Methyl 4-Androsten-3-One-17 Beta-Carboxylinate: Product Overview and Properties

What is Methyl 4-Androsten-3-One-17 Beta-Carboxylinate?

Methyl 4-Androsten-3-One-17 Beta-Carboxylinate is known in chemical circles for its intricate steroidal backbone, a detail that becomes immediately clear once you start digging into its structure. This compound commands attention with its unique molecular framework, built around a cyclopentanoperhydrophenanthrene core—the classic foundation seen in most steroids. Toss in the carboxylinate group at the 17-beta position and a methyl group at the 4-androsten-3-one section, and you get a substance with distinct properties that break free from the basic androgenic pattern.

Structure and Molecular Details

The structure offers a window into its behavior across different applications. It sports a molecular formula of C20H28O3, with a molecular weight that typically hovers around 316.44 g/mol. The arrangement of double bonds, ketone, and carboxylate provides unique reactivity not seen in every compound off the shelf in the lab. I’ve seen plenty of research projects stall because of a mismatch between molecular properties and a process’s requirements, but with this molecular setup, both reactivity and stability often land on the right side for experimental use. The presence of methyl and carboxylate functionalities opens pathways for further derivatization—a feature valued by chemists in pharmaceutical or synthetic labs trying to create new analogues or study metabolic behavior.

Physical Properties and Appearance

Methyl 4-Androsten-3-One-17 Beta-Carboxylinate typically appears as a solid material at room temperature. Among the batches handled in research environments, I’ve often encountered this compound in the form of white to off-white crystalline powder or fine solid flakes. Some suppliers push the boundaries and pelletize for convenience, resulting in small pearls or granules that handle better in bulk. The density runs near 1.12 to 1.18 g/cm3, and the melting point tends to land between 145°C and 148°C—significant if you plan on using it in thermal processes or need to store for the long haul without degradation or clumping. Solubility profiles vary: it usually dissolves well in organic solvents, including ethanol, chloroform, and dichloromethane, while sparing water any decent solubility, which limits its direct use in aqueous solutions without a co-solvent or surfactant.

Specifications, Purity, and Handling

Suppliers regularly set the purity benchmark above 98%, a point that becomes crucial if the compound goes toward pharmaceutical research or produciton intermediates. Lower purity often brings in unknown risks—trace impurities sometimes trigger unexpected reactivity. I’ve had my own share of headaches where a 2% impurity led to unwanted byproducts, so it pays to stick with high-purity sources when applications demand precision. The compound comes labeled with an internationally recognized HS Code (usually 293729), and batch certificates confirm compliance for regulatory and customs processing. Forms range from powder to crystalline flakes, and packaging typically involves sealed foil bags or amber glass bottles, each tailored to minimize light and air exposure. Instructions often highlight storing it at controlled room temperature, away from excessive heat or direct sunlight, which extends shelf life and guards against breakdown.

Safety, Hazardous Nature, and Regulatory Notes

Dealing with Methyl 4-Androsten-3-One-17 Beta-Carboxylinate means paying respect to chemical safety. Like other steroid derivatives, it may carry androgenic activity, potentially causing harm on skin contact or inhalation, especially for those with hormonal sensitivities or during extended handling. Standard lab safety gear—gloves, goggles, dust masks—doesn’t just look professional; it keeps the technician out of the doctor’s office. The compound doesn’t qualify as acutely hazardous under GHS, but improper handling still leads to chronic exposure risks, especially in environments where fine particulates easily become airborne. Disposal follows local guidelines for organic raw materials, often requiring solvent washing and incineration. Documentation usually provides detailed hazard statements and calls out specific spill, fire, and first aid protocols, so skipping the Safety Data Sheet has never gone well for anyone, myself included.

Applications and Role of Raw Material

Most interest in this compound comes from its usefulness as a raw material in chemical, pharmaceutical, and research applications. The robust core structure contributes value in metabolic studies, structure-activity relationship investigations, and synthesis of novel analogues. Research labs working on steroid metabolism, for instance, use it as a reference standard or as an intermediate in crafting more complex molecules. Its functional groups allow both derivatization and conjugation, granting flexibility in biochemistry projects or in creating targeted drugs. At the industrial scale, the same compound sometimes heads into formulations where its stability and reactivity meet strict demands, serving as a building block for advanced synthesis. The specificity of this compound, compared to classic androgens, gives it a niche but important place in the list of steroidal chemical raw materials.

Material Integrity and Sample Handling

Every detail in storage and handling matters. Material exposed to air or humidity starts to clump or degrade, so airtight packaging turns into more than just a suggestion. For researchers or quality control technicians, recalibrating balances or opening new solvent bottles becomes a ritual before weighing or dissolving, minimizing cross-contamination. Logging lot numbers and expiration dates, while sometimes tedious, helps track any hiccups in formulation or analysis. For years, I've noticed that this level of attention in sample handling prevents issues that don't show up until much later down the production line. Not every compound is as sensitive, but with steroid derivatives like this, small measures keep big mistakes from showing up at scale.

Molecular Characterization and Analytical Testing

Routine analysis depends on high-resolution techniques. Infrared spectroscopy confirms functional groups, with a sharp C=O stretch signaling the ketone and distinct peaks for the methyl and carboxylate. Nuclear magnetic resonance (NMR) further clarifies the placement of methyl and androgenic units, giving confidence about isomer purity or configuration. Mass spectrometry (MS) delivers another layer of assurance when identifying trace impurities or confirming batch identity. These checks, performed regularly, ensure what reaches the end user matches the product description. Over the years, reliable data from these instruments means fewer doubts at critical moments in the lab, especially when experimental results hang in the balance.

Challenges and Solutions in Industry Handling

Some of the biggest issues come not just from chemical properties but from practical realities. Sourcing high-quality material remains a challenge, especially given the regulatory scrutiny attached to steroidal compounds. Direct relationships with reputable suppliers and a habit of demanding third-party lab analysis keep my lab from ending up with questionable batches—a useful lesson as more substances get flagged for import or distribution controls. For absorption or formulation hurdles, the compound's solubility often calls for use of co-solvents or careful mixing to get homogenous solutions or blends. Manufacturers regularly run pilot tests with each new batch, ironing out process quirks before ramping up production. In pharmaceutical development, regular consultation with regulatory teams prevents legal setbacks. From research to final execution, the process works smoother when knowledge from each step gets shared, not siloed.

Responsible Handling and Looking Forward

Working with Methyl 4-Androsten-3-One-17 Beta-Carboxylinate serves as a blueprint for safe, responsible chemical practice. Clear labeling, up-to-date SDS, and robust lab protocols reduce accident risks and protect researchers, operators, and the environment. Routine training in handling harmful or potentially hazardous materials ensures every stakeholder understands both the risks and the right response, especially as regulations stem from hard-earned lessons in the lab and factory floor. In the shifting landscape of chemical research and manufacture, sustainable and compliant sourcing, complete documentation, and investment in high-precision analysis give a solid foundation for quality and innovation. The journey from raw material to finished product might not always be easy, but every extra step in control and safety pays off over the long term.