# Anilin – Addendum: Reevaluierung des BAT-Wertes und Evaluierung einer Schwangerschaftsgruppe zum BAT-Wert: Beurteilungswerte in biologischem Material

**Authors:** Britta Brinkmann, Rüdiger Bartsch, Sandra Michaelsen, Gerlinde Schriever-Schwemmer, Hans Drexler, Andrea Hartwig

PMC · DOI: 10.34865/bb6253d10_1ad · The MAK Collection for Occupational Health and Safety · 2025-03-31

## TL;DR

This paper reevaluates the biological tolerance value for aniline and assigns it to a pregnancy risk group based on toxicological effects.

## Contribution

The study confirms the BAT value for aniline and assigns it to Pregnancy Risk Group B due to potential developmental risks.

## Key findings

- The BAT value of 500 μg aniline/l urine is confirmed based on methaemoglobin levels.
- Aniline exposure is assigned to Pregnancy Risk Group B due to potential risks to the unborn child.
- A urinary concentration of 30 μg aniline/l is considered safe for the embryo or fetus.

## Abstract

The German Senate Commission for the Investigation of Health Hazards of Chemical Compounds in the Work Area (MAK Commission) re-evaluated the data for aniline [62-53-3] to verify the biological tolerance value (BAT value) of 500 μg aniline/l urine and to assign the BAT value to a pregnancy risk group, considering all toxicological end points. Relevant studies were identified from a literature search. The critical effect of aniline exposure in humans is considered to be the formation of methaemoglobin. It must be ensured that the methaemoglobin value remains below 5%, even if the BAT value is maintained. In an experimental study, the methaemoglobin content in human blood rose from 0.72% to an average methaemoglobin value of 1.2% (maximum of 2.07% methaemoglobin) during six hours of exposure to 2 ml aniline/m3 (corresponding to the maximum concentration at the workplace, MAK value). With linear extrapolation an excretion of 224 μg aniline/l would be expected at the end of an eight-hour exposure period. Consideration of the increased respiratory volume and the critical methaemoglobin increment results in a concentration of 500 μg aniline (after hydrolysis)/l urine. The BAT value has therefore been confirmed. Due to acute toxic effects, the BAT value must be regarded as the maximum value, i. e. it must be ensured that this value is not exceeded. Sampling should take place at the end of exposure or the end of a shift.

Because the no observed adverse effect concentration (NOAEC) for methaemoglobin content in relation to developmental toxicity in humans is not known, a risk for the unborn child cannot be ruled out, even in cases of compliance with the BAT value. The BAT value is therefore assigned to Pregnancy Risk Group B. As an indication of the prerequisite for an assignment to Pregnancy Risk Group C, a concentration of 30 µg aniline/l urine has been calculated from the lowest value of the natural background range of mean methaemoglobin values in (pregnant) women. At this urinary aniline concentration, damage to the embryo or foetus is unlikely.

## Linked entities

- **Chemicals:** aniline (PubChem CID 6115)

## Full-text entities

- **Genes:** CYB5A (cytochrome b5 type A) [NCBI Gene 1528] {aka CYB5, MCB5, METAG}, CYB5R3 (cytochrome b5 reductase 3) [NCBI Gene 1727] {aka B5R, DIA1}, BAAT (bile acid-CoA:amino acid N-acyltransferase) [NCBI Gene 570] {aka BACAT, BACD1, BAT, FHCA3, HCHO}, DECR1 (2,4-dienoyl-CoA reductase 1) [NCBI Gene 1666] {aka DECR, NADPH, SDR18C1}, MAK (male germ cell associated kinase) [NCBI Gene 4117] {aka RP62}
- **Diseases:** toxicity (MESH:D064420), Hypotonie (MESH:D009123), fetalem distress (MESH:D012128)
- **Chemicals:** Atemminutenvolumen (-), NADH (MESH:D009243), SO2 (MESH:D013458), NO2 (MESH:D009585), aniline (MESH:C023650)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Thr117Ser

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12823119/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12823119/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12823119/full.md

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Source: https://tomesphere.com/paper/PMC12823119