Ethanol has reached the final stages of the review process and is now undergoing a crucial phase of regulatory scrutiny. The Working Groups have concluded that ethanol meets the exclusion criteria for carcinogenicity and reproductive toxicity, but a decision on mutagenicity is still pending. The classification of ethanol as category 1A or 1B for carcinogenicity and reproductive toxicity remains unresolved, with further discussions planned.

Regardless of the final classification, ethanol is now considered a candidate for substitution (CfS) under Article 10(1). In light of this, it is essential to assess whether viable substitutes exist.

ECHA has opened a consultation on alternatives for this substance, with a deadline for input set for 28 April 2025.

The outcome of this review could significantly impact ethanol's market presence, potentially leading to serious consequences for a key substance used in various applications, particularly those aimed at protecting human health. Regulatory strategies intended to safeguard public health may, paradoxically, have counterproductive effects if ethanol’s use becomes restricted or removed from the market.

Whether you are seeking to adapt to the new regulatory requirements or aiming to ensure that your products remain compliant and competitive in the market, our biocides regulatory compliance experts can provide the necessary support and guidance. We’ll keep you at the forefront of regulatory developments – supporting your business with; risk assessments, dossier updates, analysis of alternatives and stakeholder engagement.

Call and speak with one of our biocide consultants today.