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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study records
Reference
Endpoint:
skin sensitisation: in vivo (LLNA)
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP- and guideline-conformant study
Qualifier:
according to guideline
Guideline:
OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
GLP compliance:
yes (incl. QA statement)
Remarks:
testing lab.
Type of study:
mouse local lymph node assay (LLNA)
Species:
mouse
Strain:
CBA
Sex:
female
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Envigo RMS B.V., Inc. (Netherlands)
- Age at study initiation: 11-12 weeks (pre-test), 8-9 weeks (main study)
- Weight at study initiation: 19.4 +/- 1 g (main study)
- Housing: by group
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 2
- Humidity (%): 45-65
- Photoperiod (hrs dark / hrs light): 12/12

Vehicle:
propylene glycol
Remarks:
purity 99%
Concentration:
Based on a pre-test with concentrations of 25% and 10% substance, 10% was the highest concentration that could be achieved whilst avoiding local skin irritation. Therefore, the main study was conducted at concentrations of 2, 5, and 10% test substance.
No. of animals per dose:
5
Parameter:
SI
Value:
1.74
Test group / Remarks:
2% test substance
Parameter:
SI
Value:
4.25
Test group / Remarks:
5% test substance
Parameter:
SI
Value:
7.67
Test group / Remarks:
10% test substance
Parameter:
EC3
Value:
3.3

The following data were obtained in the local lymph node assay (calculated per group):

Test substance concentration

mean DPM per animal

(2 lymph nodes)$

SD

S.I.

Vehicle control

1169.2

281.5

1.00

2% 1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3)

2035.0

800.8

1.74

5%1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3)

4965.4

1516.4

4.25

10%1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3)

8969.8*

4310.1

7.67

DPM, Radioactive disintegrations per minute

S.I., stimulation index

$Mean DPM/animal was determined by dividing the sum of the measured values from lymph nodes of all animals within a group by the number of animals in that group (5 animals)

* mean DPM value for the group was significantly higher than the corresponding control value (ANOVA Dunnett-test, p=0.000)

Calculation of the EC3 value:

 

Test substance concentration

S.I.

Test group 2

1.58% (a)

1.74 (b)

Test group 3

5%(c)

4.25 (d)

EC3 = (a-c) [(3-d)/(b-d)] + c = 3.3% (w/w)

 

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

1,3,5-Benzenetricarboxylic acid, copper (2+) salt (2:3) was tested in the LLNA at concentrations of 2, 5, and 10%, resulting in stimulation indices of 1.74, 4.25, and 7.67. The calculated EC3 value was 3.3% (w/w).


Migrated from Short description of key information:
LLNA (OECD 429, BASF SE, 2015): positive

Justification for selection of skin sensitisation endpoint:
GLP- and guideline-conformant study

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

Testing of 1,3,5 -Benzenecarboxylic acid, copper (2 +) salt (2:3) derived an EC3 value of 3.5% in the LLNA. According to Regulation (EU) 1272/2008, classification as skin sensitizer (Cat. 1B, H317) is warranted.