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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
skin sensitisation: in vivo (LLNA)
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2014
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: well performed OECD study with GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2014
Report date:
2014

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
GLP compliance:
yes
Type of study:
mouse local lymph node assay (LLNA)

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyl p-toluate
EC Number:
202-784-1
EC Name:
Methyl p-toluate
Cas Number:
99-75-2
Molecular formula:
C9H10O2
IUPAC Name:
methyl 4-methylbenzoate
Details on test material:
purity: 97.8%
expiry date: 2015-10-15

In vivo test system

Test animals

Species:
mouse
Strain:
CBA
Sex:
female
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Charles River UK Ltd
- Age at study initiation: 9 - 11 weeks
- Weight at study initiation: 15.86 g - 20.92 g
- Housing: individually, in solid floor standard polysulfone cages (Size: Approximately L 360 x B 205 x H 140 mm)
- Diet: Ssniff mice pellet food – Ssniff Spezialdiäten GmbH., Ferdinand-Gabriel-Weg 16, D-59494 Soest, Germany (ad libitum)
- Water: deep bore-well water passed through activated charcoal filter and exposed to UV rays (ad libitum)
- Acclimation period: 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 22
- Humidity (%): 64 - 65
- Air changes (per hr): 13.4
- Photoperiod: 12 hrs dark / 12 hrs light

Study design: in vivo (LLNA)

Vehicle:
dimethylformamide
Concentration:
0, 10, 25, 75 %
No. of animals per dose:
6
Positive control substance(s):
hexyl cinnamic aldehyde (CAS No 101-86-0)

Results and discussion

Positive control results:
25% α – Hexylcinnamaldehyde (HCA) in DMF SI = 7.43+-1.15

In vivo (LLNA)

Resultsopen allclose all
Parameter:
SI
Remarks on result:
other: see above
Parameter:
other: disintegrations per minute (DPM)
Remarks on result:
other: see Remark
Remarks:
Group and Dose concentration No. of mice DPM/Mouse SI G1 vehicle DMF 6 554+-90 1.00+-0.26 G2 25% HCA in DMF 6 4116+-640 7.43+-1.15 G3 10% substance in DMF 6 1096+-166 1.98+-0.30 G4 25% substance in DMF 6 2180+-562 3.93+-1.01 G5 75% substance in DMF 6 3023+-521 5.45+-0.94

Any other information on results incl. tables

  EC3calculation:

                       EC3  = XL+ [(3-YL)/ (Yh-YL)](Xh-XL)

                Where, YL = SI value below 3

                             XL = chemical concentration that elicits YL

                               Yh =  SI value above 3

                             Xh = chemical concentration that elicits Yh

EC3 value for the substance is 17.85%

Applicant's summary and conclusion

Interpretation of results:
sensitising
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The test item demonstrated skin sensitization potential in the mouse LLNA, as the lymph nodes draining the area of topical application elicit a proliferative response greater than the threshold (SI ≥ 3, i.e. 3-fold greater proliferation than vehicle control).
Executive summary:

The substance was tested for skin sensitisation according to OECD guideline 429 (Local lymph node assay, LLNA) in DMF.

In a sceening study the vehicle- N,N-dimethylformamide (DMF), 5, 10, 25, 50 and 75% w/v of the substance in DMF were applied to one animal at each dose level for 3 days. There were no clinical signs, no erythema at the site of application, no significant increase in the ear thickness and ear punch weights and no effect on body weight.

In the LLNA main study six female CBA/Ca mice/group received the vehicle  (DMF) or 25% α-hexylcinnamaldehyde (HCA: positive control in DMF) or  10, 25 and 75%w/v test item in DMF on days 1 to 3. On day 6, uptake of3H-methyl thymidine into the auricular lymph nodes draining the site of test item application was measured approximately five hours post administration. Proper conduct of the LLNA was confirmed via a positive response using 25% α-hexylcinnamaldehyde, a contact sensitizer, which elicited proliferation with a Mean Stimulation Index (SI) value of 7.43, in comparison to vehicle-treated mice.

There were no clinical signs, no local skin reactions,no significant increase in  % ear thickness and ear punch weight at the tested concentrations and treatment had no significant effect on body weight gain.

The test item at dose concentrations of 10, 25 and 75% w/v elicited proliferative response with SI of 1.98, 3.93 and 5.45, respectively in comparison with the vehicle-treated mice. The EC3value was 17.85%.