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Agency
DAC
USP
Quality Level
vapor density
4.9 (vs air)
product line
EMPROVE® ESSENTIAL
form
solid
pH
8.7-9.3 (25 °C, 50 g/L in H2O)
mp
48 °C (Elimination of water of crystallisation)
solubility
154 g/L
density
1.68 g/mL at 25 °C (lit.)
application(s)
liquid formulation
ophthalmics
pharmaceutical
semi-solid formulation
solid formulation
storage temp.
2-30°C
SMILES string
O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O
InChI
1S/2Na.H3O4P.7H2O/c;;1-5(2,3)4;;;;;;;/h;;(H3,1,2,3,4);7*1H2/q2*+1;;;;;;;;/p-2
InChI key
PYLIXCKOHOHGKQ-UHFFFAOYSA-L
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This Item | 1.47574 | 8210-OP | 1.37092 |
|---|---|---|---|
| application(s) liquid formulation | application(s) liquid formulation | application(s) - | application(s) liquid formulation |
| agency DAC, USP | agency DAC, USP | agency - | agency DAC, USP |
| form solid | form granular | form crystalline powder (Fine) | form solid |
| density 1.68 g/mL at 25 °C (lit.) | density 1.68 g/mL at 25 °C (lit.) | density 1.68 g/mL at 25 °C (lit.) | density 1.68 g/mL at 25 °C (lit.) |
| product line EMPROVE® ESSENTIAL | product line EMPROVE® EXPERT | product line - | product line EMPROVE® EXPERT |
| solubility 154 g/L | solubility - | solubility - | solubility - |
General description
As part of our Emprove® Program, our raw materials are offered with extensive documentation facilitating compliance of your pharma and biopharma product, full supply chain transparency and risk mitigation. Our SAFC® portfolio of high-quality products for biopharmaceutical and pharmaceutical formulation and production withstands strict quality control procedures and is produced according to applicable cGMP guidelines.
Application
Legal Information
related product
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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