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ECHA Recommends Eight Substances for Authorisation List

Once substances are added to the list, companies will need to apply for authorisation to continue using them.

On April 12, 2023, ECHA submitted its 11th recommendation to the European Commission, which recommends the inclusion of 8 substances to the REACH Authorisation List to protect people and the environment.

The proposed list of substances are:

Substance nameCAS No.EC No.SVHC property

Ethylenediamine

107-15-3

203-468-6

Respiratory sensitiser

2-(4-tert-butylbenzyl) propionaldehyde and its individual stereoisomers

--

Toxic for reproduction

Lead

7439-92-1

231-100-4

Toxic for reproduction
Glutaral111-30-8203-856-5Respiratory sensitiser

2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one

71868-10-5400-600-6Toxic for reproduction

2-benzyl-2-dimethylamino-4'-morpholinobutyrophenone

119313-12-1404-360-3Toxic for reproduction

Diisohexyl phthalate 

71850-09-4276-090-2Toxic for reproduction

Orthoboric acid, sodium salt

13840-56-7237-560-2Toxic for reproduction

As early as 2014, ECHA has prioritised these substances in the Candidate List of substances of very high concern (SVHC). On February 2, 2022, the draft recommendation for inclusion of 8 substances was published by ECHA for consultation. Certain issues concerning the uses of these substances, their possible exemptions from the authorisation requirement and on the structure and complexity of their supply chains were discussed and requested for further information.

Once adopted, this recommendation would subject lead metal to the same regulatory requirements as other lead compounds with similar uses and have already been recommended for addition to the Authorisation List.

Background

ECHA has the legal obligation to regularly recommend substances from the Candidate List for the EU Commission to include in the Authorisation List. Substances recommended to be included in the Authorization List are considered to be of very high concern (SVHC), either because of their hazardous properties or because of their widespread use in consumer products.

 

Once a substance is included in the Authorisation List, producer, importer or downstream users need to apply for authorization before the latest application date to continue using or placing it on the European Economic Area (EEA) market. Without authorisaiton, its use or placement will be banned after given sunset date. 

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