Detailed view of Tramadol impurity E CRS

Catalogue Code Y0000157
Name Tramadol impurity E Batches
Current batch number 4

Unit quantity 15 mg
Sale unit 1
Used in monograph(s) 1681
Assigned content
Additional information (2RS)-2-[(dimethylamino)methyl]cyclohexanone
Leaflet click to download the leaflet
SDS Click to download SDS
CAS Registry Number n/a
Presentation
Origin click to download Origin Of Goods.pdf
Proposed Import HS code 292219
EDQM long term storage conditions +5°C ± 3°C
Dispatching conditions Ambient temp.
UN Code 2811
Shipping group A1A
Price 79 EUR
Availability Available
Sales restriction No

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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 or *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 3.3.2 c


    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 Chemical Substances and Biological Preparations provided by the EDQM are exclusively supplied as European Pharmacopoeia Reference Standards or Reagents (i.e. Chemical Reference Substances, Herbal Reference Standards, Biological Reference Preparations, Biological Reference Reagents, Reference Spectra) for use as standards or reference substance 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 See leaflet for the value and explanations on use. 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 and information in case of suppression or replacement of a standard.

    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 (SDS) are provided for occupational health and environment protection in accordance with CLP and UNECE/GHS and applicable to hazardous chemicals only. SDS is not applicable to harmless chemicals and biological/herbal preparations where a safety data statement is provided instead. Additional information on SDS is provided in our Terms and conditions for EDQM safety documentation and their use.

    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 and are not provided systematically. 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 any batches.

    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- Proposed Import HS code To be checked for your import customs clearance. The HS code stated for each product is a proposal of the Council of Europe (EDQM). The accuracy of HS code cannot be guaranteed.
    The importer shall be personally responsible for the tariff classification in the country of import and will assume the ensuing regulatory, fiscal, health and safety obligations.

    15- EDQM long term Storage conditions Those are the recommended storage conditions as used by EDQM. Our storage conditions are in most cases more stringent than those given in the monograph.

    16- Dispatching conditions includes information on special dispatching conditions required by the item.

    17- UN Code Classification for the shipment of the dangerous goods (only stated if a shipper's declaration for Dangerous Goods is required for this item with the stated unity quantity). Please refer to (Transport information) of the SDS.

    18- Shipping group Shipping group A parcel can only be composed of products with the same shipping group. In addition, dangerous goods will be splitted according to UN code.

    Shipping
    group
    Description
    L Reference spectrum
    A1a Shipment at ambient temperature for no controlled and no dangerous
    A1b Shipment at ambient temperature for no controlled and dangerous goods
    A2a Shipment at ambient temperature for * psy and * narc and no dangerous goods
    A2b Shipment at ambient temperature for * psy and * narc and dangerous goods
    A3a Shipment at ambient temperature for drug precursor and no dangerous goods
    A3b Shipment at ambient temperature for drug precursor and dangerous goods
    B1a Shipment under Ice +5C (products kept refrigerated) for no controlled and no dangerous goods
    B1b Shipment under Ice +5C (products kept refrigerated) for no controlled and dangerous goods
    B2a Shipment under Ice +5C (products kept refrigerated) for * psy and * narc and no dangerous goods
    B2b Shipment under Ice +5C (products kept refrigerated) for * psy and * narc and dangerous goods
    B3a Shipment under Ice +5C (products kept refrigerated) for drug precursor and no dangerous goods
    B3b Shipment under Ice +5C (products kept refrigerated) for drug precursor and dangerous goods
    C1a Shipment under Ice -20C (products kept frozen) for no controlled and no dangerous goods
    C2a Shipment under Ice -20C (products kept frozen) for * psy and * narc and no dangerous goods
    C3a Shipment under Ice -20C (products kept frozen) for drug precursor and no dangerous goods
    D1a Shipment with Dry-Ice for no controlled and no dangerous goods
    D1b Shipment with Dry-Ice for no controlled and dangerous goods
    D2a Shipment with Dry-Ice for * psy and * narc and no dangerous goods
    D2b Shipment with Dry-Ice for * psy and * narc and dangerous goods
    D3a Shipment with Dry-Ice for drug precursor and no dangerous goods
    D3b Shipment with Dry-Ice for drug precursor and dangerous goods