Cyclohexanone stands as an organic compound, appearing most commonly as a clear to slightly yellowish liquid. Its molecular formula is C6H10O, with a molecular weight of about 98.15 g/mol. In the world of chemical raw materials, cyclohexanone lands among the most industrially significant substances, especially in the production of nylon intermediates. Chemists describe its structure as a six-membered carbon ring with a single ketone group. In commercial applications, this product flows as a liquid but reaches solid or crystalline form at colder temperatures. Lab workers recognize its slightly sweet, pungent odor right away, giving a clear signal of its presence, which matters for safe work environments.
With a boiling point of 155.6°C and a melting point of -31°C, cyclohexanone transitions smoothly between liquid and solid under different storage or shipping conditions. The density sits around 0.9478 g/cm3 at 20°C, which stands relatively high compared to many organics of similar size. This density indicates the tight atomic packing in its ring structure. As a solvent, it dissolves well with alcohols, ethers, and esters, and partially with water. Unlike some solvents, cyclohexanone resists forming loose emulsions with water, which matters for technicians who want clear separation in industrial processes. High purity grades carry very low water content and minimal side products, crucial for downstream polymer manufacturing. Cyclohexanone moves fast through supply chains, usually shipped in drum containers or tankers, and every drum comes with a precise label for traceability — something anyone in logistics or chemical plants learns to appreciate after enough audits.
Looking closely at its molecular structure, chemists see cyclohexanone as a ketone with the carbonyl group sitting at one position of the cyclohexane ring. This placement leaves the remaining carbon atoms saturated with hydrogen, giving the molecule a stable, yet reactive, backbone. The molecule’s shape gives it a balance between flexibility and rigidity, allowing selective reactions at the carbonyl carbon but resisting unwanted ring-breaking. This unique arrangement explains why factories pick it for oxidizing or polymerizing into more valuable compounds, such as caprolactam and adipic acid — both gateway materials for nylon fibers. In research labs, cyclohexanone’s slightly polar nature lets it act as a go-between, dissolving both aromatic and aliphatic materials without stripping away volatiles or leaving harmful residues.
Most suppliers offer cyclohexanone as a clear colorless liquid, but in colder climates or in poorly sealed containers, it may crystallize, forming clear or white solid flakes. Some users encounter it as a powder, pearls, or small crystalline aggregates, depending on storage and manufacturing methods. Solid forms typically mean exposure to low temperatures or impurity precipitation, and safe handling demands slow warming to redissolve crystals evenly. Large factories and bulk chemical users almost always prefer the liquid form, thanks to easy pumping and mixing. But labs and smaller producers value powder and crystalline cyclohexanone for precise measurement, especially in analytical procedures where weight accuracy outweighs convenience. During daily checks, quality control professionals look for unexpected color, odor, or haziness to catch contamination early, as these signs often signal water absorption or unwanted byproducts.
On the international trade scene, cyclohexanone moves under the HS Code 29142200. Customs officers and supply managers know this number by heart. It helps smooth out import and export paperwork, avoids legal trouble, and ensures correct tariff calculation. Regulations vary by region, but governments often group cyclohexanone with other ketones for purposes of transport classification, storage rules, and worker safety. Safety Data Sheets list cyclohexanone as a hazardous chemical, so bulk shipments demand labeling and warnings in accordance with local laws. This product sometimes ranks as a controlled precursor because of its use in pharmaceutical synthesis and potential diversion to illicit activities. Down at the warehouse, proper documentation and clear records matter — avoiding headaches during inspections.
Anyone working around cyclohexanone wears gloves and goggles, and experienced workers understand that even short-term exposure can cause skin, eye, or respiratory irritation. Its vapor can build up silently in enclosed spaces, so all storage rooms need good ventilation. Chemical plants typically install gas detectors, with regular air quality checks, and use closed systems or local exhaust to cut down on accidental release. If spilled, cyclohexanone speeds into drains and low areas because of its density and liquid nature, potentially contaminating groundwater or soil. Clean-up teams rely on absorbent pads and chemical neutralizers. Any facility storing large amounts needs spill containment procedures and trained first responders. Cyclohexanone ignites in the presence of an ignition source; fires involving this material produce hazardous fumes. Fire extinguishers suitable for alcohols and ketones — like foam or dry chemical — should sit nearby. Following these measures means keeping people out of emergency rooms and labs running safely.
This material does not rank among the deadliest chemicals, but no one shrugs off its hazards. Skin absorption carries risk, and repeated breathing of vapor causes headaches, nausea, and dizziness. Research shows that chronic exposure leads to liver and kidney damage, especially in those working without proper protection. Cyclohexanone’s harmful effects extend beyond people. Disposing of waste or rinsing containers into sewer systems creates environmental headaches. Even small spills threaten aquatic ecosystems, where the material interferes with fish gill function and plant respiration. Modern chemical operators follow strict rules on air and liquid effluent, with real penalties for violators. Waste treatment plants use biological and chemical neutralization before drainoff. Responsible companies invest in regular monitoring and emergency response teams to stay prepared for leaks or accidents. Environmental stewardship connects directly to long-term business health, keeping operations sustainable and building public trust.
Cyclohexanone serves as an essential raw material in the synthesis of nylon, with most of the annual global output heading straight to caprolactam and adipic acid production. These chemicals form the backbone for nylon fibers, which become everything from carpets and clothes to industrial hoses and parachutes. Paint and coating industries draw on cyclohexanone as a solvent, especially where high purity and controlled evaporation rates matter. Its reactivity allows for customization in fine chemical manufacturing — think specialty pharmaceuticals, adhesives, and plastics. This versatility shapes purchasing decisions. Production managers keep close watch on delivery timelines and batch quality because hiccups in cyclohexanone supply ripple through the entire value chain. Real-world experience teaches that substituting another ketone rarely gives the same performance, proving the irreplaceable position of cyclohexanone in today’s chemical sector.
Solving issues around cyclohexanone boils down to education, investment in safer technology, and real accountability for spills or accidents. Training staff in emergency procedures cuts down on response times. Advanced drum seals and bulk storage tanks with automatic leak detection prevent large-scale losses. Monitoring equipment lets plant managers catch small leaks before they become environmental disasters. Research into greener processes — both for cyclohexanone synthesis and waste management — offers hope for reducing both workplace hazards and overall environmental impact. Making these investments does not just protect workers and the environment; it secures the long-term viability of cyclohexanone-based industries by building safer and more sustainable processes into every step.