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HS Code |
919337 |
| Cas Number | 100-52-7 |
| Molecular Formula | C7H12O |
| Molecular Weight | 112.17 g/mol |
| Iupac Name | Cyclohexanecarboxaldehyde |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 175-177°C |
| Melting Point | -38°C |
| Density | 0.930 g/cm³ at 25°C |
| Solubility In Water | Slightly soluble |
| Flash Point | 63°C (closed cup) |
| Refractive Index | 1.454 at 20°C |
| Vapor Pressure | 0.4 mmHg at 25°C |
| Smiles | C1CCC(CC1)C=O |
| Synonyms | Hexahydrobenzaldehyde |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited Cyclohexanecarboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Cyclohexanecarboxaldehyde comes in a 100 mL amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | Cyclohexanecarboxaldehyde should be shipped in tightly sealed containers, away from heat, sparks, and open flames. It must be kept in a cool, well-ventilated area and protected from moisture. Proper labeling and documentation are required, and it should be handled as a flammable liquid according to applicable regulations during transportation. |
| Storage | Cyclohexanecarboxaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as oxidizing agents. Protect from direct sunlight and moisture. Store under an inert atmosphere if possible. Keep away from heat and open flames, and ensure the storage area is equipped for spill containment and fire safety. |
Applications of Cyclohexanecarboxaldehyde in Industrial ManufacturingCyclohexanecarboxaldehyde finds consistent use as a high-value intermediate in several downstream manufacturing sectors. Its unique aldehyde structure enables it to participate in controlled syntheses, particularly where aromatic, alicyclic, or functionalized end-products are required. Below, we outline key industrial scenarios where this compound delivers critical value, based on real-world processing, formulation, and quality control demands. 1. Fragrance Ingredient ManufacturingMajor aroma chemical facilities use cyclohexanecarboxaldehyde to synthesize core building-blocks for high-performance fragrances. The compound’s cycloaliphatic backbone provides essential olfactive notes in musk, floral, and herbal accord molecules, especially where thermal and oxidative stability are necessary. The substance is processed via catalytic condensation, acetalization, and further derivatization within closed, monitored environments. Batch records, impurity control, and traceability are strictly managed throughout the operation. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Plant Growth Regulator Intermediates)Downstream agrochemical manufacturers utilize cyclohexanecarboxaldehyde in the multi-step synthesis of selective herbicides and growth regulators. Its structural features allow controlled nucleophilic addition or oxidation to introduce specific functional groups necessary for final pesticidal activity. All operations in this sector apply stringent monitoring for trace aldehyde carryover, and waste management is closely regulated due to national environmental directives. Industry compliance standards
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3. Pharmaceutical Intermediate for API SynthesisIn API manufacturing, cyclohexanecarboxaldehyde serves as a defined-stage intermediate for selected alicyclic or aromatic API classes, where specific aldehyde derivatives are required for stereochemical or functional group incorporation. The compound’s use is fully integrated into validated process steps, with batch integrity, impurity profiling, and trace metal analysis documented for every batch destined for regulated drug synthesis. Industry compliance standards
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4. Fine Chemical Synthesis for Dye and Pigment IntermediatesCyclohexanecarboxaldehyde is integral to downstream dye and pigment manufacturing, where manufacturers incorporate it as a starting material for the synthesis of saturated alicyclic dye intermediates. Its chemical reactivity is leveraged in Knoevenagel condensation and related fine chemical syntheses, allowing the introduction of functional chromophores and improving the thermal stability of organic pigment systems. Batch quality is checked for color index consistency, and residue solvent profiles are tightly controlled. Industry compliance standards
Typical usage ratio
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Sourcing and producing Cyclohexanecarboxaldehyde demands commitment to purity, process know-how, and steady quality. Drawing from years of chemical manufacturing, our team has witnessed subtle shifts in demand and specification for this intermediate. Laboratories and industrial plants come to us with strict requirements, often based on downstream synthesis challenges. We work closely with their chemists, pointing out trace impurity risks during standard Grignard reactions and how to best avoid by-product formation in scale-up.
One of the central appeals of Cyclohexanecarboxaldehyde is its unique profile: a six-membered saturated ring joined to an aldehyde group delivers valuable reactivity without the volatility or high toxicity seen in many open-chain aldehydes. Customers rely on our consistent supply for work in fragrance compounds, agrochemical actives, and as a precursor for complex heterocycles. What sets this aldehyde apart from benzaldehyde or heptanal comes down to its well-controlled balance between ring rigidity and functional group accessibility.
Our routine batch analysis focuses on keeping the main product above 98% by GC, as minor impurities can trigger unwanted side-products for any downstream user attempting fine organic transformations. Maintaining water content below 0.1%, especially during humid months, is harder than it looks. Years back, we watched nearly a full tank go off-spec due to undetected condenser issues during distillation. That strict loss led to increased in-line instrumentation and reinforced inspection protocols for every batch.
Color and clarity matter, even for materials meant for further transformation. We have learned that even faint yellow hints can result from over-oxidation or iron traces, so we maintain all transfer lines and process vessels to eliminate any risk of rust or stuck organics. Cyclohexanecarboxaldehyde leaves our site as a clear, near-colorless liquid, free from floating debris and haze, reassuring downstream partners they are starting with the cleanest possible feed.
Several customers approach us after working with linear aldehydes such as hexanal, only to find ring-based molecules like Cyclohexanecarboxaldehyde bring less risk of uncontrolled polymerization or unwanted side-chain reactions. Our team has supported companies shifting away from benzaldehyde for synthesis of non-aromatic intermediates, building more stable ring-structures that mimic natural products without the complexity of extra aromatic reactivity.
Production workers and R&D chemists working with our Cyclohexanecarboxaldehyde have reported fewer handling incidents compared to lower molecular weight aldehydes, which often evaporate rapidly and generate hazardous atmospheres. The slight heaviness of the cyclohexane ring reduces volatility, and its modest odor remains manageable with ordinary fume extraction. We put a premium on keeping exposures low, and understand why many fine chemical makers now favor this compound in route scouting and process design.
Fragrance houses frequently specify our highest grades. Cyclohexanecarboxaldehyde becomes the backbone for cyclohexyl-derived alcohols and ketones that deliver stable, warm notes without oxidizing or decomposing during package storage. Its structural similarity to musks and woody nuances makes it a favorite for perfumers looking for subtle, long-lasting effects with less environmental scrutiny than nitro musks or polycyclic musks from prior decades. We respond to perfumery buyers by running extended stability studies, sometimes stretching over a year in high humidity. Old experience tells us to avoid any batch holding more than a few weeks; freshly distilled aldehyde simply outperforms older material.
Agrochemical researchers use Cyclohexanecarboxaldehyde as a bridge. Its ring structure allows the well-placed addition of halogens, oxygen groups, and other substituents, creating robust APIs that stand up to soil and sunlight. Several familiar weed controls and insecticides grow out of this aldehyde’s carbon backbone. Having supported pilot launches for three crop science multinationals, we know each client values traceability. We offer batch-specific impurity profiles for process mapping, recall prevention, and regulatory documentation — not because of a rule, but thanks to demands for foolproof quality auditing.
Transforming cyclohexane derivatives into the desired aldehyde means close attention to every step, from reactant selection to final purification. A single step out of place — be it the initial cyclohexanecarboxylic acid source or the use of questionable reducing agents — can leave behind unreacted starting material or secondary alcohols. We experienced this firsthand, once finding an unexpected chromatogram peak during routine QC, which we traced to a lax supplier of upstream alcohol. After that season, our vetting procedures for all incoming intermediates became more rigorous.
Our site’s process involves a controlled oxidation, followed by targeted distillation under reduced pressure to limit decomposition. We monitor temperature ramps minute by minute, using decades-old tricks learned from retired supervisors — tricks you won’t always find in literature, such as reading the faintest sulfuric notes in vent off-gas as an early marker for decomposing side streams. We switched to jacketed glass-lined reactors to minimize trace metal catalysis, yielding a purer end product and longer reactor life. These decisions reflect hard-won lessons from trial, error, and cross-generational knowledge sharing.
Meaningful differences between Cyclohexanecarboxaldehyde and more common open-chain aldehydes become obvious at larger scales. Hexanal, for instance, polymerizes faster and needs more inhibitor. Isovaleraldehyde gives off a sharp, choking odor and is far harder to contain. We’ve run side-by-side tests for regional customers shifting their feedstock to cyclohexane-based aldehydes and observed smoother reactions, more predictable isolation, and steadier yields — especially for acid- or base-catalyzed condensation chemistries. That predictability makes a big difference when operating 24/7 lines where any downtime stings the bottom line.
We keep tight control over packaging. Glass still gets called for in analytical labs, but bulk shippers rely on lined drums and tanks that won’t bleed plasticizers or corrode with time. Through seasonal changes, we alter storage protocols: winter demands constant agitation to avoid crystallization near freezing, and summers push us to accelerate turnover. Pro-active transport planning has spared us repeated headaches, since worldwide logistics remain a moving target.
Custom manufacturing runs for pharmaceutical intermediates make up roughly one third of annual production. Cyclohexanecarboxaldehyde’s robust ring makes it less likely to engage in unwanted rearrangements, giving drug synthesis chemists a forgiving starting point for hydrogenation, reductive amination, and cross-coupling routines. Since many of our pharma partners develop APIs for regulated markets, each new project drills down into traceability. We keep warehoused reference samples and take real pride in being able to verify any batch origin, even several years after delivery.
Engine oil additive formulators have also found value in this molecule, using its backbone to tweak lubricity and viscosity profiles in finished products. We collaborate closely, always testing for aldehyde reactivity with sulfur- or phosphorus-rich additives. Years ago, a major customer found that improper blending at elevated temperatures could generate off-odors. We invested in running closed-loop blending systems, sharply cutting volatilized loss and enhancing batch uniformity.
Feedback from buyers and R&D teams spurs us to continually examine upstream and downstream impact. One multinational buyer requested greater transparency on solvent residues. We responded by tightening our final purification and running third-party analysis on every multi-ton batch. Another fragrance user flagged a faint but persistent aroma, traced back to a non-obvious dicarboxylic impurity. Tweaks to our column packing and slow-cooling protocols yielded marked improvements in odor neutrality. The process pays off in credibility and trust, built on addressing real concerns with tangible process shifts.
In the world of chemical manufacturing, not every specification comes from a standard. Many arise from collaboration, with an end-user explaining an operational challenge or hinting at a hard-to-see impurity that only shows up in a finished product. These conversations guide us as much as any formal requirement.
Stringent safe handling rules are built into our routines. Since Cyclohexanecarboxaldehyde sits between commodity chemicals and specialty intermediates in hazard profiles, we treat every drum and bulk shipment as a priority. Our bulk operators receive refresher hazardous material training annually, and each new worker shadows a supervisor through entire receiving and blending cycles. Persistent efforts to keep spills contained, emissions low, and exposures at near background set our safety record apart from industry averages. Near-miss incidents are openly discussed in weekly meetings without blame; mistakes become lessons, not secrets.
Environmental performance builds on the same ethic. We recovered and recycled waste streams for a decade before formal regulations demanded it, aiming to cut landfill and minimize raw chemical use. Analytical chemists at our site run periodic wastewater and air tests, reporting real figures. An unexpected finding several years ago — trace aldehyde in stormwater outflows — led us to isolate and scrub a vent pipe left open during truck offloading. There is no shortcut: Clean and well-cared for facilities underpin both product credibility and community acceptance.
End-uses for Cyclohexanecarboxaldehyde continue to evolve. Green chemistry pushes us to find lower-impact routes, with hydrogen donors derived from renewable feedstocks becoming a larger part of our process each year. Recent R&D projects aim to switch to bio-cyclic intermediates, including pilot fermentation projects growing out of customer requests in the fine fragrance and natural flavor sectors. Early results show promise, though raw material pricing can be volatile.
Continual cooperation with regulatory bodies helps ensure batch records, safety data, and impurity profiles measure up to rising global requirements. Auditors visit our site, and we walk them through every step, openly sharing issues encountered and how they were resolved. Inspection readiness isn’t a slogan; regular practice enables our team to address gaps before they snowball into bigger problems.
We see Cyclohexanecarboxaldehyde as not just a molecule, but a relationship built around reliability, performance, and open communication with our downstream partners. Every order reflects the cumulative experience of technicians, engineers, and managers who live the realities of production and appreciate chemistry that works as promised — whether destined for new agricultural actives or an original perfume accord. The real strength of our approach rests in the trust and skills developed batch after batch, shipment after shipment. By taking ownership of the entire process, from sourcing and synthesis to on-time delivery and customer feedback, we ensure that each drum carries consistent quality and meets the high expectations set by diverse industries that depend on our expertise.