Leuprolide Acetate EP Impurity F

Product Name Leuprolide Acetate EP Impurity F
Alternate Names Leuprolide Impurities, Impurities of Leuprolide
CAT No. CS-P-05067
CAS No. 1872435-00-1
Category Impurities
Stock IN-Stock
Mol. Wt. 1209.40 g/mol
Mol. For. C₅₉H₈₄N₁₆O₁₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Leuprolide
Purity Not less than 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.C(=O)(C(F)(F)F)O
InchIKey VIKVLAJTEHLRFY-QHQZFDTASA-N
Inchl InChI=1S/C59H84N16O12.C2HF3O2/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;3-2(4,5)1(6)7/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);(H,6,7)/t40-,41-,42-,43+,44-,45-,46+,47+,48-;/m0./s1
IUPAC (2S)-N-[(2R)-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;2,2,2-trifluoroacetic acid
Controlled No
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Leuprolide Acetate EP Impurity F is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard in the quality control and analysis of Leuprolide Acetate, a medication used to treat certain types of cancer and endometriosis. This impurity is a byproduct of the manufacturing process of Leuprolide Acetate and is considered to be an unwanted substance that needs to be removed during the production process. Leuprolide Acetate EP Impurity F is also known as N-Acetyl-Leu-Lys(3-pyridyl)-D-Ala-Leu-Lys-(4-pyridyl)-D-Ala-Lys-Lys- N-6-(4,4-dimethyl-2,6-dioxocyclohex-1-yl)-L-Lys-L-Leu-L-Arg-Pro-NH2 acetate salt. It has a molecular weight of 1877.1 g/mol and its chemical formula is C88H128N28O21. This compound is a synthetic peptide that contains eleven amino acid residues and two pyridine rings. The usage of Leuprolide Acetate EP Impurity F in the pharmaceutical industry is crucial as it helps ensure the safety and efficacy of Leuprolide Acetate. Its chemical information is also important in identifying and quantifying impurities in the drug product. The standardization of the manufacturing process of Leuprolide Acetate with the help of reference standards like Leuprolide Acetate EP Impurity F ensures that the final product is of high quality and free from harmful impurities.

Related Compounds

Pyr-His-Trp-Ser-Tyr-OMe | Pyr-His-Trp-Ser-Tyr-OH | Leuprolide Acetate Impurity J | Leuprolide Acetate EP Impurity E | Des-pGlu-Leuprolide | Leuprolide Acetate EP Impurity D TFA salt | Leuprolide Impurity 1 | Des-Pyr-Leuprolide | D-Ser-leuprolide | leuprolide 2-oxo-Trp impurity | Leuprolide Acetate EP Impurity I | L-Leu6-Leuprolide trifluoroacetate salt | Leuprolide Acetate EP Impurity J | Leuprorelin - Impuritry G | Des-1,2,3-Leuprolide | D-Leu-Leu-Arg-Pro-NHEt | Leuprolide Acetate EP Impurity K | L-Leu- leuprolide |

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