Sitagliptin FP Impurity D

Product Name Sitagliptin FP Impurity D
Alternate Names Sitagliptin Impurities, Impurities of Sitagliptin
CAT No. CS-AQ-00108
CAS No. 1253056-18-6
Category Impurities
Stock IN-Stock
Mol. Wt. 390.28 g/mol
Mol. For. C₁₆H₁₂F₆N₄O
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Sitagliptin
Purity 95%
Therapeutic Antibiotics
Smileys C1CN2C(=NN=C2C(F)(F)F)CN1C(=O)C=CCC3=CC(=C(C=C3F)F)F
Canonical Smiles C1CN2C(=NN=C2C(F)(F)F)CN1C(=O)C=CCC3=CC(=C(C=C3F)F)F
InchIKey QSSHJJFVCWMIKH-HNQUOIGGSA-N
Inchl InChI=1S/C16H12F6N4O/c17-10-7-12(19)11(18)6-9(10)2-1-3-14(27)25-4-5-26-13(8-25)23-24-15(26)16(20,21)22/h1,3,6-7H,2,4-5,8H2/b3-1+
IUPAC (E)-1-[3-(trifluoromethyl)-6,8-dihydro-5H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl]-4-(2,4,5-trifluorophenyl)but-2-en-1-one
Controlled No
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Sitagliptin FP Impurity D is a chemical compound that is commonly used in the pharmaceutical industry. It is an impurity of Sitagliptin, a medication used to treat type 2 diabetes. The impurity is formed during the manufacturing process of Sitagliptin and is usually found in small quantities in the final product. The usage of Sitagliptin FP Impurity D is primarily for analytical purposes. It is used as a reference material for the identification and quantification of Sitagliptin in pharmaceutical formulations. It is also used in the development and validation of analytical methods for Sitagliptin analysis. In terms of chemical information, Sitagliptin FP Impurity D is a heterocyclic compound with a molecular weight of 435.49 g/mol. Its chemical formula is C20H28N8O2S2. The impurity is usually identified and quantified using high-performance liquid chromatography (HPLC) coupled with mass spectrometry (MS). It is important to note that the presence of Sitagliptin FP Impurity D in Sitagliptin formulations should be controlled and kept at low levels, as its presence may impact the efficacy and safety of the medication. Therefore, the analytical methods used for the detection and quantification of the impurity are crucial in ensuring the quality of Sitagliptin formulations.

Related Compounds

Sitagliptin EP Impurity C | Rac-Sitagliptin Triazecine Analog | Sitagliptin N-formyl impurity | Sitagliptin Fumarate Adduct | Sitagliptin Styrylacetyl Analogue | N-Nitroso Sitagliptin Fumarate Adduct | Sitagliptin impurity I | Sitagliptin Impurity 84 | Sitagliptin impurity F | Sitagliptin Pyrazine Impurity | Sitagliptin impurity K | Sitagliptin impurity L | Sitagliptin isopropyl ester impurity | Sitagliptin Impurity 61 | Sitagliptin impurity N | Sitagliptin Impurity 93 | Sitagliptin phosphate (Monohydrate) | Sitagliptin EP Impurity A | Sitagliptin EP Impurity C Phosphate | Sitagliptin tartrate hemihydrate | Oxo Sitagliptin | Sitagliptin impurity R | Sitagliptin Amide impurity | Sitagliptin N-Acetyl Impurity | Sitagliptin FP Impurity D (Z)-Isomer | Sitagliptin impurity G | Sitagliptin Dioxo SODIUM Impurity | Sitagliptin Phosphate Hydrate | Sitagliptin Acid Pivaloyl impurity | Sitagliptin Impurity 28 | Sitagliptin impurity T | Sitagliptin impurity H Hydrochloride | Nitroso Sitagliptin | Sitagliptin impurity D | Sitagliptin Triazecine Analog-D4 | Sitagliptin Triazecine Analog | Sitagliptin impurity J | Sitagliptin EP Impurity C | SITAGLIPTIN FORMIC ACID ADDUCT | Sitagliptin Amino Acid Impurity | Sitagliptin impurity-4 | Sitagliptin hydroxylimine impurity | Sitagliptin EP Impurity E | Sitagliptin Impurity 40 | Sitagliptin Impurity 62 | Sitagliptin dioxo impurity | Sitagliptin nitroso impurity | Sitagliptin Enamine Impurity | Sitagliptin Impurity 39 | Sitagliptin Impurity H |

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