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Clarithromycin EP Impurity P

CAS 123967-58-8 Cat. no. C4X-100215 Formula C39H71NO13 MW 761.98 In stock
Documents on file — click to open, no login needed:Certificate of analysis (COA)Safety data sheet (SDS)
Chemical structure of Clarithromycin EP Impurity P, CAS 123967-58-8
Structure of Clarithromycin EP Impurity P, CAS 123967-58-8 — click to open the full-size image

An impurity of the macrolide antibiotic clarithromycin, Clarithromycin EP Impurity P carries the European Pharmacopoeia designation used to identify this specific related substance. Pharmaceutical laboratories obtain it to demonstrate that their separation resolves the parent drug from individual impurities and to establish which peak corresponds to which known substance during release and stability testing. Its principal uses are related-substance method development and validation, system suitability and resolution checks, peak identification and quantitative determination of the impurity in drug substance and finished product. The compound is a white solid with the formula C39H71NO13 and a molecular weight of 761.98. It is kept at -20 °C ± 5 °C and shipped with ice packs, and can be supplied in pack sizes from 1 mg through 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 50 mg, 55 mg, 60 mg, 100 mg, 150 mg, 200 mg and 300 mg. A quotation or additional documentation is available on request.

Also known as

Clarithromycin Impurity P. Further pharmacopoeial and trivial names are recorded on the certificate of analysis.

Pack sizes and lead time

Pack sizeAvailabilityQuote
1 mgIn stock
10 mg10 days
15 mg10 days
20 mg10 days
25 mg10 days
30 mg10 days
35 mg10 days
50 mg10 days
55 mg10 days
60 mg10 days
100 mg10 days
150 mg56 days
200 mg56 days
300 mg56 days
Content and purity for each pack size are stated per lot on the certificate of analysis. Prices are quoted per enquiry so that pack size, documentation and shipping requirements can be confirmed together — no price is published on this site.

What the documents contain

  • Certificate of analysis — issued per lot: catalogue and lot number, the value assigned to the material and the analytical basis for it.
  • Safety data sheet — supplied for the catalogue item, and the basis for the transport classification used on the shipment.
  • Storage and shipping conditions for this item: -20℃±5℃, Shipping with Ice Packs.

Frequently asked questions

Is a certificate of analysis (COA) available for Clarithromycin EP Impurity P?

Yes. A batch-specific COA and the MSDS are issued for every lot of Clarithromycin EP Impurity P (catalogue number C4X-100215). Use the COA link on this page, or email chao.lu@cato-chem.com with the lot number printed on your label and we will send the matching document.

What pack sizes and lead times are offered?

Pack sizes 1 mg are held in stock and typically ship within 1–2 working days Other sizes (10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 50 mg, 55 mg, 60 mg, 100 mg, 150 mg, 200 mg, 300 mg) are quoted with a lead time of approximately 10 days, 56 days.

How is the purity of Clarithromycin EP Impurity P documented?

Purity is determined per batch and stated on the COA together with the analytical data used for its assignment. If your method requires a specific grade or a particular pharmacopoeial naming, tell us the requirement when you enquire and we will confirm suitability.

Can you supply a larger quantity or a custom synthesis?

Yes. Quantities above the listed pack sizes are quoted on request, and custom synthesis or isolation from related starting materials can be discussed for compounds not held in stock. Contact chao.lu@cato-chem.com with the target quantity and required delivery date.

How is Clarithromycin EP Impurity P shipped?

Shipping conditions for this item: Shipping with Ice Packs. Shipments are packed to maintain the specified storage condition, and the SDS is provided for transport classification.

Related products

Same molecular formula (C39H71NO13)