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Pharmacopeial Impurities (EP / USP / BP)Reference Standard In stock

Candesartan Cilexetil EP Impurity I

Synonyms: Methyl 1-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-carboxylate · Methyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate · Candesartan Methyl Ester · Methyl candesartan

CAS No.139481-69-9
FormulaC25H22N6O3
Mol. weight454.50
Catalogue No.VQ-006281
Purity96.2%
HSN38229090

Candesartan Cilexetil EP Impurity I (CAS 139481-69-9) – Candesartan impurity standard, 96.2%. C25H22N6O3, MW 454.5. Vaqora Chemicals: COA, global shipping.

Pack sizesPrice on quotation · bulk available
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25 mg
50 mg
100 mg
250 mg
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16-section GHS SDS
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DG-compliant packing

About Candesartan Cilexetil EP Impurity I

Vaqora Chemicals supplies Candesartan Cilexetil EP Impurity I, a pharmacopeial impurity of Candesartan registered under CAS number 139481-69-9 with a typical assay of 96.2%. Formula C25H22N6O3, molecular weight 454.5 g/mol. The IUPAC name is methyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate. It is also known as Candesartan Methyl Ester or Methyl candesartan.

It is supplied as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. The GHS classification uses the signal word “Warning”, so appropriate gloves, eye protection and ventilation are recommended.

As a characterised impurity of Candesartan, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide. Stock is available for quick dispatch.

Typical applications

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

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Related to Candesartan

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

Candesartan impurities

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Specifications & identifiers

Chemical identifiers
Product nameCandesartan Cilexetil EP Impurity I
Catalogue No.VQ-006281
CAS Number139481-69-9
IUPAC namemethyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate
Molecular formulaC25H22N6O3
Molecular weight454.5 g/mol
Exact mass454.1753
GradeReference Standard
Purity / assay96.2%
HSN code38229090
InChIKeyRBPFEPGTRLLUKI-UHFFFAOYSA-N
SMILESCCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)OC
PubChem CID15654696
Physical properties
Physical formSolid
LogP (XLogP3)4.4
H-bond donors / acceptors1 / 7
TPSA108 Ų
SynonymsMethyl 1-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-carboxylate, Methyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate, Candesartan Methyl Ester, Methyl candesartan, Candesartan cilexetil impurity I, Methyl 1-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)-2-ethoxybenzimidazole-7-carboxylate, Methyl 2-ethoxy-1-((2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl)benzimidazole-7-carboxylate, Ethyl-2-ethoxy-1-[[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]benzimidazole]-7-carboxylate, ethyl2-ethoxy-1-[[2'-(1h-tetrazol-5-yl)methyl]benzimidazole-7-carboxylate, Methyl 2-ethoxy-1-[[2'-(1 H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate, methyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]-methyl]benzimidazole-7-carboxylate, methyl 2-ethoxy-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methylbenzimidazole-7carboxylate

Safety & hazard information (GHS)

GHS08 Health hazard
Health hazard

Signal word: Warning

Hazard statements

  • H361Suspected of damaging fertility or the unborn child

Precautionary statements: P203, P280, P318, P405, 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 Candesartan Cilexetil EP Impurity I?

The CAS Registry Number of Candesartan Cilexetil EP Impurity I is 139481-69-9. It is also known as Methyl 1-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-carboxylate, Methyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate, Candesartan Methyl Ester.

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

Candesartan Cilexetil EP Impurity I has the molecular formula C25H22N6O3 and a molecular weight of 454.5 g/mol. Its IUPAC name is methyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate.

What is Candesartan Cilexetil EP Impurity I used for?

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

We supply Candesartan Cilexetil EP Impurity I in Reference Standard (96.2%) grade, in 10 mg, 25 mg, 50 mg, 100 mg, 250 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Candesartan Cilexetil EP Impurity I?

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

Yes. Candesartan Cilexetil EP Impurity I 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.

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