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1,6-Dichlorohexane

    • Product Name 1,6-Dichlorohexane
    • Alias Hexamethylene dichloride
    • Einecs 211-888-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
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    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    547021

    Cas Number 2162-98-3
    Iupac Name 1,6-Dichlorohexane
    Molecular Formula C6H12Cl2
    Molar Mass 155.07 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 220-222 °C
    Melting Point -30 °C
    Density 1.113 g/cm³ at 20°C
    Flash Point 99 °C (closed cup)
    Solubility In Water Insoluble
    Refractive Index 1.456 at 20°C
    Vapor Pressure 0.37 mmHg at 25°C

    As an accredited 1,6-Dichlorohexane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,6-Dichlorohexane is packaged in a 500 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 1,6-Dichlorohexane is shipped according to hazardous material regulations due to its flammability and toxicity. It should be transported in tightly sealed, clearly labeled containers, typically drums made from compatible materials. The package must include appropriate hazard labels, and shipping documents must comply with local, national, and international transport regulations.
    Storage 1,6-Dichlorohexane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, sparks, open flames, and incompatible substances such as strong oxidizers. Keep the container upright to prevent leaks. Ensure proper labeling and avoid exposure to moisture. Store away from direct sunlight and utilize appropriate secondary containment to prevent spills.
    Application of 1,6-Dichlorohexane

    Applications of 1,6-Dichlorohexane in Industrial Manufacturing

    1,6-Dichlorohexane serves as a specialized intermediate for diversified industries. Its dual chloro functionality and six-carbon chain enable precision in polymerization, crosslinking, and targeted alkylation processes. As the direct manufacturer, we supply this material to sectors with stringent quality controls and advanced downstream integration.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers commonly utilize 1,6-dichlorohexane for forming hexamethylene linkages in molecular frameworks of specific APIs, especially in the antihypertensive and antitumor segments. The chloro groups allow for controlled nucleophilic substitution, supporting stepwise construction under regulated GMP conditions. During multi-step synthesis, our material enters alkylation phases, enabling precise chain extension while minimizing byproduct formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP requirements
    • US FDA 21 CFR 210/211 for finished pharmaceuticals
    • USP/NF monograph requirements for impurity control

    Typical usage ratio

    • 1,6-dichlorohexane is typically used at a molar ratio just above the target amine or nucleophile (1.05:1 to 1.2:1), adjusted to maintain complete conversion and limit residual chloride content at final purification stages based on reaction yield and impurity profile.

    Downstream process integration

    • Material is introduced during the intermediate coupling or chain extension step, often following a protection–deprotection sequence. After alkylation, downstream steps include purification, crystallization, and analytical verification to meet pharmacopeial standards.

    Final product types

    • Antihypertensive agents (e.g., certain sartans)
    • Oncological APIs employing hexamethylene moieties
    • Small-molecule linker drugs
    • Pharmaceutical intermediates for CDMO contracts

    2. Polyamide Engineering Plastics Manufacturing

    Producers of high-performance polyamides choose 1,6-dichlorohexane as a reactive chain extender and crosslinker, particularly in formulations seeking improved flexibility and chemical resistance. The material reacts with diamines in interfacial polymerization or melt condensation, supporting the synthesis of specialty nylons and copolyamides with controlled molecular weights, consistent mechanical performance, and precise end-group functionalities required by the automotive and electronics sectors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive 2011/65/EU for hazardous substances
    • REACH Regulation (EC) No 1907/2006 for registration and traceability
    • UL 94 flammability classification for plastics

    Typical usage ratio

    • Used at 2–8% by total monomer weight. Ratio depends on targeted polymer chain length, crosslinking density, and mechanical property specifications as required by the final material datasheet.

    Downstream process integration

    • Introduced during monomer feeding prior to polymerization. Thorough pre-mixing ensures uniform reactivity. Monitored by in-process near-IR or Raman spectroscopy for confirmation of full conversion and residual chlorine minimization.

    Final product types

    • Specialty nylon grades (e.g., PA6, PA6/6, PA612 derivatives)
    • High-temperature engineering plastics for automotive connectors
    • Printed circuit substrate materials
    • Wire and cable insulation compounds

    3. Quaternary Ammonium Compound Synthesis for Biocides

    Chemical formulators use 1,6-dichlorohexane as a bifunctional alkylating agent to prepare hexamethylene-bridged quaternary ammonium salts. In controlled batch or continuous synthesis, it provides uniform chain lengths and facilitates the production of high-purity biocidal actives. Regulatory oversight governs the choice of production parameters, ensuring traceability and residue control for end-use in disinfectants and preservatives.

    Industry compliance standards

    • US EPA FIFRA for biocidal active substances
    • BPR Regulation (EU) No 528/2012 for biocidal products
    • ISO 14001:2015 Environmental Management
    • REACH Annex XVII restrictions on persistent organic pollutants

    Typical usage ratio

    • Used at equimolar or slight excess (1.0–1.1:1) relative to tertiary amine precursors to minimize mono-functional or unreacted intermediates, balancing target active content with regulatory-imposed impurity thresholds.

    Downstream process integration

    • Added in synthesis reactors following pre-neutralization of amine substrates. Monitored for complete substitution by HPLC or NMR before salt precipitation and purification. All processes logged for regulatory traceability.

    Final product types

    • Hexamethylene-linked quats for surface disinfectants
    • Preservatives for cooling tower water treatment
    • Antimicrobial additives in polymer masterbatches
    • Household and institutional biocide ingredients

    4. Crosslinker for Polyurethane Elastomers

    Producers of specialized polyurethane systems employ 1,6-dichlorohexane as a chain extender or crosslinker to impart increased toughness, hydrolysis resistance, and process stability. The material is incorporated in prepolymer mixing stages, reacting with active hydrogen donors. Sector-specific crosslinking requirements drive precise raw material selection and documentation, with quality controls tailored to high-performance elastomer production for demanding industrial applications.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing procedures
    • DIN EN ISO 4597 testing of polyurethane elastomers
    • REACH Substances of Very High Concern (SVHC) compliance
    • RoHS compliance for electronics-adjacent elastomers

    Typical usage ratio

    • Used at 1–5% by prepolymer weight, depending on the desired crosslink density, tensile strength, and elongation-at-break. Proportion adjusted according to MDI/TDI ratios and processing temperature.

    Downstream process integration

    • Integrated in prepolymer blending, immediately prior to final cast or molded polymer formation. Real-time monitoring ensures consistent dispersion and reactivity, with post-curing to achieve specified final material characteristics.

    Final product types

    • Industrial rollers and wheels
    • Vibration-dampening gaskets and pads
    • Mining conveyor belt elastomers
    • Specialized automotive bushings

    5. Linker in Agrochemical Synthesis

    Agrochemical producers utilize 1,6-dichlorohexane for constructing selective herbicide and insecticide intermediates, particularly those requiring a six-carbon spacer for molecular alignment on target active sites. Accurate dosing and stringent impurity controls underpin compliance with international pesticide registration requirements. The material is favored for its stability under reaction conditions and its track record in scalable manufacturing for regulatory submissions worldwide.

    Industry compliance standards

    • FAO/WHO JMPR guidelines for technical materials
    • OECD GLP principles for manufacturing traceability
    • China GB 2763 Maximum Residue Limits compliance
    • National pesticide registration requirements (e.g., US EPA PRIA standards)

    Typical usage ratio

    • Applied at 1.05–1.2 equivalents relative to coupling partners in key condensation or alkylation steps, adjusted based on analytical monitoring of conversion and regulatory specification for pesticide grade intermediates.

    Downstream process integration

    • Introduced in the active synthesis or salt formation phase. Downstream processing involves solvent exchange, purification, and stability testing according to agrochemical application files.

    Final product types

    • Intermediates for selective herbicides
    • Raw materials for systemic insecticides
    • Precursor molecules for fungicidal actives
    • Formulation additives for crop protection
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    Certification & Compliance
    More Introduction

    1,6-Dichlorohexane: Substance Overview and Practical Commentary from the Production Floor

    Real-World Experience with 1,6-Dichlorohexane

    On the factory floor, the journey from raw feedstock to high-purity 1,6-dichlorohexane never follows a simple script. This consistent molecule, often delivered at a purity above 99% by gas chromatography, stakes its claim in specialty synthesis and intermediate production more than in any old commodity chemical slot. In our hands, genuine 1,6-dichlorohexane comes off the line clear and colorless, stable for long-term warehouse storage if sealed away from light and moisture. As workers responsible for the process from reaction vessel to drum, we routinely monitor not only the molecular formula C6H12Cl2 and boiling point, but also subtle physical signs—odor, viscosity, presence of fine haze—that say as much about process integrity as any data printout.

    Long-standing customers in pharma, flavor, or high-tech resins don’t just ask for a CAS number. The questions turn to batch consistency, trace impurities, and whether the sample really holds up when the downstream chemist tries to make a specialty monomer or a pharmaceutical intermediate. Production teams hear these questions daily. Unlike generalized dihaloalkanes, 1,6-dichlorohexane carries a unique distribution of reactive centers—two chlorines precisely on the terminal carbons of the six-carbon chain. What this means in practice is greater flexibility in controlled chain extension and ring-closing chemistry compared to shorter or branched dichloroalkanes.

    How We Achieve High Purity and Batch Reliability

    Day to day, maintaining that high degree of purity is a balancing act—minimizing side reactions, optimizing the chlorination pathway, and constantly checking for over-chlorinated byproducts. We source hexanediol or hexanol grades that meet narrow contaminant tolerances and run reactors under tightly regulated temperature and solvent conditions. The real procedure rarely matches textbook yields. Certain reaction byproducts—especially 1,2-, 1,3-, or 1,4-dichlorohexane isomers—creep in if the process drifts. Our experience taught us that even minor isomer impurities can jeopardize polymerization or precision alkylation reactions, and trouble can show up as batch failures downstream.

    Regular staff training, close raw material screening, and QC protocols built around running GC-FID comparisons, not just basic titrations, separate a manufacturer’s assurance from bulk traders’ casual repackaging. Each year, we fine-tune fractionation columns, employ extra vacuum distillation steps, and constantly improve drying methods to ensure water and chlorinated side products stay out of final containers. This attention to purification isn’t just a cost—it’s become crucial as downstream users employ more sensitive catalysts or seek regulatory compliance for medicinal or high-spec electronics uses.

    Key Usage: Role in Polymer and Pharmaceutical Chemistry

    1,6-Dichlorohexane finds few generic industrial applications compared to certain mass-market solvents or plasticizers. Instead, it slots into roles that demand exact carbon chain length and substitution pattern. A mainstay application: serving as a bifunctional alkylating agent for producing specialty polymers and resins, where the dual terminal chlorine arrangement enables controlled step-growth polymerization. Polyamide and polyurethane researchers, in particular, require the clean terminal-chlorinated chains for building block assembly. The difference from 1,2- or 1,3-dichloroalkanes often shows up in lower crosslinking density and increased flexibility in final products.

    In the pharmaceutical world, its utility comes from its clean, easily traceable reactivity. A small but influential group of drug process chemists select this molecule for building ladders to secondary amines, specialty heterocycles, or for introducing hexamethylene spacers in patent-bound drug frameworks. The reactivity profile—neither too labile nor too sluggish—offers process windows that shorter-chain dichloroalkanes simply can’t access without risking toxicity or unwanted byproduct formation.

    We frequently receive requests for application-specific documentation or detailed impurity profiles, not only to satisfy regulatory expectations but also to answer narrower questions on catalyst compatibility or reactivity in high-pressure synthesis settings. By working directly with R&D teams on bespoke lots, we often help them troubleshoot side-product formation or optimize yields when moving from gram to kilogram scale. In decades of plant experience, we have seen process failures arising from small, unmeasured impurities or overlooked moisture content, leading to extra cleaning, wasted time, and bottlenecks never listed in catalog technical sheets.

    Comparing 1,6-Dichlorohexane to Other Dihaloalkanes from a Processing Perspective

    Comparisons with other dihaloalkanes rarely come in neat tables and often demand a closer look at reactivity, safety, and application specificity. Take 1,2-dichloroethane—its simpler two-carbon chain and boiling point around 84°C make it a popular base for vinyl chloride, but in specialty synthesis it reacts far too readily and brings higher toxicity concerns. Chain-extension and flexibility in the final molecular backbone are much more limited with short-chain dichlorinated molecules, so they often fall outside consideration for high-performance polymer or pharma intermediates.

    Moving to 1,4-dichlorobutane or 1,5-dichloropentane, most users notice differences in downstream processing. These intermediates, while structurally similar, don’t offer the balance between flexibility and process reliability. Their melting and boiling points shift operational parameters, change storage requirements, and—for customers developing new resins or exploring patent strategies—bring unpredictable reactivity in end-group substitutions.

    Our longtime technical staff point out other distinctions that rarely appear in outside reference guides. 1,6-Dichlorohexane brings run-of-line handling advantages: it stores and transports safely in standard steel or HDPE drums, takes up less fume extraction burden compared to highly volatile chlorinated ethanes, and rarely fouls batch reactors or transfer equipment with persistent residues or tars. Where our own experience diverges from that of distributors is in tracking tiny side products from halogen rearrangement or partial dehalogenation—a difference that might lead to color or odor changes, or, worse, unpredictable reactivity in a customer's synthesis vessel.

    In process optimization, an operator who’s managed both 1,6-dichlorohexane and similar molecules will note—often from years of trial and oversight—the relative ease of cleaning tanks and reactors post-batch. Residue carries lower chlorine contamination risk, and batch variability arising from storage time is noticeably more manageable. These are headaches seldom felt by traders or resellers, yet drive real production choices when reliability matters for quarterly planning or for running multi-week batch campaigns.

    Understanding Specifications in Real-World Terms

    Our standard output meets or exceeds 99% assay by gas chromatography, with water content typically controlled below 0.05% w/w via Karl Fischer titration. Color stability holds due to our stepwise distillation and filtration regimen—not just through off-the-shelf stabilizers, but by tuning process parameters for each annual feedstock lot. We screen heavy metals and chlorinated hydrocarbons far beyond baseline compliance, as downstream polymer makers report yield loss from contaminants at sub-ppm levels.

    From the vantage point of actual production, every specification takes on practical meaning. Chlorine distribution means more than a position on the label—it controls how the molecule drops into new reactions, how it stands up to high-temperature extrusion, and how it interacts with sensitive organometallic catalysts. Too much volatility, loose isomer content, or residual water will spell wrecked yields and off-spec polymer runs—costing end users precious time and product.

    In our work, we also learned that shipping and storage practices impose silent but critical expectations. For 1,6-dichlorohexane, oxygen and light exposure can catalyze slow decomposition and color shift, with effects showing up months after initial production. Our tanker and drum protocols, built around nitrogen blanketing and opaque containerization, grew from years of customer feedback and hands-on troubleshooting—not from theoretical shelf-life tables.

    Challenges and Factory-Grown Solutions

    Not all processing runs go as planned, and seasoned staff face real hurdles: exothermic spikes during chlorination, product loss through side venting, and filtration bottlenecks caused by tiny polymeric byproducts. Success comes not from rigid protocol, but from staff who adapt procedure to deal with small deviations—reactor jacket coolant adjusts here, alternative vacuum levels there. We rely on bench analytics and on-the-spot troubleshooting to hit tight targets for appearance, GC area, moisture, and color. Decades at the line taught us that some tweaks go unmentioned in general chemical bulletins: short cooling flushes, longer static settling, or mid-batch GC checks performed by shift leads as needed.

    To tackle recurrent issues, we set up feedback sessions with end users. Over the past three years, input from resin manufacturers and API synthesis engineers prompted us to re-examine filtration methods, enhance remote monitoring equipment, and invest in better labeling for drum traceability. These changes grew not from corporate white papers but from honest, boots-on-the-ground insights passed via support calls or site visits. Batch-to-batch reproducibility—down to fraction-of-percent deviations—remains our true measure of reliability. New investment in in-line sensors and trace analysis brought real, visible gains in customer satisfaction.

    Where sector changes outpace best practices, we’ve built flexibility into process design rather than rely only on approved historical routes. Recent shifts in sustainable chemistry, with demand for recyclable and lower-toxicity alternatives, nudge us to consider feedstock upgrades, halogen source reduction, and solvent recycling. By analyzing waste streams and working up process metrics, we target both efficiency and plant safety, aiming to anticipate shifts in environmental or health regulations instead of racing to catch up.

    Industry Demand and Evolving Standards

    Customers using 1,6-dichlorohexane aren’t pursuing generic volume—they are often developing new chemistry or securing patent protection for novel resins, APIs, and specialty intermediates. This brings us regular conversations about technical documentation, analytical traceability, and even process audits by third parties whose standards reach beyond published regulatory documents. We routinely support validation efforts with detailed COAs, secondary reference spectra, and organized chain-of-custody for larger lots.

    A recurring request among research groups: tighter control of trace chlorinated hydrocarbons and documentation showing undetectable levels of certain regulated impurities. These contracts often run on small-batch cycles with high scrutiny, where single-digit kilogram runs need the same consistency as metric ton-scale lots. Responding to such demand, we expanded our dedicated cleanroom and microanalysis facility, granting access to more advanced NMR and high-resolution GC-MS tools than most regional competitors offer.

    Local and global regulation, especially in pharmaceutical and high-performance materials sectors, drives up expectations for both process transparency and documentation. Supply to multinational buyers increasingly requires demonstration of traceability and legal compliance from raw input through to output packaging—a trend accelerated by both government mandate and client-side risk management. We developed standard operating procedures for sample archiving and documentation that provide back-audit capabilities for years, not just single customer orders.

    Supporting Long-Term End User Success

    A commitment to client support, from initial trial shipments to full-scale adoption, defines manufacturing partnerships in this space. Our technical staff field queries not only about UPLC or FTIR compatibility, but also plant integration, cleaning schedules, and disaster recovery in the event of spills or process shutdowns. Many production challenges—unexpected reactivity, fouling, or yield drop—trace back to small, unobserved differences in starting material that distributors and traders cannot fully explain or mitigate. Over years of customer engagement, we’ve absorbed as much from their troubleshooting experience as we provided through process support and tailored batch production.

    Supporting new applications means not just filling orders but tracking long-term supply, anticipating raw material availability shifts, and maintaining storage capabilities for off-schedule orders. Seasonal swings in feedstock supply, evolving safety expectations, and breakthrough requests for new end groups or lower-halogen materials turn into production roadmap updates. By staying close to both the chemistry and the customer, we continue adapting both our production capabilities and staff skills to meet the evolving shape of demand.

    The Manufacturer’s Difference in Ownership and Accountability

    A real manufacturer stands apart in accountability. Every finished drum, every correction to a gas chromatogram, directly links to someone who stands by the process and outcome. As plant operators and technical leads, the dialogue with customers doesn’t end at shipment; it stretches into post-lot support, collaborative process refinement, and shared investigation when something downstream changes. We operate within regulatory rules and respect strict site safety, but personal and organizational pride keeps the process sharp and output trustworthy.

    Unlike traders or third-party brokers, we don’t hide behind generic supplier lists. Factory staff own each batch’s reliability and go into annual reviews knowing the QC history, customer feedback, and batch narratives in detail. Raw material changes, energy interruptions, or unusual process interruptions each lead to lessons learned—and process fixes that support continual improvement. That history, known and lived by the production team, shapes how we advise users, respond to custom requests, and deliver the next order of 1,6-dichlorohexane.

    Looking Forward: Ensuring Quality and Reliability for the Future

    Our ongoing commitment centers on maintaining and raising the standard of quality, batch integrity, and transparency for users of 1,6-dichlorohexane across industries. Whether deployed in breakthrough API synthesis, specialty polymer research, or advanced materials manufacturing, close alignment with industry needs—grounded in hands-on factory experience and an open channel for user feedback—guarantees both flexibility and security for tomorrow’s innovators. As manufacturing gains in complexity and regulatory attention only intensifies, maintaining purity, delivering honest documentation, and ensuring safe, predictable supply of 1,6-dichlorohexane remain as demanding as they are rewarding.