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?? ??? ????? ??
- ???
- <0°C
- ?? ?
- 100°C
- ??
- 1.40 g/mL at 20 °C
- ???
- 0Pa at 20℃
- ?? ??
- room temp
- ???
- H2O: 5 M, ??, ??
- ??? ??
- ??
- ??
- ???
- ??????(pH)
- 4.0 - 4.5 (25℃, 50g/L in water)
- ?? ?? (pKa)
- (1) 2.15, (2) 6.82, (3) 12.38 (at 25℃)
- ??
- 100.00%. ?? ??
- ???
- ?? ?????. ???, ??? ? ?????? ???? ????.
- ??
- Hygroscopic
- ?? ??(λmax)
- λ: 260 nm Amax: ≤0.025
λ: 280 nm Amax: ≤0.02
- Merck
- 14,8660
- BRN
- 3903772
- ???
- ????. ???, ??? ???? ????.
- InChIKey
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M
- LogP
- -2.148 (est)
- CAS ??????
- 7558-80-7(CAS DataBase Reference)
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- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | Xi | ||
---|---|---|---|
?? ???? ?? | 36/37/38-36 | ||
????? | 26-36-39 | ||
WGK ?? | 1 | ||
RTECS ?? | WA1900000 | ||
F ?????? | 3 | ||
TSCA | Yes | ||
HS ?? | 28352200 | ||
?? ?? ??? | 7558-80-7(Hazardous Substances Data) | ||
?? | LD50 orally in Rabbit: 8290 mg/kg LD50 dermal Rabbit > 7940 mg/kg | ||
???? ?? | KE-31577 |
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White, slightly deliquescent crystals or granules.??? ??
Anhydrous salt: white crystalline powder; slightly hygroscopic; forms sodium acid pyrophosphate, Na2H2P2O7 on heating above 225°C and sodium metaphosphate (NaPO3)n at about 350 to 400°C; very soluble in water, aqueous solution acidic.Monohydrate: white orthorhombic crystals or granules; density 2.04 g/cm3; loses its water of crystallization at 100°C; very soluble in water, pH of 1% solution 4.5; insoluble in alcohol.
Dihydrate: large transparent crystals; orthorhombic bisphenoidal structure; density 1.915 g/cm3; decomposes at 60°C; very soluble in water; insoluble in alcohol.
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Sodium phosphate monobasic monohydrate is used as sequestrant, emulsifier, mordant in dyeing, reagent and buffer in foods and analytical chemistry. It was applied as a fireproofing agent and for weighting silk in tanning. It is employed in manufacturing of enamels, ceramics, detergents, boiler compounds, in soldering and brazing instead of borax.?? ??
Monobasic sodium phosphate can be prepared by partial neutralization of phosphoric acid with sodium hydroxide in equimolar amounts: H3PO4 + NaOH → NaH2PO4 + H2OIt also can be made by treating disodium hydrogen phosphate with phosphoric acid in proper stoichiometric amount: Na2HPO4 + HPO4 → 2NaH2PO4.
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Monobasic sodium phosphate is prepared by adding phosphoric acid to a hot, concentrated solution of disodium phosphate until the liquid ceases to form a precipitate with barium chloride. This solution is then concentrated and the monobasic sodium phosphate is crystallized.?? ??
Sodium phosphate monobasic is an effective oral osmotic laxative at minimal concentration. It is used for colonic cleansing before endoscopic examination of colon.Pharmaceutical Applications
Monobasic sodium phosphate is used in a wide variety of pharmaceutical formulations as a buffering agent and as a sequestering agent. Therapeutically, monobasic sodium phosphate is used as a mild saline laxative and in the treatment of hypophosphatemia.Monobasic sodium phosphate is also used in food products, for example, in baking powders, and as a dry acidulant and sequestrant.
Safety Profile
Poison by intramuscular route. Mdly toxic by ingestion. A human and experimental eye irritant. When heated to decomposition it emits toxic fumes of POx and Na2O. See also PHOSPHATES.Safety
Monobasic sodium phosphate is widely used as an excipient in parenteral, oral, and topical pharmaceutical formulations.Phosphate occurs extensively in the body and is involved in many physiological processes since it is the principal anion of intracellular fluid. Most foods contain adequate amounts of phosphate, making hypophosphatemia virtually unknown except in certain disease states or in patients receiving total parenteral nutrition. Treatment is usually by the oral administration of up to 100 mmol of phosphate daily.
Approximately two-thirds of ingested phosphate is absorbed from the gastrointestinal tract, virtually all of it being excreted in the urine, and the remainder is excreted in the feces. Excessive administration of phosphate, particularly intravenously, rectally, or in patients with renal failure, can cause hyperphosphatemia that may lead to hypocalcemia or other severe electrolyte imbalances. Adverse effects occur less frequently following oral consumption, although phosphates act as mild saline laxatives when administered orally or rectally (2–4 g of monobasic sodium phosphate in an aqueous solution is used as a laxative). Consequently, gastrointestinal disturbances including diarrhea, nausea, and vomiting may occur following the use of monobasic sodium phosphate as an excipient in oral formulations. However, the level of monobasic sodium phosphate used as an excipient in a pharmaceutical formulation is not usually associated with adverse effects.
LD50 (rat, IM): 0.25 g/kg(10)
LD50 (rat, oral): 8.29 g/kg
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Monobasic sodium phosphate is chemically stable, although it is slightly deliquescent. On heating at 100°C, the dihydrate loses all of its water of crystallization. On further heating, it melts with decomposition at 205℃, forming sodium hydrogen pyrophosphate, Na2H2P2O7. At 250℃ it leaves a final residue of sodium metaphosphate, NaPO3.Aqueous solutions are stable and may be sterilized by autoclaving.
Monobasic sodium phosphate should be stored in an airtight container in a cool, dry place.
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Monobasic sodium phosphate is an acid salt and is therefore generally incompatible with alkaline materials and carbonates; aqueous solutions of monobasic sodium phosphate are acidic and will cause carbonates to effervesce.Monobasic sodium phosphate should not be administered concomitantly with aluminum, calcium, or magnesium salts since they bind phosphate and could impair its absorption from the gastrointestinal tract. Interaction between calcium and phosphate, leading to the formation of insoluble calcium phosphate precipitates, is possible in parenteral admixtures.
Regulatory Status
GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (injections; infusions; ophthalmic, oral, topical, and vaginal preparations). Included in nonparenteral and parenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.?? ??? ????? ?? ?? ? ???
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