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Toxicological information

Genetic toxicity: in vivo

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Administrative data

in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
Type of genotoxicity: chromosome aberration
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Study period:
June to July 1991
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: well documented study according to OECD test guideline

Data source

Reference Type:
study report
Report date:

Materials and methods

Test guideline
according to guideline
OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
Version / remarks:
adopted May 1983
GLP compliance:
Type of assay:
micronucleus assay

Test material

Constituent 1
Reference substance name:
Sodium cumenesulphonate
EC Number:
EC Name:
Sodium cumenesulphonate
Cas Number:
sodium 2-phenylpropane-2-sulfonate
Details on test material:
- Name of test material (as cited in study report): NATRIUM-CUMOLSULFONAT (40%-ig in Wasser)
- Substance type: 40% aqueous solution of pure active substance
- Physical state: clear liquid
- Lot/batch No.: 3630/81312
- Expiration date of the lot/batch: March 1992
- Storage condition of test material: ambient temperature

Test animals

other: BOR:NMRI (SPF)
Details on test animals or test system and environmental conditions:
- Source: Winkelmann, Borchen, Germany
- Age at study initiation: young adults
- Weight at study initiation: 30.4 +/- 1.7 g (males); 24.3 +/- 1.5 g (females)
- Assigned to test groups randomly: no data
- Fasting period before study: no
- Housing: 5 animals per cage, gender separated, macrolone cages Type III
- Diet : Ssniff R10 exclusive diet for rats (ad libitum); supplied by Ssniff Spezialfutter GmbH, Soest, Germany
- Water: drinking water (ad libitum)
- Acclimation period: one week

- Temperature (°C): 20 +/- 3
- Humidity (%): 30-70
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12

IN-LIFE DATES: From: July 9, 1991 To: July 18, 1991

Administration / exposure

Route of administration:
oral: gavage
- Vehicle(s)/solvent(s) used: water
- Justification for choice of solvent/vehicle: no data
- Concentration of test material in vehicle: 40 %
- Amount of vehicle: 16.8 ml/kg bw
Frequency of treatment:
single oral application
Post exposure period:
24, 48 and 72 hours
Doses / concentrations
Doses / Concentrations:
4467 mg/kg bw
actual ingested
No. of animals per sex per dose:
Control animals:
yes, concurrent vehicle
Positive control(s):
- Justification for choice of positive control(s): no data
- Route of administration: oral by gavage
- Dose: 100 mg/kg bw
- Vehicle: water
- Total application volume: 10 ml/kg bw
- post exposure period: 24 hours


Tissues and cell types examined:
bone marrow; polychromatic erythrocytes (PCE), normochromatic erythrocytes (NCE)
Details of tissue and slide preparation:
CRITERIA FOR DOSE SELECTION: The maximum tolerable dose (MTD)* was selected as dose.

The MTD was determined in a dose range finding study :
Phase 1: Limit test with 5000 mg/kg bw
Phase 2: Determination of the TMTD range with reduced animal number
Phase 3: Determination of the MTD with 5 animals/sex/dose

*MTD is defined as dose with no mortality but clear clinical symptoms within 3 days after application

TREATMENT AND SAMPLING TIMES ( in addition to information in specific fields):
24, 48 and 72 hours after treatment the animals were killed by cervical dislocation and tissue was sampled.

The femora were removed and the bone marrow was suspended in fetal calf serum. The cell suspensions were centrifuged with 160 x g for 5 minutes and the supernatand discarded. The serum was resuspended and the suspension purified using a cellulose chromatographic column. The eluate was centrifuged at 800 x g for 10 minutes and the pellet in fetal calf serum /25 mM EDTA suspended. From this suspension 3-4 smears per animals were prepared on slides which were dried for at least 24 hours and stained with May-Grünwald/Giemsa solution.

The cell analysis was performed by means of a Zeiss miscroscope at a 1000fold magnification (oil immersion). At least 1000 polychromatic erythrocytes (PCE) per animal were examined to determine the frequency of micronucleated cells. The ratio of PCE to normochromatic cells (NCO) was determined for a sample of 1000 erythrocytes. The number of micronucleated cells in counted NCE was determined.
Evaluation criteria:
For the identification of micronuclei the following criteria were considered:
a) roundish and clear contour by the nuclear membrane
b) diameter of about 1/20 of the size of the polychromatic erythrocyte
c) lays in the same focus layer as the observed erythrocyte

The micronucleus test is regarded as positive (test substance induces micronuclei in polychromatic erythrocytes) if the frequency of mucronucleated polychromatic erythrocytes of at least one tretament group is statistically significantly increased compared to the negative control and the increase is biologically relevant.

Mean values and standard deviations were calculated for the following parameters:
a) number of polychromatic erythrocytes (PCE) containing micronuclei
b) ratio of PCE/NCE

Comparison of treatment groups with different post exposure periods with negative controls of respective post exposure periods. After control of the relative frequency of micronuclei in the treatment groups on homogeneity with the mean relative frequency a statistical analysis of micronucleus frequency using a 2 x 2 contingency table with chi² test and continuity table according to Yates was performed (see [1]).
The differences of miconucleus frequencies in the positive control were reassessed in the two-sided t-test. This test was also used for the statistical analysis of the PCE/NCE-ratio.

Results and discussion

Test results
Vehicle controls validity:
Negative controls validity:
not examined
Positive controls validity:
Additional information on results:
- Dose range:
Phase 1: males and females: 5000 mg/kg bw (limit test);
Phase 2: males: 1585, 1995, 2512, 3162 and 3981 mg/kg bw; females: 3162, 3548, 3981, 4467 and 5000 mg/kg bw.
Phase 3: males and females: 3981, 4467 and 5000 mg/kg bw.

- Clinical signs of toxicity in test animals:
Phase 1: 4/5 male and 1/5 female animals died. The males died within 4 hours after application, the female died within 24 hours after application of the test substance. Clinical signs as hunched posture, ruffled fur, closed eyes and diarrhea were observed.
Phase 2: 1/5 female at 3981 mg/kg bw died. At high doses clinicals signs as hunched posture, ruffled fur, closed eyes and diarrhea were observed.
Phase 3: 2/5 male and 2/5 female animals died at 500 mg/kg bw. At 4467 mg/kg bw no mortality occured but severe toxic effects.

- Clinical signs of toxicity in test animals:
Hunched posture, ruffled fur, closed eyes and diarrhea were observed. One day after application the effects subsided and two days after application all animals were free of clinical symptoms. One male and one female animal died 24 and 5.5 hours after application, respectively. These animals were replaced with mice of a concurrent satellite group also treated with the test substance. One male of the satellite group died 5 hours after application.

- Induction of micronuclei:
Positive control: Significantly increased number of polychromatic erythrocytes (PCE) with miconuclei both in male and female animals.
Test substance: No significant increase in the number of PCE with micronuclei after 24 and 48 hours in both males and females and after 72 hours in males. After 72 hours a statistically significant increase of the number of micronuclei in PCEs in females were observed. If the results of males and females were combined no significant difference in the frequency of micronuclei between treatment group and combined vehicle control group is observed. (Tables 1, 2 and 3)

- Ratio of PCE/NCE: Neither in the positive control group nor in the treated males a significant difference of PCE/NCE ratio compared to the control group is observed. In the females of the treatment groups no difference was observed 24 and 48 hours after treatment. After 72 hours the PCE/NCE ratio was decreased compared to vehicle control group but still was above the typically observed ratio of 1.0. (Tabels 1, 2 and 3)
- Appropriateness of dose levels and route: The selected dose level investigated as the maximum tolerable dose (MTD) induced clear toxic symptoms and was lethal in two animals. According to the guideline the recommended criteria for the dose level were fulfilled. The route of administration was appropriate as systemic availability could be demonstrated by clinical signs.

Any other information on results incl. tables

The statistically significant increase in frequency of micronuclei is considered to be of no biological relevance for the following reasons:

- The frequency of micronuclei at this sampling time point (0.18%) is not above the frequency of micronuclei of controls generally observed in this test laboratory (0.07 - 0.22%). The statistical significance in this case is caused by the low frequency of micronuclei in the control group (0.02%) which deviates downwards from the so far observed frequencies for controls. After addition of male and female animals of sampling time point 72 h into one group there is no more a statistically significant difference.

- A delayed effect based on slow excretion is improbable for sodium cumenesulphonate as sulphonic acids in general are readily absorbed and do not show any tendency for accumulation. But this kind of detention is regarded as prerequisite to explain based on the kinetic of erythrocyte maturation an impact on micronuclei frequency at sampling time point of 72 hours.

The results of the positive control affirm the sensitivity of the mouse strain to mutagenic substances.The frequency of micronuclei in polychromatic erythrocytes was considerably increased compared to the control group.

Table 1: Results of in vivo micronucleus test for male animals (mean ± standard deviation)

      Neg. control   test substance 4467 mg/kg bw      Pos. control
  sampling time    24 h  48 h  72 h  24 h  48 h  72 h 24 h 
micronuclei in 1000 PCE  0.8  ± 0.8 1.8  ± 0.8   0.4 ± 0.5 0.6 ± 0.5    0.8  ± 0,8   0.2  ± 0.4 48.0* ± 19.6
 % PCE with micronuclei 0.08  0.18  0.04 0.06  0.08 0.02  4.8
PCE / NCE  1.0 ± 0.2 1.4 ± 0.3  1.6 ± 0.3  1.0 ± 0.3 1.1 ± 0.4   1.9 ± 0.9 0.8  ± 0.1

*p < 0.05

Table 2: Results of in vivo micronucleus test for female animal (mean ± standard deviation)

      Neg. control   test substance 4467 mg/kg bw      Pos. control
  sampling time    24 h  48 h  72 h  24 h  48 h  72 h 24 h 
micronuclei in 1000 PCE 1.4  ± 1.7 1.8  ± 1.1   0.2 ± 0.4 2.2 ± 1.1    1.2  ± 0,8   1.8*  ± 1.5 36.8* ± 9.8
 % PCE with micronuclei 0.14  0.18  0.02 0.22  0.12 0.18 3.6
PCE / NCE  1.2 ± 0.2 1.4 ± 0.2  2.4 ± 0.6  1.0 ± 0.2 1.3 ± 0.3   1.3 ± 0.5 1.0  ± 0.1

*p< 0.05

Table 3: Results of in vivo micronucleus test for male + female animals (mean ± standard deviation)

      Neg. control   test substance 4467 mg/kg bw      Pos. control
  sampling time    24 h  48 h  72 h  24 h  48 h  72 h 24 h 
micronuclei in 1000 PCE  1.1  ± 1.3 1.8  ± 0.9  0.3 ± 0.5 1.4 ± 1.2    1.0  ± 0.8   1.0  ± 1.3 42.4* ± 15.7
 % PCE with micronuclei 0.11  0.18  0.03 0.14  0.10 0.10  4.24
PCE / NCE  1.1 ± 0.2 1.4 ± 0.3  2.0 ± 0.6  1.0 ± 0.2 1.2 ± 0.4   1.6 ± 0.8 0.9  ± 0.1

* p < 0.05

Applicant's summary and conclusion

Interpretation of results (migrated information): negative
All male mice treated with the test substance showed no statistically significant increase in micronucleus frequency at any sampling time compared to control animals. For the female mice treated with the test substance at sampling times 24 and 48 hours after treatment also no statistically significant increase in micronucleus frequency was observed. Only at sampling time point 72 hours a statistically significant increase of polychromatic erythrocytes with micronuclei compared to control animals was observed. This effect was regarded as biologically not relevant as this increase ís based on the exceptional low micronucleus frequency of vehicle control group.
Sodium cumenesulphonate under these test conditions is regarded as not mutagenic in the micronucleus test.