|
24.2.2011 |
EN |
Official Journal of the European Union |
L 49/52 |
Corrigendum to Commission Regulation (EU) No 143/2011 of 17 February 2011 amending Annex XIV to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (‘REACH’)
( Official Journal of the European Union L 44 of 18 February 2011 )
On page 5, the Annex is replaced by the following text:
‘ANNEX
In Annex XIV to Regulation (EC) No 1907/2006 the following table is inserted:
|
‘Entry Nr |
Substance |
Intrinsic property(ies) referred to in Article 57 |
Transitional arrangements |
Exempted (categories of) uses |
Review periods |
||||||||||
|
Latest application date (1) |
Sunset date (2) |
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|
1. |
5-tert-butyl-2,4,6-trinitro-m-xylene (Musk xylene) EC No: 201-329-4 CAS No: 81-15-2 |
vPvB |
21 February 2013 |
21 August 2014 |
— |
— |
|||||||||
|
2. |
4,4’-Diaminodiphenylmethane (MDA) EC No: 202-974-4 CAS No: 101-77-9 |
Carcinogenic (category 1B) |
21 February 2013 |
21 August 2014 |
— |
— |
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|
3. |
Hexabromocyclododecane (HBCDD) EC No: 221-695-9, 247-148-4, CAS No: 3194-55-6 25637-99-4 alpha-hexabromocyclododecane
beta-hexabromocyclododecane
gamma-hexabromocyclododecane
|
PBT |
21 February 2014 |
21 August 2015 |
— |
— |
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|
4. |
Bis(2-ethylhexyl) phthalate (DEHP) EC No: 204-211-0 CAS No: 117-81-7 |
Toxic for reproduction (category 1B) |
21 August 2013 |
21 February 2015 |
Uses in the immediate packaging of medicinal products covered under Regulation (EC) No 726/2004, Directive 2001/82/EC, and/or Directive 2001/83/EC. |
|
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|
5. |
Benzyl butyl phthalate (BBP) EC No: 201-622-7 CAS No: 85-68-7 |
Toxic for reproduction (category 1B) |
21 August 2013 |
21 February 2015 |
Uses in the immediate packaging of medicinal products covered under Regulation (EC) No 726/2004, Directive 2001/82/EC, and/or Directive 2001/83/EC. |
|
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|
6. |
Dibutyl phthalate (DBP) EC No: 201-557-4 CAS No: 84-74-2 |
Toxic for reproduction (category 1B) |
21 August 2013 |
21 February 2015 |
Uses in the immediate packaging of medicinal products covered under Regulation (EC) No 726/2004, Directive 2001/82/EC, and/or Directive 2001/83/EC. |
|
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(1) Date referred to in Article 58(1)(c)(ii) of Regulation (EC) No 1907/2006.
(2) Date referred to in Article 58(1)(c)(i) of Regulation (EC) No 1907/2006.’ ’