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Sodium dihydrogen phosphate

Sodium Dihydrogen Phosphate
Chemical / Technical Name:
Sodium Dihydrogen Phosphate Monohydrate / Sodium Dihydrogen Phosphate Anhydrous
(Monosodium phosphate; NaH₂PO₄·H₂O / NaH₂PO₄)
Common / Alternative Names:
Monosodium Phosphate, Sodium Biphosphate, Sodium Phosphate Monobasic
Category:
Inorganic phosphate salt · Acidifying agent · Buffering agent · Electrolyte · Excipient / Nutraceutical / Pharmaceutical ingredient
Raw Material Type:
Inorganic mineral salt (synthetic; pharmaceutical, nutraceutical & food grade)
Key Active Constituents (Typical):
Sodium Dihydrogen Phosphate ≥ 98.0–102.0%
Phosphate content (as PO₄³⁻): grade-specific
Sodium content (elemental): grade-specific
(Assay compliant with USP / EP / IP / BP specifications)

Formulation: Ingredients & Claim Values

Vitamin A - 50mg, Vitamin D - 30mcg

Packing Size

mg, ml, gram, oz, lbs

Packaging Type

Quantity

1000, 2000, 5000, 10000

SKU: sodium-dihydrogen-phosphate Category: Brand:
Description

Description

Technical & Manufacturing Relevance:
Sodium dihydrogen phosphate is widely used as an acidifying and buffering agent in pharmaceutical, nutraceutical, food, and medical formulations. It is a key component of phosphate buffer systems, often used in combination with dibasic sodium phosphate to achieve precise pH control.
From a manufacturing perspective, sodium dihydrogen phosphate is highly water-soluble, chemically stable, and compatible with a wide range of APIs, vitamins, and minerals. It is commonly used in oral liquids, effervescent systems, powders, sachets, and injectable formulations (where permitted). Selection between monohydrate and anhydrous forms depends on moisture sensitivity, flow characteristics, and formulation pH requirements. Careful control of phosphate intake is necessary in formulations intended for renal-sensitive populations.
Applicable Dosage Forms:
Tablets (as excipient or active, where permitted)
Powders & sachets
Oral liquids & solutions
Effervescent tablets & granules
Medical & clinical nutrition products
Pharmaceutical intermediates
Pharmacopoeial / Quality Notes:
USP / EP / IP / BP grades available
White crystalline powder or granules
Freely soluble in water; insoluble in alcohol
Stable under recommended processing and storage conditions
Monohydrate loses water on heating (hydration control required)
Controlled for heavy metals, fluoride, chloride, and microbial limits
Supplied with complete quality documentation as per international regulatory standards
Animal-Origin Declaration:
Non-animal origin · Vegan / Vegetarian compliant
No bovine, porcine, gelatin, or animal-derived processing aids involved
Manufacturing Support:
Available for bulk supply, contract manufacturing, third-party manufacturing, and private labeling (subject to regulatory permissions). Comprehensive support includes formulation feasibility and pH optimization, pilot and commercial-scale production, excipient compatibility assessment, customized packaging and labeling, and complete regulatory documentation (COA, MSDS / SDS, TDS, stability data, and batch traceability) required for easy resale and distribution in any country worldwide.