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Trans-1,2-Cyclohexanedicarboxylic Acid

    • Product Name Trans-1,2-Cyclohexanedicarboxylic Acid
    • Alias trans-1,2-CHDA
    • Einecs 205-508-3
    • 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
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    Specifications

    HS Code

    696925

    Chemical Name Trans-1,2-Cyclohexanedicarboxylic Acid
    Molecular Formula C8H12O4
    Molar Mass 172.18 g/mol
    Cas Number 1464-53-5
    Appearance White crystalline solid
    Melting Point 195-199°C
    Solubility In Water Slightly soluble
    Odor Odorless
    Boiling Point Decomposes before boiling
    Density 1.3 g/cm3
    Pka Values 3.95, 5.63
    Structure Trans isomer of 1,2-substituted cyclohexane dicarboxylic acid
    Synonyms trans-1,2-Cyclohexanedicarboxylic acid; trans-cyclohexane-1,2-dicarboxylic acid

    As an accredited Trans-1,2-Cyclohexanedicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Trans-1,2-Cyclohexanedicarboxylic Acid is supplied in a sealed amber glass bottle, 100 g, with secure screw cap and labeling.
    Shipping Trans-1,2-Cyclohexanedicarboxylic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be kept away from incompatible materials, excessive heat, and direct sunlight. Proper labeling, hazard identification, and compliant documentation are required, following safety and transport regulations for chemicals. Handle and store according to SDS guidelines.
    Storage Trans-1,2-Cyclohexanedicarboxylic Acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Keep the container protected from moisture and direct sunlight. Ensure the storage area is secure and labeled appropriately to prevent accidental exposure or mixing with incompatible chemicals.
    Application of Trans-1,2-Cyclohexanedicarboxylic Acid

    Applications of Trans-1,2-Cyclohexanedicarboxylic Acid in Industrial Manufacturing

    Trans-1,2-Cyclohexanedicarboxylic Acid plays a critical role in specialized industrial fields where controlled diacid components improve product structure, compliance, and performance. Below, we outline specific downstream sectors where our high-purity material is processed into finished goods using rigorously managed processes and formulas.

    1. Plasticizer Intermediate Manufacturing for Non-Phthalate PVC Compounds

    Producers of non-phthalate plasticizers use this molecule as a structural acid in the synthesis of cyclohexane dicarboxylic acid esters, particularly for soft PVC and flexible vinyl products requiring stringent control over migration, volatility, and phthalate-free certification. The acid is directly esterified with mixed alcohols, forming key intermediates used in toy, medical, and food contact films. Strict raw material identity and traceability are required to meet migration limits and regulatory bans on ortho-phthalates. The acid’s inclusion influences final ester purity and dosing in fusion with plastic resin blends.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 (Plastic Materials for Food Contact)
    • US FDA 21 CFR 177.2600 (Rubber Articles for Repeated Use)
    • EN 71-3:2019 (Migration of Certain Elements in Toys)
    • China GB 4806.7-2016 (Food Contact Plastic Material)
    • REACH Annex XVII (Restriction of Phthalates)

    Typical usage ratio

    • 20–38% by weight in acid:alcohol feed for esterification, modulated to control plasticizer softness and migration depending on downstream flexibility and volatility requirements; exact ratio based on alcohol chain length and PVC grade.

    Downstream process integration

    • Dosed into esterification reactors with alcohols and catalyst under nitrogen, post-reaction purification through vacuum stripping, filtration, and QC for acid value before blend into customer PVC compounder’s plasticizer mixers.

    Final product types

    • Medical IV tubings and blood bags
    • Child-safe flooring and wallcoverings
    • Toys and childcare articles
    • Food wrap films and commercial conveyor belting

    2. Curing Agent in Epoxy Resin and Powder Coating Formulations

    Epoxy system specialists use this dicarboxylic acid as an anhydride-free, low-color curing agent for hardener blends in BPA-free epoxy coatings and powder systems for household appliances, automotive components, and electrical encapsulation. The cycloaliphatic diacid structure provides controlled reactivity and improved thermal stability compared to aromatic anhydrides, with favorable flow and gloss. Regulatory audits require confirmation of non-hazardous status and monitoring of residual acids.

    Industry compliance standards

    • ISO 8130-1 (Powder Coating Thermoset Systems)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 (Flammability of Plastic Materials)
    • ASTM D3029 (Epoxy Powder Coatings for Electrical Applications)
    • EN 60335-1 (Household Electrical Appliance Safety)

    Typical usage ratio

    • 8–16% by total epoxy resin content, adjusted according to target crosslink density, powder flow characteristics, and final cured hardness parameters; optimized by stoichiometric analysis with epoxy equivalents.

    Downstream process integration

    • Blended into the hardener phase during premix, or melt-mixed with resin and additives in twin-screw extruders, milled to fine powder, sieved, and conveyed to coating lines or molding facilities.

    Final product types

    • Whitegoods and appliance housings
    • Automotive primer and topcoat powders
    • High-gloss architectural panels
    • Encapsulated circuit boards and transformer resins

    3. Monomer for Polyamide and Polyimide Engineering Plastics

    Chemical companies utilize the diacid as a co-monomer in step-growth polymerization with diamines for specialty polyamides (nylons) and polyimides, yielding improved hydrolysis resistance and color stability in high-performance molded parts. The product allows precise backbone engineering for end uses requiring FDA, UL, and automotive OEM approval. Formula and charge ratios require careful stoichiometric balance to maintain polymer chain integrity and mechanical properties.

    Industry compliance standards

    • ISO 1874-1 (Polyamide Molding Materials)
    • US FDA 21 CFR 177.1500 (Nylon Resins in Food Contact)
    • Automotive OEM material specifications (e.g., Volkswagen TL 52361)
    • UL Yellow Card (Polymer Recognition Program)

    Typical usage ratio

    • Equimolar ratio with diamine (1:1.02 acid:amine typical for linearity); percentage of overall diacid feed adjustable (10–25%) to tune crystallinity and melting point for end-use temperature requirements.

    Downstream process integration

    • Introduced into polycondensation reactors with coacid and diamine charges, operating under inert gas, with temperature ramp and vacuum distillation to drive chain extension, followed by pelletizing and post-polymerization stabilization depending on grade.

    Final product types

    • Automotive fluid connectors and sensor housings
    • High-temperature wire insulation
    • Food processing machinery gears
    • Electronic socket and connector housings

    4. Synthesis Intermediate in Specialty Plasticizer Esters for Adhesives and Sealants

    Producers of industrial and consumer adhesives and sealants select this dicarboxylic acid to synthesize softening esters where non-aromatic, low-migration properties are necessary in contact adhesives, caulks, and polymer-modified sealants. The ester intermediate enables low odor and greater UV stability, increasing end product acceptance in sensitive installations. Manufacturing requires careful catalyst selection and residue management to pass adhesive migration standards for flooring and wall systems.

    Industry compliance standards

    • ASTM D4236 (Labeling for Art Materials)
    • Association of American Adhesive Manufacturers (AAMA 800 series)
    • REACH SVHC Screening (Adhesives and Sealants)
    • ISO 11600 (Sealants for Building and Glazing)

    Typical usage ratio

    • 22–30% by weight in esterification feed; adjusted depending on resin type and desired viscosity modification; balance with alcohol selection dictates flexibility and compatibility in finished adhesive matrix.

    Downstream process integration

    • Charged into direct esterification batch reactors, followed by neutralization and stripping; purified ester dispersed into adhesive or sealant polymer base under controlled mixing and temperature, with QC for acid value and migration index prior to final formulation packaging.

    Final product types

    • Solventborne and waterborne contact adhesives
    • Interior architectural glazing sealants
    • Flooring adhesives for textile and vinyl tiles
    • Low-emission construction caulks

    5. Intermediate for Cyclohexane-Based Surface Treatment Agents

    Manufacturers of anti-corrosion coatings and conversion agents for metals deploy this cycloaliphatic acid as a chelating and buffering component within proprietary treatment baths, particularly for aluminum and zinc surfaces in architectural and automotive finishing lines. The material’s dual acid groups enable surface complex formation, supporting the creation of thin conversion layers that enhance subsequent paint adhesion and corrosion resistance. Production must adhere to monitoring protocols for effluent and workplace exposure.

    Industry compliance standards

    • ISO 12944-5 (Protective Paint Systems for Steel Structures)
    • EU REACH Regulation (Registration of Surface Chemicals)
    • China GB/T 22391-2018 (Metallic Coating Conversion Layers)
    • VW TL 211 (Corrosion Protection for Automotive Parts)

    Typical usage ratio

    • 0.8–2.5% w/v in conversion bath solutions; ratio varies with substrate surface area and target layer thickness, adjusted during continuous process by titration and bath life monitoring records.

    Downstream process integration

    • Dosed into aqueous conversion baths with metal accelerators, operated under continuous filtration; substrate parts are immersed or spray-treated, then rinsed and oven-dried before downstream paint or sealant application.

    Final product types

    • Pre-treated automotive body panels
    • Galvanized roofing and façade panels
    • Architectural building profiles
    • Heavy-duty industrial machine frames
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    Certification & Compliance
    More Introduction

    Trans-1,2-Cyclohexanedicarboxylic Acid: A Closer Look at Quality, Consistency, and Application

    Experience on the Factory Floor

    Producing Trans-1,2-Cyclohexanedicarboxylic Acid every week in our plant, I see firsthand the rigors and rewards tied to this fine-tuned process. Unlike some simpler dicarboxylic acids, every kilogram reflects careful control over isomer ratios and purity. Teams in the plant understand how even a modest shift in reaction conditions can swing the balance between trans and cis isomers, or add unwanted byproducts. Keeping variables steady takes constant attention, and operators know just how crucial each parameter can be.

    What Sets This Molecule Apart

    Trans-1,2-cyclohexanedicarboxylic acid isn’t like phthalic acid or cis-1,2-cyclohexanedicarboxylic acid. They share the core six-carbon ring and two carboxylic groups, but the geometric arrangement sets trans- apart for certain chemistries. In the trans configuration, both carboxyl groups point away from each other, which affects solubility, melting point, and crystallization behavior. These physical properties shape reactivity and make this compound valuable for distinct synthetic routes.

    In processes we support, that extra spatial difference often determines success in building high-performance polyesters, resins, and plasticizers. We've watched customers try to substitute cis isomers or phthalic derivatives, only to return when their polymers lost mechanical strength or clarity. The trans isomer resists unwanted crosslinking and gives more predictable polymerization, which matters in coatings or specialty plastics—both in performance and reliability tests.

    Specifications We Stand Behind

    We monitor and refine purity levels lot by lot. With our current equipment and methods, we keep the content of trans-1,2-cyclohexanedicarboxylic acid above 99.5% on a dry basis, and minimize trace organics and inorganic salts. Moisture content—so often ignored—is tracked closely here, since even small amounts can affect crystallization and downstream yield. Typical melting point sits above 195°C, and our team screens visually and by HPLC to make sure every bag matches control benchmarks before release.

    Particle size and flow can differ from batch to batch, so we listen when our customers run into mixing or dissolution hiccups. Some want the material milled finer for faster blending, while others find that extra surface area unnecessary. Both ends of the spectrum get a say on our line, and we log every technical request for future orders.

    Decoding Uses, Not Just Listing Them

    Polymers that demand durability see big improvements from trans-1,2-cyclohexanedicarboxylic acid. I’ve walked through R&D labs using this acid to synthesize cycloaliphatic polyesters or plasticizers, where the trans geometry brings not just structural flexibility, but also scratch resistance, UV stability, and transparency other cyclic diacids can’t quite match.

    Take flexible PVC systems as an example. Standard phthalate plasticizers have drawn regulatory scrutiny and face ever more limits in food packaging and toys. Customers approach us with long lists of sustainability goals, and our acid enters plasticizer synthesis because of its non-aromatic backbone. It translates to softer, cleaner, and above all, compliant plastics that avoid migration issues common with some phthalates.

    Beyond plasticizers, our material often becomes an intermediate for specialty adhesives and high-end paints, where a precise combination of flexibility and heat resistance matter. Waterborne alkyds, for instance, show less yellowing and a smoother finish once formulators choose a trans over a cis dicarboxylate. Electronic encapsulants and insulation compounds have called for our acid due to electrical properties; we respond with certificates tracing each batch’s purity all the way to the lot number.

    Why Structural Isomers Matter

    People sometimes underestimate the effect of isomerism at a commercial scale. Technicians outside the plant see “cyclohexanedicarboxylic acid” on a label and assume any isomer fits the bill. In our practice, the mix of trans and cis shapes melting points, solubility in solvents like DMSO or DMF, and the way intermediates form esters with glycols.

    Trans-1,2 provides a more rigid foundation for synthesis, holding its shape as chains grow longer. During polycondensation, that geometry keeps reactivity high and unwanted branching under control. We’ve tested side by side with cis-rich samples: product consistency drops, mechanical testing shows softer and less resilient polymers, and the surface quality changes enough that even end-users notice. Sticking to the trans isomer isn’t dogma, it’s a lesson learned batch after batch.

    Echoes from the Laboratory and the End User

    Formulation chemists tell us which tweaks help or hinder their work. Some years, flame retardancy sits atop customer priorities; others, clarity or reduced VOC profiles come to the fore. We have supported transitions from older aromatic dicarboxylic acids because trans-1,2-cyclohexanedicarboxylic acid enables new, stricter compliance with global environmental and health standards.

    End users place as much value in predictability as in top-end properties. Unexpected variability derails production and raises costs—even causing months-long reformulations. Our field visits and after-sales support keep everyone in the loop and build trust, because batch-to-batch reliability reduces downtime and improves scale-up success.

    Our Roots in Process Control

    We didn’t always run the stable, high-yield reaction pathways we rely on now. Years ago, scale-up hurdles kept yields modest, and controlling side-products was a never-ending concern. Platform changes, newer catalysts, and process automation made a dramatic difference. Now, all critical reaction variables—temperature, pressure, feed rates—track tighter to spec, which shows in the lower impurity content in each lot.

    Seeing the batch reports reminds us how much every variable counts. We’ve been able to trim waste, recover solvents economically, and answer customer calls for more sustainable production. Our solvents recycle internally, waste gas is scrubbed before venting, and byproduct streams go to certified handlers, all tying in to the larger commitment from factory crew to management.

    Customers Drive Improvements

    We take direction from the issues and innovations our long-term partners bring up. One coatings producer pointed out how even small levels of residual catalyst could affect curing rates and color. After a series of lab trials, we tightened our workup and secondary purification, spelled out trace content limits, and linked these specs directly to outgoing COA sheets. Another customer building medical polymers provided feedback on extractables; together, we set new benchmarks for compliance verification.

    Customers in Europe, the Americas, and East Asia push for lower thresholds not just on heavy metals but on trace aromatic content. Our analytical lab responds—spending more hours per week screening for residue, validating against up-to-date standards, and reporting specifics that weren’t tracked a decade ago. Those records give procurement and safety teams evidence to carry into their audits and filings.

    Global Shifts Shape Production Methods

    Regulatory changes and supply chain headlines shape raw materials selection at every step. Phthalate restrictions opened an avenue for new dicarboxylic acids, but not every producer could meet the purity and consistency that industries need. Legislation in the EU and North America doesn’t just target phthalates; new lists evaluate even trace constituents in plasticisers and other polymer additives.

    Downstream, electrical and electronic companies have set ever stricter criteria—not only for RoHS compliance, but for heat-aging, dielectric breakdown, and moisture uptake in encapsulants. We have responded by testing each production lot against those endpoints. Our pilot reactors mimic custom end uses, allowing us to validate material performance long before shipment.

    Root Cause Insights and Solutions

    Troubleshooting problems on the production line usually points back to a handful of root causes: deviations in feedstock purity, reaction side products, or insufficient drying before final packing. We invest heavily in cleaning protocols and in tracking moisture down to parts-per-million levels, which helps address two major failure points—lumping in high-humidity storage and uneven melt during polymerization.

    Labs pick up on certain recurring challenges; a notched DSC profile, for example, can signal the wrong ratio of trans to cis isomer. Such small signs save engineers hours troubleshooting polymer melt behavior or explaining why clarity drops. Quality assurance teams stay vigilant, repeating these checks not just for compliance, but because we’ve fixed more than one headache early this way.

    Looking Beyond Routine Applications

    Pitching trans-1,2-cyclohexanedicarboxylic acid solely as a mainstream ingredient for polyesters and plasticizers undersells its versatility. We’ve found customers exploring uses from chelation agents in battery electrolytes to innovative, lower-emission adhesives for electronics. Developing these new use cases sometimes takes years, but our lab teams take on the challenge. On more than one occasion, our incremental gains in drying or impurity control have enabled pilot runs for specialty applications never considered during product launch.

    Performance in these non-traditional fields usually circles back to small differences in isomer ratio, trace content, or even packaging format. We design bulk bags and drums for easier handling and lower dust generation, based on feedback from production operators exposed to fine powders and potential spills. These changes might seem small, but they support safer workplaces and greater confidence in material consistency.

    Continuous Improvement Philosophy

    Many in the chemical industry view dicarboxylic acids like utilities—basic, unchanging feedstocks. In our experience, real improvement starts with a willingness to see each batch as a chance to better serve end users. We solicit and act on feedback from manufacturers, R&D scientists, and conversion facilities, then look for underlying themes. Over time, our operation has shifted toward even tighter in-process monitoring and sample validation.

    We joined a consortium last year to benchmark analytical methods against peers, focusing on cis/trans isomer analysis and ultra-trace contaminant detection. The result: leaner processes, fewer reworks, and measurable boosts in customer satisfaction. Key partners tell us they value that sense of lived experience—that real people with shop-floor knowledge guide improvements and respond when questions arise.

    Investing in the Next Generation

    Our commitment to training keeps us ahead of new regulatory, environmental, and user-based challenges. Every operator understands the steps that influence isomer composition, impurity load, and even powder flow at scale. Lab teams cross-train with process engineers and maintenance staff. This kind of culture allows us to identify problems earlier in the cycle, instead of waiting for downstream failures or complaints.

    Local technical schools and university labs often reach out for partnership. Our teams guide internships, provide research samples, and hold technical sessions for up-and-coming chemists. These collaborations help drive innovation, bridging gaps between fundamental research and plant-scale reality.

    Final Thoughts From Practice, Not Theory

    Trans-1,2-cyclohexanedicarboxylic acid isn’t just a specification number on a docket. In the real world, its unique structure, tight control, and clean synthesis shape countless end products from medical devices to next-generation electronics to safe, compliant toys. Not all dicarboxylic acids manage this blend of performance and regulatory acceptance.

    From the viewpoint of a manufacturer who’s solved problems batch by batch on the shop floor, achieving high-purity trans-1,2-cyclohexanedicarboxylic acid isn’t a formulaic process. It means taking responsibility for every variable, consulting with those who put the product to use, and recognizing how even small changes influence downstream properties. That steady drive toward better, safer, more reliable chemistry keeps our team moving forward—making sure every kilogram counts toward the next breakthrough, and the confidence of every partner who counts on us.