Buspirone EP Impurity E (HCl salt)
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100 % Datengenauigkeit
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0 % Toleranz bei der Produktqualität

Lagerstandorte

  • New Jersey, USA
  • Czech Republic, EU
  • Mumbai, India

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Dokumentation

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Enthält: HPLC, MASS/LC-MS, 1H-NMR, FT-IR, Gehalt, Structure Elucidation Report (SER) sowie zusätzliche analytische Daten je nach Produkt.

257877-46-6Buspirone EP Impurity E (HCl salt)

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Katalog-Nr.::VE0022308
CAS-Nr.::257877-46-6
Summenformel::C21H34ClN5O3
Molare Masse::439.98 g/mol

Zusätzliche Informationen zu CAS 257877-46-6

Parent drug

Buspirone

IUPAC-Name

2-(1-(2-Oxo-2-((4-(4-(pyrimidin-2-yl)piperazin-1-yl)butyl)amino)ethyl)cyclopentyl)acetic acid hydrochloride

Pharmakopöe-Synonyme

N/A

Other Synonyms

seco-(8, 9)-Buspirone Carboxylic Acid; [1-[2-Oxo-2-[[4-[4-(pyrimidin-2-yl)piperazin-1-yl]butyl]amino]ethyl]cyclopentyl]acetic Acid Hydrochloride

SMILES

O=C(CC1(CC(O)=O)CCCC1)NCCCCN(CC2)CCN2C3=NC=CC=N3.Cl

InChI

InChI=1S/C21H33N5O3.ClH/c27-18(16-21(17-19(28)29)6-1-2-7-21)22-8-3-4-11-25-12-14-26(15-13-25)20-23-9-5-10-24-20;/h5, 9-10H, 1-4, 6-8, 11-17H2, (H, 22, 27)(H, 28, 29);1H

Beschreibung

Buspirone EP Impurity E (HCl salt) | also known as seco-(8 | 9)-Buspirone Carboxylic Acid; [1-[2-Oxo-2-[[4-[4-(pyrimidin-2-yl)piperazin-1-yl]butyl]amino]ethyl]cyclopentyl]acetic Acid Hydrochloride is a highly characterized reference material. It fully complies with stringent regulatory standards | including those set by USP | EMA | JP | and BP. This product is essential for use in Abbreviated New Drug Applications (ANDA) | New Drug Applications (NDA) | and the commercial production of Buspirone. Moreover | it comes with a detailed Structure Elucidation Report (SER) | ensuring its accuracy and reliability for a wide range of analytical applications.

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