Ranitidine Impurity N6
process impurity reference standard
Specifications
- Product name
- Ranitidine Impurity N6
- CAS number
- 1197-40-6
- Catalogue number
CP106551- Molecular formula
- C9H8O2
- Molecular weight
- 148.16
- Purity (HPLC)
- >90%
- Physical form
- Black Liquid
- Storage
- 2-8 °C
- SMILES
O1C=CC=C1CC1=CC=CO1- Available pack sizes
- Quoted on request
- 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
Ranitidine Impurity N6 (CAS 1197-40-6) is supplied by ImpurityLab as a process impurity standard, covering impurities that are neither pharmacopoeially lettered nor degradation products of the parent substance. Catalogue number CP106551. It is related to Ranitidine.
Parent drug substance. Ranitidine. Browse the full Ranitidine impurity and related compound standards held by ImpurityLab.
The material is issued against molecular formula C9H8O2, molecular weight 148.16 g mol−1, physical form described as black liquid.
Structural notation: O1C=CC=C1CC1=CC=CO1
Process impurities are controlled through the ICH Q3A reporting, identification and qualification thresholds, or through the equivalent thresholds in ICH Q3B for the drug product. The limits depend on the maximum daily dose of the product rather than on the impurity itself.
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. Quoted on request. 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 CP106551 when requesting either document.
Documentation
Documents are issued per lot. The COA you receive describes the lot that ships, not a representative sample.
Regulatory reference
Process impurity, not pharmacopoeially lettered. Set the limit from your own ICH Q3A or Q3B assessment and confirm against the current method.
References are provided to help you map a standard to a pharmacopoeial method. Confirm the acceptance criteria against your own method before use.