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Agency
BP
ChP
JP
Ph. Eur.
USP
Quality Level
product line
EMPROVE® EXPERT
form
solid
autoignition temp.
410 °C
pH
5-7 (20 °C, 100 g/L in H2O)
bp
290-295 °C/4 hPa
mp
167-170 °C (lit.)
solubility
213 g/L
application(s)
liquid formulation
ophthalmics
parenterals
pharma/biopharma processes
pharmaceutical
semi-solid formulation
solid formulation
storage temp.
2-25°C
SMILES string
OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
InChI
1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4-,5-,6-/m1/s1
InChI key
FBPFZTCFMRRESA-KVTDHHQDSA-N
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This Item | 1.05980 | 1.37162 | 1.05988 |
|---|---|---|---|
| application(s) liquid formulation | application(s) liquid formulation | application(s) liquid formulation | application(s) liquid formulation |
| agency BP, JP, USP, ChP, Ph. Eur. | agency BP, ChP, JP, Ph. Eur., USP | agency BP, ChP, JP, Ph. Eur., USP | agency BP, JP, Ph. Eur., USP |
| form solid | form fine powder | form solid | form fine powder |
| product line EMPROVE® EXPERT | product line EMPROVE® ESSENTIAL | product line EMPROVE® EXPERT | product line EMPROVE® ESSENTIAL |
| solubility 213 g/L | solubility 213 g/L | solubility 213 g/L | solubility - |
| autoignition temp. 410 °C | autoignition temp. 410 °C | autoignition temp. - | autoignition temp. 410 °C |
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
Due to its low microbial and endotoxin limits, D(-)-Mannitol Emprove® Expert is especially suitable for high-risk applications.
Biochem/physiol Actions
Legal Information
related product
used together
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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