© 2026 Sinochem Nanjing Corporation,
All Right Reserved
Pargyline Hydrochloride stands out as a specialty chemical recognized for its function as a monoamine oxidase inhibitor. Many in the pharmaceutical and research communities might call it by its molecular formula, C11H14ClN, and note its typical form—a white, crystalline powder. Suppliers and laboratories alike encounter it most often as a solid, though its structure means it can sometimes show up as fine flakes or as a compressed material ready for further application. With a specific molecular weight of approximately 195.69 g/mol, it holds a reputation for predictable and manageable handling during research and development phases.
Anyone working with Pargyline Hydrochloride learns its density lands close to 1.1 g/cm3. In the jar or sample bag, the crystalline form easily dissolves in water, forming a clear, stable solution. Researchers who spend years at the bench come to notice subtle differences between similar hydrochloride salts—pargyline’s behavior under standard laboratory conditions includes modest hygroscopicity, so storage in a dry, cool space makes a world of difference for long-term stability. Its melting point typically sits in the range of 138-142°C, a figure that sticks in mind for those needing reproducible synthesis results. This material owes some of its solid-state stability to well-organized ionic lattice structures, visible under polarized-light microscopy.
Looking at Pargyline Hydrochloride on paper, the molecule’s structure offers clues to its role in inhibiting monoamine oxidase. Built from a phenyl-propylamine backbone and stabilized by a hydrochloride group, the compound’s atoms arrange themselves in a way that targets specific neurotransmitter pathways. The hydrochloride moiety improves overall water solubility and makes dosing in biological studies more precise. Its pearl-like crystals hardly betray the compound’s function, but anyone handling it regularly appreciates its reliable, almost unchanging appearance between batches. Researchers note that, under normal laboratory lighting, the powder reflects just enough light to signal purity—cloudy or yellowed samples could hint at oxidation or contamination, both of which threaten downstream applications.
Across chemical catalogs, Pargyline Hydrochloride carries the HS Code 29214990, signaling its classification as an organic compound akin to other amines. Its consistent molecular profile makes it an ideal raw material for pharmaceutical development, as well as neurobiological research. The specification sheets read like a short list: purity not less than 98%, chloride content verified through titration, and a loss on drying that rarely exceeds 1%. Many longtime research chemists have run the same suite of quality tests, confirming the absence of heavy metals and organic solvent residues. In practical use, when prepared in aqueous solution—maybe at 10 mg/mL—Pargyline Hydrochloride flows with little resistance, delivering predictable concentrations for both analytical and preclinical work.
Despite its value in laboratories and industry, nobody should underestimate Pargyline Hydrochloride’s safety profile. Like many synthetic amines, it carries a mild but real risk if inhaled, swallowed, or absorbed through the skin. Long-term experience reminds professionals to wear gloves, goggles, and dust masks, especially during weighing or transfer. Its MSDS lists potential central nervous system effects at higher exposures—a trait tied directly to its mode of action. While not volatile in the way of solvents or caustic liquids, the fine powder can spread inadvertently, calling for the use of clean benches or laminar hoods. Proper labeling and storage in sealed, chemically resistant containers help prevent unnecessary spills. Disposal follows standard protocols for hazardous organics, protecting both human health and the environment from any possible residues.
Over my years working with raw materials, Pargyline Hydrochloride stood out for its batch-to-batch consistency, a result of strict manufacturing standards at synthesis labs. Some suppliers even share spectral graphs—HPLC, NMR, and IR spectra—that match reference materials almost perfectly. That trust in traceability means fewer delays, and more reliable results for clinical trial work or more exploratory research activities. As demand for insight into neuromodulation and monoamine pathways grows, the continued supply of high-grade, certified Pargyline Hydrochloride remains a linchpin for both public and private research programs.
