Manufacturer for Sofosbuvir - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai
Manufacturer for Sofosbuvir - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai Detail:
| Product name | Valganciclovir hydrochloride |
| Synonyms | L-Valine,2-[(2-aMino-1,6-dihydro-6-oxo-9H-purin-9-yl)Methoxy]-3-hydroxypropylester,hydrochloride(1:1);2-[(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy]-3-hydroxypropyl(2S)-2-amino-3-methylbutanoatehydChemicalbookrochloridehydrate;L-Valine,2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]-3-hydroxypropylester,monohydrochloridehydrate |
| CAS No. | 175865-59-5 |
| Appearance | White or off-white crystalline powder |
| Molecular Formula | C14H22N6O5.HCl |
| Molecular Weight | 390.83 |
| Usage | Pharmaceutical Grade or Research purpose |
| Packing | As per your request |
| Storage | Preserve in tight,light-resistant containers in a cool place |
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Valganciclovir hydrochloride Cas: 175865-59-5 |
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Items |
Standard |
Results |
| Appearance | White or off-white crystalline powder | white powder |
| Identification | Infrared Absorption:Corresponds to that of reference standardUltraviolet Absorption:Corresponds to that of reference standardA solution in water (1 in 20) meets the requirements of the tests for Chloride | Complies Complies
Complies |
| Isopropyl alcohol | ≤1.0% | 0.13% |
| Water | ≤8.0% | 4.5% |
| Heavy metals | ≤20ppm | Complies |
| Pd | ≤10ppm | ＜10ppm |
| Residue on ignition | ≤0.1% | 0.02% |
| Related impurities | Valganciclovir: /Ganciclovir: ≤1.5%Guanine: ≤1.5%
Methoxymethylguanine: ≤0.3% Isovalganciclovir: ≤0.5% Monoacetoxyganciclovir: ≤0.15% Bis-valine easter of ganciclovir: ≤0.1% Homologue of valganciclovir: ≤0.25% Imp H: ≤0.1% Imp I: ≤0.1% Ganciclovir monopropionate: ≤0.15% Valganciclovir dimer (stereoisomer A): ≤0.1% Valganciclovir dimer (stereoisomer B): ≤0.1% Valganciclovir dimer (stereoisomer C): ≤0.1% Single other identified impurity: ≤0.1% Total other identified impurity: ≤0.1% Ganciclovir mono-N-methyl valinate (Test 2):≤0.3% Single unidentified impurity (Test 1 and 2): ≤0.1 % Total unidentified impurity (Test 1 and 2): ≤0.25% Total impurities (Test 1 and Test 2): ≤3.0 |
/0.02%0.01%
0.03% 0.02% ND 0.04% 0.01% 0.01% 0.004% ND ND ND ND Max 0.04% 0.04%
0.02% Max 0.02% 0.13% 0.78% |
| Diastereomer ratio | 45:55 to 55:45 | 54:46 |
| Enantiomeric purity of valganciclovir | ≥97.0% | 99.9% |
| HPLC assay | 97.0%～102.0% | 98.8% |
| Conclusion: complies with USP40. | ||
Company Information
√ Management layer’s full experience in factory and skilled technicians followers; √ Quality is always our top consideration, Strict QC system; √ 11 years experienced exporting sales team; √ Independent R&D lab; √ Two signed long term GMP workshops; √ Rich resources of plenty idle factories for customized project; √ High Efficiency working team with consistent path.
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With the "Client-Oriented" business philosophy, a rigorous quality control system, advanced manufacturing equipment and a strong R&D team, we always provide high quality products, excellent services and competitive prices for Manufacturer for Sofosbuvir - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai , The product will supply to all over the world, such as: Miami, Iran, Australia, We seriously promise that we provide all the customers with the best quality products, the most competitive prices and the most prompt delivery. We hope to win a resplendent future for customers and ourselves.
By Olga from Cannes - 2018.11.02 11:11
This supplier's raw material quality is stable and reliable, has always been in accordance with the requirements of our company to provide the goods that quality meet our requirements.
By Bess from Philadelphia - 2018.06.05 13:10
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