Substance Information

Substance Infocard

IC

Ethylene oxide

Help Substance identity

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.

EC (European Community) Number

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.

CAS (Chemical Abstract Service) registry number

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.

Molecular formula

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.

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.: 200-849-9

CAS no.: 75-21-8

Mol. formula: C2H4O

formula
Help Hazard classification and labelling

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.

Please note:

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:

  • Substances may have impurities and additives that lead to different classifications. If at least one company has indicated that the substance classification is affected by impurities or additives, this will be indicated by an informative sentence. However, substance notifications in the InfoCard are aggregated independently of the impurities and additives.
  • Hazard statements were adapted to improve readability and may not correspond textually to the hazard statements codes description in the European Union Specific Hazard Statements (EUH) or the UN Global Harmonised System (GHS).

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.

More help available here.

Harmonised classification and labelling (CLH)

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.

Classification and labelling under REACH

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.

Notifications under the Classification Labelling and Packaging (CLP) Regulation

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.

GHS02: Flammable GHS05: Corrosive GHS08: Serious Health Hazard GHS06: Acute Toxicity

Danger! According to the harmonised classification and labelling (ATP14) approved by the European Union, this substance is toxic if swallowed, causes severe skin burns and eye damage, is toxic if inhaled, may cause genetic defects, may cause cancer, may damage fertility and is suspected of damaging the unborn child, causes damage to organs through prolonged or repeated exposure, is an extremely flammable gas, causes serious eye damage, may cause respiratory irritation and may cause drowsiness or dizziness.

GHS04: Gas under Pressure

Additionally, the classification provided by companies to ECHA in REACH registrations identifies that this substance may damage fertility or the unborn child, is an extremely flammable gas and may react explosively even in the absence of air, contains gas under pressure and may explode if heated and causes skin irritation.

Helpful information About this substance

This section provides an overview of the calculated volume at which the substance is manufactured or imported to the European Economic Area (EU28 + Iceland, Liechtenstein and Norway). Additionally, if available, information on the use of the substance and how consumers and workers are likely to be exposed to it can also be displayed here.

The use information is displayed per substance life cycle stage (consumer use, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites or in manufacturing). The information is aggregated from the data coming from REACH substance registrations provided by industry.

For a detailed overview on identified uses and environmental releases, please consult the registered substance factsheet.

Use descriptors are adapted from ECHA guidance to improve readability and may not correspond textually to descriptor codes described in Chapter R.12: Use Descriptor system of ECHA Guidance on information requirements and chemical safety assessment.

The examples provided are generic examples and may not apply to the specific substance you are viewing. A substance may have its use restricted to certain articles or products and therefore not all the examples may apply to the specific substance. Furthermore, some substances can be found in an article, but with unlikely exposure (e.g. inside a watch) or with very low concentrations considered not to pose risks to human health or the environment.

Please note:

For readability purpose, only non-confidential use descriptors occurring in more than 5% of total occurrences are displayed.

The described Product category (i.e. the products in which the substance may be used) may refer to uses as intermediate and under controlled conditions, for which there is no consumer exposure.

More help is available here.

This substance is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 000 tonnes per annum.

This substance is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Biocidal Uses

This substance is being reviewed for use as a biocide in the EEA and/or Switzerland, for: disinfection.

Consumer Uses

This substance is used in the following products: inks and toners and fillers, putties, plasters, modelling clay.
Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use as processing aid.

Article service life

Release to the environment of this substance can occur from industrial use: manufacturing of the substance, formulation in materials, as an intermediate step in further manufacturing of another substance (use of intermediates) and for thermoplastic manufacture.
This substance can be found in complex articles, with no release intended: vehicles.

Widespread uses by professional workers

This substance is used in the following products: plant protection products, laboratory chemicals, coating products, inks and toners, adhesives and sealants and fertilisers.
This substance is used in the following areas: agriculture, forestry and fishing, building & construction work and scientific research and development.
This substance is used for the manufacture of: chemicals.
Release to the environment of this substance can occur from industrial use: manufacturing of the substance.
Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).

Formulation or re-packing

This substance is used in the following products: polymers, inks and toners, coating products, fuels, non-metal-surface treatment products, paper chemicals and dyes and washing & cleaning products.
Release to the environment of this substance can occur from industrial use: formulation of mixtures and formulation in materials.

Uses at industrial sites

This substance is used in the following products: polymers, inks and toners, washing & cleaning products, non-metal-surface treatment products and paper chemicals and dyes.
This substance has an industrial use resulting in manufacture of another substance (use of intermediates).
This substance is used for the manufacture of: chemicals.
Release to the environment of this substance can occur from industrial use: for thermoplastic manufacture and as an intermediate step in further manufacturing of another substance (use of intermediates).

Manufacture

Release to the environment of this substance can occur from industrial use: manufacturing of the substance.

Help Properties of concern

The ‘Properties of concern’ section shows ECHA-assigned graphical indicators for certain substance properties that are regarded as being of relevance or importance to human health and/or the environment based on the information provided to the Agency.

Properties of concern are calculated at four "levels" of certainty:

  • "Recognised" - meaning that the concern is indicated in an official source. Recognised concerns are illustrated with a dark red icon. Sources for these are either a Harmonised C&L (CLP Regulation Annex VI) or in the Candidate list of substances of very high concern for authorisation (REACH).
  • "Potential" - again comes from official sources only. Potential concerns are illustrated with a light red icon. For (C), (M), and (R) it means that the concern is suspected in a Harmonised C&L (CLP Regulation Annex VI), as Carc. 2, Muta. 2, or Repr. 2. For (PBT) and (ED) Potential means that the concern is under assessment in the PBT or ED assessment list, and the outcome indicates a potential ED. There are no potential (Ss) or (Sr)s.
  • "Broad agreement" - comes from data submitted by industry to ECHA, and indicates that the data submitted is aligned, with >= 50% of the data submitters providing the same concern. Broad agreement concerns are illustratated with a solid outlined circle icon.
  • "Minority position" - comes from data submitted by industry to ECHA, and indicates that the data submitted is not aligned. > 5% and < 50% of the data submitters have provided the concerns indicated at this "level". Minority position concerns are illustrated with a greyed out circle icon.

The following properties of concern are calculated:

  • Carcinogenic (C) – Recognised carcinogen: comes from a harmonised C&L classifying the substance as Carc. 1A or 1B and/or an entry in the Candidate list. Potential carcinogen: comes from a harmonised C&L classifying the substance as a suspected carcinogen Carc.2. Broad agreement: comes from industry data where a majority of data submitters agree the substance is carcinogenic. Minority position: comes from industry data where a minority of data submitters indicate the substance is carcinogenic. More information about carcinogenicity here.
  • Mutagenic (M) – Recognised mutagen: comes from a harmonised C&L classifying the substance as Muta. 1A or 1B and/or an entry in the Candidate list. Potential mutagen: comes from a harmonised C&L classifying the substance as a suspected mutagen Muta. 2. Broad agreement: comes from industry data where a majority of data submitters agree the substance is mutagenic. Minority position: comes from industry data where a minority of data submitters indicate the substance is mutagenic. More information about mutagenicity here.
  • Toxic to Reproduction (R) – Recognised as toxic to reproduction: comes from a harmonised C&L classifying the substance as Carc. 1A or 1B and/or an entry in the Candidate list. Potentially toxic to reproduction: comes from a harmonised C&L classifying the substance as suspected toxic to reproduction Repr. 2. Broad agreement: comes from industry data where a majority of data submitters agree the substance is toxic to reproduction. Minority position: comes from industry data where a minority of data submitters indicate the substance is toxic to reproduction. More information about reproductive toxicity here.
  • Skin sensitising (Ss) – Recognised skin sensitiser: comes from a harmonised C&L classifying the substance as Skin Sens. 1, 1A, or 1B. Broad agreement: comes from industry data where a majority of data submitters agree the substance is a skin sensitiser. Minority position: comes from industry data where a minority of data submitters indicate the substance is skin sensitising. More information about skin sensitiser here.
  • Respiratory sensitising (Sr) – Recognised respiratory sensitiser: comes from a harmonised C&L classifying the substance as Resp. Sens. 1, 1A, or 1B and/or an entry in the Candidate list. Broad agreement: comes from industry data where a majority of data submitters agree the substance is a respiratory sensitiser. Minority position: comes from industry data where a minority of data submitters indicate the substance is a respiratory sensitiser. More information about respiratory sensitiser here.
  • PBT – Recognised Persistent, bioaccumulative and toxic (PBT) (or vPvB): comes from an entry in the Candidate list. Potential PBT: is shown for substances under assessment, and comes from an entry in the PBT assessment list. Broad agreement: comes from industry data where a majority of data submitters agree the substance is PBT. Minority position: comes from industry data where a minority of data submitters indicate the substance is PBT. More information about persistent, bioaccumulative and toxic substances here.
  • ED – Recognised Endocrine Disruptor (ED): comes from an entry in the Candidate list. Potential ED: is shown for substances under assessment, and comes from an entry in the ED assessment list, if the outcome is not final and “Not ED”. At this time there is no industry submitted data taken into account to display an ED property of concern. More information about endocrine disrupting substances here.
  • POP – Recognised Persistent Organic Pollutant (POP): comes from an entry in the Annex I, II or III to the POPs Regulation and/or an entry in the Annex A, B or C to the Stockholm Convention. 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. Note that proposals that have been set aside, either before their submission by the EU to the Convention, or by the POP Review Committee are still indicated as "Potentially a POP".

The substance properties displayed in this section are derived from Harmonised classification and labelling (CLH) data, entries in the Candidate list of substances of very high concern for authorisation, the PBT assessment list, the ED assessment list, REACH registered dossier data and from notifications made under CLP. A prioritisation hierarchy means that data is taken from harmonised C&L data and regulatory lists first, then REACH registrations and finally from CLP notifications.

Impurities or additives: When a specific critical property is calculated from industry data and where the majority of data submitters have indicated that the property relates to cases containing impurities and/or additives, then the respective critical property icon is modified with an asterisk (*).

  • C

Carcinogenic

  • M

Mutagenic

  • R

Toxic to Reproduction

  • ED

Under assessment as Endocrine Disrupting

Help Important to know

This section highlights four regulatory activities or outcomes under REACH – Registration, Evaluation, Authorisation and Restriction of Chemicals – Regulation (EC) No 1907/2006:

  • Community rolling action plan - indicates if the substance is or was included in the Community rolling action plan (CoRAP). The CoRAP list includes substances that could pose a risk to human health or the environment and whose (potentially hazardous) properties are to be evaluated by the Member States in the next three years. After evaluation, proposals may be made for further regulatory action regarding the substance.
  • Candidate List - indicates if the substance is included in the candidate list of substances of very high concern (SVHCs). 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.
  • Authorisation list (Annex XIV to REACH) - indicates if the substance is included in the Authorisation list. 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.
  • Restriction list (Annex XVII to REACH) - indicates if the substance is included in the Restriction List. 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.

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.

More help available here.

Help How to use it safely

This section provides links to the list of precautions (precautionary statements) and to the guidance on safe use, if they have been provided in REACH registration dossiers.

  • Precautionary statements - describe recommended measures to minimise or prevent adverse effects resulting from exposure to a hazardous product or improper storage or handling of a hazardous product.
  • Guidance on safe use - recommendations by substance registrant on the proper use of the substance in various situations. Examples include recommended measures on fire-fighting, transport and recycling and disposal.

Please note: Precautionary measures and guidance on safe use concern the use and handling of the specific substance as such, not of the presence of the substance in other articles or mixtures. The precautionary measures and guidance on safe use are as submitted to ECHA by registrants under the REACH Regulation. Information on precautionary measures and the safe use is submitted by the registrant of a substance and the registrant is solely responsible for its accuracy and completeness.

More help available here.

about INFOCARD - Last updated: 14/10/2021 InfoCard

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.

More help available here.

Help Help

Key datasets

HELP HELP

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):

REACH - Registration, Evaluation, Authorisation and Restriction of Chemicals Regulation
CLP - Classification, Labelling and Packaging
  • Harmonized C&L
    CLP Regulation Annex VI
    Substances for which an agreed set of classification and labelling data has been agreed at EU level by Member States.
  • Substances for which classification and labelling data have been notified to ECHA by manufacturers or importers. Such notifications are required for hazardous substances, mixtures, or articles, manufactured or imported at over 1 kg per annum.
  • Proposals for new, or updates to existing harmonised classification and labelling of substances.
  • Seveso Annex I
    Seveso III Directive Annex I
    Substances for which industrial accident prevention and reporting requirements have been established.
BPR - Biocidal Products Regulation
Previous Legislations
  • Substances listed in the EINECS, ELINCS, or NLP inventories.
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
mg/m3 ppm f/ml mg/m3 ppm f/ml
European Union CMD - Carcinogens and Mutagens Directive 1.8 1.0 Yes
Active Implantable Medical Devices Directive
  • Active Implantable Medical Devices Directive - Hazardous Substances
    EU. 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.

Aerosol Dispensers Directive
  • Aerosols Directive - Flammable Contents - Labelling Requirements
    EU. 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.

CAD - Chemical Agents Directive
  • CAD - Chemical Agents Directive, Article 2(b)(i) - Hazardous Agents
    EU. 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.

CMD - Carcinogens and Mutagens Directive
  • CMD - Carcinogens and Mutagens Directive, Annex III - OELVs
    EU. OELs for Certain Carcinogens & Mutagens: Annex III, Directive 2004/37/EC (CMD), as amended by Directive 2019/983/EU, 20 June 2019

    This list contains occupational exposure limit values (OELs) for carcinogens and mutagens pursuant to Annex III of Directive 2004/37/EC (CMD). 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.

  • Carc and Muta Directive, Annex I - Substances, Mixtures & Processes
    EU. Substances, Mixtures, Related Processes: Annex I & Article 2, Directive 2004/37/EC (CMD), as amended by Directive 2019/130/EU, 31 January 2019

    This list contains a non-exhaustive inventory of substances based on Art. 2 carcinogen and mutagen (CM) definitions and Annex I of the Carcinogens and Mutagens Directive. Category 1A and 1B carcinogens and mutagens 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.

Construction Products Regulation
  • Construction Product Regulation - Annex I (3) - Hazardous Substances
    EU. 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.

  • Construction Product Regulation - Article 6(5) - SDS and Declaration
    EU. 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.

Cosmetic Products Regulation
  • Cosmetic Products Regulation, Annex II - Prohibited Substances
    EU. Prohibited Substances: Annex II, Regulation 1223/2009/EC on Cosmetic Products, as amended by Regulation (EU) 2021/1099, 6 July 2021

    This list contains substances which are banned from use in any cosmetic products marketed for sale or use in the European Union.

EU Ecolabel Regulation
  • Ecolabels - Restrictions for Hazardous Substances/Mixtures
    EU. 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.

End-of-Life Vehicles Directive
  • End-of-Life Vehicles Directive - Hazardous Substances
    EU. 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.

Food Contact Active and Intelligent Materials and Articles Regulation
  • Active and Intelligent Materials - CMR Substances not allowed for use
    EU. 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).

Food Contact Recycled Plastic Materials and Articles Regulation
  • FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use
    EU. 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.

General Product Safety Directive
  • General Product Safety Directive - Hazardous Substances
    EU. 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.

In Vitro Diagnostic Medical Devices Directive
  • In Vitro Diagnostic Medical Devices Directive - Hazardous Substances
    EU. 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).

Inland Transport of Dangerous Goods Directive
  • Inland Transport of Dangerous Goods Directive, Annex I - ADR
    EU. 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).

  • Inland Transport of Dangerous Goods Directive, Annex II - RID
    EU. 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).

  • Inland Transport of Dangerous Goods Directive, Annex III - ADN
    EU. 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).

Marine Environmental Policy Framework Directive
  • Marine Environmental Policy Framework Directive - Hazardous Substances
    EU. 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).

Medical Devices Directive
  • Medical Devices Directive - Hazardous Substances
    EU. 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.

PPPR - Plant Protection Products Regulation
  • Annex of co-formulants not accepted for inclusion in PPPs
    EU. 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.

Pesticide Residues Regulation
  • Annexes II, III, IV, VII - Defined & Temporary Maximum Residue Levels
    EU. Pesticides. Maximum Residue Levels: Annexes II, III, IV, VII, Regulation 396/2005/EC, last amended by Regulation (EU) 2021/590, 13 April 2021

    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.

Plastic Materials and Articles Regulation
  • FCM and Articles Regulation, Annex I - Authorised Substances
    EU. 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.

Pressure Equipment Directive
  • Pressure Equipment Directive - Group 1 Fluids Hazardous Substances
    EU. 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.

Protection of Pregnant and Breastfeeding Workers Directive
  • Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II
    EU. 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.

Protection of Young People Directive
  • Physical, Biological and Chemical Agents & Processes and Work
    EU. 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.

Safety and Health of Workers at Work Directive
  • Safety and Health of Workers at Work Directive - Hazardous Substances
    EU. 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.

Safety and/or Health Signs at Work Directive
  • Workplace Signs - minimum requirements & signs on containers and pipes
    EU. 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.

WFD - Waste Framework Directive
  • Waste Framework Directive, Annex III - Waste - Hazardous Properties
    EU. 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.

Help Help

Substance names and other identifiers

Regulatory process names
Ethylene oxide
EC Inventory, Substance Evaluation - CoRAP, PIC, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID, Cosmetic Products Regulation, Annex II - Prohibited Substances, source-name.EU-PLANT_PROTECTION-ANX_III, CMD - Carcinogens and Mutagens Directive, Annex III - OELVs, Other, FCM and Articles Regulation, Annex I - Authorised Substances, FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use
ETHYLENE OXIDE
Substance Evaluation - CoRAP, PIC, Inland Transport of Dangerous Goods Directive, Annex III - ADN, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID, Cosmetic Products Regulation, Annex II - Prohibited Substances, source-name.EU-PLANT_PROTECTION-ANX_III, CMD - Carcinogens and Mutagens Directive, Annex III - OELVs, Other, FCM and Articles Regulation, Annex I - Authorised Substances, FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use
Ethylene oxide
Substance Evaluation - CoRAP, PIC, Biocidal active substances, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID, Cosmetic Products Regulation, Annex II - Prohibited Substances, source-name.EU-PLANT_PROTECTION-ANX_III, CMD - Carcinogens and Mutagens Directive, Annex III - OELVs, Other, FCM and Articles Regulation, Annex I - Authorised Substances, FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use
ethylene oxide
Substance Evaluation - CoRAP, PIC, Pre-Registration process, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID, Cosmetic Products Regulation, Annex II - Prohibited Substances, source-name.EU-PLANT_PROTECTION-ANX_III, CMD - Carcinogens and Mutagens Directive, Annex III - OELVs, Other, FCM and Articles Regulation, Annex I - Authorised Substances, FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use
ETHYLENE OXIDE WITH NITROGEN up to a total pressure of 1 MPa (10 bar) at 50 °C
Inland Transport of Dangerous Goods Directive, Annex III - ADN, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID
ethylene oxide; oxirane
FCM Active and Intelligent Materials - CMRs not allowed for use, Aerosols Directive - Flammable Contents - Labelling Requirements, CAD - Chemical Agents Directive, Art. 2(b)(i) - Hazardous Agents, Construction Product Regulation - Annex I (3) - Hazardous Substances, Construction Product Regulation - Art. 6(5) - SDS and Declaration, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, End-of-Life Vehicles Directive - Hazardous Substances, Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances, Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II, Pressure Equipment Directive - Group 1 Fluids Hazardous Substances, General Product Safety Directive - Hazardous Substances, Workplace Signs - minimum requirements & signs on containers and pipes, Safety and Health of Workers at Work Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties, Carc and Muta Directive, Annex I - Substances, Mixtures & Processes, Fertiliser Regulation- Annex I, E.3 (chelating and complexing agents)
ethylene oxide;oxirane
C&L Inventory
Translated names
Ethyleenoxide (nl)
Biocidal active substances
ethyleenoxide;oxiraan (nl)
C&L Inventory
Ethylene oxide (no)
Biocidal active substances
ethylenoxid (cs)
Biocidal active substances
ethylenoxid (da)
Biocidal active substances
Ethylenoxid (de)
Biocidal active substances
ethylenoxid;oxiran (cs)
C&L Inventory
ethylenoxid;oxiran (da)
C&L Inventory
Ethylenoxid;Oxiran (de)
C&L Inventory
Etilen oksid (hr)
Biocidal active substances
Etilen oksid (sl)
Biocidal active substances
etilen oksid;oksiran (sl)
C&L Inventory
etilen-oksid;oksiran (hr)
C&L Inventory
etileno oksidas;oksiranas (lt)
C&L Inventory
Etilenoksidas (lt)
Biocidal active substances
Etilén-oxid (hu)
Biocidal active substances
etilén-oxid;oxirán (hu)
C&L Inventory
Etilēnoksīds (lv)
Biocidal active substances
etilēnoksīds;oksirāns (lv)
C&L Inventory
Etyleenioksidi (fi)
Biocidal active substances
Etyleenioksidi;oksiraani (fi)
C&L Inventory
Etylenoxid (sv)
Biocidal active substances
etylenoxid;oxiran (sv)
C&L Inventory
etylénoxid (sk)
Biocidal active substances
etylénoxid;oxirán (sk)
C&L Inventory
Etüleenoksiid (et)
Biocidal active substances
etüleenoksiid;oksiraan (et)
C&L Inventory
Ossido di etilene (it)
Biocidal active substances
ossido di etilene;ossirano (it)
C&L Inventory
ossidu tal-etilen;ossiran (mt)
C&L Inventory
Ossidu tal-etilene (mt)
Biocidal active substances
Oxid de etilenă (ro)
Biocidal active substances
oxid de etilenă;oxiran (ro)
C&L Inventory
Oxyde d'éthylène (fr)
Biocidal active substances
oxyde d'éthylène;oxirane (fr)
C&L Inventory
Tlenek etylenu (pl)
Biocidal active substances
tlenek etylenu;oksiran (pl)
C&L Inventory
Óxido de etileno (es)
Biocidal active substances
Óxido de etileno (pt)
Biocidal active substances
Óxido de etileno;oxirano (es)
C&L Inventory
óxido de etileno;oxirano (pt)
C&L Inventory
Αιθυλενοξείδιο (el)
Biocidal active substances
αιθυλενοξείδιο·οξιράνιο (el)
C&L Inventory
Етиленов оксид (bg)
Biocidal active substances
етиленов оксид;оксиран (bg)
C&L Inventory
CAS names
Oxirane
Other
IUPAC names
EO
Registration dossier
EO as monomer for Victawet 12
Registration dossier
ethene oxide
Registration dossier
ethylene
Registration dossier
Ethylene oxid
Registration dossier
Ethylene Oxide
C&L Inventory, Registration dossier
Ethylene oxide
C&L Inventory, Registration dossier
ethylene oxide
C&L Inventory, Registration dossier
Ethylene Oxide
Registration dossier
Ethylene oxide
Registration dossier
ethylene oxide
Registration dossier
Ethylene oxide (EO)
Registration dossier
Ethylene Oxide based Polymers
Registration dossier
Ethylene oxide monomer
Registration dossier
Ethylene oxide or oxirane
Registration dossier
Ethylene Oxide with nitrogen
Registration dossier
Ethylene oxide, Dimethylene oxide
Registration dossier
ethylene oxide, EO
Registration dossier
ethylene oxide; oxirane
C&L Inventory
Ethylene_oxide
Registration dossier
ethylene_oxide
Registration dossier
Ethylenoxid
C&L Inventory
Ethylenoxide
Registration dossier
ethylenoxide
Registration dossier
Hexanedioic acid, diester with ethoxylated butanol (3-4-EO)
C&L Inventory
Oxirane
C&L Inventory, Registration dossier, Other
oxirane
C&L Inventory, Registration dossier, Other
Oxirane
Registration dossier, Other
oxirane
Registration dossier, Other
Oxirane / ethylene oxide
Registration dossier
Trade names
1, 2- Epoxyethane
Registration dossier
1,2 Epoxyethane
Registration dossier
1,2-Epoxyethane
Registration dossier
CHINT: EO
Registration dossier
Cremophor polymer
Registration dossier
Dihydooxirene
Registration dossier
Dihydrooxirene
Registration dossier
Dihydroxooxirene
Registration dossier
Dimethylene oxide
Registration dossier
dimethylene oxide
Registration dossier
DOW Ethylene Oxide
Registration dossier
EO
Registration dossier
Epoxyethane
Registration dossier
epoxyethane
Registration dossier
Ethene Oxide
Registration dossier
Ethene oxide
Registration dossier
Ethleneoxy (6Cl)
Registration dossier
ETHYLENE OXIDE
Registration dossier
Ethylene Oxide
Registration dossier
Ethylene oxide
Registration dossier
ethylene oxide
Registration dossier
Ethylene Oxide (8CI)
Registration dossier
Ethylene oxide (8CI)
Registration dossier
Ethylene Oxide (8CL)
Registration dossier
Ethylene Oxide (8Cl)
Registration dossier
Ethylene oxide (8Cl)
Registration dossier
Ethylene Oxide (EO)
Registration dossier
ethylene oxide HP
Registration dossier
Ethyleneoxy (6CI)
Registration dossier
EthyleneOxy (6Cl)
Registration dossier
Ethyleneoxy (6Cl)
Registration dossier
Ethylenoxid
Registration dossier
Ethylenoxid Reinst
Registration dossier
Ethylenoxide
Registration dossier
Etyleneoxy (6CI)
Registration dossier
Etylenoxid
Registration dossier
HEC
Registration dossier
Makrogel 6000
Registration dossier
Not relevant, the substance is imported and placed on the market only bound in a polymer
Registration dossier
O0825
Registration dossier
Oxacyclopropane
Registration dossier
Oxane
Registration dossier
Oxidoethane
Registration dossier
Oxiran
Registration dossier
Oxirane
Registration dossier
oxirane
Registration dossier
Oxirane (9CI)
Registration dossier
Oxirane (9CL)
Registration dossier
Oxirane (9Cl)
Registration dossier
Oxirene, Dihydro
Registration dossier
Oxirene, dihydro
Registration dossier
Oxirene, dihydro-
Registration dossier
PEG 400
Registration dossier
PEO
Registration dossier
Phase I REACH Expertenentscheidung
Registration dossier
Phase I REACH Kandidat
Registration dossier
Pluronic polymer
Registration dossier
Resin 8020 A
Registration dossier
Resin 8020 B
Registration dossier
Resin 8095 A
Registration dossier
Resin 8095 A-LP
Registration dossier
Resin SG 95 A
Registration dossier
Resin SG 95 A-LP
Registration dossier
Resin SG 95 NA
Registration dossier
This substance is a monomer in an imported polymer, therefore no trade names are available and/or relevant.
Registration dossier
Vinkocell
Registration dossier
W1
Registration dossier
Other identifiers
142175-32-4
Other
CAS number
142175-32-4
Other
Deleted CAS number
184288-32-2
Other
CAS number
184288-32-2
Other
Deleted CAS number
19034-08-3
Other
CAS number
19034-08-3
Other
Deleted CAS number
2910 10 00
PIC
Combined Nomenclature Code
2910 10 00
PIC
Combined Nomenclature Number
2910.10
PIC
Harmonised System Code
37341-05-2
Other
CAS number
37341-05-2
Other
Deleted CAS number
3808.50 -- 3824.81
PIC
Harmonised System Code (Mixture)
436859-78-8
Other
CAS number
436859-78-8
Other
Deleted CAS number
603-023-00-X
C&L Inventory
Index Number
75-21-8
EC Inventory, C&L Inventory, Substance Evaluation - CoRAP, PIC, Biocidal active substances, Registration dossier, Pre-Registration process, FCM Active and Intelligent Materials - CMRs not allowed for use, Aerosols Directive - Flammable Contents - Labelling Requirements, CAD - Chemical Agents Directive, Art. 2(b)(i) - Hazardous Agents, Construction Product Regulation - Annex I (3) - Hazardous Substances, Construction Product Regulation - Art. 6(5) - SDS and Declaration, Cosmetic Products Regulation, Annex II - Prohibited Substances, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, End-of-Life Vehicles Directive - Hazardous Substances, Active Implantable Medical Devices Directive - Hazardous Substances, Inland Transport of Dangerous Goods Directive, Annex III - ADN, Inland Transport of Dangerous Goods Directive, Annex I - ADR, Inland Transport of Dangerous Goods Directive, Annex II - RID, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances, source-name.EU-PLANT_PROTECTION-ANX_III, FCM and Articles Regulation, Annex I - Authorised Substances, Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II, Pressure Equipment Directive - Group 1 Fluids Hazardous Substances, General Product Safety Directive - Hazardous Substances, FCMs Recycled Plastic & Articles Regulation - Annex I - Authorised Use, Workplace Signs - minimum requirements & signs on containers and pipes, Safety and Health of Workers at Work Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties, CMD - Carcinogens and Mutagens Directive, Annex III - OELVs, Carc and Muta Directive, Annex I - Substances, Mixtures & Processes, Fertiliser Regulation- Annex I, E.3 (chelating and complexing agents), Other
CAS number
99932-75-9
Other
CAS number
99932-75-9
Other
Deleted CAS number