Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Description of key information

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (sensitising)
Additional information:

3,5-Lutidine was tested in female BALB/c mice in a local lymph node assay (LLNA) and found to be weakly sensitizing, with a SI of 5 after topical exposure of 50% in vehicle. However, this substance was found not to be irritating in a preliminary screening assay measuring mouse ear swelling after topical exposure. The weak response and the absence of irritation lead to questioning the validity of the findings.


Migrated from Short description of key information:
Weakly sensitizing, stimulation index (SI) = 5 at highest dose tested.

Justification for selection of skin sensitisation endpoint:
Experimental result

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available
Additional information:
Migrated from Short description of key information:
no study available

Justification for classification or non-classification

3,5-Lutidine was tested in BALB/c mice in a LLNA and found to be weakly positive, with a SI of 5, at the highest dose tested (50% in vehicle). There is strong evidence that the substance is corrosive or strongly irritating in specific assays for skin irritation and acute dermal toxicity. However, in the LLNA, the substance was found to be nonirritating when in the acetone/olive oil vehicle, in the screening assay performed prior to LLNA dosing. There is anecdotal evidence from immunotoxicologists in contract research organizations that chemicals which cause dermal irritation can result in false positive findings in the LLNA. Considering that, in general, pyridine and methyl pyridines are not sensitisers, the accuracy of this one test finding is questioned and the substance is not classified.