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关于此项目
Quality Level
agency
BP, ChP, Ph. Eur., USP
vapor pressure
0.11 hPa ( 20 °C)
product line
EMPROVE® EXPERT
assay
≥99.5% (GC)
form
liquid
autoignition temp.
371 °C
expl. lim.
2.4-17.4 % (v/v)
refractive index
n20/D 1.43
pH
6-8 (20 °C, 100 g/L in H2O)
bp
188 °C/1013 hPa
mp
-59 °C
transition temp
flash point 99 °C
density
1.04 g/cm3 at 20 °C
application(s)
liquid formulation
ophthalmics
parenterals
parenterals
pharmaceutical
semi-solid formulation
storage temp.
2-30°C
SMILES string
OC(CO)C
InChI
1S/C3H8O2/c1-3(5)2-4/h3-5H,2H2,1H3
InChI key
DNIAPMSPPWPWGF-UHFFFAOYSA-N
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
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存储类别
10 - Combustible liquids
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
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商品
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.
相关内容
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.