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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Specific investigations: other studies

Currently viewing:

Administrative data

Endpoint:
biochemical or cellular interactions
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study well documented

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Unnamed
Year:
1988
Report date:
1988
Reference Type:
study report
Title:
Unnamed
Year:
1988
Report date:
1988

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Study of DNA adduct formation in vivo
GLP compliance:
no
Type of method:
in vivo
Endpoint addressed:
carcinogenicity

Test material

Constituent 1
Chemical structure
Reference substance name:
Acrylic acid
EC Number:
201-177-9
EC Name:
Acrylic acid
Cas Number:
79-10-7
Molecular formula:
C3H4O2
IUPAC Name:
prop-2-enoic acid
Details on test material:
Acrylic acid was 2,3-14C labelled. No further data

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: 0.1 M Na2HPO4
Details on exposure:
130 µL [2,3-14CJacrylic acid was dissolved in 1.9 mL 0.1 M Na2HP04 and the pH was adjusted about 5.5 with 0.2 mL 27% NaOH.
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
once
Frequency of treatment:
single
Post exposure period:
24 h
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
233/ 257 mg/kg bw
Basis:
actual ingested
Remarks:
Doses / Concentrations:
7.9-8.7*10e9 dpm/kg bw
Basis:
actual ingested
No. of animals per sex per dose:
2
Control animals:
yes, concurrent vehicle

Results and discussion

Details on results:
No DNA adducts were detectable neither in the liver nor in the stomach.

Any other information on results incl. tables

Based on the limit of detection, a maximum possible DNA binding of AA will be at least 100,000 times below the DNA binding potency of the standard carcinogen aflatoxin B1.

Applicant's summary and conclusion