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Risperidone EP Impurity D

EP impurity reference standard

CAS1199589-74-6
Risperidone EP Impurity D chemical structure
Cat. no. C4X-111111 Purity >95% HPLC Form White to Light Beige Solid

Specifications

Product name
Risperidone EP Impurity D
CAS number
1199589-74-6
Catalogue number
C4X-111111
Molecular formula
C23H27FN4O2
Molecular weight
410.48
Purity (HPLC)
>95%
Physical form
White to Light Beige Solid
Storage
2-8 °C
SMILES
C1CC2=NC(C)=C(CCN3CCC(C4C5=CC(F)=CC=C5ON=4)CC3)C(=O)N2CC1
Available pack sizes
1 mg / 25 mg / 50 mg / 100 mg / 200 mg / 10 mg / 20 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

Risperidone EP Impurity D (CAS 1199589-74-6) is supplied by ImpurityLab as a European Pharmacopoeia impurity standard, identified by letter against the monograph for its parent substance. Catalogue number C4X-111111. It is related to Risperidone.

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

The material is issued against molecular formula C23H27FN4O2, molecular weight 410.48 g mol−1, physical form described as white to light beige solid.

Structural notation: C1CC2=NC(C)=C(CCN3CCC(C4C5=CC(F)=CC=C5ON=4)CC3)C(=O)N2CC1

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. 1 mg / 25 mg / 50 mg / 100 mg / 200 mg / 10 mg / 20 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-111111 when requesting either document.

Documentation

Certificate of analysis (per lot)COA-C4X-111111Download
Safety data sheet (SDS)SDS-C4X-111111Download

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

Regulatory reference

EP Impurity D. 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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