Tadalafil EP Impurity A

Product Name Tadalafil EP Impurity A
Alternate Names Tadalafil Impurities, Impurities of Tadalafil
CAT No. CS-O-08227
CAS No. 171596-27-3
Category Impurities
Stock IN-Stock
Mol. Wt. 389.4 g/mol
Mol. For. C22H19N3O4
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Tadalafil
Purity 95%
Therapeutic Erectile dysfunction
Smileys O=C(N1[C@@H](C2=C(C[C@]1(C3=O)[H])C4=CC=CC=C4N2)C5=CC6=C(C=C5)OCO6)CN3C
Canonical Smiles CN1CC(=O)N2C(C1=O)CC3=C(C2C4=CC5=C(C=C4)OCO5)NC6=CC=CC=C36
InchIKey WOXKDUGGOYFFRN-HRAATJIYSA-N
Inchl InChI=1S/C22H19N3O4/c1-24-10-19(26)25-16(22(24)27)9-14-13-4-2-3-5-15(13)23-20(14)21(25)12-6-7-17-18(8-12)29-11-28-17/h2-8,16,21,23H,9-11H2,1H3/t16-,21+/m0/s1
IUPAC (2R,8S)-2-(1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.03,8.011,16]heptadeca-1(10),11,13,15-tetraene-4,7-dione
Controlled No
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Tadalafil EP Impurity A is a chemical substance that is commonly used in the pharmaceutical industry for the development of drugs that treat erectile dysfunction, pulmonary arterial hypertension, and other similar medical conditions. This impurity is often used as a reference standard in the quality control of tadalafil formulations. Tadalafil EP Impurity A is a highly purified substance that is obtained through various purification processes, including chromatography and crystallization. It is a white to off-white crystalline powder that has a molecular formula of C22H19N3O4 and a molecular weight of 393.4 g/mol. Chemically, Tadalafil EP Impurity A is a structural isomer of tadalafil, which is a phosphodiesterase type 5 (PDE5) inhibitor. This impurity shares the same core structure as tadalafil, but with subtle differences in the arrangement of its functional groups. When used as a reference standard, Tadalafil EP Impurity A is typically analyzed using various analytical techniques, such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and nuclear magnetic resonance (NMR) spectroscopy. These techniques are used to confirm the identity and purity of the impurity, as well as to ensure that it meets the necessary quality standards for use in pharmaceutical formulations. Overall, Tadalafil EP Impurity A is a vital component in the development and quality control of tadalafil-based drugs, and its chemical properties and usage are critical for ensuring the safety and efficacy of these medications.

Related Compounds

Tadalafil Impurity D (S,S)Isomer | Tadalafil EP Impurity C | Tadalafil Ketolactam | Tadalafil Related Compound 2 | Tadalafil impurity F | Tadalafil Impurity 7 | N-Desmethyl Tadalafil | Tadalafil chloroacetyl Impurity | Tadalafil impurity E | N-Ethyl tadalafil | Tadalafil EP Impurity I | Tadalafil Impurity 13 | Tadalafil Acid Impurity (HCl) | N-Nitroso Chloropretadalafil | Tadalafil EP Impurity D | Tadalafil Impurity 5 | Tadalafil Impurity 4 | Tadalafil impurity G | Tadalafil EP Impurity B | Amino Tadalafil | Tadalafil EP Impurity I | Tadalafil Impurity 3 | Tadalafil Impurity 4 | Chloropropanoylpretadalafil | Tadalafil EP Impurity C hydrochloride trihydrate | Chloropretadalafil (S,S-isomer) | Tadalafil Nitroso Impurity 1 | Tadalafil EP Impurity I (Hydrate) | Tadalafil Impurity H | Tadalafil Impurity 6 | Tadalafil Impurity 10 | Tadalafil Hydroxypiperidone | N-nitroso Tadalafil | Tadalafil Impurity 14 | Tadalafil Impurity 37 | Tadalafil Desmethylene Impurity |

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