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Xitai Ammonium Chloride BP EP USP Pharma Grade stands out as a high-purity inorganic compound, with the formula NH4Cl. In daily operations across laboratories and industries, Ammonium Chloride serves as a staple raw material within several processes. From my experience in chemical manufacturing, the significance of pharmaceutical grade ammonium chloride hinges on thorough purity checks and compliance with British Pharmacopoeia (BP), European Pharmacopoeia (EP), and United States Pharmacopeia (USP) standards. These standards make a difference for anyone relying on consistent chemical behavior, especially when patient health and strict safety depend on trace-level impurity management.
Xitai Ammonium Chloride often appears in different physical forms. It takes shape as free-flowing powder, glossy crystals, compressed flakes, small pearls, and even in formulated solutions with exact concentrations specified by liters. Each form comes with unique handling and storage concerns. For instance, working on a packaging line, I noticed how powder flows rapidly, demanding dust management, while flakes can clump under humidity, requiring air-tight containers. In every format, colorless or faintly white appearance becomes a marker for purity that buyers and regulators expect. This balance between form and purity guides its acceptance for pharmaceutical acts.
The molecular structure of Ammonium Chloride finds roots in one ammonium ion (NH4+) bonded with a chloride ion (Cl-), which makes the formula NH4Cl easy to remember and identify in material inventories. Under a microscope or during chemical tests, these crystals show a cubic shape and clarity that speaks for minimal contaminants. Bulk density tends to vary, commonly in the range of 0.85–0.95 g/cm3 for powders. Purity above 99.5% always finds clear mention in specification sheets, giving assurance to anyone sending the product for pharmaceutical blending or reagent supply. Moisture content, residue after ignition, and heavy metal traces anchor specification tables, giving labs a concrete grip on batch-to-batch consistency.
Xitai Ammonium Chloride for pharma grade shipment appears under the Harmonized System code (HS Code) 2827.10. This regulatory code labels the product globally, smoothing past customs checks for pharmaceutical manufacturers and raw material importers. Such identification reinforces the accountability of the supply chain, making recalls rare and helping regulatory compliance. Facing audits and customs processes, I found that detailed HS coding left no room for delays or misinterpretations. This brings peace of mind for regulatory affairs managers who deal with international shipment and clearance tasks.
Pharmaceuticals demand more than purity; they also require safety data that supports each material transition. Xitai Ammonium Chloride holds a moderate risk profile. In solid form—flakes, crystals, powder, or pearls—the substance remains stable but may irritate respiratory systems on inhalation, calling for careful handling and dust masks. Dust clouds should stay under check because even pharmaceutical grade ammonium chloride shares hazardous traits seen in lower grades. Liquid or solution forms, by contrast, reduce the inhalation hazard but spill control and absorption become more pressing. From experience in workplace safety programs, nothing replaces well-ventilated spaces, strong local exhausts, and routine personal protective equipment during load-in sessions.
The product deserves respect for its mild corrosiveness, particularly when dissolved in water or introduced to reactive compounds. Chemical compatibility charts recommend keeping it away from strong alkalis and oxidizers. In pharmaceutical plants, emergency showers and eye wash stations nearby turn out less a luxury, more a baseline. Xitai Ammonium Chloride’s GHS labelling focuses on acute toxicity, environmental harm, and eye irritation, placing it into a clear risk category. It neither causes combustion nor feeds fire, which keeps it out of the most hazardous warehouse sections, but comprehensive chemical spill training remains vital.
The molecular weight of NH4Cl lands at 53.49 g/mol, a number that matters for compounding pharmacists and chemical analysts making standards for laboratory use or pharmaceutical batch mixing. Solubility in water—always a defining factor—comes in at about 37 g per 100 mL at 20°C, giving clear indication of how fast and fully batches dissolve during buffer solution prep. Experience shows that this fast solubility accelerates process efficiency, helping technicians move through schedules without annoying residue or clogged lines. Specific gravity for solid Ammonium Chloride stands around 1.527, while aqueous solutions depend on concentration, staying above water but dissolving with little agitation.
Xitai Ammonium Chloride BP EP USP achieves pharmaceutical certification by rigorous analytical controls—loss on drying, acidity/alkalinity, and tests for arsenic, lead, mercury, and sulfate. Each batch brings a verification trail, not just a generic manufacturer’s promise. Lot-specific certificates of analysis clarify trace contaminants and standard compliance, offering a direct paper trail for pharmacovigilance and medical device safety.
Across the pharmaceutical sector, Xitai’s product becomes an acidifier in urine, an electrolyte replenisher in intravenous solutions, and a buffering agent for injection preparations where it counters pH drifts. Beyond medicine, Ammonium Chloride plays a role in metalwork fluxes, textile printing, battery electrolyte formulation, and fire extinguisher mixtures—making regulatory and supply teams appreciate its grade distinctions even more. In the lab or on a filling line, familiarity with granular behavior, safety risks, and chemical integrity makes the difference between batch success and costly recalls.
No pharmaceutical or medical device company can ignore the need for verified raw materials. Ammonium Chloride’s presence in excipients and injectable products raises the bar for both sourcing transparency and supply stability. Over years of supplier audits, I found that production records, batch traceability, and robust quality management systems separate dependable suppliers from unreliable ones. The smooth transfer of goods from plant to pharmacy relies on certified production lots, advanced analytical methods, and tight container sealing to control environmental exposure.
Getting the most value from Xitai Ammonium Chloride BP EP USP comes down to careful process integration, tested health and safety protocols, and a deep-rooted respect for the hazards inherent in chemicals—even those as familiar as NH4Cl. With global supply chains tightening on both regulatory and sustainability fronts, those handling this compound will benefit from supplier partnerships, third-party testing, and ongoing employee safety training. Safe handling, meticulous recordkeeping, and clear batch verification remain essential for all teams in the industry, from bench chemists to quality assurance specialists.
Chengguan District, Lanzhou, Gansu, China
