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Citalopram EP Impurity C; Citalopram Related Compound C

3-Oxo Citalopram Oxalate; EsCitalopram EP Impurity C; Citalopram USP Related Compound C; 3-[3-(Dimethylamino)-1-propyl](4-fluorophenyl)-6-cyano-1(3H)-isobenzofuranone oxalate;

Citalopram-EP-Impurity-C

Specifications:

CAS No.

: 1440961-11-4; 372941-54-3 (free base)

Mol F.

: C20H19FN2O2 (base), C22H21FN2O6 (oxalate salt)

Mol W.

: 338.38,428.41(oxalatesalt)

Cat No.

: SA17007

Appearance

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Product Name

: Citalopram EP Impurity C; Citalopram Related Compound C

CAS No.

: 1440961-11-4; 372941-54-3 (free base)

Mol F.

: C20H19FN2O2 (base), C22H21FN2O6 (oxalate salt)

Mol W.

: 338.38,428.41(oxalatesalt)

Cat No.

: SA17007

Appearance

Synonyms

: 3-Oxo Citalopram Oxalate; EsCitalopram EP Impurity C; Citalopram USP Related Compound C; 3-[3-(Dimethylamino)-1-propyl](4-fluorophenyl)-6-cyano-1(3H)-isobenzofuranone oxalate;

Related API

: Citalopram

Category

Citalopram EP Impurity C product with CAS: 1440961-11-4; 372941-54-3 (free base) is also known as Citalopram USP Related Compound C. This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Citalopram EP Impurity C is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Citalopram and its related formulations. Moreover, Citalopram USP Related Compound C is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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