Buspirone EP Impurity H (Dioxalate)
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100 % Datengenauigkeit
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0 % Toleranz bei der Produktqualität

Lagerstandorte

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

* Vorbehaltlich Verfügbarkeit

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.

2724726-70-7Buspirone EP Impurity H (Dioxalate)

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Katalog-Nr.::VE0022416
CAS-Nr.::2724726-70-7
Summenformel::C33H50N8O4.2C2H2O4
Molare Masse::802.87 g/mol

Zusätzliche Informationen zu CAS 2724726-70-7

Parent drug

Buspirone

IUPAC-Name

Bis[4-[4-(pyrimidin-2-yl)piperazin-1-yl]butyl] (Cyclopentane-1, 1-diyl)diacetate Dioxalate

Pharmakopöe-Synonyme

N/A

Other Synonyms

N/A

SMILES

O=C(OCCCCN1CCN(C2=NC=CC=N2)CC1)CC3(CC(OCCCCN4CCN(C5=NC=CC=N5)CC4)=O)CCCC3.O=C(O)C(O)=O

InChI

InChI=1S/C12H18N2O3S.ClH/c1-4-5-13-6-9(15)14-10-8(2)7-18-11(10)12(16)17-3, /h7, 13H, 4-6H2, 1-3H3, (H, 14, 15), 1H

Beschreibung

The compound Buspirone EP Impurity H (Dioxalate) is a well-documented reference standard that adheres to strict regulatory requirements set by USP EMA JP and BP. It’s highly suited for use in various applications like analytical method development method validation (AMV) and quality control (QC) especially when manufacturing Buspirone. Whether you’re preparing for ANDA or NDA submissions | this product provides the accuracy you need. Plus | it comes with a comprehensive Structure Elucidation Report (SER) | which ensures its reliability for precise analytical work.

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