Food additives, flavourings, processing aids and materials in contact with food (AFC)

The Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (the Panel) is asked to advise the Commission on the implications for human health of
chemically defined flavouring substances used in or on foodstuffs in the Member States. In particular, the Scientific Panel is asked to evaluate 58 flavouring substances in the Flavouring Group
Evaluation, Revision 1 (FGE.03Rev1), using the procedure as referred to in the Commission Regulation (EC) No 1565/2000. These 58 flavouring substances belong to chemical groups 1, 2 and 4 of
Annex I of the Commission Regulation (EC) No 1565/2000.

The present Flavouring Group Evaluation deals with 56 acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated or unsaturated
aldehydes, one orthoester of formic acid and one ester of a hemiacetal.
Thirty-two of the 58 flavouring substances possess one or more chiral centres. For 30 of these substances the stereoisomeric composition has not been specified.

One of the 58 substances can exist as a geometrical isomer [FL-no: 06.063] and no indication has been given that one of the possible isomers has preponderance in the commercial flavouring
material. Fifty-seven of the flavouring substances are classified into structural class I and the orthoester [FL-no: 06.096] into structural class III.
Fifty-one of the substances in the present group of 58 substances have been reported to occur naturally in a wide range of food items.
In its evaluation, the Panel as a default used the Maximised Survey-derived Daily Intakes (MSDIs) approach to estimate the per capita intakes of the flavouring substances in Europe. However,
when the Panel examined the information provided by the European Flavouring Industry on the use levels in various foods, it appeared obvious that the MSDI approach in a number of cases would
grossly underestimate the intake by regular consumers of products flavoured at the use level reported by the Industry, especially in those cases where the annual production values were reported
to be small. In consequence, the Panel had reservations about the data on use and use levels provided and the intake estimates obtained by the MSDI approach.
In the absence of more precise information that would enable the Panel to make a more realistic estimate of the intakes of the flavouring substances, the Panel has decided also to perform an
estimate of the daily intakes per person using a modified Theoretical Added Maximum Daily Intake (mTAMDI) approach based on the normal use levels reported by Industry. In those cases where the
mTAMDI approach indicated that the intake of a flavouring substance might exceed its corresponding threshold of concern, the Panel decided not to carry out a formal safety assessment using the
Procedure. In these cases the Panel requires more precise data on use and use levels.
According to the default MSDI approach, the 57 flavouring substances have intakes in Europe from 0.001 to 14 microgram/capita/day, which are below the threshold of concern value for structural
class I of 1800 microgram/person/day. Likewise the estimated level of intake for the orthoester [FL-no: 06.096] of 0.013 microgram/capita/day is below the threshold of concern for structural
class III of 90 microgram/person/day.
Adequately reported genotoxicity studies are only available for one of the flavouring substances. These studies do not give rise to safety concern with respect to genotoxicity of the flavouring
substance in this Flavouring Group Evaluation. Consideration was given to methanol, formaldehyde, ethanol, and acetaldehyde that are potential hydrolysis products of several of the acetals in
the present Flavouring Group Evaluation. Because of the natural occurrence in food and the endogenous formation in humans of considerably larger amounts of these compounds, their formation from
hydrolysis of the acetals were not considered to be of safety concern with respect to genotoxicity at their estimated levels of intakes, based on the MSDI approach.
The 58 candidate substances are expected to be metabolised to innocuous products.
There are no toxicological studies available on the 58 flavouring substances or on structurally related acetals other than data on acute toxicity.
On the basis of the default MSDI approach the Panel concluded that the 56 acetals, the orthoester and the ester of a hemiacetal would not give rise to safety concerns at levels of intake
arising from their use as flavouring substances.
When the estimated intakes were based on the mTAMDI approach they ranged from 3 to 4900 microgram/person/day for the 57 substances from structural class I. For 15 of the substances the intakes
were above the threshold of concern for structural class I of 1800 microgram/person/day. For the one substance from structural class III [FL-no: 06.096] the mTAMDI is 1600 microgram/person/day,
which is above the threshold of concern for structural class III of 90 microgram/person/day.

Thus, for 16 of the 58 flavouring substances considered in this opinion, the intakes, estimated on the basis of the mTAMDI, exceed the relevant threshold for their structural class to which the
flavouring substance has been assigned. Therefore, for these 16 substances more reliable exposure data are required. On the basis of such additional data, these flavouring substances should be
reconsidered using the Procedure. Subsequently, additional data might become necessary.

In order to determine whether this evaluation could be applied to the materials of commerce, it is necessary to consider the available specifications.
Adequate specifications including complete purity criteria and identity tests for the materials of commerce have been provided for 41 of the 58 flavouring substances, except that information on
geometrical isomerism/chirality is missing for 31 substances. The specifications are not adequate for 17 substances [FL-no: 03.023, 06.041, 06.042, 06.043, 06.045, 06.046, 06.047, 06.063,
06.105, 06.106, 06.107, 06.109, 06.115, 06.123, 06.124, 06.128, 06.129].

Thus, the final evaluation of the materials of commerce cannot be performed for 34 substances ([FL-no: 03.023, 06.041, 06.042, 06.043, 06.044, 06.045, 06.046, 06.047, 06.048, 06.049, 06.050,
06.063, 06.079, 06.082, 06.083, 06.084, 06.085, 06.086, 06.091, 06.092, 06.105, 06.106, 06.107, 06.109, 06.111, 06.114, 06.115, 06.123, 06.124, 06.127, 06.128, 06.129, 06.130, 06.131], pending
further information. The remaining 24 substances [FL-no: 06.051, 06.052, 06.053, 06.054, 06.055, 06.057, 06.058, 06.059, 06.061, 06.062, 06.064, 06.065, 06.066, 06.067, 06.069, 06.070, 06.071,
06.073, 06.074, 06.075, 06.076, 06.096, 06.100 and 06.125] would present no safety concern at the levels of intake estimated on the basis of the MSDI approach.


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