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1-Hexanethiol

    • Product Name 1-Hexanethiol
    • Alias Hexyl mercaptan
    • Einecs 211-875-5
    • 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
    Specifications

    HS Code

    487825

    Cas Number 111-31-9
    Iupac Name Hexane-1-thiol
    Molecular Formula C6H14S
    Molar Mass 118.24 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Strong, unpleasant (thiol-like)
    Melting Point -94 °C
    Boiling Point 151 °C
    Density 0.845 g/cm³ at 25 °C
    Solubility In Water Insoluble
    Refractive Index 1.440 at 20 °C
    Flash Point 41 °C (closed cup)
    Vapor Pressure 3.2 mmHg at 25 °C

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

    Packing & Storage
    Packing 1-Hexanethiol is packaged in a 100 mL amber glass bottle with a secure screw cap and clear hazard labeling.
    Shipping 1-Hexanethiol is shipped in tightly sealed containers, typically glass or compatible plastic, to prevent leaks and exposure. It is classified as a hazardous material and should be packed according to regulations for flammable and toxic substances. Proper labeling, safety documentation, and secure handling are required to ensure safe transportation and storage.
    Storage 1-Hexanethiol should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as oxidizing agents. Keep the container tightly closed and properly labeled. Protect it from direct sunlight and moisture. Use appropriate chemical-resistant containers and avoid contact with air to prevent oxidation. Store in accordance with local regulations for flammable and toxic substances.
    Application of 1-Hexanethiol

    Purity 98%: 1-Hexanethiol with purity 98% is used in organic synthesis for pharmaceuticals, where it ensures high reaction yields and minimized impurities.

    Boiling Point 151°C: 1-Hexanethiol featuring a boiling point of 151°C is applied in solvent extraction processes, where it allows efficient separation of metal ions.

    Molecular Weight 118.25 g/mol: 1-Hexanethiol with molecular weight 118.25 g/mol is utilized in surface modification of nanoparticles, where it enhances dispersion stability in colloidal systems.

    Stability Temperature up to 40°C: 1-Hexanethiol stable up to 40°C is used in manufacturing of lubricating additives, where it maintains chemical integrity during blending.

    Low Sulfur Content: 1-Hexanethiol with low sulfur content is employed in flavor and fragrance synthesis, where it minimizes off-odors during production.

    Density 0.84 g/cm³: 1-Hexanethiol with density 0.84 g/cm³ is used in the formulation of specialized coatings, where it provides controlled rheological properties.

    Viscosity 1.6 mPa·s: 1-Hexanethiol with viscosity 1.6 mPa·s is used in polymerization reactions, where it facilitates uniform chain transfer for consistent polymer growth.

    Flash Point 48°C: 1-Hexanethiol with flash point 48°C is used in agrochemical formulations, where it offers safe handling under controlled conditions.

    Refractive Index 1.442: 1-Hexanethiol with refractive index 1.442 is employed in chemical sensor manufacturing, where it improves detection sensitivity via tailored optical properties.

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    Certification & Compliance
    More Introduction

    Getting to Know 1-Hexanethiol: A Closer Look at a Unique Chemical Building Block

    What Makes 1-Hexanethiol Stand Out

    In my years of working with specialty chemicals, there are certain compounds that tend to crop up time and again in both research and manufacturing. 1-Hexanethiol is one of those understated, yet critical, molecules that quietly enables progress in many fields. The structure is simple: a six-carbon alkyl chain capped by a thiol group. Yet this simplicity is precisely what fuels its versatility. If you’re in a lab or a production environment that demands reliable sulfur chemistry or surface functionalization, odds are that you’ve encountered this clear, strong-smelling liquid before.

    Most folks start out thinking of alcohols or amines as go-to functional groups for alteration or surface attachment. But once you work with gold surfaces or want to build self-assembled monolayers, you realize alcohols and amines don’t always cut it – they lack that strong, sulfur-based “grab” that thiols offer. Here’s where 1-Hexanethiol steps up. That terminal SH group isn’t just reactive; it forms bonds with gold so robust that even repeated rinsing or harsh solvents often can’t break them. Anyone fabricating nanoscale sensors or electronic devices quickly learns the value of this reliability.

    1-Hexanethiol in the Lab: Everyday Uses

    I’ve watched researchers spend hours trying to control the properties of a surface. With 1-Hexanethiol, a simple immersion of a gold-coated slide transforms the entire interface. The molecule forms a dense, ordered monolayer, creating a hydrophobic barrier that resists water and many chemicals. This sounds abstract until you see droplets bead up differently or see a sensor’s signal-to-noise ratio jump after functionalization.

    It isn’t only about gold – copper and silver surfaces can also benefit. The binding doesn’t always reach the same intensity, but the ability to modulate wettability or introduce new reactive sites can’t be overstated. I’ve seen hydrophobic patterns used to direct the growth of certain nanostructures, create defined channels for microfluidics, or simply to protect delicate surfaces from oxidation. In the world of organic synthesis, the presence of that reactive sulfur also opens the door to new coupling strategies and cross-linking reactions.

    How Model and Purity Impact Real-World Results

    Quality varies across suppliers. Sometimes folks treat all 1-Hexanethiol as interchangeable, but the model and specifications set the stage for every downstream application. High-purity variants with fewer trace contaminants like disulfides or lighter thiols ensure cleaner, more reproducible surface modifications—especially in demanding fields like electronics or analytical chemistry. Purity matters most where electrical properties are sensitive, since a few impurities can throw off impedance or even short devices at the micro- or nano-scale.

    Storage conditions factor in, too. The compound can oxidize on exposure to air, leading to disulfide formation and degraded performance. In practice, storing in airtight containers under an inert gas atmosphere makes a difference. I’ve learned to buy smaller bottles that get used up quickly or split larger purchases with colleagues just to keep batches fresh over time.

    Differences That Shape Performance

    A common mistake is to treat alkane thiols as a single class, as if the only thing that changes is the carbon chain length. The difference between 1-Hexanethiol and shorter (like 1-Propanethiol) or longer (such as 1-Dodecanethiol) chain thiols goes far beyond volatility or ease of handling. Chain length alters the packing density, stability, and fluidity of self-assembled layers. I remember troubleshooting a project that never quite worked until we swapped out the chain length – suddenly, the packing tightness suited our needs, and the gold sensors started to perform as advertised.

    Short-chain thiols remain more volatile, and their films tend to be less robust. Films from longer chains may be more stable, but their higher melting points and increased viscoelasticity can limit their utility in dynamic settings. With 1-Hexanethiol, there’s a sweet spot: the molecule stays manageable at room temperature, doesn’t evaporate in a blink, and gives monolayers that hold up under typical lab and field conditions.

    Sector-Specific Benefits and Realities

    Academia will always push the boundaries on what a molecule like 1-Hexanethiol can do. In my own work with undergraduate researchers, there was that moment of realization – a simple bottle held solutions to months of effort, once we took seriously how the thiol’s unique chemistry played out in real-world setups.

    In biotechnology, 1-Hexanethiol becomes a linker or a blocking group. By controlling how proteins or enzymes array themselves on a gold chip, you shape the entire outcome of a biosensor experiment. Without a reliable thiol, signal drift and background noise mask the signal. In materials science, the same compound might be cast as a stabilizer – helping nanoparticles stay discrete and preventing agglomeration that would otherwise ruin an experimental batch.

    Industrial scale-up brings new concerns. Quality assurance routines tighten up, as cross-contamination or lot-to-lot variability can undercut batch yields or lead to regulatory headaches. Here, consistent modeling and transparent documentation really matter. Teams can trace results back to a molecular lot and tweak processes as needed to maintain reliability.

    Supporting Data and Current Understanding

    Multiple studies on thiol-gold chemistry have shown how 1-Hexanethiol reliably forms highly ordered, crystalline monolayers. The sulfur end binds directly to the gold, while the hydrocarbon tail points outward. This organized structure plays out in changes to contact angle and surface roughness, which researchers can actually measure and relate to sensor sensitivity, catalytic activity, or even corrosion resistance.

    Patents for nanoelectronics routinely cite the benefits of hexanethiol monolayers. In tip-based nanolithography, the ability to use the compound to block or direct chemical reactions at nanoscales speeds up fabrication and leads to new device designs. Empirical data continues to confirm what chemists saw decades ago: 1-Hexanethiol is a dependable workhorse for molecular assembly and surface engineering.

    Challenges and Areas for Growth

    Despite, or perhaps because of, its widespread utility, there’s always room to improve how 1-Hexanethiol is handled and deployed. One challenge that sticks out is the distinct, pungent odor – anyone who has cracked open a bottle knows it lingers. Fume hoods and personal protective equipment help, but large-scale handling still calls for technological fixes or better solvents to minimize vapor loss.

    Health and safety standards remain another ongoing discussion. Chronic exposure to thiol vapors can cause headaches or more severe effects over time. Careful training, explicit labeling, and engineering controls cut down on incidents. Over the years, industry groups have responded by updating recommended exposure limits and refining monitoring tools, but vigilance matters at every stage.

    Transparency, Traceability, and Quality in the Modern Market

    One reason I trust certain suppliers more than others is their willingness to share data. They provide certificates of analysis, lot tracking, and third-party verification of purity levels, which lets researchers and purchasing managers spot trends and identify problems early. An open approach aligns with current best practices and fosters confidence that each bottle will match specifications, batch after batch.

    With mounting pressure to ensure both effectiveness and safety, many firms now invest in independent testing or allow academic labs to publish third-party verifications. These partnerships build trust and support a culture of accountability. Open lines of communication between users and producers help flag emerging issues, such as supply chain disruptions or new regulatory thresholds.

    Environmental Responsibility and Disposal

    Over the past decade, there’s been an increasing push to consider the full lifecycle of specialty chemicals. The disposal of organosulfur compounds has long raised environmental questions, especially since they can persist or react unpredictably. Environmental engineers and compliance teams look for cleaner synthetic routes and advocate for reclaiming or neutralizing leftover thiol residues instead of flushing them through municipal waste channels. I’ve seen partnerships with waste management specialists evolve, with some facilities now reprocessing or incinerating spent thiol solutions under controlled conditions to prevent atmospheric release.

    It’s not just about proper handling after use. Greener synthesis methods that minimize byproducts and energy consumption are beginning to displace older, more wasteful routes. Supporting this kind of innovation often comes from within the industry, with scientists and engineers suggesting improvements as they balance yield, efficiency, and environmental footprint.

    Comparisons with Similar Compounds: Not All Thiols Are Equal

    The category of alkane thiols includes a broad spread of compounds, yet each has different strengths and weaknesses in practical use. I’ve worked with 1-Octanethiol and 1-Dodecanethiol in situations where longer alkyl chains were preferred for increased hydrophobicity or thicker self-assembled layers. There are trade-offs: longer chains sometimes reduce solubility in standard solvents and complicate processing, while shorter chains can suffer from volatility or reduced surface coverage. The mid-length of 1-Hexanethiol lends flexibility – not too volatile, nor too rigid on the surface.

    Other sulfur-based molecules, such as thioethers or mercaptans with branched chains, behave differently again. They may offer advantages in selectivity for certain catalytic or binding applications but typically don’t form ordered monolayers as predictably as straight-chain thiols do. In semiconductor processing, for example, those differences can make or break a delicate patterning step.

    Trends in Research and Industry

    A major shift in the past few years is the growing use of 1-Hexanethiol in interdisciplinary contexts. Chemists now collaborate with physicists and electrical engineers to create hybrid systems, controlling interfaces at an unprecedented scale. Emerging work on nano-circuitry, plasmonic sensors, and new materials all depend on robust, reproducible chemical surfaces. I’ve heard more frequent discussions about customizing mixed monolayers or modulating end-group chemistry for multifunctional interfaces.

    The trajectory suggests more tailored molecules may eventually replace simple thiols in some specialties, as researchers chase even tighter control over electronic, optical, or catalytic properties. Yet, for many standard applications, the blend of availability, cost, and proven results keeps 1-Hexanethiol in regular rotation.

    Solutions and Recommendations

    In my experience, working with 1-Hexanethiol is most effective with a focus on education and informed handling. Teaching young scientists how to calculate surface coverage, mitigate vapor release, and store chemicals away from oxidizing environments pays dividends in both performance and safety. Purchasing high-purity variants and demanding detailed certificates of analysis support research integrity and ensure device yield meets industry expectations.

    Another practical step involves integrating environmental responsibility at every stage. Plan for safe disposal and source suppliers with transparent supply chains who support sustainable chemistry goals. Encourage open dialogue between producers, users, and regulators to keep improving quality, reliability, and sustainability.

    Laboratories and industries that prioritize clear protocols and continuous learning will reap the benefits in reproducible results, worker health, and minimized environmental impact. 1-Hexanethiol may not have the flash of newly discovered molecules, but its ongoing relevance speaks to a chemical that just works, year after year, across an ever-growing range of settings.