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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: oral

Currently viewing:

Administrative data

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

Data source

Reference
Reference Type:
other: Predicted data
Title:
R: QSAR Toolbox 2.3.0.1132 prediction for "Effect LOEL" read across evaluation for 27375-52-6
Author:
Sustainability Support Services (Europe) AB
Year:
2012
Bibliographic source:
QSAR Toolbox version 2.3

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity Study in Rodents)
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide
EC Number:
248-433-6
EC Name:
N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide
Cas Number:
27375-52-6
Molecular formula:
C10H13NO4S
IUPAC Name:
N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide
Details on test material:
- Name of test material (as cited in study report): N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide
- Substance type: Organic
- Physical state: Solid

Test animals

Species:
rat
Strain:
Fischer 344
Sex:
male/female

Administration / exposure

Route of administration:
oral: drinking water
Vehicle:
not specified
Duration of treatment / exposure:
90 days
Control animals:
not specified

Results and discussion

Results of examinations

Body weight and weight changes:
effects observed, treatment-related
Description (incidence and severity):
Body weight decreased

Effect levels

Dose descriptor:
LOEL
Effect level:
1 738.437 other: mg/kg/day
Based on:
test mat.
Sex:
male/female
Basis for effect level:
other: Effect : Body weight decreased

Target system / organ toxicity

Critical effects observed:
not specified

Any other information on results incl. tables






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

("a" and ("b" and "c" ) )

Domain logical expression index: "a"

Similarity boundary:Target: c1(S(=O)(=O)CCO)ccc(NC(C)=O)cc1
Threshold=50%,
Dice(Atom pairs)

Domain logical expression index: "b"

Parametric boundary:The target chemical should have a value of log Kow which is >= -0.967

Domain logical expression index: "c"

Parametric boundary:The target chemical should have a value of log Kow which is <= 1.27

Applicant's summary and conclusion

Conclusions:
Repeated dose toxicity LOEL (Lowest observed effect level) of N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide to rat by the oral route was estimated at a dose concentration of 1738.437 mg/kg bw/day.On the basis of this LOEL value it is concluded that the test substance is not toxic to rat by oral route below the above mentioned dose.
Executive summary:
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Repeated dose toxicity LOEL (Lowest observed effect level) of N-[4-[(2-hydroxyethyl)sulphonyl]phenyl]acetamide to rat by the oral route was estimated at a dose concentration of 1738.437 mg/kg bw/day.On the basis of this LOEL value it is concluded that the test substance is not toxic to rat by oral route below theabove mentioned dose.