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Agency
BP
ChP
USP
质量水平
产品线
EMPROVE® ESSENTIAL
表单
solid
pH值(酸碱度)
4.1-4.5 (25 °C, 50 g/L in H2O)
溶解性
850 g/L
密度
2.04 g/cm3 at 20 °C
应用
liquid formulation
ophthalmics
pharmaceutical
semi-solid formulation
solid formulation
储存温度
15-25°C
SMILES字符串
[Na+].[H]O[H].OP(O)([O-])=O
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此商品 | 31277 | 202185 | V800125 |
---|---|---|---|
form solid | form solid | form crystals or chunks | form solid |
assay ≥97%, 97.0-102.0% (KT) | assay 98-102% | assay - | assay ≥98% |
Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level - |
vapor pressure 40 mmHg ( 0 °C) | vapor pressure 40 mmHg ( 0 °C) | vapor pressure 40 mmHg ( 0 °C) | vapor pressure 40 mmHg ( 0 °C) |
anion traces nitrate (NO3-): ≤0.01%, sulfate (SO42-): ≤0.007% | anion traces nitrate (NO3-): ≤100 mg/kg, sulfate (SO42-): ≤50 mg/kg | anion traces - | anion traces sulfate (SO42-): ≤0.03% |
cation traces Ni: ≤0.15%, Zn: ≤0.05%, Fe: ≤0.005% | cation traces Ca: ≤50 mg/kg, Cu: ≤20 mg/kg, Fe: ≤50 mg/kg, K: ≤50 mg/kg, Mg: ≤10 mg/kg, Mn: ≤50 mg/kg, Na: ≤100 mg/kg, Ni: ≤500 mg/kg, Pb: ≤5 mg/kg, Zn: ≤25 mg/kg | cation traces - | cation traces Fe: ≤0.01% |
一般描述
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.
应用
法律信息
储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
什么是Emprove®程序?
Emprove® 程序是提供我们过滤器、一次性组件、制药原料和初始材料的全面而详尽文档的系统。
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