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Pharmacopeial Impurities (EP / USP / BP)

Erlotinib EP Impurity I

Reference StandardAvailable on request

Buy Erlotinib EP Impurity I (CAS 183322-20-5) from Zemixal. Request a quote with price, lead time and documents. Packs from 10 mg.

Pack sizes
Erlotinib EP Impurity I chemical structure
CAS number183322-20-5
FormulaC13H14Cl2N2O3
Molar mass317.16 g/mol
Physical formSolid
HS code38229090
InChIKeyHFGVHQGBDDTDIJ-UHFFFAOYSA-N
IUPAC name4-chloro-7-(2-chloroethoxy)-6-(2-methoxyethoxy)quinazoline

About Erlotinib EP Impurity I

Analytical teams working on Erlotinib use Erlotinib EP Impurity I as a qualified comparison standard. For your records (Reference Standard), the material is defined by CAS 183322-20-5, formula C13H14Cl2N2O3 and molar mass 317.16 g/mol. It is handled as a solid.

Typical applications

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

Available as 10 mg, 25 mg, 50 mg and 100 mg. Larger or split packs can be arranged. You receive a certificate of analysis with characterisation data with each order. Add it to your quote list and our team replies with price, lead time and shipping options within one business day.

Reference standards for Erlotinib

See every impurity, metabolite and related compound we list for this API.

Erlotinib standards

Typical uses

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

Applications

Pharmaceutical Manufacturing and QCResearch Labs and Universities

Grade guides

Ph. Eur. Grade (European Pharmacopoeia)

Specifications and identifiers

Specifications of Erlotinib EP Impurity I
Product nameErlotinib EP Impurity I
Catalogue numberZX-029306
CAS number183322-20-5
IUPAC name4-chloro-7-(2-chloroethoxy)-6-(2-methoxyethoxy)quinazoline
Molecular formulaC13H14Cl2N2O3
Molar mass317.16 g/mol
Exact mass316.0381
GradeReference Standard
Physical formSolid
XLogP32.9
H-bond donors / acceptors0 / 5
Topological polar surface area53.5 Ų
HS code38229090
InChIKeyHFGVHQGBDDTDIJ-UHFFFAOYSA-N
SMILESCOCCOC1=C(C=C2C(=C1)C(=NC=N2)Cl)OCCCl
PubChem CID18925091
SynonymsErlotinib Hydrochloride - Impurity I, Erlotinib Impurity 48, 4-chloro-7-(2-chloroethoxy)-6-(2-methoxy-ethoxy)quinazoline, Quinazoline, 4-chloro-7-(2-chloroethoxy)-6-(2-methoxyethoxy)-

Lot values are stated on the batch certificate of analysis. Ask for a typical COA with your quotation.

Safety and GHS hazards

No GHS classification is on file for this item. Handle it as an unknown laboratory chemical and request the SDS with your quotation.

Pack sizes

Pack sizes of Erlotinib EP Impurity I
10 mgQuoted on request
25 mgQuoted on request
50 mgQuoted on request
100 mgQuoted on request

Need a different size? Bulk drums and custom packing are quoted on request through the quote form on this page.

Questions about Erlotinib EP Impurity I

Which CAS number identifies Erlotinib EP Impurity I?
Erlotinib EP Impurity I is registered under CAS 183322-20-5. You may also see it listed as Erlotinib Hydrochloride - Impurity I, Erlotinib Impurity 48, 4-chloro-7-(2-chloroethoxy)-6-(2-methoxy-ethoxy)quinazoline. Our catalogue number for this item is ZX-029306.
What are the formula and molar mass of Erlotinib EP Impurity I?
For Erlotinib EP Impurity I, its formula is C13H14Cl2N2O3 and its molar mass is 317.16 g/mol. The systematic (IUPAC) name is 4-chloro-7-(2-chloroethoxy)-6-(2-methoxyethoxy)quinazoline. InChIKey HFGVHQGBDDTDIJ-UHFFFAOYSA-N lets you match it in any structure database.
How is Erlotinib EP Impurity I used in pharmaceutical QC?
Erlotinib EP Impurity I is a characterised reference material linked to Erlotinib. Laboratories use it to identify and quantify this impurity during method development and validation, stability work, batch release testing and regulatory submissions.
What grade and pack sizes are available for Erlotinib EP Impurity I?
This listing is Reference Standard grade. Standard packs are 10 mg, 25 mg, 50 mg, 100 mg. Larger quantities and custom packing can be quoted on request.
Which documents come with Erlotinib EP Impurity I?
Each lot ships with a batch certificate of analysis and a 16-section GHS safety data sheet. A typical COA or specification sheet can be shared with the quotation before you order.
Can Zemixal ship Erlotinib EP Impurity I to my country?
Yes. Erlotinib EP Impurity I ships worldwide by express courier, air cargo or sea freight, quoted on the Incoterm you prefer, with full export documents.

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