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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
Remarks:
Type of genotoxicity: DNA damage and/or repair
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Scientifically valid publication in peer reviewed journal that lacks details of test conditions reporting

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1980

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
Deviations:
not specified
GLP compliance:
no
Type of assay:
micronucleus assay

Test material

Constituent 1
Reference substance name:
chromic nitrate
IUPAC Name:
chromic nitrate
Constituent 2
Chemical structure
Reference substance name:
Chromium trinitrate
EC Number:
236-921-1
EC Name:
Chromium trinitrate
Cas Number:
13548-38-4
Molecular formula:
Cr.3HNO3
IUPAC Name:
chromium trinitrate
Test material form:
other: aqueous solution
Details on test material:
no data reported in publication

Test animals

Species:
mouse
Strain:
Balb/c
Sex:
male
Details on test animals or test system and environmental conditions:
age of animals: 8-12 weeks

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
chromium trinitrate was provided as aqueous solution
Details on exposure:
0.5 ml applied, dose 500 Cr(NO3)3*9H2O mg/kg bw and 250 Cr(NO3)3*9H2O mg/kg bw
Duration of treatment / exposure:
single application
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
500 mg/kg bw
Basis:
analytical conc.
Cr(NO3)3 * 9H2O
Remarks:
Doses / Concentrations:
250 mg/kg bw
Basis:
analytical conc.
Cr(NO3)3 * 9H2O
No. of animals per sex per dose:
5 male animals per dose were used
Control animals:
yes
Positive control(s):
no positive controls but another substance tested in this array (K2Cr2O7) was found positive.

Examinations

Tissues and cell types examined:
Erythrocytes
Details of tissue and slide preparation:
The cells of the bone marrow were extracted from the femour and suspended in serum of featal calf. After centrifugation at 1000 rpm during 8 minutes the supernatant was removed and the cells were transferred to a slide and coloured by May-Gruenwald and by Giemsa.
Evaluation criteria:
The young erythrocytes which have matured in the last 24 hours can be made visible because of their polychromatophily.
Statistics:
Method not reported in publication but statistics was applied.

Results and discussion

Test results
Sex:
male
Genotoxicity:
negative
Toxicity:
no effects
Vehicle controls validity:
not applicable
Negative controls validity:
valid
Positive controls validity:
other: K2Cr2O7 was found positive in this test array

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative
Under the conditions of this test chromium trinitrate was found not to affect micronuclei development in vivo.
Executive summary:

In the in-vivo micronucleus test in mice reported in this publication three chromium salts were investigated for their mutagenic potential. Whereas chromium trinitrate was found to be negative, potassium dichromate (chromiumVI) was confirmed to be positive and thus can be seen as positive control in this study. In conclusion, it can be stated that chromium trinitrate was negative in the in-vivo mouse micronucleus test.