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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: via oral route - systemic effects

Link to relevant study records
Reference
Endpoint:
sub-chronic toxicity: oral
Type of information:
(Q)SAR
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Justification for type of information:
QSAR prediction: migrated from IUCLID 5.6
Qualifier:
according to guideline
Guideline:
other: Estimated data
Principles of method if other than guideline:
QSAR prediction is done using the QSAR toolbox version 3.0
GLP compliance:
not specified
Species:
mouse
Strain:
B6C3F1
Sex:
male/female
Route of administration:
oral: gavage
Vehicle:
corn oil
Duration of treatment / exposure:
98 days
Frequency of treatment:
once daily
Remarks:
Doses / Concentrations:
0.00, 75.00, 150.00, 300.00
Basis:
nominal in diet
Dose descriptor:
LOEL
Effect level:
292.468 other: mg/kg bw/day
Based on:
test mat.
Sex:
male/female
Basis for effect level:
other: body weight decrease
Critical effects observed:
not specified





The prediction was based on dataset comprised from the following descriptors: "effect LOEL"
Estimation method: Takes average value from the 5 nearest neighbours
Domain logical expression:Result: In Domain

((((("a" and "b" ) and ("c" and ( not "d") ) ) and "e" ) and ("f" and ( not "g") ) ) and ("h" and "i" ) )

Domain logical expression index: "a"

Similarity boundary:Target: C(=O)(O)CCCCC(=O)O_C1CNCCN1
Threshold=50%,
Dice(Atom pairs)

Domain logical expression index: "b"

Referential boundary: The target chemical should be classified as No superfragment by Superfragments

Domain logical expression index: "c"

Referential boundary: The target chemical should be classified as Not possible to classify according to these rules (GSH) by Protein binding potency

Domain logical expression index: "d"

Referential boundary: The target chemical should be classified as Highly reactive (GSH) OR Highly reactive (GSH) >> 2-Alken-1-als (MA) OR Highly reactive (GSH) >> Cinnamaldehydes (MA) OR Moderately reactive (GSH) OR Moderately reactive (GSH) >> Substituted 1-Alken-3-ones (MA) by Protein binding potency

Domain logical expression index: "e"

Referential boundary: The target chemical should be classified as High (Class III) AND Low (Class I) by Toxic hazard classification by Cramer (with extensions)

Domain logical expression index: "f"

Referential boundary: The target chemical should be classified as Non-Metals by Groups of elements

Domain logical expression index: "g"

Referential boundary: The target chemical should be classified as Alkali Earth OR Halogens by Groups of elements

Domain logical expression index: "h"

Parametric boundary:The target chemical should have a value of log Kow which is >= -0.392

Domain logical expression index: "i"

Parametric boundary:The target chemical should have a value of log Kow which is <= 0.666

Conclusions:
Based on the prediction done for piperazine adipate for repeated dose via oral route for subchronic value on mouse, the estimated lowest observed effect level (LOEL) is 292.46 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via oral route for the above mentioned dose.
Executive summary:

Based on the prediction done for piperazine adipate for repeated dose via oral route for subchronic value on mouse, the estimated lowest observed effect level (LOEL) is 292.46 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via oral route for the above mentioned dose.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Study duration:
subchronic
Species:
mouse
Quality of whole database:
K2 data is predicted using the OECD QSAR toolbox version 3.0

Repeated dose toxicity: inhalation - systemic effects

Link to relevant study records
Reference
Endpoint:
short-term repeated dose toxicity: inhalation
Type of information:
(Q)SAR
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Justification for type of information:
QSAR prediction: migrated from IUCLID 5.6
Qualifier:
according to guideline
Guideline:
other: Estimated data
Principles of method if other than guideline:
QSAR prediction is done using the QSAR toolbox version 3.0
GLP compliance:
not specified
Species:
rat
Strain:
other: Sprague-Dawley;F344;Wistar;CD
Sex:
male/female
Route of administration:
inhalation: vapour
Type of inhalation exposure:
not specified
Vehicle:
not specified
Duration of treatment / exposure:
28 days
Frequency of treatment:
6 hours/day and 5 days/week
Remarks:
Doses / Concentrations:
0.00, 3.10, 9.90, 30.00, 98.00
Basis:
nominal conc.
Dose descriptor:
LOEL
Effect level:
152.49 other: mg/kg/day
Based on:
test mat.
Sex:
male/female
Basis for effect level:
other: Decrease in body weight
Critical effects observed:
not specified





The prediction was based on dataset comprised from the following descriptors: "effect LOEL"
Estimation method: Takes average value from the 5 nearest neighbours
Domain logical expression:Result: In Domain

(((("a" and ("b" and ( not "c") ) ) and "d" ) and "e" ) and ("f" and "g" ) )

Domain logical expression index: "a"

Similarity boundary:Target: C(=O)(O)CCCCC(=O)O_C1CNCCN1
Threshold=50%,
Dice(Atom pairs)

Domain logical expression index: "b"

Referential boundary: The target chemical should be classified as No alert found by Protein binding by OECD

Domain logical expression index: "c"

Referential boundary: The target chemical should be classified as Acylation OR Acylation >> Direct Acylation Involving a Leaving group OR Acylation >> Direct Acylation Involving a Leaving group >> Acetates OR Acylation >> Isocyanates and Related Chemicals OR Acylation >> Isocyanates and Related Chemicals >> Isocyanates OR Michael addition OR Michael addition >> Polarised Alkenes OR Michael addition >> Polarised Alkenes >> Polarised alkene - esters OR SN2 OR SN2 >> Epoxides and Related Chemicals OR SN2 >> Epoxides and Related Chemicals >> Epoxides OR SN2 >> SN2 reaction at a sulphur atom OR SN2 >> SN2 reaction at a sulphur atom >> Thiols OR SN2 >> SN2 reaction at sp3 carbon atom OR SN2 >> SN2 reaction at sp3 carbon atom >> alpha-Halocarbonyls by Protein binding by OECD

Domain logical expression index: "d"

Referential boundary: The target chemical should be classified as No superfragment by Superfragments

Domain logical expression index: "e"

Referential boundary: The target chemical should be classified as High (Class III) AND Low (Class I) by Toxic hazard classification by Cramer (with extensions)

Domain logical expression index: "f"

Parametric boundary:The target chemical should have a value of log Kow which is >= -0.484

Domain logical expression index: "g"

Parametric boundary:The target chemical should have a value of log Kow which is <= 1.81

Conclusions:
Based on the prediction done for piperazine adipate for repeated dose via inhalation route for subacute value on rat, the estimated lowest observed effect level (LOEL) is 152.49 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via inhalation route for the above mentioned dose.
Executive summary:

Based on the prediction done for piperazine adipate for repeated dose via inhalation route for subacute value on rat, the estimated lowest observed effect level (LOEL) is 152.49 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via inhalation route for the above mentioned dose.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Study duration:
subacute
Species:
rat
Quality of whole database:
K2 data is predicted using the OECD QSAR toolbox version 3.0

Repeated dose toxicity: dermal - systemic effects

Link to relevant study records
Reference
Endpoint:
repeated dose toxicity: dermal
Data waiving:
other justification
Justification for data waiving:
other:
Critical effects observed:
not specified
Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for selection of repeated dose toxicity via oral route - systemic effects endpoint:

Based on the prediction done for piperazine adipate for repeated dose via oral route for subchronic value on mouse, the estimated lowest observed effect level (LOEL) is 292.46 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via oral route for the above mentioned dose.

Justification for selection of repeated dose toxicity inhalation - systemic effects endpoint:

Based on the prediction done for piperazine adipate for repeated dose via inhalation route for subacute value on rat, the estimated lowest observed effect level (LOEL) is 152.49 mg/kg bw/day for body weight decrease effect. Based on this value it can be conclued that piperazine adipate is not toxic via inhalation route for the above mentioned dose.

Justification for classification or non-classification