Substance Information
Substance Information
Substance Infocard
Confidential or not yet assessed substance
EC / List no.: -
CAS no.: -
Mol. Formula:

Regulatory context
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):
- ECHA Legislations
- Occupational Exposure limits (OELs)
- Emission Limit Values (ELVs)
- Other chemical legislations
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Substances assessed for potential regulatory needs.
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Details of dossier compliance checks and testing proposal evaluation.
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PACT - Public activities Co-ordination ToolPublic (risk management) activities co-ordination tableTool showing an overview of substances in various key regulatory processes that authorities are working on.
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Proposals for new, or updates to existing harmonised classification and labelling of substances.
Region | Legislation | Long-term Exposure Limit (LTEL) Values | Short-term Exposure Limit (STEL) Values | Skin Designation | Dermal Sensitization | Respiratory Sensitization | Work Sector | Effective Date | Expiration Date | Miscellaneous Notes | |||||
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mg/m3 | ppm | f/ml | mg/m3 | ppm | f/ml | ||||||||||
European Union | CMD - Carcinogens and Mutagens Directive | 3.25 | 1.0 | Yes | 05 April 2024 | ||||||||||
European Union | CMD - Carcinogens and Mutagens Directive | 0.66 | 0.2 | Yes | 05 April 2026 | ||||||||||
European Union | CMD - Carcinogens and Mutagens Directive | 1.65 | 0.5 | Yes | 05 April 2024 | 05 April 2026 |
Region | Legislation | Emission medium | Process/equipment | Maximum emissions | Average emissions | Notes | |||
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Maximum limit | Maximum sampling duration | Average limit | Average sampling duration | ||||||
European Union | Ambient Air Quality Directive | 5.0 µg/m3 | 1.0 yr | Without prejudice to Annex I the criteria for 'Required proportion of valid data' shall be used for checking validity when aggregating data and calculating statistical parameters Margin of tolerance: 5 µg/m3 (100 %) on 13 December 2000 decreasing on 1 January 2006 and every 12 months thereafter by 1 µg/m3 to reach 0 % by 1 January 2010 Date by which limit value is to be met: 1 January 2010 'Year' in Averaging period referes to 'calendar year' The requirements for the calculation of annual mean do not include losses of data due to the regular calibration or the normal maintenance of the instrumentation The required proportion of valid data for the Limit Value refers to the one hour values or (if not available) 24-hour values over the year Average Limit is the Limit Value a level fixed with the aim of avoiding preventing or reducing harmful effects on human health and/or the environment and not to be exceeded once attained | |||||
European Union | Water Environmental Quality Standards Directive | Inland surface waters | 50.0 µg/l | 10.0 µg/l | 1.0 yr | Unless otherwise specified the EQS parameter expressed as an annual average value (AA-EQS) applies to the total concentration of all isomers. Inland surface waters encompass rivers and lakes and related artificial or heavily modified water bodies. | |||
European Union | Water Environmental Quality Standards Directive | Surface waters other than inland surface waters | 50.0 µg/l | 8.0 µg/l | 1.0 yr | Unless otherwise specified the EQS parameter expressed as an annual average value (AA-EQS) applies to the total concentration of all isomers. Inland surface waters encompass rivers and lakes and related artificial or heavily modified water bodies. |
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Active Implantable Medical Devices Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of Directive 90/385/EEC on Active Implantable Medical Devices, 20 July 1990, amended by Directive 2007/47/EC, 21 September 2007
This list contains hazardous substances for purposes of Directive 90/385/EEC on active implantable medical devices, particularly as regards Article 3 and Annex I (Essential Requirements). This non-exhaustive database is derived from: Table 3 of Annex VI to CLP, REACH Candidate List of SVHCs, and Directive 2000/54/EC's Annex III (Biological Agents list). Please note that Regulation (EU) 2017/745 on medical devices has repealed Directive 90/385/EEC and begun to apply from 26 May 2021. Nevertheless, Article 120 of the Regulation provides for a transitional period allowing medical devices, under specified conditions (e.g., placed on the market prior to 26 May 2021), to continue to comply with the Directive. In accordance with the fourth paragraph of Article 120, this period ends 26 May 2025.
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Aerosols Directive - Flammable Contents - Labelling RequirementsEU. Flammable Contents/Aerosols (1.8, 1.9, 2.2 of Annex), Aerosol Dispensers Directive 75/324/EEC, 9 June 1975, amended by Directive 2016/2037/EU, 22 November 2016
This list contains a subset of Table 3-listed substances in Annex VI to the CLP Regulation (1272/2008/EC). The non-exhaustive list is based on: (1) the flammable content, and (2) flammable aerosol definitions in sections 1.8 and 1.9, and (3) the labelling requirements given in section 2.2, of the Annex to the Aerosol Dispensers Directive 75/324/EEC.
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Ambient Air Quality Directive, Annex X - Ozone Precursor SubstancesEU. Ambient Air. Ozone Precursor Substances: Annex X, Section B, Directive 2008/50/EC, last amended by Directive 2015/1480/EU, 29 August 2015
This list contains ozone precursor substances, including nitrogen oxides (NO and NO2) and volatile organic compounds (VOC) that shall be measured to analyze any trend in ozone precursors, to check the efficiency of emission reduction strategies, to check the consistency of emission inventories and to help attribute emission sources to observed pollution concentrations.
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Annexes II VII XI XII XIII XIV - Assessment Thresholds & Limit ValuesEU. Limit, Critical, Target, Long-term Values; Alert, Info. and Assessment Thresholds - Anxes II A; VII B&C; XI B; XII A&B; XIII; XIV C, D&E, Dir 2008/50/EC, amended by Dir 2015/1480/EC, 29 Aug 2015
This list contains the Limit, Critical, Target and Long-term Values on ambient air for protection of human health and vegetation. It also contains the Alert, Information and Upper and Lower Assessment thresholds for sulphur dioxide, nitrogen dioxide, benzene, carbon monoxide, lead, PM2.5, PM10 and ozone.
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CAD - Chemical Agents Directive, Article 2(b)(i) - Hazardous AgentsEU. Hazardous Substances - Article 2(b)(i), Directive 98/24/EC on Protection of Workers from Chemical Agent-related Risks, 5 May 1998 (Table 3 of Annex VI to CLP, as amended)
This list contains a non-exhaustive inventory based on the list of substances with harmonised classification and labelling (i.e., Table 3 of Annex VI to the CLP Regulation 1272/2008/EC). While the harmonised list covers many hazardous substances, others not listed may also meet the classification criteria in accordance with the CLP Regulation.
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CMD - Carcinogens and Mutagens Directive, Annex III - OELVsEU. OELs for Certain Carcinogens, Mutagens, Reprotoxins: Annex III, Directive 2004/37/EC (CMRD), as amended by Directive (EU) 2022/431, 16 March 2022
This list provides occupational exposure limit values (OELVs) for carcinogens, mutagens and reprotoxic substances pursuant to Annex III 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.
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Carc and Muta Directive, Annex I - Substances, Mixtures & ProcessesEU. Substances, Mixtures, Related Processes: Annex I & Art. 2, Dir 2004/37/EC (CMRD), as amended by Dir (EU) 2022/431, 16 March 2022
This list contains a non-exhaustive inventory of substances based on Art. 2 carcinogen, mutagen and reprotoxin (CMR) definitions and Annex I of the Carcinogens, Mutagens and Reprotoxins Directive (CMRD). Category 1A and 1B CMRs are derived from the CLP Regulation's Table 3 of Annex VI (1272/2008/EC). Employers are obligated to minimize worker exposure to these agents as far as possible, and must arrange for medical surveillance of workers exposed to these substances.
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Construction Product Regulation - Annex I (3) - Hazardous SubstancesEU. Hazardous Substances for Purposes of Annex I (3) (Requirements for Construction Works), Regulation 305/2011/EU on Marketing of Construction Products, amended by Regulation 574/2014/EU, 28 May 2014
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.
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Construction Product Regulation - Article 6(5) - SDS and DeclarationEU. Hazardous Substances Subject to Declaration (Article 6(5)), Regulation 305/2011/EU on Marketing of Construction Products, amended by Regulation 574/2014/EU, 28 May 2014
This list contains a non-exhaustive inventory of substances originating from: (1) Table 3 of Annex VI to CLP (i.e., the list of harmonised substances); (2) the Candidate List of Substances of Very High Concern (SVHCs); and REACH Annex XIV (Authorisation List). This list is compiled on the basis of Article 6(5) of Regulation 305/2011/EC on Marketing of Construction Products. This provision requires SDSs and information on hazardous substances (i.e., SVHCs) contained in construction products be provided with the declaration of performance.
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Cosmetic Products Regulation, Annex II - Prohibited SubstancesEU. Prohibited Substances: Annex II, Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation (EU) 2021/1902, OJ L 387 of 3 November 2021
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Ecolabel - Restrictions for Hazardous Substances/MixturesEU. Hazardous Substances which may Preclude Goods from the Ecolabel Award as per Article 6(6) of Regulation 66/2010/EC, L 27/1, 30 January 2010
This list contains a non-exhaustive inventory of substances based on the list of hazardous substances with harmonised classification and labelling (i.e. Table 3 of Annex VI to the CLP Regulation), and the Candidate List of substances of very high concern (SVHCs). Pursuant to Article 6(6) of the EU Ecolabel Regulation, the ecolabel must not be awarded to goods containing substances or mixtures classified according to the CLP as toxic; hazardous to the environment; and carcinogenic, mutagenic, or toxic for reproduction (CMRs). Nor are products allowed the ecolabel award when they contain SVHCs (per Article 57 of REACH). While the CLP's harmonised list contains many such substances, other ones not listed in Table 3 may also meet the criteria specified for classification under the CLP.
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End-of-Life Vehicles Directive - Hazardous SubstancesEU. Hazardous Substances per Article 2(11) of End-of-Life Vehicles Directive 2000/53/EC, 21 October 2000, amended by Directive 2020/363/EU, 5 March 2020 (based on Table 3/Annex VI of CLP)
This list contains a non-exhaustive inventory of hazardous substances as defined by Article 2(11) of the End-of-Life Vehicles Directive 2000/53/EC. It is based on the relevant subset of substances with harmonised classification listed in Table 3 of Annex VI to the CLP Regulation 1272/2008/EC.
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Active and Intelligent Materials - CMR Substances not allowed for useEU. Carcinogens, Mutagens and Reproductive substances Not Allowed for Use in Components of Active and Intelligent Materials and Articles (Article 5(2)(c)(i)), Regulation 450/2009/EC, 30 May 2009
This list contains a non-exhaustive list of Carcinogens, Mutagens and Reproductive substances (CMRs) that are not allowed for use in components of active and intelligent materials and articles per Art. 5(2)(c)(i) of Regulation 450/2009/EC. The list is derived from a subset of substances on Table 3 of Annex VI to the CLP Regulation (1272/2008/EC).
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FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised UseEU. Plastic Food Contact Materials (FCMs) per Regulation 10/2011/EU (Union List), Directive 282/2008/EC on Recycled Plastic FCMs, 28 March 2008, amended by Regulation 2015/1906/EU, 23 October 2015
This list contains the Annex I Plastic Food Contact Materials (FCMs) authorised for use in the European Union under Regulation 10/2011/EU. Pursuant to Art. 4(b) of Directive 282/2008/EC on recycled plastic FCMs, plastic recycling processes can only be authorised if input originates from plastic materials and articles manufactured in accordance with EU legislation on plastic food contact materials and articles.
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General Product Safety Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of General Product Safety Directive (2001/95/EC), 15 January 2002, amended by Reg 596/2009/EC, 18 July 2009
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.
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In Vitro Diagnostic Medical Devices Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of Article 3 & Annex I (Essential Requirements), Directive 98/79/EC on In Vitro Diagnostic Medical Devices, 7 December 1998
This list contains a non-exhaustive inventory of hazardous substances for purposes of essential requirements (Article 3 and Annex I) for general safety, design, manufacture and hazard communication of in vitro diagnostic medical devices. It is derived from: Table 3 of Annex VI to CLP, REACH Candidate List of SVHCs, and Directive 2000/54/EC's Annex III (Biological Agents list). Note that Regulation 2017/746/EU on in vitro diagnostic medical devices was published in the EU Official Journal on 5 May 2017. With few exceptions specified in Articles 112 and 113 of this Regulation, Directive 98/79/EC is repealed, and the rules pursuant to 2017/746/EU apply, from 26 May 2022.
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IPPC - Industrial Emissions Directive, Annex II - Polluting SubstancesEU. Polluting Substances: Annex II, Directive 2010/75/EU on Industrial Emissions (IPPC), 17 December 2010
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.
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Inland Transport of Dangerous Goods Directive, Annex I - ADREU. Dangerous Goods List (ADR, Chap. 3.2, Table A), Directive 2008/68/EC, last amended by Directive 2020/1833/EU, 4 December 2020
This list contains the ADR Dangerous Goods List, as implemented by the European Union's Directive 2008/68/EC. This Directive applies the European Agreements on the international transport of dangerous goods by road (ADR) and inland waterways (ADN), and the regulations concerning the international carriage of dangerous goods by rail (RID). Any specific CAS linked as members for substances where the list refers to finished material/article/compound/component are representative examples, but not exhaustive.
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Inland Transport of Dangerous Goods Directive, Annex II - RIDEU. Dangerous Goods List (RID, Chap. 3.2, Table A), Directive 2008/68/EC, last amended by Directive 2020/1833/EU, 4 December 2020
This list contains the RID Dangerous Goods List, as implemented by the European Union's Directive 2008/68/EC. This Directive applies the European Agreements on the international transport of dangerous goods by road (ADR) and inland waterways (ADN), and the regulations concerning the international carriage of dangerous goods by rail (RID). Any specific CAS linked as members for substances where the list refers to finished material/article/compound/component are representative examples, but not exhaustive.
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Inland Transport of Dangerous Goods Directive, Annex III - ADNEU. Dangerous Goods List (ADN, Chap. 3.2, Table A), Directive 2008/68/EC, last amended by Directive 2020/1833/EU, 4 December 2020
This list contains the ADN Dangerous Goods List, as implemented by the European Union's Directive 2008/68/EC. This Directive establishes rules for the safe transport of dangerous goods between EU countries by road (ADR) and inland waterways (ADN), and the regulations concerning the international carriage of dangerous goods by rail (RID). Any specific CAS linked as members for substances where the list refers to finished material/article/compound/component are representative examples, but not exhaustive.
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Marine Environmental Policy Framework Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of Directive 2008/56/EC (Marine Strategy Framework Directive), 25 June 2008, amended by Directive 2017/845/EU, 18 May 2017
This list contains a non-exhaustive inventory of hazardous substances for purposes of the Marine Strategy Framework Directive, especially as it concerns Art. 3(8), and Annexes I and III. The listed substances meet the European Union's definitions as hazardous, 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 Annex XIV (Authorisation List).
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Medical Devices Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of Medical Devices Directive 93/42/EEC, 12 July 1993, amended by Directive 2007/47/EC, 21 September 2007
This list contains hazardous substances in accordance with the Medical Devices Directive's (MDD) design and construction requirements pursuant to Annex I, Part II (7) & (8) (i.e., chemical, physical and biological properties; and infection and microbial contamination). Specifically, the non-exhaustive database is derived from: Table 3 of Annex VI to CLP, REACH Candidate List of SVHCs, and Directive 2000/54/EC's Annex III (Biological Agents list). Please note that Regulation (EU) 2017/745 on medical devices has repealed Directive 93/42/EEC and begun to apply from 26 May 2021. Nevertheless, Article 120 of the Regulation provides for a transitional period allowing medical devices, under specified conditions (e.g., placed on the market prior to 26 May 2021), to continue to comply with the Directive. In accordance with the fourth paragraph of Article 120, this period ends 26 May 2025.
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Medical Devices Regulation - Hazardous SubstancesEU. Hazardous Substances for Purposes of Medical Devices Regulation 2017/745/EU, 5 May 2017, as amended by Regulation 2020/561/EU, 24 April 2020
This list contains hazardous substances for purposes of the Medical Devices Regulation (MDR), based on the legislation's Annex I general safety and performance requirements, including for chemical, physical and biological properties. Specifically, the non-exhaustive database is derived from: Table 3 of Annex VI to CLP, REACH Candidate List of SVHCs, and Directive 2000/54/EC's Annex III (Biological Agents list).
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Annex of Approved Active Substances for Plant Protection ProductsEU. Annex of Approved Active Substances, Regulation 540/2011/EU implementing Regulation 1107/2009/EC, last amended by Implementing Regulation (EU) 2022/378, OJ L 72, 7 March 2022
This list contains the active substances approved under Regulation 1107/2009/EC, as listed in Regulation 540/2011/EU. The list is separated into five parts: Part A (deemed to have been approved under 1107/2009/EC); Part B (approved under 1107/2009/EC); Part C (basic substances); Part D (low-risk active substances); and Part E (candidates for substitution). Entries include common & IUPAC names, identifiers (e.g., CAS, CIPAC), purity information, and approval and approval expiration dates.
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Annex of co-formulants not accepted for inclusion in PPPsEU. Co-formulants not accepted for inclusion in Plant Protection Products Regulation (PPPR): Annex III, Regulation 1107/2009/EC, as amended by Regulation 2021/383/EU, 4 March 2021
This list contains the PPPR's Annex III co-formulants that are not accepted for inclusion in plant protection products (PPPs), as referred to in Article 27 of Regulation 1107/2009/EC (PPPR). Authorisations granted for PPPs containing co-formulants listed in Annex III shall be amended or withdrawn from the EU market no later than 24 March 2023.
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Annexes II, III, IV, VII - Defined & Temporary Maximum Residue LevelsEU. Pesticides. Maximum Residue Levels: Annexes II, III, IV, VII, Regulation 396/2005/EC, last amended by Regulation (EU) 2022/93, OJ L 16 of 25 January 2022
This list contains the maximum residue level (MRLs) entries as listed in the following annexes of Regulation (EC) No 396/2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC: (1) Annex II: Maximum Residue Levels; (2) Annex III: Temporary MRLs; (3) Annex IV: Active Substances for Which No MRLs Are Required; and (4) Annex VII: Active Substance/Product Combinations.
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FCM and Articles Regulation, Annex I - Authorised SubstancesEU. Union List of Authorised Substances: Annex I, Plastics Food Contact Regulation 10/2011/EU, as amended by Regulation 2020/1245/EU, 3 September 2020
This list contains the Union list of authorised monomers, other starting substances, macromolecules obtained from microbial fermentation, additives and polymer production aids. It is taken from Annex I of the Commission Regulation (EU) No 10/2011 on plastic materials and articles intended to come into contact with food.
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Pressure Equipment Directive - Group 1 Fluids Hazardous SubstancesEU. Group 1 Fluids per Article 13(1)(a), Directive 2014/68/EU on Pressure Equipment, 27 June 2014
This list contains a non-exhaustive inventory of hazardous substances based on Article 13(1)(a) of Directive 2014/68/EU, defining Group 1 fluids for purposes of classifying pressure equipment in accordance with the Directive. The list is derived from a subset of the substances with harmonised classifications, as listed on Table 3 of Annex VI to the CLP Regulation 1272/2008/EC.
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Protection of Pregnant and Breastfeeding Workers Directive, Annex I+IIEU. Chemical Agents: Annexes I & II, Directive 92/85/EEC on Pregnant Workers, 28 November 1992 (updated by table 3 of Annex VI to CLP, 5 October 2018)
This list contains a non-exhaustive inventory of substances to which pregnant workers and workers who have recently given birth or are breastfeeding may not be exposed. Employers are obligated to prevent the exposure of these workers to any agents that may have adverse health effects on either mother or child. The inventory originates from Table 3 of Annex VI to the CLP.
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Physical, Biological and Chemical Agents & Processes and WorkEU. Non-Exhaustive List of Banned Substances, Directive 94/33/EC on Young People at Work, 20 August 1994, as amended by Dir 2014/27/EU, March 5, 2014 (Based on Table 3 of Annex VI to CLP, inter alia)
This list contains biological and chemical agents, in accordance with Art. 7 and points 2 and 3 of the Annex to Directive 94/33/EC, to which young persons (under 18 years of age) may not be exposed at the workplace. The list is a non-exhaustive inventory of such substances based on: 1) agents of risk groups 3 and 4 under Directive 2000/54/EC; 2) Table 3 of Annex VI to the CLP Regulation; 3) and Annex I of Directive 2004/37/EC.
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Safety and Health of Workers at Work Directive - Hazardous SubstancesEU. Hazardous Substances for Purposes of Directive 89/391/EEC, 29 June 1989, amended by Regulation 1137/2008/EC, 21 November 2008 (Table 3/Annex VI, CLP; Annex III, 2000/54/EC)
This list contains a non-exhaustive inventory of substances that fall within the scope of the European Union's definition of hazardous chemical and biological substances, as provided on: (1) Table 3 of Annex VI to the CLP Regulation 1272/2008/EC; and (2) Annex III of Directive 2000/54/EC (Biological Agents). The EU's Occupational Safety and Health (OSH) Framework Directive 89/391/EEC applies to risks arising from chemical, physical and biological agents at the workplace.
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Workplace Signs - minimum requirements & signs on containers and pipesEU. Workplace Signage: Annexes I and III, Directive 92/58/EEC, last amended by Directive 2014/27/EU, 5 March 2014
This list contains hazardous substances based on Table 3 of Annex VI to the CLP Regulation 1272/2008/EC. According to the annexes to Directive 92/58/EEC, storage areas and containers containing chemical substances or mixtures that are classified as hazardous according to the CLP Regulation must be duly marked and/or labeled. Directive 92/58/EEC requires employers to ensure proper signage is posted in areas where hazards cannot be avoided or reduced.
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Statistics on Pesticides Regulation - Annex III Harmonised C&LEU. Harmonized Classification of Substances: Annex III, Regulation 1185/2009/EC, as amended by Regulation (EU) 2021/2010, OJ L 410, 18 November 2021
This list contains Annex III of Regulation 1185/2009/EC. It provides the substances with harmonised classifications to be covered to produce European statistics on the sales and use of pesticides.
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Annex II, Sec III - Allergenic Fragrances Banned/Restricted in ToysEU. Allergenic Fragrances Banned or Restricted in Toys, Directive 2009/48/EC, OJ L 170/1, 30 June 2009, last amended by Directive (EU) 2020/2089, OL L 423, 15 December 2020
This list contains allergenic fragrances whose use in toys is banned or restricted in the European Union in accordance with point 11, Part III of Annex II (Particular Safety Requirements) to Directive 2009/48/EC on toy safety. For each entry in the list, the substance name, CAS number and, where applicable, notes on restrictions are provided.
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Waste Framework Directive, Annex III - Waste - Hazardous PropertiesEU. Substances according to Hazardous Waste Properties: Annex III, Directive 2008/98/EC, 22 November 2008, amended by Directive 2018/851/EU, 14 June 2018
This list contains substances that have been assigned hazard property (HP) waste codes 1-15, as defined in terms of the hazard class and category, hazard (H) statement, and/or concentration limits provided in Annex III of the Waste Framework Directive 2008/98/EC. The classifications of the substances listed in the list are based on their harmonised classifications per Table 3 of Annex VI to the CLP Regulation 1272/2008/EC.
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Annex I, Part A - Priority Substances & Pollutants in waterEU. Environmental Quality Standards (EQS) for Priority Substances: Annex I, Part A, Directive 2008/105/EC, 24 December 2008, amended by Directive 2013/39/EU, 24 August 2013
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.
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Water Framework Directive, Annex X - Priority SubstancesEU. Annex X to Directive 2000/60/EC, Priority Substances in the Field of Water Policy, as amended by Directive 2013/39/EU, OJ L 226/1, 24 August 2013
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.
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Water for Human Consumption Directive - Quality CriteriaEU. Quality Criteria for Water for Human Consumption, Directive 98/83/EC, as amended by Directive 2015/1787/EU, 27 October 2015
This list contains the Annex I parameters from the Drinking Water Directive 98/83/EC, which concerns the quality of water intended for human consumption. Its objective is to protect human health from adverse effects of any contamination of water intended for human consumption by ensuring that it is wholesome and clean.
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