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The European Chemicals Agency (ECHA) proposes to add 8 substances to the REACH Annex XIV authorized substance list

2022-02-18 00:00:00
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On February 2, 2022, the European Chemicals Agency (ECHA) proposed to add 8 new substances to Annex XIV (List of Authorized Substances) of the REACH Regulation (EC) No 1907/2006 and launched a public consultation. The deadline for public consultation is May 2, 2022.


The eight substances proposed for inclusion in the list of authorized substances are as follows:

substance

Intrinsic properties associated with SVHC

EC number

CAS number

Examples of uses within the scope of the license

Ethylenediamine

Respiratory sensitization

Ethylenediamine

Ethylenediamine

It is used as a processing aid, purifying agent in refinery gas streams, corrosion inhibitors, process aids, and for odor control emissions

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

Reproductive toxicity

--

--

Fragrances in washing and cleaning products, air care products, perfumes, cosmetics

lead

Reproductive toxicity

231-100-4

7439-92-1

Battery production, cable sheathing, welding, production of different components for vehicles, machines, furniture

Glutaraldehyde

Respiratory sensitization

203-856-5

111-30-8

Leather tanning, cleaning agents, for polymers, X-ray film developers

2-Methyl-1-(4-methylthiophenyl)-2-morpholino-1-acetone

Reproductive toxicity

400-600-6

71868-10-5

Photoinitiators in UV-curable coatings, inks, and adhesives

2-Benzyl-2-dimethylamino-1-(4-morpholinophenyl)butanone

Reproductive toxicity

404-360-3

119313-12-1

Photoinitiators in UV-curable coatings, inks, and adhesives

Diisohexylphthalates

Reproductive toxicity

276-090-2

71850-09-4

It is not currently registered under REACH

Sodium orthoborate

Reproductive toxicity

237-560-2

13840-56-7

It is not currently registered under REACH

The comments received during the public consultation will help ECHA define its recommendations to the European Commission. In the spring of 2023, ECHA's recommendations will be submitted to the European Commission, which will decide which substances to include in the list of authorized substances.

If a substance is included in the list of authorized substances, after a certain date, the substance can only be placed on the market or used for a specific purpose after the authorization has been granted. Companies that use, manufacture, or import these substances should apply for authorization.




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