Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: chromosome aberration
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable publication which meets basic scientific principles

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Micronucleus tests in mice on 39 food additives and eight miscellaneous chemicals
Author:
Hayashi M et al.
Year:
1988
Bibliographic source:
Fd. Chem. Toxic., 26, 487-500
Reference Type:
publication
Title:
SIDS Initial Assessment Report For SIAM 17
Author:
OECD
Year:
2006
Bibliographic source:
OECD SIDS AMMONIUM CHLORIDE

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
Deviations:
yes
Remarks:
limited data
GLP compliance:
no
Type of assay:
micronucleus assay

Test material

Constituent 1
Reference substance name:
Ammonium chloride
EC Number:
235-186-4
EC Name:
Ammonium chloride
Cas Number:
12125-02-9
IUPAC Name:
ammonium chloride
Details on test material:
- Name of test material (as cited in study report): Ammonium chloride
- Supplier: Japan Food Additive Association
- Analytical purity: purity 99.7%

Test animals

Species:
mouse
Strain:
other: ddY
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Shizuoka Agricultural Cooperative Association for Laboratory Animals, Shizu
- Age at study initiation: 8 weeks
- Diet (e.g. ad libitum): food pellets CE-2 (Japan Clea, Toky); ad libitum
- Water (e.g. ad libitum): water; ad libitum

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
- Vehicle(s)/solvent(s) used: saline
Duration of treatment / exposure:
24 h
Frequency of treatment:
Trial 1: one application
Trial 2: 4 injections every 24 h
Post exposure period:
24 h
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
62.5, 125, 250, 500 mg/kg bw
Basis:
nominal conc.
single injections
Remarks:
Doses / Concentrations:
31.3, 62.5, 125, 250 mg/kg bw
Basis:
nominal conc.
four injections with 24-h intervals
No. of animals per sex per dose:
6
Control animals:
yes
Positive control(s):
mitomycin C;
- Route of administration: i.p.
- Doses / concentrations: 2.0 mg/kg bw

Examinations

Tissues and cell types examined:
bone marrow of femur
Details of tissue and slide preparation:
CRITERIA FOR DOSE SELECTION:
The maximum dose of NH4Cl was determined by pilot experiments using the multisampling at multi-dose levels method. Dose up to MTD (maximum tolerance dose)

DETAILS OF SLIDE PREPARATION:
Femoural marrow cells were flushed out with fetal bovine serum and fixed with methanol and stained with Giemsa.

METHOD OF ANALYSIS:
One thousand polychromatic erythrocytes per mouse were scored using a light microscope and the number of micronucleated erythrocytes (MNPCE) was recorded.
Evaluation criteria:
A positive result was recorded only when one or more treatment group(s) showed a statistically significant difference (P < 0.01) from the spontaneous level of MNPCEs and the trend test indicated a positive dose response (P < 0.05).
Statistics:
Data were compared with the binomial distribution specified by historical data from laboratory followed by Armitage trend test (Armitage, 1955)

Results and discussion

Test results
Sex:
male
Genotoxicity:
negative
Toxicity:
not specified
Vehicle controls validity:
valid
Negative controls validity:
not specified
Positive controls validity:
valid

Any other information on results incl. tables

Results:

Number of doses Dose (mg/kg bw) MNPCE (%) PC (%) Mortality
1 Saline 0.18 ± 0.18 56.8 ± 4.7 0/6
62.5 0.12 ± 0.12 60.9 ± 4.2 0/6
125 0.15 ± 0.14 61.7 ± 3.8 0/6
250 0.13 ± 0.05 64.3 ± 2.5 0/6
500 0.12 ± 0.08 56.9 ± 8.3 0/6
2.0 MMC 4.18 ± 1.30* 52.3 ± 4.6 0/6
4 Saline 0.20 ± 0.09 59.9 ± 8.3 0/6
31.3 0.25 ± 0.19 67.2 ± 13.5 0/6
62.5 0.17 ± 0.10 63.7 ± 4.5 0/6
125 0.20 ± 0.18 64.0 ± 9.2 0/6
250 0.17 ± 0.08 61.6 ± 6.9 0/6
2.0 MMC 7.15 ± 3.92* 32.2 ± 11.0 0/6

*: significantly different from the historical negative control : (P <0.01)

MNPCE: micronucleated polychromatic erythrocytes

PCE: polychromatic erythrocyt

MMC: Mitomycin C

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information): negative