Citalopram EP Impurity F Oxalate

Name: Citalopram EP Impurity F Oxalate
Brand: Vaqora Chemicals
SKU: VQ-024995

About Citalopram EP Impurity F Oxalate

Citalopram EP Impurity F Oxalate is a pharmacopeial impurity of Citalopram carrying the CAS registry number 64372-43-6. With the molecular formula C21H23BrFNO5, it has a molar mass of 468.3 g/mol. Common synonyms include Citalopram EP Impurity F (Oxalate salt) and Citalopram EP Impurity F.

It is supplied as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Good laboratory practice and suitable PPE are recommended during handling.

Pharmaceutical QC and development laboratories use this impurity standard of Citalopram to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. Our customers for this product work in pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Citalopram EP Impurity F Oxalate in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports worldwide.

Typical applications

Pharmacopeial method verification
Impurity profiling
QC release testing
ANDA / DMF filings

Industries

Related to Citalopram

View every impurity, metabolite and intermediate we list for Citalopram.

Citalopram impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product name	Citalopram EP Impurity F Oxalate
Catalogue No.	VQ-024995
CAS Number	64372-43-6
IUPAC name	3-[5-bromo-1-(4-fluorophenyl)-3H-2-benzofuran-1-yl]-N,N-dimethylpropan-1-amine;oxalic acid
Molecular formula	C₂₁H₂₃BrFNO₅
Molecular weight	468.3 g/mol
Exact mass	467.0744
Grade	Reference Standard
HSN code	38229090
InChIKey	ARDGNZSILLRUSV-UHFFFAOYSA-N
SMILES	CN(C)CCCC1(C2=C(CO1)C=C(C=C2)Br)C3=CC=C(C=C3)F.C(=O)(C(=O)O)O
PubChem CID	12371044

Physical properties
Physical form	Solid
H-bond donors / acceptors	2 / 7
TPSA	87.1 Å²

Documents

Safety Data Sheet (SDS)16-section GHS · on request Certificate of AnalysisTypical / batch COA · on request Specification sheetTDS / MOA · on request

Frequently asked questions

What is the CAS number of Citalopram EP Impurity F Oxalate?

The CAS Registry Number of Citalopram EP Impurity F Oxalate is 64372-43-6. It is also known as Citalopram EP Impurity F (Oxalate salt), Citalopram EP Impurity F, Citalopram Hydrobromide - Impurity F (Oxalate).

What is the molecular formula and molecular weight of Citalopram EP Impurity F Oxalate?

Citalopram EP Impurity F Oxalate has the molecular formula C21H23BrFNO5 and a molecular weight of 468.3 g/mol.

What is Citalopram EP Impurity F Oxalate used for?

Citalopram EP Impurity F Oxalate is supplied as a characterised reference material related to Citalopram. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.

Which grade and pack sizes of Citalopram EP Impurity F Oxalate can I order?

We supply Citalopram EP Impurity F Oxalate in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Citalopram EP Impurity F Oxalate?

Yes. Every lot of Citalopram EP Impurity F Oxalate is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.

Can Citalopram EP Impurity F Oxalate be shipped internationally?

Yes. We export Citalopram EP Impurity F Oxalate worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.