1.02994
Sorbitol
liquid, (sorbitol syrup, crystallizing), EMPROVE® ESSENTIAL, Ph. Eur., BP, USP, E 420
Agency
BP
Ph. Eur.
USP
Quality Level
vapor density
<1 (vs air)
vapor pressure
<0.1 mmHg ( 25 °C)
product line
EMPROVE® ESSENTIAL
form
liquid
viscous liquid
pH
6 (20 °C in H2O, 50% solution)
mp
98-100 °C (lit.)
density
1.3 g/cm3
application(s)
liquid formulation
pharmaceutical
storage temp.
15-25°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-JGWLITMVSA-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
Legal Information
related product
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
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Articles
Medicine for children poses unique formulation challenges compared to adults. Consider developmental physiology and age specifics when designing pharmaceuticals. Quality issues can severely impact patient safety. Therefore, excipient quality, supplier selection, and supply chain security are crucial, particularly for pediatric formulations.
Related Content
Developing formulations specifically for infants and children is increasingly important. To help you master these challenges effectively, we offer an extensive portfolio of well-established high-quality excipients and APIs for pediatric pharmaceutical formulations that are proven in practice.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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