3-CHLORO-1-PHENYL-1-PROPANOL is a versatile organic compound with the molecular formula C9H11ClO. Its chemical structure features a phenyl group attached to a three-carbon chain, which includes both a chlorine atom and a hydroxyl group. Many in the chemistry and materials sectors use this compound, recognizing the importance of clear identification and reliable supply. Whether in research, pharmaceutical manufacturing, or specialty chemical applications, the value of understanding the core physical and chemical profile of 3-CHLORO-1-PHENYL-1-PROPANOL cannot be understated.
This substance usually appears as a white or off-white crystalline solid at room temperature. The powdered or flake form shows up in reaction vessels across industrial labs, often creating a striking contrast against other raw materials. Its density typically lands in the range of 1.2–1.3 g/cm³. Depending on the supplier and method of production, you might see it described as flakes, solid, powder, pearls, or crystals. Melt point remains a key piece of data for those working on temperature-controlled processes, hovering around 44–48°C. Many appreciate the scentless, stable nature of the pure material, making it straightforward to deal with in both liquid and solid phases. Though some might think of dangerous fumes or unpredictable behavior from the word “chlorine,” this molecule handles manipulation with the right gear and remains manageable under the lab’s standard chemical safety protocols.
The chemical structure of 3-CHLORO-1-PHENYL-1-PROPANOL holds significance for anyone diving into advanced organic synthesis or quality control. The benzene ring gives it aromatic properties, known to many chemists as a signature of stability and reactivity at the same time. The molecule’s backbone shows a clear three-carbon chain, with a chlorine atom fixed to the third carbon and a hydroxyl group (alcohol) on the first. This arrangement plays a big role in how the substance interacts with other chemicals, as it presents both polar and nonpolar traits. Its formula, C9H11ClO, tells you straight out of the gate what elements are in play, which lets chemists predict its behavior across dozens of reaction types.
Suppliers provide 3-CHLORO-1-PHENYL-1-PROPANOL in formats tailored for industrial, academic, and pharma needs. Often, the substance comes in tightly sealed containers as a solid or powder, though solutions sometimes show up for those preferring easier dispensing. In practice, a liter of stock solution or a few grams of solid can support extensive research or bulk production. Reliable documentation covers purity (typically above 98%), melting and boiling points, and trace impurities. Standard packaging units—ranging from a few grams for laboratory testing to kilo quantities for industrial use—allow for tailored procurement.
The Harmonized System (HS) Code plays a critical role in global logistics. For 3-CHLORO-1-PHENYL-1-PROPANOL, businesses shipping across borders use codes falling within the range for organic chemicals, usually listed under 2903, which covers halogenated derivatives of hydrocarbons. Clarity in shipping and customs avoids hefty fines and delays. Those of us who have spent long hours sorting import paperwork know the relief of seeing an accurate HS Code on the invoice.
When dealing with any chemical holding a halogen group and an alcohol moiety, proper handling stands as a must. Safety data consistently highlight the need for gloves and goggles, as skin and eye irritation ranks as a primary hazard. Inhalation of fine powders can present a risk, underlining the value of a fume hood and sound laboratory technique. The compound does not combust easily, yet prudent storage—away from strong bases, acids, and oxidizing agents—keeps both professionals and students out of trouble. Careful labeling contributes to safe workflows in teaching labs and production floors. While not classed as extremely toxic, the substance qualifies as harmful upon prolonged exposure, often prompting facilities to keep Material Safety Data Sheets (MSDS) close at hand. Emergency procedures focus on skin and eye flushing, as well as ventilating any area with unintended release.
3-CHLORO-1-PHENYL-1-PROPANOL often appears as a raw material in the synthesis of more complex pharmaceuticals or specialty chemicals. The dual reactivity of the chlorinated and alcoholic groups serves as a launchpad for further derivatization. Custom chemical synthesis shops find value in its use for generating stereospecific intermediates, while pharmaceutical teams employ it in routes leading to beta-blockers and other active molecules. Academic projects that push boundaries in organic chemistry sometimes rely on this compound for mechanism studies and proof-of-concept syntheses. In industry, raw material sourcing teams appreciate transparency about density, purity, and safe packaging, knowing that up-to-date technical documentation reduces downtime and waste. Only through precise knowledge of the product’s physical and chemical profile can scientists and engineers achieve the repeatability and safety today's regulatory environments demand.
Continued focus on improved packaging, clear hazard labeling, and comprehensive SDS access supports safer and more productive use. Those in charge of training also see the benefits when new lab members receive hands-on practice with this and similar aromatic halogenated alcohols. Sourcing teams support innovation and resilience by demanding transparent supplier documentation and consistent batch quality. Investing in robust quality assurance, focusing on purity checks and regular re-certification of storage facilities, narrows risks and builds confidence for everyone involved. Through teamwork and an honest approach to raw chemical fundamentals, scientists and industry staff get better long-term results in projects that depend on 3-CHLORO-1-PHENYL-1-PROPANOL as a workhorse material.
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