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Laurocapram (Oil-Soluble/Water-Soluble) BP EP USP Pharma Grade: Comprehensive Look at a Raw Material

What Is Laurocapram?

Laurocapram takes its place in the pharmaceutical world as both an oil-soluble and water-soluble raw material, known for its versatility. The compound’s presence in formulations stretches across topical medications, creams, and transdermal drug delivery systems, pointing to a chemical that adapts well to many settings. Its molecular formula, C18H35NO, draws from a foundation of eighteen carbon atoms, thirty-five hydrogens, one nitrogen, and one oxygen. The substance contains an amide group, contributing to both its solubility and reactivity. As a synthetic compound, laurocapram walks the line between function and safety. Chemically speaking, laurocapram acts as more than just a carrier: many in the healthcare and cosmetics industries use it to help active ingredients reach their target more effectively.

Physical Characteristics and Appearance

Users typically find laurocapram as a white to off-white solid, present in forms such as flakes, powder, pearls, or crystals. Temperature has a direct impact on its state; it melts down to become a clear, nearly colorless liquid, and this transition allows for flexibility in handling and processing. Its density has been measured in the range of about 0.801 to 0.810 grams per milliliter at 25°C, and users can dissolve it in both oil-phase and water-phase formulations. Those working in the lab handle laurocapram as both a solution and as a raw material in solid form, depending on the application. Oil solubility allows laurocapram to interact well with lipid-based formulations, while its water solubility opens up more options across cream bases and gels.

Product Specifications and Structure

The structure of laurocapram, also known by its INCI name Azone, centers on a twelve-carbon lauric acid amide, branched to a six-membered caprolactam ring. Chemists appreciate the clarity that comes from its molecular arrangement, since this directly relates to its function as a penetration enhancer. A melting point that falls near 40°C means the material changes form at body temperature, making it a useful tool for topical preparations. The HS Code, used in global commerce for tracking and classification, often catalogs laurocapram under 2924.29 for chemical raw materials. Laurocapram BP EP USP Pharma Grade adheres to pharmaceutical standards, showing low impurity levels and confirming identity through IR spectrum and purity tests. Users across Europe, the United States, and Asia see consistent labeling and documentation as a sign of reliability that matters during audits and regulatory review.

Properties that Demand Attention

Laurocapram stands out because it breaks the skin barrier gently and temporarily, welcoming active molecules, especially in drugs and certain cosmetic products. The amphiphilic nature lets the substance blend in with lotions and multilayered materials, reducing the friction that many active ingredients face at the skin’s surface. Many studies support laurocapram’s performance — scientists at universities and in commercial labs have tested penetration rates, measuring its effect on various drugs, including anti-inflammatory agents and topical anesthetics. Recognizing both its oil-soluble and water-soluble characteristics, I’ve seen formulators turn to laurocapram to tweak the release profile of drugs, ensuring a steady effect over time. This approach often cuts waste and enhances control, matching the expectations of patients and regulators alike.

Safety, Hazards, and Handling Concerns

Anyone dealing with chemicals, even those with a history of safe pharmaceutical use, should always check the safety data. Laurocapram generally receives a low toxicity score and is not considered a hazardous substance by most regulatory bodies. Material Safety Data Sheets usually recommend wearing gloves, goggles, and lab coats, particularly at scale, since skin and eye irritation have been recorded in rare cases. Storage takes place at room temperature, ideally in tightly sealed, light-resistant containers. I’ve watched industry colleagues set rules for bulk storage—spill control plans and waste minimization help keep both workers and the environment out of harm’s way. Importantly, this chemical does not classify as flammable, another check in its favor during transport and manufacturing. No raw material comes without risk, but constant training and clear labeling help remove uncertainty from day-to-day use.

Density, Solutions, and Application Notes

Density impacts how laurocapram behaves in mixtures, especially when combining with other oils, solvents, or aqueous systems. Its measured density of around 0.8 g/mL makes the substance lighter than water, so mixing protocols often account for layer formation and dissolution times. Solution concentrations depend on the end product — topical creams might use as little as 1% for effective results, while transdermal patches sometimes call for a greater amount to promote absorption. As a solid, it’s easy to transport in large quantities without risk of spillage or evaporation. Those familiar with pharmaceutical compounding know how small differences in density and solubility can change the spreadability, appearance, and delivery profile of a formulation. Solutions made with laurocapram have a reputation for stability, often retaining activity through months of storage and regular handling.

Raw Material Considerations and Environmental Impact

Any conversation around the long-term use of synthetic raw materials should include an honest look at origin, disposal, and end-of-life scenarios. Laurocapram, synthesized through established chemical routes, doesn’t pose a major threat to the environment in small quantities. Still, the pharmaceutical and cosmetics industries keep a close watch on synthetic ingredients, tracking not just direct human safety, but also breakdown products and waste streams. The rise in green chemistry forces suppliers to publish more transparent lifecycle data, tracing laurocapram from raw ingredient stock to final waste treatment. As a raw material, documentation around manufacturing—batch numbers, certificates of analysis, safety documentation—remains crucial for end users. In my own work, I’ve seen audit teams put a spotlight on traceability and non-toxicity, making it clear that regulatory clarity and cleaner disposal methods drive buying decisions.

Conclusion

Laurocapram BP EP USP Pharma Grade emerges as a reliable and versatile pharmaceutical raw material, offering unique solubility and penetration properties valued across medicine and cosmetics. With a clear chemical structure, measurable properties, and consistent adherence to regulatory standards, it finds its way into many daily-use formulations. While safety remains strong in typical applications, ongoing considerations around sourcing, disposal, and long-term health impact push this compound’s users to maintain rigorous standards from lab to finished product. As innovation continues, laurocapram’s performance record gives formulators both a trusted baseline and a springboard for new solutions.