Safety assessment of the substance N,N′‐(2‐(4‐(2‐aminobenzamido)butyl)pentane‐1,5‐diyl)bis(2‐aminobenzamide) for use in plastic food contact materials

The EFSA Panel on Food Contact Materials assessed the safety of N,N'-(2-(4-(2-aminobenzamido)butyl)pentane-1,5-diyl)bis(2-aminobenzamide) to be used at up to 650 mg/kg in polyethylene terephthalate (PET) to scavenge acetaldehyde (AA). Final articles are intended for contact with aqueous, acidic and low-alcoholic beverages for long-term storage at room temperature and below. The migration of the substance from PET bottles into 20% ethanol was 0.0038 mg/kg food. The Panel calculated the potential migration of the summed reaction products not to exceed 0.02 mg/kg food. From experimental studies, the Panel excluded genotoxicity concerns for the substance, for 2-aminobenzamide +1 formaldehyde and 2-aminobenzamide +1 AA, both with desaturation. In silico predictions, previous EFSA evaluations and the use of the threshold of toxicological concern (TTC) excluded genotoxicity concerns for 15 other impurities/reaction products. A tentatively identified by-product was predicted as possible DNA-reactive in vitro mutagen and clastogen, due to its aromatic hydroxylamine group. Its modelled migration would not exceed 0.14 μg/kg food, leading to a potential exposure below the TTC of 0.0025 μg/kg body weight per day. Non-identified reaction products are expected to be structurally related to the identified ones and, hence, not to raise concern for genotoxicity. The Panel concluded that the substance is not of safety concern for the consumer, if it is used as an additive at up to 650 mg/kg in PET intended for contact with foods simulated by simulants A, B and C, for storage above 6 months at room temperature and below, including hot-fill conditions and/or heating up to 70°C ≤ <i>T</i> ≤ 100°C for maximum <i>t</i> = 120/2<sup>((<i>T</i>-70)/10)</sup> minutes. The substance should not be used for infant formula (including water used for reconstitution) and human milk. The migration of the substance should not exceed 0.05 mg/kg food. The substance should not contain aromatic hydroxylamine derivatives at more than 0.15% w/w.

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Publication Details

Journal
EFSA Journal
Published
2025-05-01
DOI
https://doi.org/10.2903/j.efsa.2025.9368
Primary Topic
Agricultural safety and regulations
Type
article
Field-Weighted Citation Impact
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article

Safety assessment of the substance N,N′‐(2‐(4‐(2‐aminobenzamido)butyl)pentane‐1,5‐diyl)bis(2‐aminobenzamide) for use in plastic food contact materials

Els Van Hoeck, Georgios Theodoridis, Mario Ščetar, Maria Rosaria Milana et al.
EFSA Journal
Agricultural safety and regulations
article

Safety assessment of the substance N,N′‐(2‐(4‐(2‐aminobenzamido)butyl)pentane‐1,5‐diyl)bis(2‐aminobenzamide) for use in plastic food contact materials

Els Van Hoeck, Georgios Theodoridis, Mario Ščetar, Maria Rosaria Milana, Riccardo Crebelli, Claude Lambré, Ronan Cariou, Gilles Rivière, Nadia Waegeneers, Remigio Marano, Evgenia Lampi, Emma Di Consiglio, Eric Barthélémy, Maria da Silva, Laurence Castle, Konrad Grob, Marja Pronk, Roland Franz
article en

Abstract

The EFSA Panel on Food Contact Materials assessed the safety of N,N'-(2-(4-(2-aminobenzamido)butyl)pentane-1,5-diyl)bis(2-aminobenzamide) to be used at up to 650 mg/kg in polyethylene terephthalate (PET) to scavenge acetaldehyde (AA). Final articles are intended for contact with aqueous, acidic and low-alcoholic beverages for long-term storage at room temperature and below. The migration of the substance from PET bottles into 20% ethanol was 0.0038 mg/kg food. The Panel calculated the potential migration of the summed reaction products not to exceed 0.02 mg/kg food. From experimental studies, the Panel excluded genotoxicity concerns for the substance, for 2-aminobenzamide +1 formaldehyde and 2-aminobenzamide +1 AA, both with desaturation. In silico predictions, previous EFSA evaluations and the use of the threshold of toxicological concern (TTC) excluded genotoxicity concerns for 15 other impurities/reaction products. A tentatively identified by-product was predicted as possible DNA-reactive in vitro mutagen and clastogen, due to its aromatic hydroxylamine group. Its modelled migration would not exceed 0.14 μg/kg food, leading to a potential exposure below the TTC of 0.0025 μg/kg body weight per day. Non-identified reaction products are expected to be structurally related to the identified ones and, hence, not to raise concern for genotoxicity. The Panel concluded that the substance is not of safety concern for the consumer, if it is used as an additive at up to 650 mg/kg in PET intended for contact with foods simulated by simulants A, B and C, for storage above 6 months at room temperature and below, including hot-fill conditions and/or heating up to 70°C ≤ <i>T</i> ≤ 100°C for maximum <i>t</i> = 120/2<sup>((<i>T</i>-70)/10)</sup> minutes. The substance should not be used for infant formula (including water used for reconstitution) and human milk. The migration of the substance should not exceed 0.05 mg/kg food. The substance should not contain aromatic hydroxylamine derivatives at more than 0.15% w/w.

EFSA JournalVol. 23(5)
Responsible consumption and production
Openalex Percentile: Top 89%
Agricultural safety and regulations
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