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UK Updates the Status of 90 Substances in the GB MCL List

HSE, the GB CLP Agency, is proposing to update the status of 90 substances in GB mandatory classification and labeling (GB MCL). It is scheduled to be effective in April 2024. These 90 substances are from the 14th and 15th ATP (Adaptation to Technical Progress, which was used to update the EU CLP Regulation) released by the European Commission. These two ATPs were published and came into force before the end of the transition period of Brexit and the HSE has already added these substances to the GB MCL list.

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EU Approves 2 Existing Active Substances Used in Biocidal Products

On January 16, 2024, trihydrogen pentapotassium di(peroxomonosulfate) di(sulfate) (CAS: 70693-62-8) was approved for use in biocidal products of product-types 2, 3, 4, and 5, in accordance with Regulation (EC) No 528/2012 of the European Parliament and the Council. Earlier on 15 January, Alkyl (C12-16) dimethylbenzyl ammonium chloride (CAS: 68424-85-1) was approved as an existing active substance for use as product-type 2, subject to the specifications in Table 2.

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ECHA Adds Five Substances Into the Candidate List of SVHCs

Helsinki, January 23, 2024 – The European Chemicals Agency (ECHA) officially announced the addition of two substances of very high concern (SVHC), bringing the total number of substances on the SVHC list (also known as the Candidate List) to 240. ECHA has also updated the existing Candidate List entry for dibutyl phthalate to include its endocrine-disrupting properties for the environment. Dibutyl phthalate (DBP) was added to the SVHC Candidate List in October 2008 in the first batch.

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ECHA stelt voor om drie benzotriazolen te beperken onder REACH

On 18 January 2024, ECHA published a screening report to assess whether the use of these four benzotriazoles in articles, including UV-328, UV 327, UV-350, and UV-320, should be restricted in accordance with REACH Article 69(2). Based on the available evidence, ECHA is considering restricting or prohibiting the use (or presence) of three out of the four substances, including UV-320, UV-350, and UV-327 in articles and preparing an Annex XV dossier for restriction. In terms of UV-328, ECHA is of the view that at present there is no need to prepare an Annex XV dossier for restriction as the substance is expected to be addressed by the EU POPs regulation.

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Heeft u een UFI-code in uw SDS opgenomen wanneer u mengsels naar de EU exporteert?

Vanaf 2023 zijn de wijzigingen in bijlage II van de REACH-verordening over veiligheidsinformatiebladen (SDS's) verplicht geworden. Dit betekent dat gerelateerde ondernemingen een unieke formule-identificatiecode (UFI) moeten aanbrengen in sectie 1.1 van hun SDS bij het exporteren van mengsels naar de EU. Mengsels die aan specifieke voorwaarden voldoen, moeten ook een melding bij het vergiftigingencentrum (PCN) invullen.

Heeft u een UFI-code in uw SDS opgenomen wanneer u mengsels naar de EU exporteert? Lees meer »

Turkije heeft officieel aangekondigd de kkdik-r te verlengen

Turkije heeft officieel aangekondigd de registratiedeadlines voor KKDIK te verlengen

Op 23 december 2023 kondigde Turkije officieel aan de KKDIK-registratiedeadline van 31 december 2023 met maximaal zeven jaar te verlengen, tussen 2026 en 2030, afhankelijk van de tonnageband en de gevarenclassificatie. Eerder in november werd een concepttekst ingediend bij de NGO waarin werd voorgesteld de KKDIK-registratiedeadlines geleidelijk te verlengen.

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Five Chemicals Will Not Be Used for Food Packaging in the United States

The United States Congress has proposed to amend a bill, adding substances including PFAS, ortho-phthalates, bisphenols, styrene, and antimony trioxide as unsafe for use in food contact materials. As an increasing number of states have enacted their own regulations on food safety, the House of Representatives has proposed to introduce an Act cited as the “No Toxic in Food Packaging Act of 2023” on October 26. The Act aims to federally prohibit the use of certain compounds in Food Contact Materials(FCMs). Notably, there is an overlap with restrictions outlined in the previously introduced U.S. Plastic Act. After several rounds of intense debate, the Congress ultimately decided to designate the following substances deemed unsafe for use as food contact substances in the Federal Food, Drug, and Cosmetic Act which comes into effect two years after the date of enactment of this Act.

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