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VAQORACHEMICALS
Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Citalopram EP Impurity C

Synonyms: Escitalopram EP Impurity C · Citalopram Hydrobromide - Impurity C · Escitalopram - Impurity C · 3-Oxocitalopram

CAS No.372941-54-3
FormulaC20H19FN2O2
Mol. weight338.40
Catalogue No.VQ-022199
PurityReference Standard
HSN38229090

Citalopram EP Impurity C (CAS 372941-54-3) – Citalopram impurity standard. C20H19FN2O2, MW 338.4. From Vaqora Chemicals, with COA and worldwide delivery.

Pack sizesPrice on quotation · bulk available
10 mg
25 mg
50 mg
100 mg
Bulk / custom pack · kg to MT
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Batch COA with every lot
16-section GHS SDS
Export to 120+ countries
DG-compliant packing

About Citalopram EP Impurity C

Listed under CAS 372941-54-3, Citalopram EP Impurity C is a pharmacopeial impurity of Citalopram available from Vaqora Chemicals. Formula C20H19FN2O2, molecular weight 338.4 g/mol. Systematically, it is named 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3-oxo-2-benzofuran-5-carbonitrile. It is also known as Escitalopram EP Impurity C or Citalopram Hydrobromide - Impurity C.

The product is provided as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. The GHS classification uses the signal word “Warning”, so appropriate gloves, eye protection and ventilation are recommended.

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. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Citalopram EP Impurity C 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 nameCitalopram EP Impurity C
Catalogue No.VQ-022199
CAS Number372941-54-3
IUPAC name1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3-oxo-2-benzofuran-5-carbonitrile
Molecular formulaC20H19FN2O2
Molecular weight338.4 g/mol
Exact mass338.1431
GradeReference Standard
HSN code38229090
InChIKeyASGSMDPSNUXWMB-UHFFFAOYSA-N
SMILESCN(C)CCCC1(C2=C(C=C(C=C2)C#N)C(=O)O1)C3=CC=C(C=C3)F
PubChem CID11484526
Physical properties
Physical formSolid
LogP (XLogP3)3.4
H-bond donors / acceptors0 / 5
TPSA53.3 Ų
SynonymsEscitalopram EP Impurity C, Citalopram Hydrobromide - Impurity C, Escitalopram - Impurity C, 3-Oxocitalopram, 3-(3-Dimethylaminopropyl)-3-(4-fluorophenyl)-6-cyano-1(3H)-isobenzofuranone, 3-Oxo Citalopram, 3-oxo-citalopram, (3RS)-6-Cyano-3-[3-(dimethylamino)propyl]-3-(4-fluorophenyl)isobenzofuran-1(3H)-one, DISCONTINUED. Please see O869983., 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3-oxo-isobenzofuran-5-carbonitrile

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed

Precautionary statements: P264, P270, P301 + P317, P330, P501

Classification is indicative (aggregated GHS notifications) and may vary by grade and concentration. Always refer to the SDS supplied with your lot.

Documents

Frequently asked questions

What is the CAS number of Citalopram EP Impurity C?

The CAS Registry Number of Citalopram EP Impurity C is 372941-54-3. It is also known as Escitalopram EP Impurity C, Citalopram Hydrobromide - Impurity C, Escitalopram - Impurity C.

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

Citalopram EP Impurity C has the molecular formula C20H19FN2O2 and a molecular weight of 338.4 g/mol. Its IUPAC name is 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3-oxo-2-benzofuran-5-carbonitrile.

What is Citalopram EP Impurity C used for?

Citalopram EP Impurity C 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 C can I order?

We supply Citalopram EP Impurity C 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 C?

Yes. Every lot of Citalopram EP Impurity C 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 C be shipped internationally?

Yes. Citalopram EP Impurity C is classified as hazardous, so it is packed in UN-approved packaging and shipped as dangerous goods under IATA/IMDG rules. We export worldwide on EXW, FOB, CIF and DAP terms.

Enquire about Citalopram EP Impurity C

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Why buyers choose Vaqora

  • Batch-traceable lots with COA
  • R&D packs to multi-tonne supply
  • IATA / IMDG dangerous-goods packing
  • EXW, FOB, CIF, DAP Incoterms
  • Custom synthesis & sourcing
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