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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: oral
Type of information:
other: Weight of evidence based on data on hydrolysis products
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Justification for type of information:
No data is available on polyglycerol-2-caprate. Data on the different constituents of the substance was used to obtain information on the acute toxicity by oral route. Because polyglycerol is a mixture consisting mainly of diglycerol, triglycerol and tetraglycerol and further information on metabolism in vivo and in vitro is available, this data is considered to be adequate for read-across. The weight of evidence document is attached below.

Data source

Reference
Reference Type:
other: weight of evidence document
Title:
Unnamed
Year:
2017
Report date:
2017

Materials and methods

Principles of method if other than guideline:
Weight of evidence analysis based on studies according to OECD guideline 401 and EPA OPPTS 870.1100

Test material

Constituent 1
Chemical structure
Reference substance name:
1,2,3-Propanetriol, homoplymer, decanoate
EC Number:
616-105-5
Cas Number:
74504-65-7
Molecular formula:
Main component: C16H32O6
IUPAC Name:
1,2,3-Propanetriol, homoplymer, decanoate
Test material form:
liquid
Details on test material:
Reaction mass of 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate and 1-(2,3-dihydroxypropoxy)-3-hydroxypropan-2-yl decanoate

Results and discussion

Effect levels
Key result
Dose descriptor:
LD50
Remarks:
rats
Effect level:
> 2 000 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Based on the weight of evidence assessment of the acute toxicity by oral route it is concluded that the reaction mass containing decanoic acid, 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl ester and decanoic acid, 1-(2,3-dihydroxypropoxy)-3-hydroxypropyl ester (Dermosoft DGMC) is of low acute oral toxicity and that no animal test is necessary. No impurities or by-products of high toxicity, its acute oral toxicity were identified in the Certificate of Analysis. Therefore, the acute oral toxicity in rats can be predicted by weight-of-evidence assessment to be higher than 2000 mg/kg body weight.
Executive summary:

No data was available on the acute toxicity by oral route for Dermosoft DGMC. Data on this endpount was therefore obtained for the main constituents in the substance as a weight of evidemce documentation of the toxicity. Thus, LD50(oral, rat) of 3320 mg/kg bw has been found for decanoic acid while a LD50(oral, rat) > 10g/kg bw was found of other polyglycerol esters of fatty acids. Based on this assessment it is concluded that the reaction mass containing decanoic acid, 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl ester and decanoic acid, 1-(2,3-dihydroxypropoxy)-3-hydroxypropyl ester (Dermosoft DGMC) is of low acute oral toxicity and that no animal test is necessary. No impurities or by-products of high toxicity, its acute oral toxicity were identified in the Certificate of Analysis. Therefore, the acute oral toxicity in rats can be predicted by weight-of-evidence assessment to be higher than 2000 mg/kg body weight.