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Document 32018R1480

    Commission Regulation (EU) 2018/1480 of 4 October 2018 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures and correcting Commission Regulation (EU) 2017/776 (Text with EEA relevance.)

    C/2018/6348

    OJ L 251, 5.10.2018, p. 1–12 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    Legal status of the document In force

    ELI: http://data.europa.eu/eli/reg/2018/1480/oj

    5.10.2018   

    EN

    Official Journal of the European Union

    L 251/1


    COMMISSION REGULATION (EU) 2018/1480

    of 4 October 2018

    amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures and correcting Commission Regulation (EU) 2017/776

    (Text with EEA relevance)

    THE EUROPEAN COMMISSION,

    Having regard to the Treaty on the Functioning of the European Union,

    Having regard to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006 (1), and in particular Article 37(5) and Article 53(1) thereof,

    Whereas:

    (1)

    Table 3.1 of Part 3 of Annex VI to Regulation (EC) No 1272/2008 contains the list of harmonised classification and labelling of hazardous substances based on the criteria set out in Parts 2 to 5 of Annex I to that Regulation.

    (2)

    Proposals to introduce harmonised classification and labelling of certain substances and to update or delete the harmonised classification and labelling of certain other substances have been submitted to the European Chemicals Agency pursuant to Article 37 of Regulation (EC) No 1272/2008. Based on the opinions on those proposals issued by the Committee for Risk Assessment of the Agency (RAC), as well as on the comments received from the parties concerned, it is appropriate to introduce, update or delete harmonised classification and labelling of certain substances.

    (3)

    Council Directive 67/548/EEC (2) and Directive 1999/45/EC of the European Parliament and of the Council (3) were repealed with effect from 1 June 2015. As a result, Part 3 of Annex VI to Regulation (EC) No 1272/2008 was amended by Commission Regulation (EU) 2016/1179 (4) to remove Table 3.2. That amendment took effect on 1 June 2017. Annex VI to Regulation (EC) No 1272/2008 was further amended by Commission Regulation (EU) 2017/776 (5) to delete references to Table 3.2, to convert references to Table 3.1 into references to Table 3 and to delete references to the repealed Directives. Under Article 2(2) of Regulation (EU) 2017/776, the majority of those amendments were to apply from 1 June 2017, while the remaining amendments were stated to apply from 1 December 2018. However, due to an oversight, Article 2(2) failed to list two further amendments that should have applied from 1 June 2017, including in particular the amendment changing the name of the Table from ‘Table 3.1’ to ‘Table 3’. The second subparagraph of Article 2(2) of Regulation (EU) 2017/776 should therefore be corrected to include reference to those two amendments. This correction, although it has the effect of applying the two amendments retroactively, does not affect the rights and obligations of manufacturers, importers, downstream users or suppliers.

    (4)

    Regulation (EU) 2017/776 also amended Annex VI to Regulation (EC) No 1272/2008 to add harmonised ‘Acute Toxicity Estimate’ (ATE) values in Table 3.1 as part of the information relating to the classification and labelling of certain substances for the purposes of the classification of mixtures. The ATE introduced for nicotine was expressed in mg/kg. In order to clarify how mixtures containing nicotine should be classified, the ATE for the oral and the dermal routes for nicotine should instead be expressed in ‘mg/kg bw’ (6). The ATEs for three other substances, namely colecalciferol, 1,2-dihydroxybenzene and pinoxaden should also be expressed in the same way. In addition, in the title of the penultimate column of Table 3.1, a footnote should be added indicating what the abbreviation ‘mg/kg bw’ stands for.

    (5)

    The Annex to Commission Regulation (EU) 2018/669 (7) provides for the translation of the names of the substances included in Table 3.1 of Annex VI to Regulation (EC) No 1272/2008. As a consequence, the title of the second column of that Table, which currently refers to ‘international chemical identifications’, should be amended to take account of the fact that the ‘international chemical identifications’ will lose their international character once the Regulation providing for their translation in Annex VI becomes applicable. For the sake of consistency, this amendment should take effect when the translation of the names in Annex VI takes effect. The new title should reflect the terminology used in Article 18 of Regulation (EC) No 1272/2008.

    (6)

    Compliance with the new or updated harmonised classifications should not be required immediately as a certain period of time will be necessary to allow suppliers to adapt the labelling and packaging of substances and mixtures to the new or revised classifications and to sell existing stocks. That period of time will also be necessary to allow suppliers to adapt to and comply with other legislative obligations resulting from the new or updated harmonised classifications, such as those set out in Article 22(f) or Article 23 of Regulation (EC) No 1907/2006 of the European Parliament and of the Council (8), those set out in Article 50 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (9) or those set out in Article 44 of Regulation (EC) No 1107/2009 of the European Parliament and of the Council (10).

    (7)

    Regulation (EC) No 1272/2008 should therefore be amended accordingly.

    (8)

    In line with the transitional provisions of Regulation (EC) No 1272/2008 which allow for new provisions to be applied at an earlier stage on a voluntary basis, suppliers should be allowed to apply the new and updated harmonised classifications, and to adapt the labelling and packaging accordingly, on a voluntary basis before the date of application of those new or updated classifications.

    (9)

    The measures provided for in this Regulation are in accordance with the opinion of the Committee established by Article 133 of Regulation (EC) No 1907/2006,

    HAS ADOPTED THIS REGULATION:

    Article 1

    Amendment to Regulation (EC) No 1272/2008

    Annex VI to Regulation (EC) No 1272/2008 is amended as set out in the Annex to this Regulation.

    Article 2

    Correction to Regulation (EU) 2017/776

    In Regulation (EU) 2017/776, the second subparagraph of Article 2(2) is replaced by the following:

    ‘In the Annex, point (1), point (2) and points (a), (b) and (c) of point (3) shall apply from 1 June 2017.’

    Article 3

    Entry into force and application

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

    Point (1) and point (a) of point (2) of the Annex shall apply from 1 December 2019.

    Points (b), (c), (d) and (e) of point (2) of the Annex shall apply from 1 May 2020.

    By way of derogation from the third paragraph of this Article, substances and mixtures may, before 1 May 2020, be classified, labelled and packaged in accordance with Regulation (EC) No 1272/2008 as amended by this Regulation.

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

    Done at Brussels, 4 October 2018.

    For the Commission

    The President

    Jean-Claude JUNCKER


    (1)   OJ L 353, 31.12.2008, p. 1.

    (2)  Council Directive 67/548/EEC of 27 June 1967 on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (OJ 196, 16.8.1967, p. 1).

    (3)  Directive 1999/45/EC of the European Parliament and of the Council of 31 May 1999 concerning the approximation of laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (OJ L 200, 30.7.1999, p. 1).

    (4)  Commission Regulation (EU) 2016/1179 of 19 July 2016 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures (OJ L 195, 20.7.2016, p. 11).

    (5)  Commission Regulation (EU) 2017/776 of 4 May 2017 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures (OJ L 116, 5.5.2017, p. 1).

    (6)  Body weight.

    (7)  Commission Regulation (EU) 2018/669 of 16 April 2018 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures (OJ L 115, 4.5.2018, p. 1).

    (8)  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).

    (9)  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).

    (10)  Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC (OJ L 309, 24.11.2009, p. 1).


    ANNEX

    Annex VI to Regulation (EC) No 1272/2008 is amended as follows:

    (1)

    in Part 1, the heading of point 1.1.1.4 is replaced by the following:

    Chemical name ’;

    (2)

    in Part 3, Table 3.1 is amended as follows:

    (a)

    the title of the second column is replaced by the following: ‘Chemical name’;

    (b)

    the title of the penultimate column is replaced by the following: ‘Specific Conc. Limits, M-factors and ATEs (*)

    (*)

    ATEs for oral and dermal exposure routes are expressed in mg/kg bw, which stands for milligram per kilogram bodyweight.’;

    (c)

    the entry corresponding to index number 607-414-00-6 is deleted;

    (d)

    the entries corresponding to index numbers 006-044-00-7, 015-101-00-5, 016-096-00-2, 017-011-00-1, 025-002-00-9, 603-180-00-4, 604-014-00-3, 604-016-00-4, 604-090-00-8, 605-003-00-6, 606-047-009, 607-096-00-9, 607-103-00-5, 607-113-00-X, 607-373-00-4, 613-167-00-5, 613-205-00-0 and 614-001-00-4 are replaced by the following entries respectively:

    Index No

    Chemical name

    EC No

    CAS No

    Classification

    Labelling

    Specific Conc. Limits, M-factors and ATEs

    Notes

    Hazard Class and Category Code(s)

    Hazard statement Code(s)

    Pictogram, Signal Word Code(s)

    Hazard statement Code(s)

    Suppl. Hazard statement Code(s)

    ‘006-044-00-7

    isoproturon (ISO);

    3-(4-isopropylphenyl)-1,1-dimethylurea

    251-835-4

    34123-59-6

    Carc. 2

    STOT RE 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H351

    H373 (blood)

    H400

    H410

    GHS08

    GHS09

    Wng

    H351

    H373 (blood)

    H410

     

    M = 10

    M = 10’

     

    ‘015-101-00-5

    phosmet (ISO);

    S-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl] O,O-dimethyl phosphorodithioate;

    O,O-dimethyl-S-phthalimidomethyl phosphorodithioate

    211-987-4

    732-11-6

    Repr. 2

    Acute Tox. 4

    Acute Tox. 3

    STOT SE 1

    Aquatic Acute 1

    Aquatic Chronic 1

    H361f

    H332

    H301

    H370 (nervous system)

    H400

    H410

    GHS08

    GHS06

    GHS09

    Dgr

    H361f

    H332

    H301

    H370 (nervous system)

    H410

     

    M = 100

    M = 100’

     

    ‘016-096-00-2

    thifensulfuron-methyl (ISO);

    methyl 3-(4-methoxy-6-methyl-1,3,5-triazin-2-ylcarbamoylsulfamoyl)thiophene-2-carboxylate

    79277-27-3

    Aquatic Acute 1

    Aquatic Chronic 1

    H400

    H410

    GHS09

    Wng

    H410

     

    M = 100

    M = 100’

     

    ‘017-011-00-1

    sodium hypochlorite, solution … % Cl active

    231-668-3

    7681-52-9

    Skin Corr. 1B

    Eye Dam. 1

    Aquatic Acute 1

    Aquatic Chronic 1

    H314

    H318

    H400

    H410

    GHS05

    GHS09

    Dgr

    H314

    H410

    EUH031

    M = 10

    M = 1

    EUH031:

    C ≥ 5 %

    B’

    ‘025-002-00-9

    potassium permanganate

    231-760-3

    7722-64-7

    Ox. Sol. 2

    Repr. 2

    Acute Tox. 4 * Aquatic Acute 1 Aquatic Chronic 1

    H272

    H361d

    H302

    H400

    H410

    GHS03

    GHS08

    GHS07

    GHS09

    Dgr

    H272

    H361d

    H302

    H410’

     

     

     

    ‘603-180-00-4

    colecalciferol;

    cholecalciferol;

    vitamin D3

    200-673-2

    67-97-0

    Acute Tox. 2 Acute Tox. 2 Acute Tox. 2

    STOT RE 1

    H330

    H310

    H300

    H372

    GHS06

    GHS08

    Dgr

    H330

    H310

    H300

    H372

     

     

    inhalation:

    ATE = 0,05 mg/L (dusts or mists)

     

    dermal:

    ATE = 50 mg/kg bw

     

    oral:

    ATE = 35 mg/kg bw

    STOT RE 1; H372: C ≥ 3 %

    STOT RE 2; H373: 0,3 % ≤ C < 3 %’

     

    ‘604-014-00-3

    chlorocresol;

    4-chloro-m-cresol;

    4-chloro-3-methylphenol

    200-431-6

    59-50-7

    Acute Tox. 4

    Skin Corr. 1C

    Eye Dam. 1

    STOT SE 3

    Skin Sens. 1B Aquatic Acute 1

    Aquatic Chronic 3

    H302

    H314

    H318

    H335

    H317

    H400

    H412

    GHS07

    GHS05

    GHS09

    Dgr

    H302

    H314

    H335

    H317

    H410

     

    M = 1’

     

    ‘604-016-00-4

    1,2-dihydroxybenzene;

    pyrocatechol

    204-427-5

    120-80-9

    Carc. 1Β

    Muta. 2

    Acute Tox. 3

    Acute Tox. 3

    Skin Irrit. 2

    Eye Irrit. 2

    H350

    H341

    H311

    H301

    H315

    H319

    GHS08

    GHS06

    Dgr

    H350

    H341

    H311

    H301

    H315

    H319

     

     

    oral:

    ATE = 300 mg/kg bw

     

    dermal:

    ATE = 600 mg/kg bw’

     

    ‘604-090-00-8

    4-tert-butylphenol

    202-679-0

    98-54-4

    Repr. 2

    Skin Irrit. 2

    Eye Dam. 1

    Aquatic Chronic 1

    H361f

    H315

    H318

    H410

    GHS08

    GHS05

    GHS09

    Dgr

    H361f

    H315

    H318

    H410

     

    M = 1’

     

    ‘605-003-00-6

    acetaldehyde;

    ethanal

    200-836-8

    75-07-0

    Flam. Liq. 1

    Carc. 1B

    Muta. 2

    STOT SE 3

    Eye Irrit. 2

    H224

    H350

    H341

    H335

    H319

    GHS02

    GHS08

    GHS07

    Dgr

    H224

    H350

    H341

    H335

    H319’

     

     

     

    ‘606-047-00-9

    2-benzyl-2-dimethylamino-4′-morpholinobutyrophenone

    404-360-3

    119313-12-1

    Repr. 1B

    Aquatic Acute 1

    Aquatic Chronic 1

    H360D

    H400

    H410

    GHS08

    GHS09

    Dgr

    H360D

    H410’

     

     

     

    ‘607-096-00-9

    maleic anhydride

    203-571-6

    108-31-6

    Acute Tox. 4

    STOT RE 1

    Skin Corr. 1B

    Eye Dam. 1

    Resp. Sens. 1

    Skin Sens. 1A

    H302

    H372 (respiratory system) (inhalation)

    H314

    H318

    H334

    H317

    GHS07

    GHS08

    GHS05

    Dgr

    H302

    H372 (respiratory system) (inhalation)

    H314

    H334

    H317

    EUH071

    Skin Sens. 1A; H317: C ≥ 0,001 %’

     

    ‘607-103-00-5

    succinic anhydride

    203-570-0

    108-30-5

    Acute Tox. 4

    Skin Corr. 1

    Eye Dam. 1

    Resp. Sens. 1

    Skin Sens. 1

    H302

    H314

    H318

    H334

    H317

    GHS07

    GHS05

    GHS08

    Dgr

    H302

    H314

    H334

    H317

    EUH071’

     

     

    ‘607-113-00-X

    isobutyl methacrylate

    202-613-0

    97-86-9

    Flam. Liq. 3

    STOT SE 3

    Skin Irrit. 2

    Skin Sens. 1B

    H226

    H335

    H315

    H317

    GHS02

    GHS07

    Wng

    H226

    H335

    H315

    H317

     

     

    D’

    ‘607-373-00-4

    quizalofop-P-tefuryl (ISO); (+/–) tetrahydrofurfuryl (R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenyloxy]propionate

    414-200-4

    200509-41-7

    Carc. 2

    Repr. 2

    Acute Tox. 4

    STOT RE 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H351

    H361fd

    H302

    H373

    H400

    H410

    GHS08

    GHS07

    GHS09

    Wng

    H351

    H361fd

    H302

    H373

    H410

     

    M = 1

    M = 1’

     

    ‘613-167-00-5

    reaction mass of 5-chloro-2-methyl-2H-isothiazol-3-one and 2-methyl-2H-isothiazol-3-one (3:1)

    55965-84-9

    Acute Tox. 2

    Acute Tox. 2

    Acute Tox. 3

    Skin Corr. 1C

    Eye Dam. 1

    Skin Sens. 1A Aquatic Acute 1

    Aquatic Chronic 1

    H330

    H310

    H301

    H314

    H318

    H317

    H400

    H410

    GHS06

    GHS05

    GHS09

    Dgr

    H330

    H310

    H301

    H314

    H317

    H410

    EUH071

    Skin Corr. 1C; H314: C ≥ 0,6 %

    Skin Irrit. 2; H315: 0,06 % ≤ C < 0,6 %

    Eye Dam. 1; H318: C ≥ 0,6 %

    Eye Irrit. 2; H319: 0,06 % ≤ C < 0,6 %

    Skin Sens. 1A; H317: C ≥ 0,0015 %

    M = 100

    M = 100

    B’

    ‘613-205-00-0

    propiconazole (ISO); (2RS,4RS;2RS,4SR)-1-{[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl]methyl}-1H-1,2,4-triazole

    262-104-4

    60207-90-1

    Repr. 1B

    Acute Tox. 4

    Skin Sens. 1

    Aquatic Acute 1

    Aquatic Chronic 1

    H360D

    H302

    H317

    H400

    H410

    GHS08

    GHS07

    GHS09

    Dgr

    H360D

    H302

    H317

    H410

     

    M = 1

    M = 1’

     

    ‘614-001-00-4

    nicotine (ISO);

    3-[(2S)-1-methylpyrrolidin-2-yl]pyridine

    200-193-3

    54-11-5

    Acute Tox. 2

    Acute Tox. 2

    Acute Tox. 2

    Aquatic Chronic 2

    H330

    H310

    H300

    H411

    GHS06

    GHS09

    Dgr

    H330

    H310

    H300

    H411

     

     

    inhalation:

    ATE = 0,19 mg/L (dusts or mists)

     

    dermal:

    ATE = 70 mg/kg bw

     

    oral:

    ATE = 5 mg/kg bw’

     

    (e)

    the following entries are inserted in the appropriate places, following the order of the entries set out in Table 3.1:

    Index No

    Chemical name

    EC No

    CAS No

    Classification

    Labelling

    Specific Conc. Limits, M-factors and ATEs

    Notes

    Hazard Class and Category Code(s)

    Hazard statement Code(s)

    Pictogram, Signal Word Code(s)

    Hazard statement Code(s)

    Suppl. Hazard statement Code(s)

    ‘604-094-00-X

    isoeugenol; [1]

    (E)-2-methoxy-4-(prop-1-enyl)phenol; [2]

    (Z)-2-methoxy-4-(prop-1-enyl)phenol [3]

    202-590-7 [1]

    227-678-2 [2]

    227-633-7 [3]

    97-54-1 [1]

    5932-68-3 [2]

    5912-86-7 [3]

    Skin Sens. 1A

    H317

    GHS07

    Wng

    H317

     

    Skin Sens. 1A; H317: C ≥ 0,01 %’

     

    ‘607-724-00-1

    2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl (1R,3R)-2,2-dimethyl-3-[(1Z)-prop-1-en-1-yl]cyclopropanecarboxylate; epsilon-metofluthrin

    240494-71-7

    Acute Tox. 4

    Acute Tox. 3

    STOT SE 1

    STOT RE 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H332

    H301

    H370 (nervous system)

    H373

    H400

    H410

    GHS06

    GHS08

    GHS09

    Dgr

    H332

    H301

    H370 (nervous system)

    H373

    H410

     

    M = 100

    M = 100’

     

    ‘607-725-00-7

    isopropyl (2E,4E,7S)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienoate; S-methoprene

    65733-16-6

    Aquatic Acute 1

    Aquatic Chronic 1

    H400

    H410

    GHS09

    Wng

    H410

     

    M = 1

    M = 1’

     

    ‘607-726-00-2

    pinoxaden (ISO);

    8-(2,6-diethyl-4-methylphenyl)-7-oxo-1,2,4,5-tetrahydro-7H-pyrazolo[1,2-d][1,4,5]oxadiazepin-9-yl 2,2-dimethylpropanoate

    243973-20-8

    Repr. 2

    Acute Tox. 4

    Acute Tox. 4

    Eye Irrit. 2

    STOT SE 3

    Skin Sens. 1A

    Aquatic Acute 1

    Aquatic Chronic 3

    H361d

    H332

    H302

    H319

    H335

    H317

    H400

    H412

    GHS08

    GHS07

    GHS09

    Wng

    H361d

    H332

    H302

    H319

    H335

    H317

    H410

     

     

    inhalation:

    ATE = 4,63 mg/L (dusts or mists)

     

    oral:

    ATE = 500 mg/kg bw

    M = 1’

     

    ‘607-727-00-8

    tetramethrin (ISO);

    (1,3-dioxo-1,3,4,5,6,7-hexahydro-2H-isoindol-2-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate

    231-711-6

    7696-12-0

    Carc. 2

    Acute Tox. 4

    STOT SE 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H351

    H302

    H371 (nervous system) (inhalation)

    H400

    H410

    GHS08

    GHS07

    GHS09

    Wng

    H351

    H302

    H371 (nervous system) (inhalation)

    H410

     

    M = 100

    M = 100’

     

    ‘607-728-00-3

    (1,3,4,5,6,7-hexahydro-1,3-dioxo-2H-isoindol-2-yl)methyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate

    214-619-0

    1166-46-7

    Carc. 2

    Acute Tox. 4

    STOT SE 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H351

    H302

    H371 (nervous system) (inhalation)

    H400

    H410

    GHS08

    GHS07

    GHS09

    Wng

    H351

    H302

    H371 (nervous system) (inhalation)

    H410

     

    M = 100

    M = 100’

     

    ‘607-729-00-9

    mesosulfuron-methyl (ISO);

    methyl 2-[(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-α-(methanesulfonamido)-p-toluate;

    208465-21-8

    Aquatic Acute 1

    Aquatic Chronic 1

    H400

    H410

    GHS09

    Wng

    H410

     

    M = 100

    M = 100’

     

    ‘607-730-00-4

    spirodiclofen (ISO);

    3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl 2,2-dimethylbutyrate

    148477-71-8

    Carc. 1B

    Repr. 2

    STOT RE 2

    Skin Sens. 1B

    Aquatic Chronic 1

    H350

    H361f

    H373

    H317

    H410

    GHS08

    GHS07

    GHS09

    Dgr

    H350

    H361f

    H373

    H317

    H410

     

    M = 10’

     

    ‘607-731-00-X

    sodium methyl [(4-aminophenyl)sulphonyl]carbamate; sodium methyl (EZ)-sulfanilylcarbonimidate; asulam-sodium

    218-953-8

    2302-17-2

    Skin Sens. 1

    Aquatic Acute 1

    Aquatic Chronic 1

    H317

    H400

    H410

    GHS07

    GHS09

    Wng

    H317

    H410

     

    M = 1

    M = 1’

     

    ‘607-732-00-5

    salicylic acid

    200-712-3

    69-72-7

    Repr. 2

    Acute Tox. 4

    Eye Dam. 1

    H361d

    H302

    H318

    GHS08

    GHS07

    GHS05

    Dgr

    H361d

    H302

    H318’

     

     

     

    ‘608-068-00-9

    flutianil (ISO);

    (2Z)-{[2-fluoro-5-(trifluoromethyl)phenyl]thio}[3-(2-methoxyphenyl)-1,3-thiazolidin-2-ylidene]acetonitrile

    958647-10-4

    Aquatic Chronic 1

    H410

    GHS09

    Wng

    H410

     

    M = 100’

     

    ‘612-293-00-8

    reaction mass of 1-[2-(2-aminobutoxy)ethoxy]but-2-ylamine and 1-({[2-(2-aminobutoxy)ethoxy]methyl}propoxy)but-2-ylamine

    447-920-2

    -

    Repr. 2

    Acute Tox. 4

    Skin Corr. 1B

    Eye Dam. 1

    H361f

    H302

    H314

    H318

    GHS08

    GHS07

    GHS05

    Dgr

    H361f

    H302

    H314

    EUH071’

     

     

    ‘613-326-00-9

    2-methylisothiazol-3(2H)-one

    220-239-6

    2682-20-4

    Acute Tox. 2

    Acute Tox. 3

    Acute Tox. 3

    Skin Corr. 1B

    Eye Dam. 1

    Skin Sens. 1A

    Aquatic Acute 1

    Aquatic Chronic 1

    H330

    H311

    H301

    H314

    H318

    H317

    H400

    H410

    GHS05

    GHS06

    GHS09

    Dgr

    H330

    H311

    H301

    H314

    H317

    H410

    EUH071

    Skin Sens. 1A; H317: C ≥ 0,0015 %

    M = 10

    M = 1’

     

    ‘613-327-00-4

    pyroxsulam (ISO);

    N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide

    422556-08-9

    Skin Sens. 1

    Aquatic Acute 1

    Aquatic Chronic 1

    H317

    H400

    H410

    GHS07

    GHS09

    Wng

    H317

    H410

     

    M = 100

    M = 100’

     

    ‘613-328-00-X

    1-vinylimidazole

    214-012-0

    1072-63-5

    Repr. 1B

    H360D

    GHS08

    Dgr

    H360D

     

    Repr. 1B; H360D: C ≥ 0,03 %’

     

    ‘616-224-00-2

    amisulbrom (ISO);

    3-(3-bromo-6-fluoro-2-methylindol-1-ylsulfonyl)-N,N-dimethyl-1H-1,2,4-triazole-1-sulfonamide

    348635-87-0

    Carc. 2

    Eye Irrit. 2

    Aquatic Acute 1

    Aquatic Chronic 1

    H351

    H319

    H400

    H410

    GHS08

    GHS07

    GHS09

    Wng

    H351

    H319

    H410

     

    M = 10

    M = 10’

     


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