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Tests under this Part shall be according to methods recognised and recommended by the competent international bodies where such recommendations exist.
If it is not technically possible or if it does not appear scientifically necessary to give information, the reasons shall be clearly stated and subject to acceptance by the competent authority.
The name of the body or bodies responsible for carrying out the studies shall be mentioned.
In addition to the information requested below, member States may, if they consider it necessary for the risk assessment, require that the notifier provides the following additional information:
vapour pressure,
daphnia acute toxicity test.
0. | IDENTITY OF MANUFACTURER AND THE IDENTITY OF THE NOTIFIER: LOCATION OF THE PRODUCTION SITE |
For substances manufactured outside the Communities and for which, for the purpose of notification, the notifier has been designated as the manufacturer’s sole representative, the identities and addresses of the importers who will be bringing the substance into the Communities. | |
1. | IDENTITY OF THE SUBSTANCE |
1.1 | Name |
1.1.1 | Names in the IUPAC nomenclature |
1.1.2 | Other names (usual name, trade name, abbreviation) |
1.1.3 | CAS number and CAS name (if available) |
1.2 | Molecular and structural formula |
1.3 | Composition of the substance |
1.3.1 | Degree of purity (%) |
1.3.2 | Nature of impurities, including isomers and by-products |
1.3.3 | Percentage of (significant) main impurities |
1.3.4 | If the substance contains a stabilizing agent or an inhibitor or other additives, specify: nature, order of magnitude: ..ppm; .. % |
1.3.5 | Spectral data (UV, IR, NMR or mass spectrum) |
1.3.6 | Chromatographic data (HPLC, GC) |
1.4 | Methods of detection and determination |
A full description of the methods used or the appropriate bibliographical references. Apart from methods of detection and determination, information shall be given on analytical methods which are known to the notifier and allow detection of a substance and its transformation products after discharge into the environment as well as determination of the direct exposure of humans. | |
2. | INFORMATION ON THE SUBSTANCE |
2.0 | Production |
Information given in the section should be sufficient to allow an approximate but realistic estimation of human and environmental exposure, associated with the production process.Precise details of the production process, particularly those of a commercially sensitive nature, are not required. | |
2.0.1 | Technological process(es) used in production |
2.0.2 | Exposure estimate related to production:
|
2.1 | Proposed uses |
Information given in this section should be sufficient to allow an approximate but realistic estimation of human and environmental exposure to the substances as associated with the proposed/expected uses. | |
2.1.1 | Types of use: description of the function and the desired effects |
2.1.1.1 | Technological process(es) related to the use of the substance (where known) |
2.1.1.2 | Exposure estimate(s) related to use (where known):
|
2.1.1.3 | Form under which the substance is marketed: substance, preparation, product |
2.1.1.4 | Concentration of the substance in marketed preparations and products (where known) |
2.1.2 | Fields of application with approximate breakdown:
|
2.1.3 | Where known and where appropriate, the identity of the recipients of the substance |
2.2 | Estimated production and/or imports for each of the anticipated uses or fields of application |
2.2.1 | Overall production and/or imports in tonnes per year:
For substances manufactured outside the Communities and for which, for the purpose of notification, the notifier has been designated as the manufacturer’s sole representative, this information must be given for each of the importers identified under section 0 above. |
2.2.2 | Production and/or imports, broken down in accordance with 2.1.1 and 2.1.2 expressed as a percentage:
|
2.3 | Recommended methods and precautions concerning: |
2.3.1 | – Handling |
2.3.2 | – Storage |
2.3.3 | – Transport |
2.3.4 | – Fire (nature of combustion gases or pyrolysis, where proposed uses justify this) |
2.3.5 | Other dangers, particularly chemical reaction with water |
2.4 | Emergency measures in the case of accidental spillage |
2.5 | Emergency measures in the case of injury to persons (e.g. poisoning) |
2.6 | Packaging |
3. | PHYSICO-CHEMICAL PROPERTIES OF THE SUBSTANCE |
3.0 | State of the substance at 20 degrees C and 101.3 kPa |
3.1 | Melting point |
3.2 | Boiling point |
3.6 | Water solubility |
3.8 | Partition coefficient n-octanol/water |
3.9 | Flash point |
3.10 | Flammability |
4. | TOXICOLOGICAL STUDIES |
4.1 | Acute toxicity |
For tests 4.1.1 to 4.1.2 one route of administration is sufficient.Substances other than gases should be treated by oral administration.Gases should be tested by inhalation. | |
4.1.1 | Administered orally |
4.1.2 | Administered by inhalation |
4.1.5 | Skin irritation |
4.1.6 | Eye irritation |
4.1.7 | Skin sensitization |
4.3 | Other effects |
4.3.1 | Mutagenicity The substance should be examined in a bacteriological (reverse mutation) test with and without metabolic activation. |
5. | ECOTOXICOLOGICAL STUDIES |
5.2 | Degradation: biotic. |
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