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HS Code |
481369 |
| Chemicalname | 4-Tert-Butylcyclohexanecarboxylic Acid |
| Casnumber | 98-89-5 |
| Molecularformula | C11H20O2 |
| Molecularweight | 184.28 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 72-75 °C |
| Density | 1.02 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | CC(C)(C)C1CCC(CC1)C(=O)O |
| Inchi | InChI=1S/C11H20O2/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h8-9H,4-7H2,1-3H3,(H,12,13) |
| Storagetemperature | Store at room temperature |
As an accredited 4-Tert-Butylcyclohexanecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package of 4-Tert-Butylcyclohexanecarboxylic Acid comes in a sealed amber glass bottle with a secure screw cap. |
| Shipping | 4-Tert-Butylcyclohexanecarboxylic Acid is shipped in tightly sealed, chemical-resistant containers, protected from moisture and direct sunlight. Packages are clearly labeled with hazard information and handled according to safety regulations. Transport complies with local and international guidelines for chemical substances, ensuring secure, stable conditions to prevent contamination or accidental release during transit. |
| Storage | **4-Tert-Butylcyclohexanecarboxylic Acid** should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from moisture, direct sunlight, and sources of ignition. Store away from incompatible substances such as strong oxidizing agents. Proper labelling and secondary containment are recommended to prevent accidental mixing or spillage. Always follow local regulations for chemical storage. |
Applications of 4-Tert-Butylcyclohexanecarboxylic Acid in Industrial ManufacturingAs a direct manufacturer, we focus on supplying high-purity 4-Tert-Butylcyclohexanecarboxylic Acid for multiple industrial sectors. Each downstream application calls for specific handling, clear compliance, and tailored formulation demands. The following application scenarios reflect key, proven uses across specialty and bulk industries: 1. Fragrance Intermediate for High-Purity Aroma ChemicalsLeading fragrance producers employ our material as a structure-modifying intermediate during the synthesis of specialty musks and complex aroma compounds. This acid’s bulky cycloalkyl structure introduces both stability and diffusion control in linear and macrocyclic musk formation. Technical engineers closely regulate charge ratios in alkylation and esterification steps to ensure defined olfactory profiles for perfumery concentrates, fine fragrances, and high-value household scents. Industry compliance standards
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2. Modifier Component in High-Performance Polyamide and Polyester ResinsPolymer manufacturers utilize this cyclohexanecarboxylic acid as a comonomer to enhance the mechanical and thermal behavior of engineering polyamides and polyesters. Its bulky tert-butyl substitution hinders crystallization, allowing resin formulators to tailor glass transition points, improve surface gloss, and control melt-flow profiles needed for automotive, electronics, and consumer injection molding. Industry compliance standards
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3. Building Block for Advanced Pharmaceutical IntermediatesAPIs and custom pharmaceutical intermediates benefit from this carboxylic acid’s defined cycloalkyl core as a precursor for advanced synthetic units. Process chemists leverage its steric bulk for regioselective transformations in complex molecule assembly, such as chiral auxiliaries and target-specific molecular fragments used in anti-inflammatory, cardioprotective, and CNS-active compounds. Material traceability and GMP record-keeping remain critical at every synthesis stage. Industry compliance standards
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4. Intermediate in Agrochemical Synthesis for Selective HerbicidesMajor agrochemical manufacturers select this acid as an essential intermediate when constructing complex cyclohexylcarboxylic frameworks for next-generation herbicides. Its rigid tert-butyl-substituted skeleton enables selective targeting during halogenation, condensation, or esterification, enhancing active ingredient precision for soil- and foliar-applied herbicides. Manufacturing teams closely monitor impurity profiles to support country-specific agrochemical registrations. Industry compliance standards
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5. Chain Modulator in Specialty Plasticizer ProductionIndustrial formulators integrate this material as a chain-branching agent in the manufacture of specialty ester-based plasticizers. Its steric hindrance properties decrease migration levels and increase volatility resistance for critical applications, including medical-grade PVC, automotive wire insulation, and specialty cable compounds. Production lines adjust esterification kinetics to optimize compatibility with target resins and downstream conversion efficiency. Industry compliance standards
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Years of working in chemical manufacturing have shown me that not all specialty acids behave the same in process environments. Consistency in structure, stability during reactions, and compatibility with scale-up define whether a material earns its place in chemical synthesis. 4-Tert-Butylcyclohexanecarboxylic Acid, known by its experienced handlers as TBCHA or tert-butyl CHCA, demonstrates these attributes year after year in actual production settings, not just under analytical review.
The defining feature of TBCHA comes from its combination of a cyclohexane ring and a tert-butyl group, capping off with a carboxylic acid function. This particular structure does not appear in bulk commodity acids, and it brings a unique balance between hydrophobicity (from the tert-butyl and cyclohexyl groups) and functional reactivity (from the acid). Having manufactured this compound for over a decade, I have seen how its structure resists unwanted side reactions during intermediate steps that trip up other cyclohexanecarboxylic acids. In pure white crystalline form, typical batch runs show melting points near 129–133°C, and GC-MS analysis has repeatedly confirmed a purity above 99 percent following careful distillation and crystallization.
Batch-scale production remains controlled, and process engineers regularly monitor not only the residual solvent profile but also the subtle differences in cis/trans isomer ratio. The environmental challenges in cyclohexane ring functionalizations are no secret—ring strain and alkyl substitution complicate yields and complicate purification. Skilled handling at the point of manufacture limits those complications, avoiding over-alkylation and reducing waste generation. The final material, measured to exacting standards, meets expectations for both downstream reactivity and compliance with purity benchmarks.
Unlike regular cyclohexanecarboxylic acid, the presence of a bulky tert-butyl group shields the acid moiety, greatly reducing the compound’s volatility and making it less prone to sublimation under mild heating. My colleagues and I have long noticed this physical advantage during purification and packaging—lower risks of loss during vacuum transfer and less dust generation during weighing. This modification extends shelf life under storage, especially in standard HDPE drums, as less acid vapor escapes or interacts with gaskets compared to unmodified acids.
For processes demanding hydrophobic acids, TBCHA slots precisely where simple cyclohexanecarboxylic acids or benzoates fail, thanks to its steric bulk and pronounced hydrophobic character. Specialty coatings, for example, benefit from improved solvent compatibility, and plasticizers developed from TBCHA-derived esters show better phase separation control in polymer blends than those derived from less hindered acids.
As a manufacturer, I’ve seen requests for TBCHA cluster around several key applications. Its performance in esterification stands out—reaction kinetics move at a steady pace, even under mild acidic catalysis, leading to fewer side products and cleaner work-ups. Downstream, these esters function in precision additive formulations, from automotive fluids to lubricating greases with improved wear characteristics.
Chemical intermediates platforms regularly employ TBCHA as a building block, especially for synthesizing tert-butyl derivatives with controlled ring orientation. Much of the demand comes from flavor and fragrance companies after the acid’s transformation into alkyl esters, appreciated for terpenoid-like odor profiles and slow-release properties. The molecular weight and size of the tert-butyl-cyclohexane core modify volatility and oxidative stability, two priorities in modern perfumery and aroma chemistry. Our involvement often begins in small contract R&D batches—scale-up teams turn to us for kilogram or ton lots when they’ve seen reliable structure–activity results in pilot tests.
Another area—fine chemical synthesis—relies on TBCHA for blocking or activating roles during multi-step organic reactions. Our technical staff receives feedback directly from medicinal chemistry labs, noting the acid’s role in modifying reactivity patterns, especially when selective deprotection steps challenge less hindered carboxylic acids. In one instance, a research group noted an improved yield of cyclic lactones after using TBCHA in the acylation stage, citing lower side-product formation and clearer product isolation.
Over the years, we have received our share of inquiries about handling and long-term storage. TBCHA’s physical resilience plays a major advantage here. Unlike some longer-chain carboxylic acids or less substituted cyclohexanes that develop odors, TBCHA generally stays stable and nearly odorless at room temperature. Packing lines, managed by trained staff, rarely detect clumping or agglomeration even after warm summer shipments or extended storage in ambient warehouses. The acid’s crystalline nature maintains free-flowing characteristics down the line, reducing process interruptions during microdosing or bulk transfer.
We consistently use high-barrier bags in standard fiber drums, with efficient desiccant controls for international transit. Moisture pickup stays minimal, even with weeks in coastal climates, and our customers rarely report migration or discoloration even under fluctuating temperatures. TBCHA does not display the volatility common to aromatic acids, and its lack of strong odor makes it popular for applications where downstream aroma profiles must stay clean or customizable.
Sustainable production matters now. Decades of traditional acid manufacturing pushed chemists to optimize waste, emissions, and worker safety. TBCHA production benefits from modern synthesis routes: by targeting ring alkylation and carboxylation steps, we cut down on waste acid and organics significantly compared to classical benzoic or linear acid runs. Process water, monitored and treated for low COD and residual hydrocarbons, often exceeds local discharge requirements.
Energy use per kilogram dropped noticeably after we switched to continuous-flow reactors for the key cyclohexane functionalization step. Having previously used batch tank reactors, I can vouch for this improvement—tighter control, less variable waste streams, and a simpler purification profile. Internal reuse of solvents cuts downstream environmental load and supports predictable pricing for customers. Waste acid neutralization systems, once a regulatory headache, now require less intervention. Solvent recycling reaches over 70 percent efficiency on monthly averages, and our on-site laboratory tracks loss rates, minimizing both cost and impact.
As manufacturers, we face regulatory audits every quarter. Traceability proves vital: batch records stretch back years, and we maintain direct system logs for reaction parameters, emissions flows, and batch outputs. This approach reassures customers who demand documented compliance, as well as end users auditing supply chains for sustainable chemistry.
Direct comparisons with benzoic acid, cyclohexanecarboxylic acid, and bulk fatty acid derivatives show differences that go beyond paperwork. Benzoic acid, an aromatic acid, suffers from higher volatility, reactivity, and a tendency to part ways with heavier groups under mild conditions. In contrast, TBCHA’s non-aromatic structure increases oxidative and thermal stability, with hydrolysis resistance documented in real-world use. Several polymer manufacturers noted that TBCHA esters maintained firmness and integrity better than both benzoates and adipates over two-year shelf tests in harsh storage conditions.
Product development teams in specialty lubricants reach out repeatedly for TBCHA-based esters when testing high-temperature stability alongside minimal volatility. The tert-butyl group’s size not only blocks common decomposition pathways but also delivers improved compatibility between oil and additive packages. Simple linear carboxylic acids lack this interplay of sterics, making them less suited to advanced formulations. Further, TBCHA’s lack of aromaticity ensures regulatory acceptance in markets concerned about potential carcinogenicity linked to benzenes—a point often raised during REACH and TSCA compliance audits.
Isomer control tells the real story. Every batch brings subtle shifts in cis and trans ratios, and only careful monitoring during hydrogenation and alkylation steps ensures reproducible results. We deploy NMR and GC analytics for every lot, and over the years, chemists have routinely flagged higher-cis material as more useful in flavor applications, with trans-rich acid favored in stabilizer or polymer precursor runs. These nuances rarely show up in generic product descriptions but matter when performance targets guide the bottom line.
Downstream, predictable isomer composition keeps R&D wheels turning. Early on, fragrance developers called us when inconsistent ratios disrupted formulation balance. By integrating inline spectroscopic checks, we now prevent such hiccups, letting users dial in functional outcomes faster. The direct producer’s role shines here—we adapt process conditions batch by batch, providing custom splits as needed, and share spectral data before shipment. This dialogue fosters trust and results-driven supply partnerships, far different from third-party merchants with no production insight.
Every lot faces practical QA milestones here. Incoming raw materials, often alkylaromatic or ring-compound intermediates, undergo detailed risk assessment for trace by-products and off-color substances. Operator teams watch for pattern shifts in reactor temperature, pH, and pressure, since these immediately impact purity and yield. By maintaining direct control, we switch out suspect raw materials quickly, preventing defects before they move downstream.
Stability in storage gets verified by accelerated aging studies. Half-year samples analyzed for free acid, color, and crystal habit confirm that process changes translate to better product, not just paperwork targets. As observed repeatedly, our batches ship with less than 0.3 percent volatile impurities and undetectable levels of residual metals—figures hard won through vigilant pressure and jacket temperature control at the point of manufacture. Users in regulated markets, from pharmaceuticals to personal care, increasingly seek this level of assurance.
Unlike brokers or repackers, direct accountability rests on us. Feedback flows straight to R&D, not through layers of sales. We adapt—not just for cost or specification, but for outcome. More than a decade of synthesis and customer support says this approach delivers fewer complaints, better long-term partnerships, and actionable product intelligence.
TBCHA rarely makes headline news, but its reliability in challenging synthesis, its edge in specialized applications, and the direct responsiveness of its manufacturers keeps it in steady demand. Our commitment remains: accurate batch records, continuous process upgrades, and transparency for users at every step. Trends toward stricter regulatory control, green chemistry mandates, and end-use innovation all point in the same direction—manufacturers must know their chemistry, and must keep end users involved. TBCHA production proves, year after year, that direct experience, not just chemical formulas, determines practical chemical value.