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EC number: 837-816-9 | CAS number: 10438-94-5
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in chemico
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 02 Sep 2019 to 06 sep 2019
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- The validated in chemico skin sensitization test is the DPRA assay, which is recommended in international guidelines (e.g. OECD) and mentioned in the ECHA guidance as the in chemico test to be performed as part of weight of evidence.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 019
- Report date:
- 2019
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 442C (In Chemico Skin Sensitisation: Direct Peptide Reactivity Assay (DPRA))
- Version / remarks:
- 18 June 2019
- Deviations:
- no
- GLP compliance:
- yes
- Type of study:
- direct peptide reactivity assay (DPRA)
- Justification for non-LLNA method:
- A validated in chemico skin sensitization test is the DPRA assay, which is recommended in international guidelines (e.g. OECD) and mentioned in the ECHA guidance as one of the non-animal tests to be performed as part of weight of evidence.
Test material
- Reference substance name:
- 3-(octyloxy)propane-1,2-diol
- Cas Number:
- 10438-94-5
- Molecular formula:
- C11H24O3
- IUPAC Name:
- 3-(octyloxy)propane-1,2-diol
- Test material form:
- liquid
- Details on test material:
- Storage Conditions: At room temperature protected from light container flushed with nitrogen.
Constituent 1
In chemico test system
- Details on the study design:
- TEST ITEM PREPARATION:
Solubility of the test item in an appropriate solvent was assessed before performing the DPRA. An appropriate solvent dissolved the test item completely, i.e., by visual inspection the solution had to be not cloudy nor have noticeable precipitate. The following solvent was evaluated: acetonitrile (ACN).
Test item stock solutions were prepared freshly for each reactivity assay.
For both the cysteine and lysine reactivity assay 34.78 mg of test item was pre-weighed into a clean amber glass vial and dissolved, just before use, in 1702 µL ACN after vortex mixing to obtain a 100 mM solution. Visual inspection of the forming of a clear solution was considered sufficient to ascertain that the test item was dissolved. The test item, positive control and peptide samples were prepared less than 4 hours before starting the incubation of the cysteine (cys) or lysine (lys) reactivity assay, respectively.
TEST SYSTEM
Test system: Synthetic peptides containing cysteine (SPCC) (Ac RFAACAA COOH) or synthetic peptides containing lysine (SPCL) (Ac RFAAKAA COOH). The molecular weight is 750.9 g/mol for SPCC and 775.9 g/mol for SPCL.
Source: JPT Peptide Technologies GmbH, Berlin, Germany.
Storage: The peptides were stored in the freezer (≤ 15°C) for a maximum of 6 months.
Incubation: The samples (reference controls, calibration solutions, co-elution control, positive controls and test item samples) were placed in the autosampler in the dark and incubated at 25±2.5°C. The incubation time between placement of the samples in the autosampler and analysis of the first RCcysB- or RClysB-sample was 24.2 hours. The time between the first RCcysB- or RClysB-injection and the last injection of a cysteine or lysine sequence did not exceed 30 hours.
Analysis: All samples were analyzed according to the HPLC method presented in Table 1. (See 'other information on materials and methods').
The HPLC sequences of the cysteine and lysine reactivity assay for the test item are presented in Table 2. (See 'other information on materials and methods').
POSITIVE CONTROL: Cinnamic aldehyde
- Purity: 99.1%
- Batch: MKCB9907
- Expiry of batch: 30 November 2021
DATA EVALUATION
The concentration of SPCC or SPCL was spectrophotometrically determined at 220 nm in each sample by measuring the peak area of the appropriate peaks by peak integration and by calculating the concentration of peptide using the linear calibration curve derived from the standards.
The Percent Peptide Depletion was determined in each sample by measuring the peak area and dividing it by the mean peak area of the relevant reference controls C according to the following formula:
Percent Peptide Depletion= [1-(Peptide Peak Area in Replicate Injection (at 220 nm))/Mean Peptide Peak Area in Reference Controls (at 220 nm))]×100
In addition, the absorbance at 258 nm was determined in each sample by measuring the peak area of the appropriate peaks by peak integration. The ratio of the 220 nm peak area and the 258 nm peak was used as an indicator of co-elution. For each sample, a ratio in the range of 90%
DATA INTERPRETATION (see Table 3 `other information on materials and method')
The mean Percent Cysteine Depletion and Percent Lysine Depletion were calculated for the test item. Negative depletion was considered as “0” when calculating the mean. By using the Cysteine 1:10 / Lysine 1:50 prediction model (see table below), the threshold of 6.38% average peptide depletion was used to support the discrimination between a skin sensitizer and a non-sensitizer.
ACCEPTABILITY CRITERIA
The following criteria had to be met for a run to be considered valid:
a) The standard calibration curve had to have a r2>0.99.
b) The mean Percent Peptide Depletion value of the three replicates for the positive control cinnamic aldehyde had to be between 60.8% and 100% for SPCC and between 40.2% and 69.0% for SPCL.
c) The maximum standard deviation (SD) for the positive control replicates had to be <14.9% for the Percent Cysteine Peptide Depletion and <11.6% for the Percent Lysine Peptide Depletion.
d) The mean peptide concentration of Reference Controls A had to be 0.50 ± 0.05 mM.
e) The Coefficient of Variation (CV) of peptide areas for the nine Reference Controls B and C in ACN had to be <15.0%.
The following criteria had to be met for a test item’s results to be considered valid:
a) The maximum SD for the test item replicates had to be <14.9% for the Percent Cysteine Depletion and <11.6% for the Percent Lysine Depletion.
b) The mean peptide concentration of the three Reference Controls C in the appropriate solvent had to be 0.50±0.05 mM.
Results and discussion
In vitro / in chemico
Resultsopen allclose all
- Key result
- Run / experiment:
- other: Cysteine Reactivity Assay
- Parameter:
- other: Mean Percentage SPCC depletion
- Value:
- 0.8
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- CV Between reference controls: 0.6%
- Positive controls validity:
- valid
- Remarks:
- mean percentage SPCC: 71.1% ± 0.2%.
- Key result
- Run / experiment:
- other: Lysine Reactivity Assay
- Parameter:
- other: Mean Percentage SPCL depletion
- Value:
- 0.4
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- CV between reference controls: 0.4%
- Positive controls validity:
- valid
- Remarks:
- Mean percentage SPCL: 62.3% ± 3.4%
- Other effects / acceptance of results:
- - Upon preparation as well as after incubation of the SPCC and SPCL test item samples, no precipitate or phase separation was observed in any of the samples.
- In the cysteine reactivity assay the test item showed 0.8% SPCC depletion while in the lysine reactivity assay the test item showed 0.4% SPCL depletion. The mean of the SPCC and SPCL depletion was 0.6% and as a result the test item was negative in the DPRA and was classified in the “no or minimal reactivity class” when using the Cysteine 1:10 / Lysine 1:50 prediction model.
Any other information on results incl. tables
Acceptability of the Direct Peptide Reactivity Assay (DPRA)
|
Cysteine reactivity assay |
Lysine reactivity assay |
||
Acceptability criteria |
Results for SPCC |
Acceptability criteria |
Results for SPCL |
|
Correlation coefficient (r2) standard calibration curve |
>0.99 |
1.000 |
>0.99 |
1.000 |
Mean peptide concentration RC-A samples (mM) |
0.50 ± 0.05 |
0.506 ± 0.002 |
0.50 ± 0.05 |
0.502 ± 0.001 |
Mean peptide concentration RC-C samples (mM) |
0.50 ± 0.05 |
0.507 ± 0.003 |
0.50 ± 0.05 |
0.501 ± 0.002 |
CV (%) for RC samples B and C |
<15.0 |
0.6 |
<15.0 |
0.4 |
Mean peptide depletion cinnamic aldehyde (%) |
60.8-100 |
71.1 |
40.2-69.0 |
62.3 |
SD of peptide depletion cinnamic aldehyde (%) |
<14.9 |
0.2 |
<11.6 |
3.4 |
SD of peptide depletion for the test item (%) |
<14.9 |
0.2 |
<11.6 |
0.2 |
RC = Reference Control; CV = Coefficient of Variation; SD = Standard Deviation.
SPCC and SPCL Depletion, DPRA Prediction and Reactivity Classification forthe Test Item
Test item |
SPCC depletion |
SPCL depletion |
Mean of SPCC and SPCL depletion |
DPRA prediction and reactivity classification |
||
Mean |
± SD |
Mean |
± SD |
Cysteine 1:10 / Lysine 1:50 prediction model |
||
Saskine ™ 80 |
0.8% |
±0.2% |
0.4% |
±0.2% |
0.6% |
Negative: No or minimal reactivity |
SD = Standard Deviation.
Applicant's summary and conclusion
- Interpretation of results:
- other: study is part of a weight of evidence approach and is not used for classification on its own
- Conclusions:
- In a DPRA performed according to OECD TG 442C the mean of the SPCC and SPCL depletion was 0.6% and the substance is classified in the “no or minimal reactivity class” when using the Cysteine 1:10 / Lysine 1:50 prediction model.
- Executive summary:
A DPRA study was performed according to the OECD TG 442C and in accordance with GLP principles. SPCC and SPCL Percent Depletion Values were calculated and used in a prediction model which allows assigning the test item to one of four reactivity classes used to support the discrimination between sensitizers and non-sensitizers. The relative peptide concentration was determined by High-Performance Liquid Chromatography (HPLC) with gradient elution and spectrophotometric detection at 220 nm and 258 nm. The validation parameters, i.e. calibration curve, mean concentration of Reference Control (RC) samples, the CV for RC samples, the mean percent peptide depletion values for the positive control with its standard deviation value and the standard deviation value of the peptide depletion for the test item, were all within the acceptability criteria for the DPRA. Since all acceptability criteria were met this DPRA is considered to be valid. No coelution of the test item with SPCC or SPCL was observed.
In the cysteine reactivity assay the test item showed 0.8% SPCC depletion while in the lysine reactivity assay the test item showed 0.4% SPCL depletion. The mean of the SPCC and SPCL depletion was 0.6% and as a result the test item was considered to be negative in the DPRA and classified in the “no or minimal reactivity class” when using the Cysteine 1:10 / Lysine 1:50 prediction model.
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