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

Carvedilol EP Impurity E

Synonyms: 2-(2-Methoxyphenoxy)ethylamine Hydrochloride · Carvedilol EP Impurity E (HCl Salt) · Carvedilol Impurity E · 1-(2-Aminoethoxy)-2-methoxybenzene Hydrochloride

CAS No.64464-07-9
FormulaC9H14ClNO2
Mol. weight203.66
Catalogue No.VQ-022039
PurityReference Standard
HSN38229090

Carvedilol EP Impurity E (CAS 64464-07-9) – Carvedilol impurity standard. C9H14ClNO2, MW 203.66. 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 Carvedilol EP Impurity E

Carvedilol EP Impurity E is a pharmacopeial impurity of Carvedilol carrying the CAS registry number 64464-07-9. Formula C9H14ClNO2, molecular weight 203.66 g/mol. It is also known as 2-(2-Methoxyphenoxy)ethylamine Hydrochloride or Carvedilol EP Impurity E (HCl Salt).

The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Under GHS it is labelled “Warning”, so handle it with suitable PPE and consult the SDS.

Pharmaceutical QC and development laboratories use this impurity standard of Carvedilol to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. It is used across pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Carvedilol EP Impurity E 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 Carvedilol

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

Carvedilol impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameCarvedilol EP Impurity E
Catalogue No.VQ-022039
CAS Number64464-07-9
IUPAC name2-(2-methoxyphenoxy)ethanamine;hydrochloride
Molecular formulaC9H14ClNO2
Molecular weight203.66 g/mol
Exact mass203.0713
GradeReference Standard
HSN code38229090
InChIKeyKNWPXZOMSZABHD-UHFFFAOYSA-N
SMILESCOC1=CC=CC=C1OCCN.Cl
PubChem CID2762734
Physical properties
Physical formSolid
H-bond donors / acceptors2 / 3
TPSA44.5 Ų
Synonyms2-(2-Methoxyphenoxy)ethylamine Hydrochloride, Carvedilol EP Impurity E (HCl Salt), Carvedilol Impurity E, 1-(2-Aminoethoxy)-2-methoxybenzene Hydrochloride, 2-(2-methoxyphenoxy)ethanamine Hydrochloride, Ethanamine, 2-(2-methoxyphenoxy)-, hydrochloride, 2-(2-methoxyphenoxy)ethan-1-amine hydrochloride, 2-(2-Methoxyphenoxy)ethylaMine Hydrochloride Hydrate, Carvedilol Impurity 5, (E)-Azobenzene HCl, 2-(2-MethOxphenOxyl)ethylamine HCl, 2-(2-Aminoethoxy)anisole Hydrochloride

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed
  • H315Causes skin irritation
  • H319Causes serious eye irritation
  • H335May cause respiratory irritation

Precautionary statements: P261, P264, P264 + P265, P270, P271, P280, P301 + P317, P302 + P352, P304 + P340, P305 + P351 + P338, P319, P321, P330, P332 + P317, P337 + P317, P362 + P364, P403 + P233, 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 Carvedilol EP Impurity E?

The CAS Registry Number of Carvedilol EP Impurity E is 64464-07-9. It is also known as 2-(2-Methoxyphenoxy)ethylamine Hydrochloride, Carvedilol EP Impurity E (HCl Salt), Carvedilol Impurity E.

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

Carvedilol EP Impurity E has the molecular formula C9H14ClNO2 and a molecular weight of 203.66 g/mol.

What is Carvedilol EP Impurity E used for?

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

We supply Carvedilol 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 Carvedilol EP Impurity E?

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

Yes. Carvedilol EP Impurity E 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 Carvedilol EP Impurity E

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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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