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Ritonavir EP Impurity J

EP impurity reference standard

CAS162849-95-8
Ritonavir EP Impurity J chemical structure
Cat. no. C4X-175110 Purity >95% HPLC Form White Powder

Specifications

Product name
Ritonavir EP Impurity J
CAS number
162849-95-8
Catalogue number
C4X-175110
Molecular formula
C28H35N3O5S
Molecular weight
525.66
Purity (HPLC)
>95%
Physical form
White Powder
Storage
2-8 °C
SMILES
C(OC(C)(C)C)(=O)N[C@](CC1C=CC=CC=1)([H])C[C@@](O)([H])[C@@](CC1C=CC=CC=1)([H])NC(=O)OCC1SC=NC=1
Available pack sizes
10 mg / 20 mg / 25 mg / 50 mg / 100 mg / 200 mg
Lead time
In stock
Intended use
Related substances and impurity testing, method development and validation, system suitability, QC release and stability testing.

Fields shown as — are not published for this item. They are left blank rather than filled with an estimate.

Description

Ritonavir EP Impurity J (CAS 162849-95-8) is supplied by ImpurityLab as a European Pharmacopoeia impurity standard, identified by letter against the monograph for its parent substance. Catalogue number C4X-175110. It is related to Ritonavir.

Parent drug substance. Ritonavir. Browse the full Ritonavir impurity and related compound standards held by ImpurityLab.

The material is issued against molecular formula C28H35N3O5S, molecular weight 525.66 g mol−1, physical form described as white powder.

Structural notation: C(OC(C)(C)C)(=O)N[C@](CC1C=CC=CC=1)([H])C[C@@](O)([H])[C@@](CC1C=CC=CC=1)([H])NC(=O)OCC1SC=NC=1

Letter designations are assigned inside a monograph for one named substance. The same molecule can carry a different letter, or a different style of name, in another pharmacopoeia. Map the material from its structure — chemical name, formula and CAS — rather than from the letter alone.

Storage. Store at 2-8 °C. Allow the container to reach room temperature before opening so that moisture does not condense onto the material. Record the date of first opening on the label.

Pack sizes. 10 mg / 20 mg / 25 mg / 50 mg / 100 mg / 200 mg. Non-standard quantities are quoted on request, normally within two working days.

Documentation. Each lot is released with a certificate of analysis that states the assay method, the water content and the form as supplied. The safety data sheet is available with the same lot number. Quote catalogue number C4X-175110 when requesting either document.

Documentation

Certificate of analysis (per lot)COA-C4X-175110Download
Safety data sheet (SDS)SDS-C4X-175110Download

Documents are issued per lot. The COA you receive describes the lot that ships, not a representative sample.

Regulatory reference

EP Impurity J. Confirm the acceptance criterion, the reporting threshold and the edition of the monograph against your own method before use.

References are provided to help you map a standard to a pharmacopoeial method. Confirm the acceptance criteria against your own method before use.

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