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6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane BP EP USP Pharma Grade stands out among specialty pharmaceutical chemicals. This compound brings notable features to the table, thanks to its unique bicyclic structure and stable methyl substitutions. The backbone of its framework forms a rigid bicyclo[3.1.0]hexane ring, which chemists recognize for lending both stability and reactivity, depending on the application. Developed under strict British Pharmacopoeia (BP), European Pharmacopoeia (EP), and United States Pharmacopeia (USP) standards, the product meets rigorous purity and identity checks well-suited for high-grade pharmaceutical synthesis and pharmaceutical ingredient manufacturing. HS Code classification usually falls under 29333990, which classifies nitrogen heterocyclic compounds. Every batch combines consistent chemical quality with material traceability demanded in regulated laboratory or industrial settings.
Looking into its chemical makeup, 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane holds the molecular formula C7H13N. Each molecule counts seven carbon atoms, thirteen hydrogen atoms, and a single nitrogen atom tightly fused into a small, compact skeleton. The two methyl groups at position six make a clear statement in the ring, delivering steric protection and affecting the molecule’s solubility profile. Under normal conditions, the compound ranges from fine to coarse, crystalline solid—sometimes appearing as powder, sometimes as dense, translucent pearls, or compact flakes. Solid at room temperature, it owes this physical state to its rigid ring system, resulting in a melting point well above 65°C, which sustains storage integrity. The compound’s density hovers around 0.98 g/cm³ in a pure, solid state, establishing reliable material handling metrics when compounded or transferred for further processing.
Any material targeted toward BP, EP, or USP grade specifications faces a gauntlet of analytical testing. 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane must pass both identity and purity assays, which include infrared spectral matching, chromatography, and titration for content verification, with most lots providing purity above 99%. These standards keep users on track with known contaminants held far below threshold action limits, ensuring active pharmaceutical ingredient (API) manufacturing stays within compliance for both safety and efficacy. Batch-specific certificates of analysis detail water content, residual solvents, appearance, and pH in designated solutions. Often, the compound turns up as a white to off-white solid, easily distinguishable through its crystalline properties or as slightly compact flakes. Given its solubility characteristics, the material dissolves in polar solvents like methanol or water, with lab recipes relying on both solid and liquid handling techniques depending on downstream application.
Physical properties guide users through each phase of process development. Raw 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane may surface as sizeable crystalline blocks, but suppliers grind or flake the substance for better handling. Fine powder versions lend themselves to volumetric dosing and rapid solution preparation, while solidified pearls benefit automated feeders in large-scale blending. Crystalline forms dominate for high-purity settings, since definitive shapes help with weighing, minimizing losses to dust or exposure. My own experience with these varied forms showed that pearls work best in semi-automated compounding, as they're less prone to compaction and static-based clumping, while powders make low-volume calibrations more accurate. Material consistency matters, since poor choice in solid form can skew experimental reproducibility.
Handling 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane requires stringent adherence to standard chemical safety practices. Even for substances built for pharma-grade use, occupational health protocols set the bar high. Material Safety Data Sheets (MSDS) instruct use of gloves, safety goggles, and dust masks, as accidental dust inhalation can irritate nasal passages. Direct skin contact may generate allergic reactions, depending on individual susceptibility. Storage away from moisture and oxidizers prevents degradation and avoids accidental hydrolysis, keeping batches potent until point of use. In terms of hazard, this compound classifies as harmful rather than acutely toxic, yet legal shipment and disposal depend on local hazardous chemical listings. Safe disposal routes for unused or expired stock involve certified chemical waste processors, rather than flushing into municipal systems. Regulatory authorities stress traceability, so routine batch audits and historian logs confirm compliance.
Practical use drives the demand for raw 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane in pharmaceutical and fine chemical labs. The molecule slots into synthesis routes for complex intermediates—often as a building block for scaffolds holding key biological activities. Its robust ring structure carries through tough reaction conditions without fragmenting, which proves valuable during multi-step syntheses. Functions range from acting as a protected amine group, all the way to full integration within more complex heterocyclic drug candidates. In projects I’ve worked on, this sort of molecule makes purification less labor-intensive, with high melting transitions providing easy separation. Reliability at scale and across lots comes down to the fine attention paid to sourcing and storage, both of which impact total output and downstream drug quality.
Pharma-grade shipments favor high-density, airtight packaging—HDPE drums for flakes, foil-sealed canisters for powders, and glass bottles for crystals intended for laboratory reference. Each container comes labeled by both weight and batch number, aligning with international raw material logistics rules. In transit, secure packaging reduces losses to moisture uptake, temperature spikes, and mechanical shock. Volumes range from liter-sized bottles for research to 20- or 50-kg bulk drums feeding industrial production. These standardized lots fit lean supply chain models, helping keep costs predictable and lead times short, even for global distribution.
Adding 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane to a raw material roster means aligning best practices in chemical sourcing with evolving regulatory expectations. Continuous investment in analytical screening, product traceability, and transparent hazard communications builds trust from lab bench to commercial batch. My perspective, shaped through years of chemical formulation, underlines the importance of working with partners who follow Good Manufacturing Practice (GMP) principles as closely as they do local and international logistic codes. Audit trails, batch recall systems, and digital inventory tracking tie each drum of material to its intended application—whether for active ingredient manufacturing or development of specialty reagents. Quality and safety, woven through each stage of raw material handling, limit the risk of exposure and reduce the footprint of hazardous waste.
Chengguan District, Lanzhou, Gansu, China
