Citalopram Didesmethyl Impurity (Free base)
✓
データの正確性100%
24時間年中無休の科学サポート
⬡
品質に対する妥協ゼロ

在庫拠点

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

* 在庫状況によります

Documentation

MSDSをダウンロード

サンプルCOAをダウンロード

内容: HPLC、MASS/LC-MS、1H NMR、FT-IR、含量、構造解析レポート(SER)、および製品に応じた追加分析データ。

62498-69-5Citalopram Didesmethyl Impurity (Free base)

● 在庫あり

カタログ番号:VE006519
CAS番号:62498-69-5
分子式:C18H17FN2O
分子量:296.37 g/mol

に関する追加情報 CAS 62498-69-5

親薬物

Citalopram

IUPAC名

1-(3-Aminopropyl)-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile

同義語

N,N-DiDesmethyl Citalopram

Pharmacopeial Synonyms

N/A

SMILES

N#CC1=CC2=C(C(C3=CC=C(F)C=C3)(CCCN)OC2)C=C1

InChI

InChI=1S/C18H17FN2O/c19-16-5-3-15(4-6-16)18(8-1-9-20)17-7-2-13(11-21)10-14(17)12-22-18/h2-7,10H,1,8-9,12,20H2

説明

Citalopram Didesmethyl Impurity (Free base), N,N-DiDesmethyl Citalopram, CAS 62498-69-5, is a primary demethylation impurity encountered during citalopram synthesis and stability studies. Characterized by LC-MS and NMR, this basic impurity requires targeted method development for accurate quantitation in API batches and formulated products. Typical control strategies include optimization of methylation steps, purification by preparative HPLC, and validated stability-indicating assays to monitor its formation under acidic or oxidative conditions. Relevant analytical parameters include retention time, mass fragmentation pattern, and limit of quantitation within regulatory thresholds. Supplied as a certified reference material, it supports impurity profiling, method validation, and regulatory submissions.

見積もり依頼

「*」は必須フィールドを示します

このフィールドは入力チェック用です。変更しないでください。
Products quotation
Name
Url