Good Quality Anti-Viral Drugs - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai
Good Quality Anti-Viral Drugs - 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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We know that we only thrive if we can easily guarantee our combined cost competiveness and high-quality advantageous at the same time for Good Quality Anti-Viral Drugs - USP 175865-59-5 Valganciclovir hydrochloride for Antiviral – Yibai , The product will supply to all over the world, such as: Algeria, Naples, Ottawa, Our company has already have pass the ISO standard and we are fully respect our customer 's patents and copyrights. If the customer provides their own designs, We will guarantee that they will be the only one can have that products. We hoping that with our good products can bring our customers a great fortune.
By Esther from Denmark - 2017.02.28 14:19
This enterprise in the industry is strong and competitive, advancing with the times and develop sustainable, we are very pleased to have a opportunity to cooperate!
By Polly from New Zealand - 2017.09.26 12:12
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