TheLawyer.sh
Tilbage

Commission Regulation (EU) 2026/1120of 26 May 2026amending Annex III to Regulation (EC) No 1107/2009 of the European Parliament and of the Council by adding twelve co-formulants which are not accepted for inclusion in plant protection products(Text with EEA relevance)

32026R1120

Den Europæiske UnionForordning2026

European Union

§ Article 57

Article 57, points (d) and (e), of Regulation (EC) No 1907/2006 of the European Parliament and of the Council

Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC (OJ L 396, 30.12.2006, p. 1, ELI: http://data.europa.eu/eli/reg/2006/1907/oj).

, substances listed as persistent organic pollutants (POPs) under Regulation (EU) 2019/1021 of the European Parliament and of the Council

Regulation (EU) 2019/1021 of the European Parliament and of the Council of 20 June 2019 on persistent organic pollutants (OJ L 169, 25.6.2019, p. 45, ELI: http://data.europa.eu/eli/reg/2019/1021/oj).

and substances not approved for use in biocidal products for product-type 6 (preservatives for products during storage) under Regulation (EU) No 528/2012 of the European Parliament and of the Council

Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (OJ L 167, 27.6.2012, p. 1, ELI: http://data.europa.eu/eli/reg/2012/528/oj).

.

(6) In accordance with Article 5 of Implementing Regulation (EU) 2023/574, the Commission listed those unacceptable co-formulants on its website.

(7) It is therefore appropriate to amend Annex III to Regulation (EC) No 1107/2009 to include the additional substances that Member States have identified as unacceptable for their use as co-formulants in plant protection products or adjuvants.

(8) Co-formulants to be listed in Annex III to Regulation (EC) No 1107/2009 may also be contained in adjuvants placed on the market. As detailed rules for the authorisation of adjuvants have not yet been established, Member States may continue to apply national provisions as regards adjuvants in accordance with Article 81(3) of that Regulation. As that Regulation aims to prevent the placing on the market or use of adjuvants containing prohibited co-formulants, it is necessary to ensure that also adjuvants, to be mixed with plant protection products, do not contain any of those unacceptable co-formulants.

(9) Member States should be provided with time to review the composition of the plant protection products and adjuvants currently authorised in their territory, to assess whether they contain any co-formulants listed in Annex III to Regulation (EC) No 1107/2009 by this Regulation and to withdraw or amend authorisations for plant protection products and adjuvants containing those co-formulants.

(10) To allow for the orderly phasing out of products and minimise potential disruption to users and supply chains, in the case of plant protection products or adjuvants containing a co-formulant listed in Annex III to Regulation (EC) No 1107/2009 by this Regulation, Member States may grant a grace period, where appropriate and in accordance with Article 46, first subparagraph, of that Regulation or, where applicable, under national provisions governing the authorisation of adjuvants.

(11) Co-formulants listed in Annex III to Regulation (EC) No 1107/2009 by this Regulation may be present as unintentional impurities in other co-formulants, which as such are acceptable for use in plant protection products or adjuvants. Therefore, the individual concentration of the unacceptable co-formulants in the finished plant protection product or adjuvant should be less than 0,1 % weight by weight (w/w) or less than a specific concentration limit related to CMR properties (carcinogenic, mutagenic and reprotoxic), when established in Annex VI to Regulation (EC) No 1272/2008 for the unacceptable co-formulant at a level lower than 0,1 % weight by weight (w/w), in order to be considered as acceptable unintentional impurity, unless a different limit is provided due to technical limitations of relevant analytical methods.

(12) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,

HAS ADOPTED THIS REGULATION:

Article 1

Annex III to Regulation (EC) No 1107/2009 is amended in accordance with the Annex to this Regulation.

Article 2

Member States which have granted authorisations for plant protection products containing co-formulants listed in Annex III to Regulation (EC) No 1107/2009 by this Regulation, shall amend or withdraw those authorisations as soon as possible and, in any case, no later than 16 June 2028.

Article 3

Member States shall not authorise the placing on the market or use of adjuvants containing co-formulants listed in Annex III to Regulation (EC) No 1107/2009, as amended by this Regulation.

Member States which have authorised adjuvants containing co-formulants listed in Annex III to Regulation (EC) No 1107/2009 by this Regulation, shall amend or withdraw those authorisations as soon as possible and, in any case, no later than 16 June 2028.

Article 4

Any grace period granted by Member States in accordance with Article 46 of Regulation (EC) No 1107/2009 or national provisions for authorisation of adjuvants shall be as short as possible and shall expire for the sale and distribution at the latest 3 months after the date of amendment or withdrawal of the authorisations referred to in Articles 2 and 3. Any grace period for the disposal, storage and use shall expire at the latest 12 months after the date of amendment or withdrawal of the authorisations referred to in Articles 2 and 3.

Article 5

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 26 May 2026.

For the Commission

The President

Ursula von der Leyen

Annex

ANNEX

Annex III to Regulation (EC) No 1107/2009 is amended as follows:

The following rows are added after row 144:

145.AcetaldehydeEthanal75-07-0200-836-8Carcinogenic cat. 1B146.Propylene oxide

1,2-epoxypropane;

methyloxirane

75-56-9200-879-2

Carcinogenic cat. 1B/

Mutagenic cat. 1B

147.Cumene(1-Methylethyl)benzene98-82-8202-704-5Carcinogenic cat. 1B148.Dodecamethylcyclohexasiloxane; (D6)540-97-6208-762-8

Persistent, bioaccumulative and toxic (REACH Article 57(d);

Very persistent and very bioaccumulative (REACH Article 57(e)

149.Decamethylcyclopentasiloxane; (D5)541-02-6208-764-9

Persistent, bioaccumulative and toxic (REACH Article 57(d);

Very persistent and very bioaccumulative (REACH Article 57(e)

150.Octamethylcyclotetrasiloxane; (D4)556-67-2209-136-7

Persistent, bioaccumulative and toxic (REACH Article 57(d);

Very persistent and very bioaccumulative (REACH Article 57(e)

151.2-(2'-hydroxy-3'-tert-butyl-5'-methylphenyl)-5-chlorobenzotriazoleBumetrizole3896-11-5223-445-4Very persistent and very bioaccumulative (REACH Article 57(e)152.Distillates (petroleum) solvent-dewaxed light paraffinic with a content of ≥ 3,0 % DMSO-extract (measured by IP 346)64742-56-9265-159-2Carcinogenic cat. 1B153.3,5,7-Triaza-1-azoniatricyclo[3.3.1.1 3,7] decane,1-(3-chloro-2-propen-1-yl)-, chloride

Methenamine

3-chloroallylochloride

(CTAC)

4080-31-3223-805-0Not approved for use in biocidal products for product-type 6 (preservatives for products during storage)154.Phosphinic acid, bis(perfluoro-C6-12-alkyl) derivatives68412-69-1270-206-5Persistent organic pollutant (POP)155.1,4-dioxane123-91-1204-661-8Carcinogenic cat. 1B156.2-(4-tert-butylbenzyl)propionaldehyde80-54-6201-289-8Toxic to reproduction cat.1B

Metadata

Type
Forordning
År
2026
Ikrafttrædelsesdato
1. januar 1970