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

Carteolol EP Impurity E

Synonyms: Carteolol HCl EP Impurity E · Carteolol Hydrochloride EP Impurity E · Carteolol Hydrochloride - Impurity E · 5,5'-((2-Hydroxypropane-1,3-diyl)bis(oxy))bis(3,4-dihydroquinolin-2(1H)-one)

CAS No.56660-90-3
FormulaC21H22N2O5
Mol. weight382.40
Catalogue No.VQ-022032
PurityReference Standard
HSN38229090

Carteolol EP Impurity E (CAS 56660-90-3) – Carteolol impurity standard. C21H22N2O5, MW 382.4. 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 Carteolol EP Impurity E

Carteolol EP Impurity E is a pharmacopeial impurity of Carteolol carrying the CAS registry number 56660-90-3. With the molecular formula C21H22N2O5, it has a molar mass of 382.4 g/mol. Systematically, it is named 5-[2-hydroxy-3-[(2-oxo-3,4-dihydro-1H-quinolin-5-yl)oxy]propoxy]-3,4-dihydro-1H-quinolin-2-one. Common synonyms include Carteolol HCl EP Impurity E and Carteolol Hydrochloride EP Impurity E.

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. Handle it with standard laboratory precautions and appropriate personal protective equipment.

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

We offer Carteolol EP Impurity E in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers worldwide.

Typical applications

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

Industries

Related to Carteolol

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

Carteolol impurities

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Specifications & identifiers

Chemical identifiers
Product nameCarteolol EP Impurity E
Catalogue No.VQ-022032
CAS Number56660-90-3
IUPAC name5-[2-hydroxy-3-[(2-oxo-3,4-dihydro-1H-quinolin-5-yl)oxy]propoxy]-3,4-dihydro-1H-quinolin-2-one
Molecular formulaC21H22N2O5
Molecular weight382.4 g/mol
Exact mass382.1529
GradeReference Standard
HSN code38229090
InChIKeyOXFQNSYUOMGLAL-UHFFFAOYSA-N
SMILESC1CC(=O)NC2=C1C(=CC=C2)OCC(COC3=CC=CC4=C3CCC(=O)N4)O
PubChem CID156613495
Physical properties
Physical formSolid
LogP (XLogP3)1.2
H-bond donors / acceptors3 / 5
TPSA96.9 Ų
SynonymsCarteolol HCl EP Impurity E, Carteolol Hydrochloride EP Impurity E, Carteolol Hydrochloride - Impurity E, 5,5'-((2-Hydroxypropane-1,3-diyl)bis(oxy))bis(3,4-dihydroquinolin-2(1H)-one), 5,5'-((2-Hydroxy-1,3-propanediyl)bis(oxy))bis(3,4-dihydro-2(1H)-quinolinone), 5,5'-((2-Hydroxypropan-1,3-diyl)bis(oxy))bis(3,4-dihydroquinolin-2(1H)-one), 5,5'-[(2-Hydroxy-1,3-propanediyl)bis(oxy)]bis[3,4-dihydro-2(1H)-quinolinone], 5,5'-[(2-hydroxypropan-1,3-diyl)bis(oxy)]bis(3,4-dihydroquinolin-2(1H)-one)

Documents

Frequently asked questions

What is the CAS number of Carteolol EP Impurity E?

The CAS Registry Number of Carteolol EP Impurity E is 56660-90-3. It is also known as Carteolol HCl EP Impurity E, Carteolol Hydrochloride EP Impurity E, Carteolol Hydrochloride - Impurity E.

What is the molecular formula and molecular weight of Carteolol EP Impurity E?

Carteolol EP Impurity E has the molecular formula C21H22N2O5 and a molecular weight of 382.4 g/mol. Its IUPAC name is 5-[2-hydroxy-3-[(2-oxo-3,4-dihydro-1H-quinolin-5-yl)oxy]propoxy]-3,4-dihydro-1H-quinolin-2-one.

What is Carteolol EP Impurity E used for?

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

We supply Carteolol EP Impurity E 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 Carteolol EP Impurity E?

Yes. Every lot of Carteolol EP Impurity E 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 Carteolol EP Impurity E be shipped internationally?

Yes. We export Carteolol EP Impurity E 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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