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Paclitaxel Idebenone & Citalopram Hydrobromide
 Paclitaxel Idebenone & Citalopram Hydrobromide |
Product Description
Paclitaxel
Test Standard Results
Appearance White to off-whitecrystalline powder White crystalline powder
Identification Infrared Absorption Conform
HPLC Conform
Solubility Insoluble in water, soluble I alcohol. Conform
Assay Not less than 97.0 bercen1. And not more than102.0 percent of calculated on the anhydrous, solvent free badis. 99.5%
Water NMT 4.0% 0.96%
Specific Rotation -49.0~ -55.0(at 20) -49.4
Residue on Ignition NMT 0.2% 0.12%
Heavy Metals NMT 0.002% NMT 0.002%
Microbial limits Total aerobic microbialNMT 100cfu/g.
Absence of Staphaureusn aureus,
Pseudomonas aeruginos, Salmonella species,
And Escherichia coli. Conform
Bacterial endotoxins 0.4EU/mg 0.2EU/mg
Related Compounds
Conclusion It conforms to enterprise standard.
Docetaxel
[Product type]: Pharmaceutical raw material
[English name]: Docetaxel
[Molecular formula]: C43H53NO14
[Molecular weight]: 807.88
[C A S]: 114977-28-5
[Quality standard]: Enterprise Standard
[Content]: e99.0%
[Appearance]: White powder
[Function and use]: The mechanism strengthens the microtubule protein polymerization and suppresses depolimerization causing stable non-functionality and thus destructing cell's mitosis.
[Usage]: Pharmaceutical raw material, be for preparation's using only
[Packing]: 200g/tin, 100g/tin
[Storage]: Shade, airtight and cold place.
Nystatin: USP28
| Company: | HongKong Henry Industry Co., Limited |
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