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More information about persistent, bioaccumulative and toxic substances here. Potentially a Persistent Organic Pollutant: is shown for substances that have been proposed for their inclusion in the Stockholm Convention and are under assessment, or for which a proposal is under preparation in the European Union. In case the substance classification is not harmonised and the substance is not registered the properties are derived from classifications provided in CLP notifications.

Please note: The icons in this section are only meant as visual indicators to help communicate information about the abovementioned critical properties. R There is broad agreement in that a majority of data submitters agree this substance is Toxic to Reproduction The regulation aims improve the protection of human health and the environment from the risks that can be posed by chemicals, while enhancing the competitiveness of the EU chemical industry.

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The REACH regulatory processes identified for the Brief Profile are: Registration Pre-registration — indicated if the substance is included in the list of pre-registered substances. Pre-registration allows companies to continue manufacturing and importing their phase-in substances for several years until the registration deadline is reached. Evaluation Dossier evaluation — indicated if at least one registered dossier for the substance has been evaluated under REACH for compliance check or testing proposal evaluation and associated decision s published on the ECHA website.

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After evaluation, proposals may be made for further regulatory action regarding the substance. Authorisation Candidate List — indicates if the substance is included in the candidate list of substances of very high concern SVHCs.

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The Candidate List includes substances that are subject to additional protocols and reporting obligations and which may eventually be included in the Authorisation list, further limiting their use. These substances cannot be placed on the market or used after a given date, unless an authorisation is granted for their specific use, or the use is exempted from authorisation.

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The Restriction list describes the conditions for the manufacture, placing on the market or use of certain substances, either on their own or in mixtures or articles.

The regulation aims to protect human health and the environment by banning or severely restricting the production and use of persistent organic pollutants in the European Union.

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List of substances proposed as POPs - Indicates if the substance has been proposed for its inclusion in the Stockholm Convention or if a proposal is under preparation in the European Union. The goal of CLP is to make sure that hazards presented by chemicals are clearly communicated to workers and consumers in the European Union through a system of classifying and labelling of chemicals.

The BPR addresses the placing on the market and use of biocidal products, which are used to protect humans, animals, materials or articles against harmful organisms, like pests or bacteria, by regulating the active substances contained in a biocidal product. The BPR regulatory processes identified for the Brief Profile are: Active substance approval — indicates if the substance is an approved biocidal active substance.

PIC administers the import and export of certain hazardous chemicals and places obligations on companies who wish to export these chemicals to non-EU countries.