Lisinopril EP Impurity E

Product Name Lisinopril EP Impurity E
Alternate Names Lisinopril Impurities, Impurities of Lisinopril
CAT No. CS-O-31221
CAS No. 85955-59-5
Category Impurities
Stock IN-Stock
Mol. Wt. 405.49 g/mol
Mol. For. C21H31N3O5
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Lisinopril
Purity 95%
Therapeutic Anti-Hypertensives
Smileys C1CC(N(C1)C(=O)C(CCCCN)NC(CCC2=CC=CC=C2)C(=O)O)C(=O)O
Canonical Smiles C1CC(N(C1)C(=O)C(CCCCN)NC(CCC2=CC=CC=C2)C(=O)O)C(=O)O
InchIKey RLAWWYSOJDYHDC-KSZLIROESA-N
Inchl InChI=1S/C21H31N3O5/c22-13-5-4-9-16(19(25)24-14-6-10-18(24)21(28)29)23-17(20(26)27)12-11-15-7-2-1-3-8-15/h1-3,7-8,16-18,23H,4-6,9-14,22H2,(H,26,27)(H,28,29)/t16-,17+,18-/m0/s1
IUPAC (2S)-1-[(2S)-6-amino-2-[[(1R)-1-carboxy-3-phenylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid
Controlled No
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Lisinopril is a widely used medication for the treatment of hypertension and congestive heart failure. It belongs to a class of drugs known as ACE inhibitors, which work by relaxing blood vessels, allowing blood to flow more easily through the body. Lisinopril EP Impurity E, also known as (2S)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]pyrrolidine-2-carboxylic acid, is a synthetic intermediate used in the production of Lisinopril. Chemically, Lisinopril EP Impurity E is a white to off-white crystalline powder with a molecular formula of C22H31N3O6. It has a molecular weight of 433.51 g/mol and a melting point of 126-129°C. It is soluble in water, methanol, and ethanol. Lisinopril EP Impurity E is used in the manufacturing process of Lisinopril, and it is important to ensure that the impurity levels in the final product comply with regulatory requirements. The presence of impurities can affect the safety and efficacy of the drug, and therefore, it is essential to monitor and control the impurity levels throughout the manufacturing process. In conclusion, Lisinopril EP Impurity E is a crucial intermediate in the production of Lisinopril, a widely used medication for the treatment of hypertension and congestive heart failure. It is important to ensure that the impurity levels in the final product comply with regulatory requirements to ensure the safety and efficacy of the drug.

Related Compounds

N-(1-Carboxy-3-phenylpropyl)-S-lisinopril (Mixture of diastereomers) | N-Benzyloxycarbonyl Lisinopril Cyclohexyl Analogue Ethyl Methyl Diester | Lisinopril EP impurity C Acetate salt | Lisinopril EP Impurity J | Lisinopril EP Impurity A | Lisinopril Intermediate | N-Benzyloxycarbonyl (S)-Lisinopril Ethyl Methyl Diester | N-trifluoroacetyl Lisinopril Intermediate | Lisinopril-D8 | Lisinopril EP Impurity A | Lisinopril EP Impurity G | Lisinopril-D4 | Lisinopril EP Impurity F | Lisinopril EP Impurity D | Lisinopril Des-Proline dimer - II | N-Benzyloxycarbonyl (S)-Lisinopril | N2-(1-Ethoxycarbonyl-3-oxo-3-phenylpropyl)-N6-trifluoroacetyl-L-lysine | Lisinopril SRS-Diastereomer | Lisinopril EP Impurity I Acetate salt |

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