Worldwide shipping · 120+ destinationsCOA & GHS SDS with every lotMon–Sat, 09:30–18:30 IST
VAQORACHEMICALS
Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Candesartan Cilexetil EP Impurity C

Synonyms: Candesartan Cilexetil - Impurity C · 2-Desethoxy-2-hydroxy-1H-1-Ethyl Candesartan Cilexetil · 2-Desethoxy-2-oxo-1H-1-ethyl candesartan cilexetil · N2-Ethyl candesartan cilexetilc

CAS No.1185255-99-5
FormulaC33H34N6O6
Mol. weight610.70
Catalogue No.VQ-021969
PurityReference Standard
HSN38229090

Candesartan Cilexetil EP Impurity C (CAS 1185255-99-5) – Candesartan impurity standard. C33H34N6O6, MW 610.7. Vaqora Chemicals: COA, global shipping.

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

About Candesartan Cilexetil EP Impurity C

Vaqora Chemicals supplies Candesartan Cilexetil EP Impurity C, a pharmacopeial impurity of Candesartan registered under CAS number 1185255-99-5. The compound has the formula C33H34N6O6, corresponding to a molecular weight of 610.7 g/mol. Alternative names: Candesartan Cilexetil - Impurity C and N2-Ethyl candesartan cilexetilc.

The product is provided as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Under GHS it is labelled “Warning”, so handle it with suitable PPE and consult the SDS.

This Candesartan impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF 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.

Typical applications

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

Industries

Related to Candesartan

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

Candesartan impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameCandesartan Cilexetil EP Impurity C
Catalogue No.VQ-021969
CAS Number1185255-99-5
IUPAC name1-cyclohexyloxycarbonyloxyethyl 3-[[4-[2-(1-ethyltetrazol-5-yl)phenyl]phenyl]methyl]-2-oxo-1H-benzimidazole-4-carboxylate
Molecular formulaC33H34N6O6
Molecular weight610.7 g/mol
Exact mass610.254
GradeReference Standard
HSN code38229090
InChIKeyDEGBAMTUFHKMQR-UHFFFAOYSA-N
SMILESCCN1C(=NN=N1)C2=CC=CC=C2C3=CC=C(C=C3)CN4C5=C(C=CC=C5NC4=O)C(=O)OC(C)OC(=O)OC6CCCCC6
PubChem CID71315578
Physical properties
Physical formSolid
LogP (XLogP3)6
H-bond donors / acceptors1 / 9
TPSA138 Ų
SynonymsCandesartan Cilexetil - Impurity C, 2-Desethoxy-2-hydroxy-1H-1-Ethyl Candesartan Cilexetil, 2-Desethoxy-2-oxo-1H-1-ethyl candesartan cilexetil, N2-Ethyl candesartan cilexetilc, Candesartan Cilexetil Impurity C, 2-Desethyl-1H-1-ethyl candesartan cilexetil

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 C?

The CAS Registry Number of Candesartan Cilexetil EP Impurity C is 1185255-99-5. It is also known as Candesartan Cilexetil - Impurity C, 2-Desethoxy-2-hydroxy-1H-1-Ethyl Candesartan Cilexetil, 2-Desethoxy-2-oxo-1H-1-ethyl candesartan cilexetil.

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

Candesartan Cilexetil EP Impurity C has the molecular formula C33H34N6O6 and a molecular weight of 610.7 g/mol. Its IUPAC name is 1-cyclohexyloxycarbonyloxyethyl 3-[[4-[2-(1-ethyltetrazol-5-yl)phenyl]phenyl]methyl]-2-oxo-1H-benzimidazole-4-carboxylate.

What is Candesartan Cilexetil EP Impurity C used for?

Candesartan Cilexetil EP Impurity C 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 C can I order?

We supply Candesartan Cilexetil 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 Candesartan Cilexetil EP Impurity C?

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

Yes. Candesartan Cilexetil 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 Candesartan Cilexetil EP Impurity C

We reply within one business day with price, pack options, lead time and documentation.

By submitting you agree to our privacy policy. We never share your details.

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
How ordering works

Related products

More in Pharmacopeial Impurities (EP / USP / BP) →