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Ziel der REACH-Verordnung ist es, den Schutz der menschlichen Gesundheit und der Umwelt vor den Risiken, die durch Chemikalien entstehen können, zu verbessern.
Die CLP-Verordnung gewährleistet, dass Arbeitnehmer und Verbraucher in der Europäischen Union durch die Einstufung und Kennzeichnung von Chemikalien eindeutig über die mit Chemikalien verbundenen Gefahren informiert werden.
Einstufungs- und Kennzeichnungsverzeichnis
Ziel der Verordnung über Biozidprodukte ist es, die Funktionsweise des Markts für Biozidprodukte in der EU zu verbessern und gleichzeitig ein hohes Schutzniveau für Mensch und Umwelt zu gewährleisten.
Genehmigung von Wirkstoffen
Zulassung von Biozidprodukten
Leitlinien und IT-Tools
Die Verordnung über die vorherige Zustimmung nach Inkenntnissetzung (PIC-Verordnung) regelt die Aus- und Einfuhr bestimmter gefährlicher Chemikalien und erlegt Unternehmen, die diese Chemikalien in Nicht-EU-Länder ausführen möchten, Verpflichtungen auf.
Liste der der PIC-Verordnung unterliegenden Chemikalien
Die POP-Verordnung verbietet bzw. schränkt die Herstellung und die Verwendung von persistenten organischen Schadstoffen in der Europäischen Union stark ein.
Listen der Stoffe
Die Grenzwerte berufsbedingter Exposition (OEL-Werte) basieren auf zwei Rechtsrahmen, die integraler Bestandteil des EU-Mechanismus zum Schutz der Gesundheit der Arbeitnehmer sind.
The Waste Framework Directive aims to protect the environment and human health from the generation and management of waste and to improve efficient use of resources.
Die überarbeitete Trinkwasserrichtlinie soll Bürger und Umwelt vor den schädlichen Auswirkungen durch verunreinigtes Trinkwasser schützen und den Zugang zu Trinkwasser verbessern.
Die ECHA organisiert Konsultationen, um Feedback von allen interessierten Kreisen einzuholen und wissenschaftliche Informationen auf möglichst breiter Ebene für die regulatorischen Verfahren zu sammeln.
Dies ist eine einzigartige Informationsquelle zu Chemikalien, die in Europa hergestellt oder dorthin eingeführt werden. Erfasst werden ihre gefährlichen Eigenschaften, ihre Einstufung und Kennzeichnung sowie Informationen zu ihrer sicheren Verwendung.
Stellungnahmen und Vereinbarungen
Der Abschnitt Unterstützung bietet Tools und praktische Anleitungen für Unternehmen, die gemäß den EU-Rechtsvorschriften für Chemikalien Pflichten zu erfüllen haben.
The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. The substance identifiers displayed in the InfoCard are the best available substance name, EC number, CAS number and/or the molecular and structural formulas.
Some substance identifiers may have been claimed confidential, or may not have been provided, and therefore not be displayed.
The EC Number is the numerical identifier for substances in the EC Inventory. The EC Inventory is a combination of three independent European lists of substances from the previous EU chemicals regulatory frameworks (EINECS, ELINCS and the NLP-list). More information about the EC Inventory can be found here.
If the substance was not covered by the EC Inventory, ECHA attributes a list number in the same format, starting with the numbers 6, 7, 8 or 9.
The EC or list number is the primary substance identifier used by ECHA.
The CAS number is the substance numerical identifier assigned by the Chemical Abstracts Service, a division of the American Chemical Society, to substances registered in the CAS registry database. A substance identified primarily by an EC or list number may be linked with more than one CAS number, or with CAS numbers that have been deleted. More information about CAS and the CAS registry can be found here.
The molecular formula identifies each type of element by its chemical symbol and identifies the number of atoms of each element found in one discrete molecule of the substance. This information is only displayed if the substance is well–defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure.
The molecular structure is based on structures generated from information available in ECHA’s databases. If generated, an InChI string will also be generated and made available for searching. This information is only displayed if the substance is well-defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure.
More help available here.
EC / List no.:
The ‘Hazard classification and labelling’ section shows the hazards of a substance based on the standardised system of statements and pictograms established under the CLP (Classification Labelling and Packaging) Regulation. The CLP Regulation makes sure that the hazards presented by chemicals are clearly communicated to workers and consumers in the European Union. The CLP Regulation uses the UN Global Harmonised System (GHS) and European Union Specific Hazard Statements (EUH).
This section is based on three sources for information (harmonised classification and labelling (CLH), REACH registrations and CLP notifications). The source of the information is mentioned in the introductory sentence of the hazard statements. When information is available in all sources, the first two are displayed as a priority.
The purpose of the information provided under this section is to highlight the substance hazardousness in a readable format. It does not represent a new labelling, classification or hazard statement, neither reflect other factors that affect the susceptibility of the effects described, such as duration of exposure or substance concentration (e.g. in case of consumer and professional uses). Other relevant information includes the following:
To see the full list of notified classifications and to get more information on impurities and additives relevant to classification please consult the C&L Inventory.
More information about Classification and Labelling is available in the Regulations section of ECHA website.
Harmonised classification and labelling is a legally binding classification and labelling for a substance, agreed at European Community level. Harmonisation is based on the substance’s physical, toxicological and eco-toxicological hazard assessment.
The ‘Hazard classification’ and labelling section uses the signal word, pictogram(s) and hazard statements of the substance under the harmonised classification and labelling (CLH) as its primary source of information.
If the substance is covered by more than one CLH entry (e.g. disodium tetraborate EC no. 215–540–4, is covered by three harmonisations: 005–011–00–4; 005–011–01–1 and 005–011–02–9), CLH information cannot be displayed in the InfoCard as the difference between the CLH classifications requires manual interpretation or verification. If a substance is classified under multiple CLH entries, a link to the C&L Inventory is provided to allow users to view CLH information associated with the substance and no text is automatically generated for the InfoCard.
It is possible that a harmonisation is introduced through an amendment to the CLP Regulation. In that case, the ATP (Adaptation to Technical Progress) number is displayed.
More info on CLH can be found here.
If available, additional information on classification and labelling (C&L) is derived from REACH registration dossiers submitted by industry. This information has not been reviewed or verified by ECHA, and may change without prior notice. REACH registration dossiers have greater data requirements (such as supporting studies) than do notifications under CLP.
If no EU harmonised classification and labelling exists and the substance was not registered under REACH, information derived from classification and labelling (C&L) notifications to ECHA under CLP Regulation is displayed under this section. These notifications can be provided by manufacturers, importers and downstream users. ECHA maintains the C&L Inventory, but does not review or verify the accuracy of the information.
Note that for readability purposes, only the pictograms, signal words and hazard statements referred in more than 5% of the notifications under CLP are displayed.
There is no harmonised classification and there are no notified hazards by manufacturers, importers or downstream users for this substance.
This section highlights four regulatory activities or outcomes under REACH – Registration, Evaluation, Authorisation and Restriction of Chemicals – Regulation (EC) No 1907/2006:
Please note: The identification of relevant regulatory activities and outcomes is done automatically and without manual verification. Substances may be grouped together under a specific regulatory activity for more efficient risk management and legislative processing (e.g. restriction on "Lead and its compounds"). In these cases, Infocards may not identify all substances in the group.Therefore it does not represent official and legally–binding information. To confirm if a substance is covered by a specific regulatory action the official publication, e.g. the electronic edition of the Official Journal of the European Union should be consulted.
The InfoCard summarises the non-confidential data of a substance held in the databases of the European Chemicals Agency (ECHA). InfoCards are generated automatically based on the data available at the time of generation.
The quality and correctness of the information submitted to ECHA remains the responsibility of the data submitter. The type of uses and classifications may vary between different submissions to ECHA and for a full understanding it is recommended to consult the source data. Information on applicable regulatory frameworks is also automatically generated and may not be complete or up to date. It is the responsibility of the substance manufacturers and importers to consult official publications, e.g. the electronic edition of the Official Journal of the European Union.
InfoCards are updated when new information is available. The date of the last update corresponds to the publication date of the InfoCard and not necessarily to the date in which the update occurred in the source data.
Here you can find all of the regulations and regulatory lists in which this substance appears, according to the data available to ECHA. This substance has been found in the following regulatory activities (directly, or inheriting the regulatory context of a parent substance):
This list contains use prohibitions of mercury and cadmium above certain thresholds in batteries and accumulators, with certain exceptions. It also captures certain labelling requirements on such products containing mercury, cadmium and lead above specified quantities.
This list contains substances assigned a binding biological exposure limit (BEL) by the European Union. National BELs for these substances may not deviate from the limits in the Directive. Annex II contains the binding BEL for lead.
This list provides the biological limit values (BLVs) pursuant to Annex IIIa of Directive 2004/37/EC (CMRD). Employers are obligated to minimize worker exposure to these agents in so far as possible, and must arrange for medical surveillance of workers exposed to these substances.
This list contains a non-exhaustive inventory of substances taken from: (1) Table 3 of Annex VI to CLP; (2) the Candidate List of SVHCs; (3) Annex XIV of REACH (Authorisation List); (4) Annex XVII of REACH (Restrictions List); (5) F-gases subject to emission limits/reporting per Regulation 517/2014/EU; and (6) volatile organic compounds (VOCs) listed in the Ambient Air Directive 2008/50/EC. The basis of the list is Annex I(3) of the Construction Products Regulation 305/2011/EC, which stipulates that construction works must not have a high impact on human health or the environment as a result of: giving off toxic gas; emissions of dangerous substances, volatile organic compounds (VOC), greenhouse gases or dangerous particles into indoor or outdoor air; release of dangerous substances into drinking water, ground water, marine waters, surface waters or soil.
This list contains substances which are banned from use in any cosmetic products marketed for sale or use in the European Union.
This list contains the Annex II material and component general use exemptions that apply to the substances prohibited from use in the manufacture of automobiles under Art. 4(2)(a) of the ELV Directive.
This list contains the specific Annex II material and component use exemptions for the substances prohibited from use in the manufacture of automobiles under Art. 4(2)(a) of the ELV Directive.
This list contains a non-exhaustive inventory of substances that fall within the European Union's hazardous substance definitions, as provided on: (1) Table 3 of Annex VI to the CLP Regulation 1272/2008/EC; (2) Annex III of Directive 2000/54/EC (Biological Agents); Candidate List of SVHCs; and REACH Annexes XIV and XVII (Authorisation and Restriction lists). They can be considered hazardous for purposes of the General Product Safety Directive 2001/95/EC.
This list contains the polluting substances for which emission limit values are assigned under Directive 2010/75/EU on Industrial Emissions (Integrated Pollution Prevention and Control - IPPC). Member States must permit all qualifying facilities in order to ensure that they minimize impact on the environment. The permit issued must provide emission limit values for pollutants on this list.
This list contains emission limit values for polluting substances in waste gases and waste water, assigned according to facility type (i.e., combustion plants (Annex V), waste incineration/co-incineration plants (Annex VI), and installations producing titanium dioxide (Annex VIII)), under Directive 2010/75/EU on Industrial Emissions (Integrated Pollution Prevention and Control - IPPC). For this list, if a substance presents 2 values in the ''Average sampling duration'' field, these indicate minimum and maximum average sampling period.
This list contains the application exemptions listed in Annexes III and IV to RoHS (2011/65/EU). Annex III contains applications exempted from the restriction in Article 4(1), while Annex IV lists applications exempted from the restriction in Article 4(1) specific to medical devices and monitoring and control instruments.
This list contains the substances listed in Annex II to the Directive on the restriction of hazardous substances in electrical and electronic equipment (RoHS - 2011/65/EU). Restricted per Art. 4(1) of RoHS, each listed substance includes a maximum concentration value tolerated by weight in homogeneous materials.
This list contains substances whose use in toys is restricted in the European Union in accordance with points 8 and 13, Part III, and Appendices A and C of Annex II (Particular Safety Requirements) to Directive 2009/48/EC on toy safety. List entries include substance name, CAS number, limit values for certain product types and, where applicable, notes on restrictions.
This list contains environmental quality standards (EQS), including annual averages and maximum allowable concentrations, for priority substances and certain other pollutants, as provided for in Article 16 of Directive 2000/60/EC establishing a framework for Community action in the field of water policy.
This list contains substances identified as priority substances that are targeted for reduction and eventual removal from waste water discharge. The list includes 'priority hazardous substances' which are subject to special restrictions.
This entry / group of substance has the following member substances:
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