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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Our well-equipped facilities and excellent quality control throughout all stages of production enables us to guarantee total customer satisfaction for Manufacturer for Sofosbuvir - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai , The product will supply to all over the world, such as: France, Honduras, Kyrgyzstan, Our products are exported worldwide. Our customers are always satisfied with our reliable quality, customer-oriented services and competitive prices. Our mission is "to continue to earn your loyalty by dedicating our efforts to the constant improvement of our products and services in order to ensure the satisfaction of our end-users, customers, employees, suppliers and the worldwide communities in which we cooperate".
By Henry from Greece - 2018.07.26 16:51
We have been cooperated with this company for many years, the company always ensure timely delivery ,good quality and correct number, we are good partners.
By Karen from luzern - 2018.06.30 17:29
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