Cetirizine EP impurity A
| Product Name | Cetirizine EP impurity A |
|---|---|
| Alternate Names | Cetirizine Impurities, Impurities of Cetirizine |
| CAT No. | CS-O-31588 |
| CAS No. | 303-26-4 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 286.80 g/mol |
| Mol. For. | C₁₇H₁₉ClN₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Cetirizine |
| Purity | >98% |
| Therapeutic | Antihistamine |
| Smileys | C1CN(CCN1)C(C2=CC=CC=C2)C3=CC=C(C=C3)Cl |
| 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 |
Cetirizine EP impurity A, also known as 1,2,3,4-tetrahydrocetirizine, is a chemical compound that is commonly used as an impurity reference standard in the pharmaceutical industry. It is a byproduct of the synthesis of cetirizine, which is an antihistamine drug used to treat allergies and hives.
Cetirizine EP impurity A is typically used in quality control and analytical testing of cetirizine drug formulations. Its chemical structure is closely related to cetirizine, containing a tetrahydrocyclopentapyrazine ring system with a hydroxyl group at the 4-position. The impurity is typically present in small amounts in cetirizine drug formulations, and its presence can affect the purity and potency of the drug.
In terms of its chemical properties, Cetirizine EP impurity A is a white to off-white solid that is soluble in water and organic solvents. Its melting point is approximately 140-145°C. The compound is stable under normal storage conditions and is not considered to be hazardous or toxic.
Overall, Cetirizine EP impurity A is an important reference standard in the pharmaceutical industry, used to ensure the purity and potency of cetirizine drug formulations. Its chemical properties and usage make it a vital component in the production and quality control of cetirizine-based medications.
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Related Compounds
Cetirizine Dimer dihydrochloride | Cetirizine 3-Chloro | Deschloro Cetirizine Dihydrochloride | Cetirizine Amide | tert-Butyl Cetirizine | Cetirizine S-Isomer | Cetirizine Methyl Ester Dihydrochloride | Cetirizine Polyethylene Glycol (PEG) Ester | Cetirizine Impurity E Sodium Salt | Cetirizine S-Isomer di HCl | Cetirizine EP impurity B | Cetirizine USP Related Compound A | Cetirizine impurity B di Hydrochloride | Cetirizine Impurity BHA | Levocetirizine Ethyl ester impurity | Cetirizine Glycerol Ester | Cetirizine Lactose Ester(Technical Grade) (α/β-mixture, mixture of diastereomers) | Levocetirizine Lactose ester | Cetirizine 1-[(4-Chlorophenyl)phenylmethyl]piperazine Amide | Cetirizine EP Impurity B Ethyl Ester | Cetirizine EP Impurity D Dihydrochloride | Cetirizine Impurity G | Levocetirizine benzyl | Cetirizine Impurity G | Cetirizine USP Related Compund A (2HCl salt) | Levocetirizine Impurity 1 | Cetirizine Sorbitol Ester Impurity Hydrochloride | Cetirizine Impurity BHT | N-Tosyl Cetirizine EP impurity A | Cetirizine Impurity 7 | Cetirizine EP Impurity E Di Hydrochloride | Cetirizine 3-Chloro Impurity | Cetirizine Impurity D | Cetirizine Glycerol Ester Impurity Hydrochloride | Cetirizine EP Impurity E | Cetirizine Impurity C Dihydrochloride | Cetirizine Lactose Ester HCl salt | Cetirizine Amide Dihydrochloride | Cetirizine EP Impurity C | Cetirizine EP Impurity F | Cetirizine Impurity 15 DiHCl |