Detailed view of Tramadol impurity E CRS
How to read this table
1- Catalogue Code designates the catalogue code that has been assigned to each Reference Standard.
2- Name lists the name of each item as designated in the European Pharmacopoeia (English version) and/or on the label.
If the suffix *psy, *narc, *Drug Precursor, or MOT(biotox) appears, export authorizations are mandatory.
Import permit / license may be needed in your country. For more details, please refer to our Terms and Conditions of supply (p. iv)
3- Current Batch Number shows the batch of the selected item being distributed as of the date of this online catalogue.
4- Unit quantity is the quantity of material provided in each container.
5- Sale unit is the number of container(s) supplied, when more than one container is supplied for each order.
6- Used in monograph(s) lists the monograph(s) and/or general method(s) of analysis for which the reference Substance is intended.
Please note that our Chemical Substances or B iological P reparations are supplied exclusively as European Pharmacopoeia Chemical Reference Substances, Biological Reference Preparations or Reference Spectra for use as standards or reference s ubstance in the tests and assay indicated above, in accordance with the official methods of the Ph. Eur. and for no other purpose .
7- Assigned content Unless otherwise stated the assigned value is given on the « as is » basis. For freeze dried standards the content of the pure substance is indicated per container.
8- Additional information includes chemical name of an impurity, synonym etc…
9- Leaflet Click on the hyperlink to download the leaflet containing the instructions for use, if available (Adobe Acrobat Reader version 5 or higher, or the corresponding browser plug-in is needed to open the file).
10- Safety Data Sheet applicable to hazardous chemicals only in accordance with UNECE/GHS. It is not applicable to other materials, but statements are issued instead. Terms and conditions.
11- CAS Registry Number The CAS registry numbers are not necessary for the European pharmacopoeia tests and assays, including the intended use of the EDQM reference standards. The EDQM does not accept any responsibility for the use of CAS registry numbers of reference standards for purposes extending beyond the description in the European Pharmacopoeia general notices 07/2014:10000: "CAS registry numbers are included for information in monographs, where applicable, to provide convenient access to useful information for users. CAS Registry Number® is a registered trademark of the American Chemical Society."
The EDQM aligns the CAS registry numbers of reference standards with the monographs. In the effort to facilitate regulatory compliance downstream (e.g. safety data sheets in accordance with the Regulations (EC) No 1272/2008 and 1907/2006), the EDQM provides CAS registry numbers occasionally also for related substance. The accuracy of CAS registry numbers cannot be guaranteed for these or any EDQM reference standards.
12 - Presentation Useful information on the production process used to prepare the batch for further handling of the standard.
13 - Origin To be checked if import permit is required in your country.
14 - Storage conditions Those are the recommended storage conditions as used by EDQM.
15 - Dispatching conditions includes information on special dispatching conditions required by the item.
16- UN Code Classification for the shipment of the dangerous goods.