Potassium Dihydrogen Phosp. Emprove
ürün Kodu : 104871.5000Sorunuz!
104871.5000
Potassium dihydrogen phosphate emprove
Ürün bilgisi | |||
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Grade | Ph Eur,BP,NF,E 340 | ||
Synonyms | mono-Potassium orthophosphate, Potassium biphosphate, Potassium phosphate monobasic | ||
Hill Formula | H2KO4P | ||
Chemical formula | KH2PO4 | ||
HS Code | 2835 24 00 | ||
EC number | 231-913-4 | ||
Molar mass | 136.08 g/mol | ||
CAS number | 7778-77-0 |
Kimyasal ve fiziksel veri | |||
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Solubility | 222 g/l (20 °C) | ||
Melting point | ca.253 °C (decomposition) | ||
Molar mass | 136.08 g/mol | ||
Density | 2.34 g/cm3 (20 °C) | ||
Bulk density | 1200 kg/m3 | ||
pH value | 4.4 (50 g/l, H2O, 20 °C) |
Güvenlik bilgisi | |||
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RTECS | TC6615500 | ||
Storage class | 10 - 13 Other liquids and solids | ||
WGK | WGK 1 slightly water endangering | ||
Disposal | 14 Inorganic salts: Container I. Neutral solutions of the these salts: Container D. Before placing in Container D, check the pH with pH-Universal indicator strips (Item No. 109535). |
Nakliye bilgisi | |||
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Declaration (railroad and road) ADR, RID | Kein Gefahrgut | ||
Declaration (transport by sea) IMDG-Code | No Dangerous Good | ||
Declaration (transport by air) IATA-DGR | No Dangerous Good |
Toksikolojik veri | |||
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LD 50 dermal | LD50 rabbit > 4640 mg/kg |
Spesifikasyonlar | |
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Assay (alkalimetric, calculated on dried substance) | 98.0 - 100.5 % |
Appearance of solution | passes test |
Identity | passes test |
Insoluble substances | ≤ 0.2 % |
pH-value - 1 %; water; 20°C |
4.2 - 4.8 |
- 5 %; water | 4.2 - 4.5 |
Chloride (Cl) | ≤ 0.02 % |
Fluoride (F) | ≤ 0.001 % |
Sulphate (SO4) | ≤ 0.03 % |
Heavy metals (as Pb) | ≤ 0.001 % |
As (Arsenic) | ≤ 0.0002 % |
Cd (Cadmium) | ≤ 0.0001 % |
Fe (Iron) | ≤ 0.001 % |
Hg (Mercury) | ≤ 0.0001 % |
Na (Sodium) | ≤ 0.10 % |
Pb (Lead) | ≤ 0.0004 % |
Residual solvents (Ph.Eur./USP/ICH) | excluded by manufacturing process |
Reducing substances | passes test |
Loss on drying (130 °C) | ≤ 1.0 % |
Residues of metal catalysts or metal reagents acc. to EMEA/CHMP/SWP/4446/2000 are not likely to be present. The product is tested according to all analytical parameters of the declared pharmacopeias including the limits for parenteral use. |