasant, thiol-like

    As an accredited 1-Heptanethiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Heptanethiol is packaged in a 100 mL amber glass bottle with a tight-seal cap and labeled with hazard and safety information.
    Shipping **Shipping of 1-Heptanethiol:** 1-Heptanethiol is shipped in tightly sealed containers, typically glass or HDPE bottles, to prevent leaks and exposure to air. It must be labeled as a flammable and toxic substance, and transported under regulations for hazardous chemicals. Avoid direct sunlight, heat sources, and strong oxidizers during storage and shipping.
    Storage 1-Heptanethiol should be stored in a tightly closed, clearly labeled container, in a cool, dry, well-ventilated area away from heat sources, sparks, and open flames. Keep away from oxidizing agents, acids, and bases. Avoid direct sunlight and moisture. Store in a designated area for flammable or sulfur-containing chemicals, ensuring appropriate secondary containment and spill response materials are available nearby.
    Application of 1-Heptanethiol

    Applications of 1-Heptanethiol in Industrial Manufacturing

    1-Heptanethiol plays a significant role in modern industrial manufacturing as a specialty alkylthiol intermediate. Downstream industries integrate this material for its reactivity in sulfur addition, surface modification, and specialty synthesis. Below are key industrial applications, with practical information for formulators and procurement teams.

    1. Lubricant Additive Synthesis

    Manufacturers of industrial and automotive lubricants use this material as a key raw ingredient for producing specialized sulfur-based extreme pressure (EP) additives. Its linear C7 alkyl chain lends particular performance advantages in anti-wear behavior and oxidation stability when incorporated into additive packages. Controlled thiol addition enables formulators to meet demanding tribological requirements for high-speed machinery and heavy-duty applications. Integration occurs during batch blending or in situ synthesis steps, tuned to base oil compatibility and end-use targets for grease, metalworking fluids, or transmission oils.

    Industry compliance standards

    • ASTM D4951 (Additive content in lubricating oils)
    • ACEA, API, and ILSAC lubricant additive standards
    • REACH Annex XVII (sulfur compound use restrictions)
    • Global Lubricant Quality standards (SAE J183 for automotive oils)

    Typical usage ratio

    • 0.05–0.8% by mass in finished oils, adjusted by base oil group and performance grade

    Downstream process integration

    • EP additive packages prepared in reaction vessels before addition to oil blends
    • Direct introduction during post-treatment blending for customized additive loadouts
    • Quality control at additive concentrate and final product phases
    • Compatibility testing with dispersants, detergents, and anti-oxidants

    Final product types

    • Multi-grade engine oils
    • Hydraulic fluids
    • Metalworking emulsion concentrates
    • Open gear greases

    2. Agrochemical Intermediates

    This raw material serves as a functionalized sulfur donor in the synthesis of specific crop protection actives, especially as a chain-transfer reagent or thiolating precursor during the assembly of herbicides and insecticides. Agrochemical producers employ controlled reactions for applications demanding balance of volatility, persistence, and bioactivity. The compound enters the synthetic route during key steps for introducing sulfur into heterocyclic rings or for alkylation of active moieties, with downstream use governed by regulatory residue limits and formulation type.

    Industry compliance standards

    • OECD GLP for pesticide intermediate synthesis
    • ISO 9001:2015 QMS for agrochemical production
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • US EPA 40 CFR Part 158 on inert ingredients and process aids

    Typical usage ratio

    • 0.1–0.5 mol per mol of final sulfur-containing active, with adjustment per synthesis pathway

    Downstream process integration

    • Batch introduction during thioether or thiol group assembly
    • Intermediate isolation and purification after key alkylation step
    • Downstream solvent stripping and neutralization prior to formulation
    • Residue risk assessment before bulk delivery to formulation plants

    Final product types

    • Selective herbicides (e.g., thiocarbamate-based)
    • Insecticidal emulsifiable concentrates
    • Fungicide active intermediates
    • Microencapsulated crop protection agents

    3. Polymer Modification and Surface Functionalization

    Specialty plastics producers employ 1-Heptanethiol for functional derivatization and end-group modification of polyolefins, latexes, and engineered elastomers. Its thiol group provides a reactive handle for grafting and crosslinking reactions, imparting hydrophobicity or tailored chemical resistance to finished films and molded goods. Addition points include late-stage latex compounding and melt-phase reactive extrusion, with in-process monitoring for conversion efficiency and property optimization in demanding environments such as automotive, electronics, and specialty packaging.

    Industry compliance standards

    • ISO 10993-5 for biocompatibility of polymer additives
    • EN 71-3:2019 for materials in contact with toys (migration of certain elements)
    • FDA 21 CFR 177.1520 for polyolefins (if used for food contact articles)
    • REACH Registration for polymer additives

    Typical usage ratio

    • 0.01–0.25% by polymer weight, tuned to target grafting density or crosslinking

    Downstream process integration

    • Direct feeding into extruder or latex blender during functional group introduction
    • Mixing with initiators or compatibilizers for in situ modification
    • On-line monitoring of thiol conversion and property advancement
    • Application-specific compounding and pelletizing

    Final product types

    • Chemically resistant cable jackets
    • Functionalized films for industrial wrapping
    • Elastomeric gaskets for harsh chemical service
    • Polyolefin resins for specialty automotive parts

    4. Metal Surface Treatment and Corrosion Inhibition

    The unique sulfur chemistry supports use as a building-block in the formulation of thiol-based surface modifiers and corrosion inhibitors for ferrous and non-ferrous metals. Blending into additive packages during pickling, cleaning, or passivation steps enables targeted monolayer deposition, enhancing corrosion resistance in petrochemical process equipment, storage tanks, and pipelines. The reactivity of the thiol group with metal surfaces fosters strong adsorption, creating a hydrophobic barrier against aggressive media in marine and industrial applications.

    Industry compliance standards

    • NACE SP0100 for corrosion inhibitor evaluation
    • ASTM G1-03 for surface cleaning processes
    • ISO 8044 for terminology in corrosion engineering
    • Quality audit under ISO 17025 for formulation QC

    Typical usage ratio

    • 10–500 ppm in circulating treatment liquids, varied by service severity and metal type

    Downstream process integration

    • Dosing into recirculating wash or pickling baths prior to metal passivation
    • Inclusion in corrosion inhibitor concentrates delivered to field service units
    • Application in closed-loop cooling towers and pipeline preservation
    • Performance monitoring by on-site film thickness and corrosion potential tests

    Final product types

    • Metal passivation liquids
    • Petrochemical pipeline corrosion inhibitors
    • Industrial degreasing and rinsing additives
    • Field-service corrosion control packs for refinery use

    5. Organic Synthesis of Pharmaceutical Intermediates

    Chemical active ingredient manufacturers select this compound as a thiolating agent or carbon chain extension component in the multi-step synthesis of certain pharmaceutical actives. It often enters the route during specific nucleophilic substitution or addition reactions for building sulfur-containing pharmacophores. Handling of the raw material takes place in validated GMP processing environments with strict batch traceability and contamination control, supporting the production of intermediates destined for APIs such as some antiviral or antithrombotic agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 for raw material handling
    • USP/NF compendial testing where applicable
    • Ph. Eur. general monographs for process intermediates

    Typical usage ratio

    • Stoichiometric addition based on target molecule route (eg: 1.05–1.10 equivalents per coupling step)

    Downstream process integration

    • Reaction charging under controlled inert atmosphere (N2/Ar)
    • Integrated purification and crystallization after sulfur introduction
    • Closed-system storage to minimize airborne exposure and cross-contamination
    • Release testing for identification and residual process impurities

    Final product types

    • Chemical intermediates for API manufacturing
    • Small-molecule building blocks for medicinal chemistry
    • Specialty batch actives for clinical development
    • Key linkers for heterocycle synthesis in drug substances
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    Certification & Compliance
    More Introduction

    Introducing 1-Heptanethiol: Experience from the Producer’s Perspective

    Shaping Quality—What We Put Into Every Batch

    Every drum of 1-heptanethiol leaving our gates starts its journey with raw materials sourced directly by our own team. Years spent fine-tuning our process have shown us just how much the purity of an organosulfur product can influence the outcome at our customers’ facilities. Molecular formula: C7H16S, CAS No. 111-31-9. Our 1-heptanethiol falls into the mid-chain length range for alkyl mercaptans, which brings certain characteristics that stand apart from shorter or longer chain alternatives. Confidence isn’t built by simply handing over a certificate; it comes from sharing real experience in synthesis, purification, storage, and integration into production lines.

    Behind the Chemistry—Why the C7 Chain Matters

    Ask anyone in the synthesis department which variable tweaks product behavior most, and you’ll hear about chain length. In the case of 1-heptanethiol, the seven-carbon backbone shapes boiling point, solubility, and reactivity. Solubility in common nonpolar solvents stays reliable across a range of temperatures, which fits practical requirements for organic synthesis and formulation labs. The boiling point—around 176°C at standard pressure—offers easier handling compared to very short-chained mercaptans, which tend to pour off as soon as the drum is opened. No two users approach thiols the same way, but this C7 chain saves us from the pungency and volatility of lower chain thiols like butanethiol, while still keeping reactivity superior to what’s seen in heavier analogs like dodecanethiol.

    Designing to Remove Residual Odor Issues

    Strong odors pose real operational challenges. 1-heptanethiol has a distinctive smell; this is the nature of all alkyl mercaptans. Our experience has demonstrated that even trace levels of oxidation byproducts amplify odor intensity, and for years, we’ve refined every stage to minimize these residues before packaging. We manage our reactors and cleaning protocols accordingly, regularly reviewing the headspace of stored lots using gas chromatography. End users in adhesive and lubricant manufacturing have told us that this control saves them headaches related to workplace environment management, since less atmospheric contamination means fewer downstream complaints.

    Why Do Formulators Choose 1-Heptanethiol?

    From batch to batch and customer to customer, the reasons vary, but certain applications lead the field. In rubber processing, 1-heptanethiol acts as a chain transfer agent, ensuring better control over molecular weights in emulsion polymerization. Colleagues from the synthesis team recall some of the earliest collaborations with tire compounders, who often noted that C7 length brought a tighter control compared to pentanethiol or hexanethiol analogs; shorter thiols frequently led to off-target side reactions and inconsistent color. In lubricant additive packages, the product’s specific sulfur content brings distinctive antiwear characteristics, allowing precise formulation without the excessive gumming issues reported with much longer mercaptans.

    The molecule also finds place in the production of surface modifiers, organic intermediates, and certain agrochemical formulations. The reactivity of the –SH group enables selective functionalization, which customers report as being more predictable than when working with longer chained thiols that offer sluggish reactivity. Instances where technical requirements evolve—a new polymer backbone, changes in solvent systems—feedback from real-world users frequently comes down to “ease of incorporation” and “predictable end results.” Both features are characteristic of a seven-carbon thiol.

    Consistency That Goes Beyond Paperwork

    Anyone can print a spec sheet with a purity threshold above 98%. Meeting and exceeding it every time is another story. Reliable synthesis methods, validated by our own years of in-house analytics, anchor our production. Our facility employs continuous distillation under reduced pressure, minimizing thermal degradation and cutting down on byproduct formation. Analytical chemists run regular GC-MS and NMR checks—not just on random lots but throughout every production campaign. This is how we keep heavy end impurities and mixed chain byproducts from ending up in your barrels.

    We’ve adjusted packaging protocols based on feedback from end users—selecting drums with specific inner lining chemistries to reduce product interaction. Specialized nitrogen blanketing neutralizes atmospheric moisture during transfer, sustaining product quality between the reactor and your shop floor. Down the line, this discipline pays off: no unexplained spots on chromatography. No mid-batch color shifts in polymer processes. No mysterious drop in sulfur content after storage.

    Comparisons—How 1-Heptanethiol Stands Among Alkyl Mercaptans

    Operators familiar with a range of alkyl mercaptans notice that differences span more than just volatility and odor. In the C4-C8 range, 1-heptanethiol offers practical volatility without the acute handling issues common to the most volatile mercaptans. Switch to products with longer hydrocarbon chains—like octanethiol or dodecanethiol—and reactivity diminishes, necessitating harsher synthesis conditions or more potent catalysts. In our own blending trials, efficiency with 1-heptanethiol holds up against unpredictable outcomes of other mid-chain alternatives, especially in surface active formulations and block-copolymer syntheses.

    Downstream processors call attention to the smoother blending experience—liquid at ambient temperatures, moderately low viscosity, and predictably sharp phase separation in multi-component systems. In adhesion modifiers, for example, 1-heptanethiol delivers a good balance of functional group availability and volatility: enough reactivity to provide a prompt cure, yet not so volatile that it flashes off long before the reaction completes. Shorter mercaptans tend to evaporate too soon for full incorporation, while longer chains lag behind, leaving tacky residues.

    Hands-on Storage and Handling Advice—Lessons from the Plant

    Years of storing 1-heptanethiol have clarified a few things about best practice. The liquid state at typical warehouse temperatures saves the operation from heating requirements common with higher alkanethiols. Tightly sealed containers keep the pervasive odor in check and moisture away from active sulfur sites. Our small-batch warehouse learned quickly that partial drums left open can darken and lose potency due to slow oxidation. We now reinforce strict sealing and nitrogen blanketing, extending shelf life and minimizing the chance of secondary reactions.

    Shipping schedules run to minimize exposure to heat, as elevated ambient temperatures can accelerate oxidation and increase pressure inside drums. Visual checks aren’t enough; we run periodic headspace monitoring using gas detection tubes to catch early traces of decomposition. End users benefit from these practices, as the material they receive matches both spec sheet and workbench experience—not just on the day of delivery, but months later, as process stocks get rotated.

    Environmental and Regulatory Responsibility—Direct Experience Counts

    Manufacturers carry a responsibility that extends beyond filling an order. 1-heptanethiol carries regulated hazards due to acute aquatic toxicity and flammability. Our team’s experience with local environmental authorities has shown how preemptively investing in emission control wins trust and reduces downtime. We fitted our scrubbers specifically to catch trace mercaptans escaping during drum filling and reactor discharge, meeting both occupational safety standards and downstream environmental controls. Site audits from outside regulatory groups have encouraged a more direct line of communication with our operations crew, increasing confidence in the reliability of controls.

    Customer Stories—From Laboratory Scale to Bulk Supply

    Early on, we supplied mainly in laboratory scale—plastic bottles of 1-heptanethiol for research chemists testing new surface modifiers. At that scale, purity makes or breaks an experiment. Analytical customers reporting unexpected spots on TLC triggered our internal review, eventually prompting a full overhaul of the distillation segment. It was their feedback, not just our own in-process analytics, that made a long-term difference in contaminant reduction.

    Scaling up for bulk petrochemical customers introduced a different set of pressures. Order requirements often arrive with tight deadlines, and production runs get backed up by any stalling along the purification chain. Our batch records show that increasing automation in distillation and shifting to closed-loop transfer systems eliminated many of the delays and batch loss events that once plagued our output. Today, production runs in the thousands of kilograms move reliably from reactor to drum, with minimal downtime. That reliability reflects lessons learned directly from early missteps.

    Troubleshooting in the Chemical Industry: What We’ve Found Matters

    Whether it’s lubricant blenders or coating producers, customers come to us when transitioning from old suppliers. Bottom line: the devil hides in the details. We’ve been called out more than once to troubleshoot material that caused process interruptions at a downstream site. Every time, root cause fell to overlooked parameters—incorrect chain length, uncontrolled water content, trace metal ions. As a producer, the real test comes in how effectively we control these variables at the source.

    Every issue prompts real changes: switching glassware types, rethinking how we dry storage tanks, tweaking transfer lines to minimize surface area where residues could form. These adjustments don’t just prevent call-backs and claims—they bring tangible improvements to yield and reproducibility. Continuous improvement doesn’t just come from chasing specs; it’s built on understanding in-plant realities and pushing back against complacency.

    Developments on the Horizon—Keeping Up with Market and Science

    There’s growing interest in applications far beyond traditional rubber compounding and specialty lubricants. Several universities have reached out to test the selective functionalization of 1-heptanethiol in building blocks for advanced materials. Our own R&D is looking into how its nucleophilicity can be harnessed in new ligand designs, which could stream into next-generation catalysis. The clean reaction profile we’ve achieved through years of plant refinement keeps us competitive in this shifting landscape; modern chemistries demand certainty in both yield and starting material consistency.

    From an operational point of view, tracking shifts in environmental regulations and safety codes influences our process tweaks just as much as evolving technical applications do. We’ve dedicated new resources to capturing and reusing vented thiols, not only limiting emissions but also providing potential side streams for lower-value applications. This kind of smarts—born from both regulation and innovation—sustains our edge and strengthens our partnership with the next generation of 1-heptanethiol users.

    Why Experience Behind the Process Matters

    A product’s journey doesn’t end with a packed drum or a signed delivery slip. We’ve watched innovation in the field leapfrog when reliable base chemicals take uncertainty off the table. Relationships with users, from specialty producers to large-scale formulators, grow with every problem solved and every adjustment made based on feedback. Over the decades, the market has seen numerous new entrants try to produce alkyl mercaptans—most stumble on the subtleties that turn on-paper specs into real-world performance.

    Manufacturers who refine process detail, commit to genuine QA improvements, and keep their door open to customer insight keep their place in the industry. We’ve seen it firsthand with 1-heptanethiol. After years of hands-on practice, we continue to believe that consistency, open communication, and a willingness to adapt have the greatest impact—long after the chemistry is finished and the paperwork is filed away.