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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Limited reporting (study summary only) of a guideline-comparable study.

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1987

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
no
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Chromic acid
EC Number:
231-801-5
EC Name:
Chromic acid
Cas Number:
7738-94-5
Molecular formula:
CrH2O4
IUPAC Name:
dihydroxy(dioxo)chromium
Details on test material:
Test material name: chromic acid
No further details reported

Test animals

Species:
rat
Strain:
Fischer 344
Sex:
male/female
Details on test animals or test system and environmental conditions:
Not reported

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
No further details reported
Doses:
0, 32, 40, 50, 63, 80 & 100 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
52 mg/kg bw
95% CL:
>= 42 - <= 62
Mortality:
Deaths occurred at 32 mg/kg bw (1M, 2F), 40 mg/kg bw (1M), 50 mg/kg bw (2M, 3F), 63 mg/kg bw (3M, 4F), 80 mg/kg bw (3M, 4F) and 100 mg/kg bw (5M, 5F), within three days of dosing.
Clinical signs:
other: Lacrimation, hunched posture, hypoactivity, soft/reduced faeces, anogenital staining, red/brown facial staining.
Gross pathology:
Findings were apparent in the stomach, intestines, brain, kidney and lungs in decedent animals in all groups, but may have been secondary effects. No effects of treatment were apparent in animals surviving to scheduled necropsy.
Other findings:
Slightly increased liver weights

Any other information on results incl. tables

The report indicates that the primary cause of death was gastrointestinal corrosion, rather than systemic toxicity.

Applicant's summary and conclusion

Interpretation of results:
other: Toxic if swallowed based on EU GHS criteria
Conclusions:
The acute oral LD50 of chromic acid was found to be 52 (42-62) mg/kg bw in the rat. Chromic acid is classified as 'Toxic if swallowed', based on the results of this study.
Executive summary:

Fischer 344 rats (5/sex/group) were gavaged with a single dose of chromic acid at dose levels of 0, 32, 40, 50, 63, 80 or 100 mg/kg bw and observed for 14 days. Deaths occurred in all dose groups, within 3 days of dosing. Reduced weight gain or initial weight loss was apparent in all groups. Gross necropsy of decedents revealed corrosive effects on the gastrointestinal tract. The acute oral LD50 of chromic acid in the rat was found to be 52 (42-62) mg/kg bw.