1.37096
D-Mannitol
EMPROVE® EXPERT, Ph. Eur., BP, ChP, JP, USP
Pharma Manufacturing
Synonym(s):
Mannite
About This Item
Recommended Products
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
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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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
Application
also commonly purchased with this product
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Articles
This overview describes the challenges when developing parenteral formulations and strategies to overcome them and reduce the risk of production.
This overview describes the challenges when developing parenteral formulations and strategies to overcome them and reduce the risk of production.
This overview describes the challenges when developing parenteral formulations and strategies to overcome them and reduce the risk of production.
This overview describes the challenges when developing parenteral formulations and strategies to overcome them and reduce the risk of production.
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