T-Butyl,3S-amino-2,3,4,5-tetrahydro-1H-[1]benaepin-2-one-1acetate-tartrate stands out for its unique molecular structure, which combines the t-butyl group with the amino-tetrahydrobenazepinone core and acetate-tartrate side chains. Chemists refer to this compound when synthesizing advanced pharmaceutical intermediates, especially for niche treatments in neurochemistry and organic synthesis. The design of the molecule introduces steric protection from the t-butyl group, while the S-amino stereochemistry matters because it means only one enantiomer—a particular “side” of the molecule—exists, making it highly selective in biological reactions. The HS (Harmonized System) Code for this chemical typically falls under bulk organic chemicals, which customs agencies use for import-export control, highlighting its status in regulated supply chains. For those in the field, it helps to remember that its long chemical name reflects the complexity chemists face, not unnecessary jargon. The way it acts comes down to the balance of its hydrophobic (t-butyl), hydrophilic (tartrate), and reactive (amino, acetate) fragments, combining into a suitable candidate for future drug design or advanced research applications. Its role as a raw material makes it a foundational building block, not just a specialty product.
This compound’s molecular formula combines several functional groups, usually written as C19H28N2O7. Its 3D structure stacks carbon, oxygen, and nitrogen atoms tightly into a semi-rigid backbone that imparts stability. The t-butyl moiety lies at the periphery, potentially encouraging solubility in nonpolar solvents or helping in controlling how it interacts in a reaction flask. As for physical form, one may encounter it as a crystalline powder, but variations like flakes, solid blocks, or even small pearls can show up from different synthesis batches or preparation methods. Sometimes, suppliers provide it dissolved in solution for immediate use in labs, which speaks to the compound’s solubility properties—soluble in some alcohols, less so in water due to steric bulk. Density averages around 1.23 to 1.32 g/cm³, though precise figures depend on purity, hydration, and form (powder or crystals). Describing molecular weight helps with accurate measurements in chemical reactions; at roughly 396.44 g/mol, it fits neatly into dosing and scaling calculations. Its appearance—off-white to pale yellow, crystalline, sometimes powdery—offers an easy visual clue chemists use for quick bench-side checks. Lab specialists value clear diagnostics: melting point around 152°C, and distinct IR and NMR signals, which make purity analysis less hassle. The acetate-tartrate portion contributes to the chiral landscape, which plays a role for advanced drug developments relying on precise structural control.
T-Butyl,3S-amino-2,3,4,5-tetrahydro-1H-[1]benaepin-2-one-1acetate-tartrate, though not reactive with air or water, calls for careful handling. Those t-butyl and acetate groups mean exposure to strong acids or bases could spark unwanted transformations—small shifts in pH or temperature sometimes lead to side reactions, especially where the amino group is exposed. Labs storing this material keep it in airtight containers at room temperature, shielded from light and moisture to avoid degradation. Many compounds with similar tartrate and acetate subgroups present low volatility, though direct inhalation or skin contact should always be avoided. Any chemist knows, despite appearing stable on the bench, accidental contamination or spillage can create persistent cleanup problems. As a powder or dust, it can scatter, so working in ventilated spaces reduces risk. I remember more than one occasion when insufficient dust control led to headaches or mild respiratory irritation after prolonged work—masking up or using a glovebox system solved those issues. The safety data sheet outlines these hazards with reminders: eye, skin, or mucous membrane contact may cause irritation, so gloves and goggles must stay on. Unlike some caustic chemicals, this compound isn't particularly volatile, so inhalation risk stays relatively low unless mishandled or ground very fine. Chemical waste disposal follows specialized protocols; running it down a drain creates real risk for the environment, so certified hazardous waste collection remains the norm in research and industry settings.
The importance of material safety goes deeper than meeting regulatory checkboxes. While t-butyl-benaepin derivatives rarely present acute toxicity at low exposure, their long-term health effects aren’t always fully understood. My own rule: treat all new organics as potentially hazardous, regardless of hazard labels. Skin contact, accidental inhalation of dust, or ingestion can cause local irritation or more significant reactions for those sensitive to amine or ester groups. Emergency wash stations and proper storage away from oxidizers and acids reduce the possibility of hazardous incidents. Regular training ensures teams know to avoid cross-contamination, particularly with raw materials that may degrade into unknown byproducts when combined—chemistry rarely forgives shortcuts. Documentation of batch numbers and origin helps reduce counterfeit or substandard supplies making their way into scientific workflows. Knowing your sources offers more than peace of mind; it lets managers track incidents to their root causes, and fix problems before they spiral. Responsible sourcing means checking that raw materials meet not only stated purity and specification but also environmental and ethical standards. Using certified supply lines, investing in closed-loop waste recovery, and participating in environmental stewardship initiatives keep chemical research sustainable. Now more than ever, buyers ask for materials with documentation of safe manufacturing, whether for drug discovery, industrial chemistry, or advanced materials research. When labs emphasize transparency, safety, and documentation alongside technical prowess, everyone benefits—from researcher down to the communities and habitat surrounding us.
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