Sitagliptin EP Impurity E
| Product Name | Sitagliptin EP Impurity E |
|---|---|
| Alternate Names | Sitagliptin Impurities, Impurities of Sitagliptin |
| CAT No. | CS-O-08191 |
| CAS No. | 936630-57-8 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 233.19 g/mol |
| Mol. For. | C₁₀H₁₀F₃NO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Sitagliptin |
| Purity | 95% |
| Therapeutic | Antibiotics |
| Smileys | FC1=C(F)C=C(F)C(C[C@@H](N)CC(O)=O)=C1 |
| Canonical Smiles | C1=C(C(=CC(=C1F)F)F)CC(CC(=O)O)N |
| InchIKey | KEFQQJVYCWLKPL-ZCFIWIBFSA-N |
| Inchl | InChI=1S/C10H10F3NO2/c11-7-4-9(13)8(12)2-5(7)1-6(14)3-10(15)16/h2,4,6H,1,3,14H2,(H,15,16)/t6-/m1/s1 |
| IUPAC | (3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic acid |
| 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 |
Sitagliptin EP Impurity E is a chemical compound that is used in the pharmaceutical industry as a reference standard for the development and quality control of Sitagliptin, a medication used to treat type 2 diabetes. It is also known as (R)-3-amino-1-(3-(trifluoromethyl)phenyl)-4-(2,4,5-trifluorophenyl)butan-1-one.
Sitagliptin EP Impurity E is a chiral compound, meaning that it has two mirror-image forms, known as enantiomers. The (R)-enantiomer of Sitagliptin EP Impurity E is the active form that is used in the body, while the (S)-enantiomer is inactive. The purity of Sitagliptin EP Impurity E is important in ensuring the quality and efficacy of Sitagliptin.
The chemical formula of Sitagliptin EP Impurity E is C16H12F6NO, and its molecular weight is 361.26 g/mol. It is a white crystalline powder that is soluble in organic solvents such as methanol and acetonitrile.
In conclusion, Sitagliptin EP Impurity E is a critical reference standard used in the development and quality control of Sitagliptin, a medication used to treat type 2 diabetes. Its chemical and physical properties, including its chiral nature and purity, are important considerations in ensuring the quality and efficacy of Sitagliptin.
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Related Compounds
Sitagliptin impurity R | Sitagliptin Enamine Impurity | Sitagliptin tartrate hemihydrate | Sitagliptin impurity D | Sitagliptin impurity L | Sitagliptin impurity I | Sitagliptin N-formyl impurity | Sitagliptin Amino Acid Impurity | SITAGLIPTIN FORMIC ACID ADDUCT | Sitagliptin Impurity 93 | Sitagliptin impurity J | Sitagliptin Dioxo SODIUM Impurity | Sitagliptin Impurity 28 | Nitroso Sitagliptin | N-Nitroso Sitagliptin Fumarate Adduct | Sitagliptin impurity N | Sitagliptin Fumarate Adduct | Sitagliptin Amide impurity | Sitagliptin Triazecine Analog-D4 | Sitagliptin FP Impurity D | Sitagliptin impurity K | Sitagliptin Impurity 84 | Sitagliptin N-Acetyl Impurity | Sitagliptin EP Impurity A | Sitagliptin Styrylacetyl Analogue | Sitagliptin Impurity H | Sitagliptin Phosphate Hydrate | Sitagliptin EP Impurity C | Sitagliptin impurity H Hydrochloride | Sitagliptin Triazecine Analog | Sitagliptin nitroso impurity | Rac-Sitagliptin Triazecine Analog | Sitagliptin impurity F | Sitagliptin Impurity 62 | Sitagliptin isopropyl ester impurity | Sitagliptin FP Impurity D (Z)-Isomer | Sitagliptin phosphate (Monohydrate) | Oxo Sitagliptin | Sitagliptin impurity G | Sitagliptin impurity-4 | Sitagliptin EP Impurity C Phosphate | Sitagliptin Impurity 39 | Sitagliptin dioxo impurity | Sitagliptin EP Impurity C | Sitagliptin Impurity 61 | Sitagliptin Acid Pivaloyl impurity | Sitagliptin Impurity 40 | Sitagliptin hydroxylimine impurity | Sitagliptin impurity T | Sitagliptin Pyrazine Impurity |