Naproxen EP Impurity H
| Product Name | Naproxen EP Impurity H |
|---|---|
| Alternate Names | Naproxen Impurities, Impurities of Naproxen |
| CAT No. | CS-O-11996 |
| CAS No. | 5111-66-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 174.20 g/mol |
| Mol. For. | C₁₁H₁₀O₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Naproxen |
| Purity | 95% |
| Therapeutic | Anti-Asthma / COPD |
| Smileys | COC1=CC2=CC=C(O)C=C2C=C1 |
| Canonical Smiles | COC1=CC2=C(C=C1)C=C(C=C2)O |
| InchIKey | WWPKRXOOVICNJY-UHFFFAOYSA-N |
| Inchl | InChI=1S/C11H10O2/c1-13-11-5-3-8-6-10(12)4-2-9(8)7-11/h2-7,12H,1H3 |
| IUPAC | 6-methoxynaphthalen-2-ol |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
Naproxen EP Impurity H is a chemical compound that is used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Naproxen drug substances and products. It is a synthetic derivative of Naproxen, a nonsteroidal anti-inflammatory drug (NSAID) that is commonly used for the treatment of pain, inflammation, and fever.
Naproxen EP Impurity H is a white to off-white powder that is soluble in organic solvents such as methanol, acetonitrile, and dichloromethane. Its chemical formula is C14H12O4 and it has a molecular weight of 244.24 g/mol. The compound is stable under normal storage conditions and has a purity level of not less than 98%.
The usage of Naproxen EP Impurity H is critical in ensuring the quality, safety, and efficacy of Naproxen drug products. It is used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC) to determine the presence and level of impurities in Naproxen drug substances and products. The impurities could arise from the synthesis process, degradation, or storage conditions.
In conclusion, Naproxen EP Impurity H is a crucial reference standard in the quality control of Naproxen drug products. Its chemical properties and usage make it an essential component in the pharmaceutical industry.
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Related Compounds
rac Naproxen 2-Propyl Ester | Desmethylnaproxen | Naproxen Impurity 11 | Naproxen Sodium impurity E | Naproxen Impurity K | Naproxen Impurity 6 | Naproxen Impurity 1 | Naproxen Impurity F | Naproxen EP Impurity J | Naproxen chloride | Naproxen 1,2-Propylene Glycol Esters (Mixture of Isomers) | rac-5-Bromo Naproxen | rac-5-Chloro Naproxen | Naproxen Glycerol Ester Impurity |