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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Skin sensitisation

Currently viewing:

Administrative data

Endpoint:
skin sensitisation: in chemico
Remarks:
The study is currently ongoing. This submission allows co-registrants to register for the deadline and the lead dossier will be spontaneously updated as soon as the result is available.
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Not yet available
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018
Report date:
2018

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 442C (In Chemico Skin Sensitisation: Direct Peptide Reactivity Assay (DPRA))
Deviations:
not specified
GLP compliance:
yes (incl. QA statement)
Type of study:
other: In Chemico skin sensitisation (DPRA)

Test material

Constituent 1
Chemical structure
Reference substance name:
3-(allyloxy)propane-1,2-diol
EC Number:
204-620-4
EC Name:
3-(allyloxy)propane-1,2-diol
Cas Number:
123-34-2
Molecular formula:
C6H12O3
IUPAC Name:
3-(allyloxy)propane-1,2-diol
Test material form:
liquid

In chemico test system

Details on the study design:
The study is currently ongoing. This submission allows co-registrants to register for the deadline and the lead dossier will be spontaneously updated as soon as the result is available

Results and discussion

In vitro / in chemico

Results
Value:
0
Vehicle controls validity:
not examined
Negative controls validity:
not examined
Positive controls validity:
not examined
Remarks on result:
no indication of skin sensitisation
Other effects / acceptance of results:
The study is currently ongoing. This submission allows co-registrants to register for the deadline and the lead dossier will be spontaneously updated as soon as the result is available

Applicant's summary and conclusion

Interpretation of results:
other: not yet available
Conclusions:
The study is currently ongoing. This submission allows co-registrants to register for the deadline and the lead dossier will be spontaneously updated as soon as the result is available
Executive summary:

The study is currently ongoing.  This  submission allows co-registrants to register for the deadline and the lead dossier will be spontaneously updated as soon as the result is available