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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute Toxicity: dermal

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1979
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1979
Report date:
1979

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Animals were dosed with 40% aqueous solutions for 24 hours and observed for 14 days.
one female rabbit was dosed with 5010 mg/kg.
one female and one male rabbit were dosed with 7940 mg/kg
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
Carboxylic acids, di-, C4-6
EC Number:
271-678-5
EC Name:
Carboxylic acids, di-, C4-6
Cas Number:
68603-87-2
Molecular formula:
C5H8O4, C4H6O4, C6H10O4
IUPAC Name:
Carboxylic acids, C4-6 di-
Details on test material:
Dibasic acid concentrate

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male/female

Administration / exposure

Type of coverage:
not specified
Vehicle:
water
Duration of exposure:
24 hours
Doses:
5010 and 7940 mg/kg
No. of animals per sex per dose:
5010 group: one female
7940 mg/kg group: one female and one male
Control animals:
not required

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD0
Effect level:
7 940 mg/kg bw

Any other information on results incl. tables

Signs of intoxication: wieght loss (two to four days)

Gross autopsy: viscera appeared normal

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
LD0 > 7940 mg/kg
Executive summary:

No mortality was reported in an acute dermal toxicity experiment in rabbits following administration of 5010 mg/kg (n=1) or 7940 mg/kg (n=2) of a 40% aqueous solution/suspension of dicarboxylic acid mixture. The only clinical signs reported were weight loss during the first 2 to 4 days. The viscera appeared normal at termination after 14 days. The LD50 was thus > 7940 mg/kg bw.