Leuprolide Acetate EP Impurity A

Product Name Leuprolide Acetate EP Impurity A
CAT No. CS-P-05062
CAS No. 62621-13-0
Category Impurities
Stock IN-Stock
Mol. Wt. 1209.42 g/mol
Mol. For. C₅₉H₈₄N₁₆O₁₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Purity 95%
Therapeutic Anti-Cancer / Oncology
Canonical Smiles CCNC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC2=CC=C(C=C2)O)NC(=O)C(CO)NC(=O)C(CC3=CNC4=CC=CC=C43)NC(=O)C(CC5=CN=CN5)NC(=O)C6CCC(=O)N6
InchIKey GFIJNRVAKGFPGQ-WQVASJQXSA-N
Inchl InChI=1S/C59H84N16O12/c1-6-63-57(86)48-14-10-22-75(48)58(87)41(13-9-21-64-59(60)61)68-51(80)42(23-32(2)3)69-52(81)43(24-33(4)5)70-53(82)44(25-34-15-17-37(77)18-16-34)71-56(85)47(30-76)74-54(83)45(26-35-28-65-39-12-8-7-11-38(35)39)72-55(84)46(27-36-29-62-31-66-36)73-50(79)40-19-20-49(78)67-40/h7-8,11-12,15-18,28-29,31-33,40-48,65,76-77H,6,9-10,13-14,19-27,30H2,1-5H3,(H,62,66)(H,63,86)(H,67,78)(H,68,80)(H,69,81)(H,70,82)(H,71,85)(H,72,84)(H,73,79)(H,74,83)(H4,60,61,64)/t40-,41-,42-,43+,44-,45-,46-,47+,48-/m0/s1
IUPAC (2S)-N-[(2S)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-5-(diaminomethylideneamino)-1-[(2S)-2-(ethylcarbamoyl)pyrrolidin-1-yl]-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]-5-oxopyrrolidine-2-carboxamide
Controlled No
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Leuprolide Acetate EP Impurity A is a synthetic peptide that is commonly used as a reference standard in various analytical applications. It is a byproduct of the manufacturing process of Leuprolide Acetate, a medication used in the treatment of prostate cancer, endometriosis, and other hormone-related conditions. The chemical formula of Leuprolide Acetate EP Impurity A is C66H87N17O15S2, and it has a molecular weight of 1465.57 g/mol. The peptide is composed of 17 amino acids and contains two disulfide bonds. Leuprolide Acetate EP Impurity A is primarily used for the identification and quantification of impurities in Leuprolide Acetate formulations. It is also used in the development and validation of analytical methods for the determination of Leuprolide Acetate and its related substances. The purity of Leuprolide Acetate EP Impurity A is crucial for its use as a reference standard in analytical testing. It is typically supplied as a white lyophilized powder and should be stored in a cool, dry place to maintain its stability. Overall, Leuprolide Acetate EP Impurity A is an essential tool for the accurate analysis of Leuprolide Acetate formulations and plays a vital role in ensuring the safety and efficacy of this important medication.

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