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

Escitalopram EP Impurity I

Synonyms: Escitalopram Olefinic impurity · Escitalopram - Impurity I (Freebase) · 4-[(1Z)-4-(Dimethylamino)-1-(4-fluorophenyl)but-1-en-1-yl]-3-(hydroxymethyl)benzonitrile · (Z)-4-(4-(dimethylamino)-1-(4-fluorophenyl)but-1-en-1-yl)-3-(hydroxymethyl)benzonitrile

CAS No.1370643-22-3
FormulaC20H21FN2O
Mol. weight324.40
Catalogue No.VQ-021173
PurityReference Standard
HSN38229090

Escitalopram EP Impurity I (CAS 1370643-22-3) – Escitalopram impurity standard. C20H21FN2O, MW 324.4. Request a quote: COA, bulk packs and worldwide export.

Pack sizesPrice on quotation · bulk available
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25 mg
50 mg
100 mg
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16-section GHS SDS
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About Escitalopram EP Impurity I

Escitalopram EP Impurity I is a pharmacopeial impurity of Escitalopram carrying the CAS registry number 1370643-22-3. Formula C20H21FN2O, molecular weight 324.4 g/mol. Systematically, it is named 4-[(Z)-4-(dimethylamino)-1-(4-fluorophenyl)but-1-enyl]-3-(hydroxymethyl)benzonitrile. It is also known as Escitalopram Olefinic impurity or Escitalopram - Impurity I (Freebase).

It is supplied as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.

Pharmaceutical QC and development laboratories use this impurity standard of Escitalopram 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.

Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Escitalopram EP Impurity I is dispatched with a Certificate of Analysis (COA) to destinations worldwide.

Typical applications

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

Industries

Related to Escitalopram

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

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Specifications & identifiers

Chemical identifiers
Product nameEscitalopram EP Impurity I
Catalogue No.VQ-021173
CAS Number1370643-22-3
IUPAC name4-[(Z)-4-(dimethylamino)-1-(4-fluorophenyl)but-1-enyl]-3-(hydroxymethyl)benzonitrile
Molecular formulaC20H21FN2O
Molecular weight324.4 g/mol
Exact mass324.1638
GradeReference Standard
HSN code38229090
InChIKeyIAICSOQOSARWDY-PVOVUMCXSA-N
SMILESCN(C)CC/C=C(/C1=CC=C(C=C1)F)\C2=C(C=C(C=C2)C#N)CO
PubChem CID11472790
Physical properties
Physical formSolid
LogP (XLogP3)3.7
H-bond donors / acceptors1 / 4
TPSA47.3 Ų
SynonymsEscitalopram Olefinic impurity, Escitalopram - Impurity I (Freebase), 4-[(1Z)-4-(Dimethylamino)-1-(4-fluorophenyl)but-1-en-1-yl]-3-(hydroxymethyl)benzonitrile, (Z)-4-(4-(dimethylamino)-1-(4-fluorophenyl)but-1-en-1-yl)-3-(hydroxymethyl)benzonitrile, 4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-buten-1-yl]-3-(hydroxymethyl)-benzonitrile, 4-[(1Z)-4-(Dimethylamino)-1-(4-fluorophenyl)-1-buten-1-yl]-3-(hydroxymethyl)benzonitrile, 4-[[Z]-4-[Dimethylamino]-1-[4-fluorophenyl]but-1-enyl]-3-[hydroxymethyl]benzonitrile

Documents

Frequently asked questions

What is the CAS number of Escitalopram EP Impurity I?

The CAS Registry Number of Escitalopram EP Impurity I is 1370643-22-3. It is also known as Escitalopram Olefinic impurity, Escitalopram - Impurity I (Freebase), 4-[(1Z)-4-(Dimethylamino)-1-(4-fluorophenyl)but-1-en-1-yl]-3-(hydroxymethyl)benzonitrile.

What is the molecular formula and molecular weight of Escitalopram EP Impurity I?

Escitalopram EP Impurity I has the molecular formula C20H21FN2O and a molecular weight of 324.4 g/mol. Its IUPAC name is 4-[(Z)-4-(dimethylamino)-1-(4-fluorophenyl)but-1-enyl]-3-(hydroxymethyl)benzonitrile.

What is Escitalopram EP Impurity I used for?

Escitalopram EP Impurity I is supplied as a characterised reference material related to Escitalopram. 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 Escitalopram EP Impurity I can I order?

We supply Escitalopram EP Impurity I 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 Escitalopram EP Impurity I?

Yes. Every lot of Escitalopram EP Impurity I 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 Escitalopram EP Impurity I be shipped internationally?

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

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