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

Oxeladin EP Impurity C

Synonyms: Oxeladin Hydrogen Citrate - Impurity C

CAS No.101778-55-6
FormulaC18H29NO2
Mol. weight291.44
Catalogue No.VQ-045132
PurityReference Standard
HSN38229090

Oxeladin EP Impurity C (CAS 101778-55-6) – Oxeladin impurity standard. C18H29NO2, MW 291.44. Request a quote: COA, bulk packs and worldwide export.

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 Oxeladin EP Impurity C

Oxeladin EP Impurity C is a pharmacopeial impurity of Oxeladin carrying the CAS registry number 101778-55-6. Its molecular formula is C18H29NO2 and its molecular weight is 291.44 g/mol. It is also known as Oxeladin Hydrogen Citrate - Impurity C.

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. Good laboratory practice and suitable PPE are recommended during handling.

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

Vaqora Chemicals supplies Oxeladin EP Impurity C 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 Oxeladin

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

Oxeladin impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameOxeladin EP Impurity C
Catalogue No.VQ-045132
CAS Number101778-55-6
Molecular formulaC18H29NO2
Molecular weight291.44 g/mol
GradeReference Standard
HSN code38229090
Physical properties
Physical formSolid

Documents

Frequently asked questions

What is the CAS number of Oxeladin EP Impurity C?

The CAS Registry Number of Oxeladin EP Impurity C is 101778-55-6. It is also known as Oxeladin Hydrogen Citrate - Impurity C.

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

Oxeladin EP Impurity C has the molecular formula C18H29NO2 and a molecular weight of 291.44 g/mol.

What is Oxeladin EP Impurity C used for?

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

We supply Oxeladin 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 Oxeladin EP Impurity C?

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

Yes. We export Oxeladin EP Impurity C worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.

Enquire about Oxeladin 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) →