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Ammonium Dihydrogen Phosphate BP EP USP Pharma Grade: Complete Product Analysis

What is Ammonium Dihydrogen Phosphate BP EP USP Pharma Grade?

Ammonium Dihydrogen Phosphate, also called monoammonium phosphate or MAP, carries the chemical formula NH4H2PO4. At a glance, this chemical appears as a clear, colorless crystal or a white granular powder. It pops up in pharmaceutical work under strict guidelines, classified under BP, EP, and USP grades, meeting some of the toughest pharmacopoeial standards. These standards insist on tight purity, particle size, handling, and trace contaminant controls, helping the product reach the safety and reliability needed for medicine and health-care production. Having worked in and around laboratories for quite a while, seeing a container of this salt always meant there was an important formulation job coming up, because it acts as a reliable pH buffer and nutrient additive where consistency counts.

Molecular Structure and Chemical Properties

Diving into its structure, NH4H2PO4 consists of an ammonium ion (NH4⁺) paired with a dihydrogen phosphate (H2PO4⁻) group. Its molecular weight comes out at 115.03 g/mol. As a solid, it transitions from a clear, sometimes pearl-shaped crystal to fine powder or flakes depending on processing. Its melting point hovers around 190°C, breaking down above that into ammonia and phosphoric acid rather than forming a true liquid. Solubility stays quite high in cold and hot water, which proves valuable for solution preparations where clear results matter and undissolved residue is not an option. Density sits at about 1.80 g/cm³, giving a good sense for both storage and mixture calculation.

Physical Appearance and Spec Forms

Ammonium Dihydrogen Phosphate often shows up in labs and storage as either fine powder, larger solid chunks, compact flakes, or, less commonly for pharma use, small pearls or granules. The transparent caps or paper sacks stashed in supply rooms don’t lie—each form responds to a different processing or blending step, something I noticed each time a supplier swapped out forms. For formulators who handle large batches, the physical state signals how the material behaves: powder pours fast, clusters together in humidity, while the crystalline or solid material holds up longer on the shelf and resists clumping. In all forms, this compound dissolves easily, an important trait for standard solutions and buffering tasks in manufacturing and research.

HS Code and Regulatory Oversight

Pharmaceutical grade Ammonium Dihydrogen Phosphate often ships under HS Code 2835.25.00, grouped as a phosphate chemical. Global trade moves this compound under strict regulatory coverage—not only for customs classification but also to track raw material sources, support pharmaceutical traceability, and make sure supply lines do not get contaminated by agricultural or technical grades. Experience in facility audits hammered home how explicit paperwork, from origin to final form, protects end-users by ensuring only the intended purity and grade ever enter a cleanroom. Where it enters as a raw material, third-party and in-house analysts both check for impurities like heavy metals, insolubles, or residual ammonium and phosphate ions that could shift pharmacological profiles.

Key Specifications and Material Safety

Specifications for BP, EP, and USP grades list minimum purity (usually above 98%), define tight tolerance for water content, set strict pH range in 5% aqueous solutions, and cap chloride, sulfate, and heavy metal levels well below hazardous thresholds. Typical impurity testing checks for substances like arsenic, lead, or mercury, as pharma guidelines take no chances with elemental toxins. Physical form is described in exacting detail—crystalline, solid, powder—because flow properties during mixing, exposure to air, and ability to absorb water all change manufacturing setups. Any product failing to match spec gets rejected, as even small deviations threaten lab controls or clinical trial consistency. In my shifts checking pharmaceutical compounds, this material only left storage after three signatures lined up, showing these technical standards exist for serious reasons.

Safe Handling and Hazard Discussion

Ammonium Dihydrogen Phosphate stays relatively safe compared to other chemicals, though workers in research or factory environments always treat it with due respect. It doesn’t burn, explode, or emit dangerous fumes without a strong external stimulus. Even so, its powderiness creates a slight inhalation risk in confined, unventilated areas. On skin or in the eyes, it can produce irritation if spilled—a risk tamed by gloves and goggles, common practice for anyone working around bulk goods or weighing stations. The real hazard comes from users overlooking the distinction between food, technical, and pharma grades, which can leak in contaminants or adulterants if not segregated. Chemical spills clean up with water and standard absorbents, but every material safety sheet still flags the minor risk: never eat, inhale, or allow contact with sensitive skin areas. In all my years, training and routine have saved more than once from missing a minor detail about safety, so I always recommend review of each product’s documentation each time supplies change.

Applications as Raw Material and Solution Preparation

As a raw material, Ammonium Dihydrogen Phosphate mainly appears in buffer solutions, intravenous nutrition, or diagnostic agents, where tight chemical fidelity shapes every final product batch. Dissolving this compound in water forms a stable, well-defined solution whose pH and phosphate content remain predictable, which keeps test results clean and enables accurate analysis. The pharma grade shows up where trace impurities and heavy metals have no room for error, such as injectable drug production, research reagents, and certain dialysis solutions. In the plant, careful measurements and consistent supply track each usage, from 5-liter beakers in a pilot plant to 1,000-liter vessels in commercial pharma runs. Like other seasoned lab workers, memories of improperly stored phosphate—caked, impure, discolored—remind how sensitive pharma formulas really are. What seems like just another white powder really sits at the keystone of reliable medicine manufacturing.

Summary Table of Key Properties

Chemical Name: Ammonium Dihydrogen Phosphate
Molecular Formula: NH4H2PO4
Molecular Weight: 115.03 g/mol
Appearance: White powder, transparent crystal, flakes, solid, sometimes as pearls
Solubility: Very soluble in water
Density: 1.80 g/cm³
Melting Point: 190°C (decomposes)
pH (5% solution): Typically between 4.2 and 4.5
HS Code: 2835.25.00
Grade: BP/EP/USP; Pharma Grade, meets international standards
Hazard Statement: Not classified as dangerous, but prolonged exposure on skin, eyes, or through inhalation may cause irritation
Main Use: Pharmaceutical raw material, pH adjustment, buffer, reagent, injectable nutrition additives, diagnostic support

Industry Value and Potential Solutions to Key Issues

Pharmaceutical grade Ammonium Dihydrogen Phosphate provides one of the most reliable and predictable compounds for controlled chemical processes, giving drug makers and laboratory teams a critical ingredient that stabilizes pH and delivers vital phosphate in a clean, manageable way. Despite its relative safety, incidents have occurred from cross-contamination with lower purity industrial forms, or mishandling due to poor storage and labeling. Keeping containers tightly sealed, rotating stock, and enforcing identity testing avoids many headaches I’ve seen over years handling similar stocks. As global pharma standards shift, digital tracking, integrated quality control, and graded packaging keep the supply chain transparent and trusted. Teams that invest in staff training, double-checking material certificates, and rapid-response documentation will find fewer surprises at regulatory reviews and will safeguard patient trust down the line.