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 Amide Dihydrochloride | Cetirizine S-Isomer | Levocetirizine Lactose ester | Cetirizine S-Isomer di HCl | Cetirizine Glycerol Ester Impurity Hydrochloride | Cetirizine 1-[(4-Chlorophenyl)phenylmethyl]piperazine Amide | Cetirizine Impurity G | Cetirizine EP impurity B | Cetirizine Impurity C Dihydrochloride | Cetirizine EP Impurity B Ethyl Ester | Cetirizine USP Related Compund A (2HCl salt) | Cetirizine Dimer dihydrochloride | Cetirizine Impurity E Sodium Salt | Cetirizine Lactose Ester(Technical Grade) (α/β-mixture, mixture of diastereomers) | Cetirizine Impurity G | Levocetirizine Impurity 1 | Cetirizine EP Impurity C | Cetirizine Impurity BHA | Cetirizine 3-Chloro Impurity | Cetirizine Sorbitol Ester Impurity Hydrochloride | Cetirizine Impurity BHT | Cetirizine EP Impurity E | Deschloro Cetirizine Dihydrochloride | Cetirizine Amide | Cetirizine Impurity D | Cetirizine EP Impurity F | Cetirizine Lactose Ester HCl salt | Levocetirizine benzyl | Cetirizine Polyethylene Glycol (PEG) Ester | Levocetirizine Ethyl ester impurity | tert-Butyl Cetirizine | Cetirizine USP Related Compound A | Cetirizine Impurity 15 DiHCl | Cetirizine 3-Chloro | N-Tosyl Cetirizine EP impurity A | Cetirizine EP Impurity E Di Hydrochloride | Cetirizine impurity B di Hydrochloride | Cetirizine Impurity 7 | Cetirizine EP Impurity D Dihydrochloride | Cetirizine Methyl Ester Dihydrochloride | Cetirizine Glycerol Ester |