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Agency
BP
JPE
Ph. Eur.
USP
Quality Level
product line
EMPROVE® ESSENTIAL
form
fine powder
particle size
(see specification)
pH
5.2-8.0 (20 °C, 50 g/L in H2O)
mp
884 °C (lit.)
density
2.68 g/mL at 25 °C (lit.)
application(s)
liquid formulation
pharmaceutical
solid formulation
storage temp.
2-30°C
SMILES string
[Na+].[Na+].[O-]S([O-])(=O)=O
InChI
1S/2Na.H2O4S/c;;1-5(2,3)4/h;;(H2,1,2,3,4)/q2*+1;/p-2
InChI key
PMZURENOXWZQFD-UHFFFAOYSA-L
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This Item | 1.28211 | 1.28225 | 798592 |
|---|---|---|---|
| application(s) liquid formulation | application(s) pharmaceutical | application(s) pharma/biopharma processes | application(s) - |
| agency BP, Ph. Eur., JPE, USP | agency BP, ChP, Ph. Eur., USP | agency BP, ChP, Ph. Eur., USP | agency - |
| form fine powder | form solid | form solid | form granular, powder |
| density 2.68 g/mL at 25 °C (lit.) | density 2.68 g/cm3 at 25 °C, 2.68 g/mL at 25 °C (lit.) | density 2.68 g/cm3 at 25 °C, 2.68 g/mL at 25 °C (lit.) | density 2.68 g/mL at 25 °C (lit.) |
| product line EMPROVE® ESSENTIAL | product line EMPROVE® ESSENTIAL | product line EMPROVE® EXPERT | product line Redi-Dri™ |
| particle size (see specification) | particle size - | particle size - | particle size - |
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
Sodium sulfate anhydrous fine powder Emprove® Essential is mainly used in highly regulated pharmaceutical applications.
Legal Information
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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