2',3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]]propionohydrazide

Toxicity to reproduction

Administrative data

Endpoint:

toxicity to reproduction

Remarks:

other: 90-day study

Type of information:

experimental study

Adequacy of study:

supporting study

Study period:

31 Jan 1983 - 25 Jan 1984

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Cross-reference

Reason / purpose for cross-reference:

reference to same study

Reference

Endpoint:

sub-chronic toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

31 Jan 1983 - 25 Jan 1984

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Qualifier:

according to guideline

Guideline:

OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity Study in Rodents)

Version / remarks:

(adopted 1981)

Deviations:

no

GLP compliance:

yes

Remarks:

Ciba-Geigy Ltd., Basle/Switzerland, GU2 Toxicology

Limit test:

no

Species:

rat

Strain:

other: F3-hybrid of RII 1/Tif x RII 2/Tif

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Tif: RAIf (SPF) rats from Animal Production, CIBA-GEIGY LTD., 4332 Stein, Switzerland
- Age at study initiation: 6 weeks
- Weight at study initiation: 190-195 g (males), 173-175 g (females)
- Housing: 5 animals per cage (Makrolon Cage Type 4)
- Diet: Pelleted, certified standard diet Nafag No. 890 Tox, ad libitum
- Water: Tap water, ad libitum
- Acclimation period: 10 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/-2
- Humidity (%): 55+/-10
- Air changes (per hr): 16-20
- Photoperiod: 12 hrs dark / 12 hrs light

Route of administration:

oral: feed

Vehicle:

unchanged (no vehicle)

Details on oral exposure:

PREPARATION OF DOSING SOLUTIONS:
The test substance was weighed on a calibrated Mettler balance. The pulverised food was then homogeneously mixed with the appropriate concentrations of the compound and 30% water was added before pelleting to ensure the necessary pellet quality. The pellets were subsequently air dried.

Analytical verification of doses or concentrations:

yes

Details on analytical verification of doses or concentrations:

Prior to the initiation of the study, pretest feed samples were analysed for concentration of test material. The same was undertaken periodically with the food batches applied during the test. The analysis were carried out in the Central Analytical Laboratories of CIBA-GEIGY LTD., Basle/Switzerland.

Duration of treatment / exposure:

90 days

Frequency of treatment:

continuous over 90 days

Dose / conc.:

400 ppm

Remarks:

Corresponding to 25 mg/kg bw in males and 27 mg/kg bw in females.

Dose / conc.:

2 000 ppm

Remarks:

Corresponding to 123 mg/kg bw in males and 127 mg/kg bw in females.

Dose / conc.:

10 000 ppm

Remarks:

Corresponding to 624 mg/kg bw in males and 667 mg/kg bw in females.

No. of animals per sex per dose:

20

Control animals:

yes, plain diet

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: twice daily on working days (mortality); daily (symptoms)

BODY WEIGHT: Yes
- Time schedule for examinations: weekly (midweek)

FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study)
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Yes

FOOD EFFICIENCY:
- mean food conversion was calculated based on weekly food consumption and midweek body weight.

WATER CONSUMPTION: Yes
- Time schedule for examinations: monthly (week 3, 7, 11)

OPHTHALMOSCOPIC EXAMINATION: Yes
- Time schedule for examinations: at the beginning and towards the end of the treatment period (day -6 and day 86 of test)
- Dose groups that were examined: in control animals and in treated animals of the highest dose level

HEARING TEST: Yes
- Time schedule for examinations: at the beginning and towards the end of the treatment period (day -6 and day 86 of test)
- Dose groups that were examined: in control animals and in treated animals of the highest dose level

HAEMATOLOGY: Yes
- Time schedule for collection of blood: At the end of the treatment period
- Anaesthetic used for blood collection: Yes (Ether anaesthesia)
- Animals fasted: Yes (20 hours before collection of blood)
- How many animals: 20 per sex and per group
- Following parameters were examined: RBC, HCT, Hb, MCV, PCV, MCH, PLT, WBC, Differential blood count, Reticulocytes, Prothrombin time

CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood: At the end of the treatment period
- Animals fasted: Yes (20 hours before collection of blood)
- How many animals: 20 per sex and per group
- Following parameters were examined: Glucose, Urea, Total Protein, Creatinine, Albumine, Globuline, A/G ratio, Sodium, Potassium, Chloride, Calcium, Phosphorus inorganic, GPT, GOT, AP, Total Cholesterol

URINALYSIS: No

NEUROBEHAVIOURAL EXAMINATION: No

Sacrifice and pathology:

GROSS PATHOLOGY: Yes
At the end of the test period all control and test animals were bled under ether anaesthesia and subjected to detailed autopsy. Liver, adrenals, brain, thymus, heart, kidneys and gonads were weighed. The following organs and tissues were preserved in 10% neutral formalin:
skin, mammary area, spleen, mesenteric lymph node, axillary lymph node, sternum with bone marrow, femur with joint, skeletal muscle, trachea, lung, heart, aorta, submandibular salivary gland, liver, pancreas, oesophagus, stomach, small intestine, large intestine, kidney, urinary bladder, prostate, seminal vesicle, testis, epididymis, uterus, ovary, pituitary gland, adrenal gland, thyroid with parathyroid gland, thymus, peripheral nerve, brain, spinal cord, eye with optic nerve, orbital gland, extraorbital lacrimal gland, organs and tissues showing macroscopical changes.
Complete autopsy with tissue preservation was performed also in all animals which died during the test period.

HISTOPATHOLOGY: Yes
After the fixation organ samples from each control and test rat were taken, embedded in paraplast, sectioned at 3-5 microns, stained with haematoxylin and eosin and subjected to microscopical examination.

Statistics:

For each time point and parameter a uni-variate statistical analysis was conducted. Due to the routine manner of the analysis system, parameter free methods were applied. Each treated group was compared to the control group in respect of dispersion and displacement (1). In addition a trend test (2) was applied considering all groups. Statistical analysis is performed to draw attention to distinct values. A statistically significant difference between two values does not necessarily imply biological relevance of that deviation and is not conclusive for a treatment related effect. Hence, the responsible scientist may not comment on statistically significant values lying within the physiological range and on the other hand may comment on statistically not significant values, which differ substantially from the expected normal values.
(1) Y. Lepage, Biometrika (1971) 58: pp. 213-217.
(2) H. R. Jonckheere, Biometrika (1954) 41: pp. 133-145

Clinical signs:

no effects observed

Description (incidence and severity):

No clinical symptoms and no signs of local and/or systemic toxicity were observed.

Mortality:

mortality observed, non-treatment-related

Description (incidence):

No death which was related to the administration of the test compound occurred in the course of the study. One animal (male no 55, group 3) died during blood withdrawal at the end of the treatment period.

Body weight and weight changes:

effects observed, non-treatment-related

Description (incidence and severity):

The mean body weight gain of all treated male and female groups was similar to that of the respective control groups, except a marginally lower weight increase in treated male group 4 (10 000 ppm), which however was not significant and within a range of 10 % of the control value.

Food consumption and compound intake (if feeding study):

no effects observed

Description (incidence and severity):

The mean food consumption of all treated male and female groups was similar to that of the respective control groups. Specific food consumption in relation to body weight in treated animals was similar to that of the respective control groups.

Food efficiency:

no effects observed

Water consumption and compound intake (if drinking water study):

no effects observed

Description (incidence and severity):

The mean water consumption of all treated male and female groups was similar to that of the respective control groups.

Ophthalmological findings:

no effects observed

Description (incidence and severity):

Ophthalmic inspections and hearing examinations performed before and towards the end of the administration period revealed no evidence of a reaction to the treatment.

Haematological findings:

effects observed, non-treatment-related

Description (incidence and severity):

Hematological investigations at week 14 showed a minimal increase in numbers of thrombocytes in females of group 4 (10000 ppm).

Clinical biochemistry findings:

effects observed, non-treatment-related

Description (incidence and severity):

Blood chemistry investigations revealed slightly lower sodium concentrations and higher concentrations of inorganic phosphorus in the females of group 4 (10000 ppm). The total protein concentration and the albumin concentration were noted to be marginally lower in the females of group 4 (10000 ppm). The globulin concentration of this group was slightly increased. The toxicological significance of these findings is doubtful.
Other parameters examined in hematology and blood chemistry achieving a level of statistical significance in their difference from control values were considered to have arisen fortuitously.

Urinalysis findings:

not examined

Behaviour (functional findings):

not examined

Immunological findings:

not examined

Organ weight findings including organ / body weight ratios:

effects observed, non-treatment-related

Description (incidence and severity):

A slight, but significant decrease of the liver weight was observed in treated male rats of groups 3 and 4 (2000 and 10000 ppm). A slight decrease of testes weight was noted in treated male group 4 (10000 ppm). Additional statistically significant differences in organ weights between treated and control groups were noted. Incidental, however statistically significant differences in organ weights between treated and control groups were noted. Since no systematic pattern emerged, these differences were attributed to spontaneous variation rather than to the treatment.

Gross pathological findings:

no effects observed

Description (incidence and severity):

No macroscopical changes were observed that were considered to be due to the administration of the test compound.

Neuropathological findings:

not examined

Histopathological findings: non-neoplastic:

effects observed, non-treatment-related

Description (incidence and severity):

Apart from an increasing incidence of nonspecific, minimal inflammatory cell infiltration in the liver in male animals of treated groups 3 and 4 (2000 and 10000 ppm) no microscopical changes were observed that were considered to be due to the administration of the test compound.

Histopathological findings: neoplastic:

not examined

Dose descriptor:

NOEL

Effect level:

400 ppm

Based on:

test mat.

Sex:

male/female

Basis for effect level:

other: At the next higher dose level, slight decrease in the liver weight and an incidence of non-specific minimal inflammatory cell infiltration were recorded.

Dose descriptor:

NOAEL

Effect level:

624 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

male

Basis for effect level:

other: no adverse effects at this dose level

Dose descriptor:

NOAEL

Effect level:

667 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

female

Basis for effect level:

other: no adverse effects at this dose level

Critical effects observed:

not specified

Table 1: Mean organ weights (g) and ratios (as a percentage of body- and brain weight) of male animals in test week 14.

Organs	Dose (ppm in food)				Trend
	0	400	2000	10000
Body	457	460	450	435
Brain	2.40	2.41	2.45	2.44
Brain/body	0.53	0.53	0.55	0.56
Heart	1.37	1.29	1.28	1.31
Heart/body	0.3	0.28*	0.285	0.31
Heart/brain	56.99	53.50*	52.37*	53.56
Liver	14.97	16.11	13.92	12.36*	X
Liver/body	3.27	3.51*	3.10*	2.85*	X
Liver/brain	624.7	670.3	570.9*	506.8*	X
Kidneys	2.79	2.79	2.80	2.74
Kidneys/body	0.61	0.61	0.62	0.63
Kidneys/brain	116.1	115.9	114.3	112.4
Adrenals	0.068	0.070	0.066	0.068
Adrenals/body	0.0148	0.0152	0.0147	0.0157
Adrenals/brain	2.83	2.91	2.70	2.78
Thymus	0.41	0.43	0.44	0.46
Thymus/body	0.090	0.093	0.098	0.105
Thymus/brain	17.10	17.83	17.96	18.72
Gonads	3.82	3.53	3.62	3.43*	X
Gonads/body	0.84	0.78	0.81	0.79
Gonads/brain	159.2	147.2	148.3*	140.6*	X

 

*: Significant difference (location and/or dispersion) between control group and test group (sign. l. = 0.05)

X: Significant negative trend from control to highest dosage group (sign. L. = 0.1)

Table 2: Mean organ weights (g) and ratios (as a percentage of body- and brain weight) of female animals in test week 14.

Organs	Dose (ppm in food)				Trend
	0	400	2000	10000
Body	302.3	312.4	315.6	298.7
Brain	2.33	2.33	2.36	2.32
Brain/body	0.774	0.749	0.757	0.780
Heart	0.972	0.974	0.970	0.916
Heart/body	0.322	0.313*	0.310*	0.308
Heart/brain	41.77	41.99	41.29	39.66
Liver	10.74	10.60	10.33	10.31
Liver/body	3.56	3.40	3.29*	3.45
Liver/brain	461.2	455.4	438.5	446.1
Kidneys	2.06	1.98	2.04	2.08
Kidneys/body	0.69	0.64*	0.65	0.70
Kidneys/brain	88.6	85.3	86.5	89.8
Adrenals	0.093	0.087	0.094	0.088
Adrenals/body	0.0308	0.0282	0.0300	0.0298
Adrenals/brain	3.99	3.76	4.00	3.82
Thymus	0.303	0.315	0.312	0.286
Thymus/body	0.101	0.101	0.099	0.096
Thymus/brain	13.08	13.59	13.33	12.38
Gonads	0.174	0.190	0.175	0.177
Gonads/body	0.058	0.062	0.056	0.060
Gonads/brain	7.49	8.20	7.42	7.66

*: Significant difference (location and/or dispersion) between control group and test group (sign. l. = 0.05)

Table 3: Summary of macroscopical findings in female and male animals.

	Dose (ppm in food)
	0		400			2000			10000
	m	f		m	f		m	f		m	f
Animals examined macroscopically	20	20		20	20		20	20		20	20
Abdominal cavity nodule (<0.5 cm)				1
Body as a whole, no changes observed	20	19		18	19		19	20		18	18
Brain Damaged during autopsy malformation		1		1
Kidney Fibrinous adhesion Small										1	1   1
Ovary Cyst (<1 cm)					1
Spleen Fibrinous adhesion small											1   1
Testis Small bilateral							1			1
Thymus Haemorrhage		1
Uterus Dilatation											1

 

 

Executive summary:

In an oral subchronic study Tif : RAIf (SPF) rats (20 per sex and dose group) were dosed for 90 days with 400, 2000 and 10000 ppm test substance added to the diet (calculated mean daily intake: 25, 123 and 624 mg/kg bw for males and 27, 127 and 667 mg/kg bw for females). No deaths related to the administration of the test compound occurred in the course of the study. No clinical symptoms and no signs of local and/or systemic toxicity were observed. The mean body weight gain of all treated male and female groups was similar to that of the respective control groups, except a marginally lower weight increase in treated male group 4 (10000 ppm), which however was not significant and within the range of 10 % of the control value. The mean food consumption of all treated male and female groups was similar to that of the respective control groups. Hematological investigations at week 14 showed a minimal increase in numbers of thrombocytes in females of group 4 (10000 ppm). Blood chemistry investigations revealed slightly lower sodium concentrations and higher concentrations of inorganic phosphorus in the females of group 4 (10000 ppm). The total protein concentration and the albumin concentration were noted to be marginally lower in the females of group 4 (10000 ppm). The globulin concentration of this group was slightly increased. The toxicological significance of these findings is doubtful. Other parameters examined in hematology and blood chemistry achieving a level of statistical significance in their difference from control values were considered to have arisen fortuitously. A slight, but significant decrease of the liver weight was observed in treated male rats of groups 3 and 4 (2000 and 10000 ppm). A slight decrease of testes weight was noted in treated male group 4 (10000 ppm). Additional statistically significant differences in organ weights between treated and control groups were noted. Since no systematic pattern emerged, these differences were attributed to spontaneous variation rather than to the treatment. Apart from an increasing incidence of nonspecific, minimal inflammatory cell infiltration in the liver in male animals of treated groups 3 and 4 (2000 and 10000 ppm) no macroscopical or microscopical changes were observed that were considered to be due to the administration of the test compound. In conclusion a NOEL of 25 (males) and 27 (females) mg/kg bw per day was derived, based on increased incidence of inflammatory cell infiltration in the liver of mainly male animals. Since no specific local or systemic effects have been observed up to the highest dose tested, the NOAEL was raised to 624 (males) and 667 mg/kg bw (females).

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1984

Report date:

1984

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

other: OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity in Rodents)

Deviations:

no

GLP compliance:

yes

Remarks:

Quality Assurance Statement available.

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

2',3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]]propionohydrazide

EC Number:

251-156-3

EC Name:

2',3-bis[[3-[3,5-di-tert-butyl-4-hydroxyphenyl]propionyl]]propionohydrazide

Cas Number:

32687-78-8

Molecular formula:

C34H52N2O4

IUPAC Name:

3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N'-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide

Details on test material:

- Physical state: solid
- Analytical purity: 100% (spectrophotometrically)

Test animals

Species:

rat

Strain:

other: F3-hybrid of RII 1/Tif x RII 2/Tif

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Tif: RAIf (SPF) rats from Animal Production, CIBA-GEIGY LTD., 4332 Stein, Switzerland
- Age at study initiation: 6 weeks
- Weight at study initiation: 190-195 g (males), 173-175 g (females)
- Housing: 5 animals per cage (Makrolon Cage Type 4)
- Diet: Pelleted, certified standard diet Nafag No. 890 Tox, ad libitum
- Water: Tap water, ad libitum
- Acclimation period: 10 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/-2
- Humidity (%): 55+/-10
- Air changes (per hr): 16-20
- Photoperiod: 12 hrs dark / 12 hrs light

Administration / exposure

Route of administration:

oral: feed

Vehicle:

unchanged (no vehicle)

Details on exposure:

PREPARATION OF DOSING SOLUTIONS:
The test substance was weighed on a calibrated Mettler balance. The pulverised food was then homogeneously mixed with the appropriate concentrations of the compound and 30% water was added before pelleting to ensure the necessary pellet quality. The pellets were subsequently airdried.

Analytical verification of doses or concentrations:

yes

Details on analytical verification of doses or concentrations:

Prior to the initiation of the study, pretest feed samples were analysed for concentration of test material. The same was undertaken periodically with the food batches applied during the test. The analysis were carried out in the Central Analytical Laboratories of CIBA-GEIGY LTD., Basle/Switzerland.

Duration of treatment / exposure:

90 days

Frequency of treatment:

continuous over 90 days

Doses / concentrations

Doses / concentrations 1

Dose / conc.:

400 ppm

Remarks:

Corresponding to 25 mg/kg bw in males and 27 mg/kg bw in females.

Doses / concentrations 2

Dose / conc.:

2 000 ppm

Remarks:

Corresponding to 123 mg/kg bw in males and 127 mg/kg bw in females.

Doses / concentrations 3

Dose / conc.:

10 000 ppm

Remarks:

Corresponding to 624 mg/kg bw in males and 667 mg/kg bw in females.

No. of animals per sex per dose:

20

Control animals:

yes, plain diet

Examinations

Parental animals: Observations and examinations:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: twice daily on working days (mortality); daily (symptoms)

BODY WEIGHT: Yes
- Time schedule for examinations: weekly (midweek)

FOOD CONSUMPTION AND COMPOUND INTAKE:
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Yes

FOOD EFFICIENCY:
- mean food conversion was calculated based on weekly food consumption anf midweek body weight.

WATER CONSUMPTION AND COMPOUND INTAKE : Yes
- Time schedule for examinations: monthly (week 3, 7, 11)

OPHTHALMOSCOPIC EXAMINATION: Yes
- Time schedule for examinations: at the beginning and towards the end of the treatment period (day -6 and day 86 of test)
- Dose groups that were examined: in control animals and in treated animals of the highest dose level

HEARING TEST: Yes
- Time schedule for examinations: at the beginning and towards the end of the treatment period (day -6 and day 86 of test)
- Dose groups that were examined: in control animals and in treated animals of the highest dose level

HAEMATOLOGY: Yes
- Time schedule for collection of blood: At the end of the treatment period
- Anaesthetic used for blood collection: Yes (Ether anaesthesia)
- Animals fasted: Yes (20 hours before collection of blood)
- How many animals: 20 per sex and per group
- Following parameters were examined: RBC, HCT, Hb, MCV, PCV, MCH, PLT, WBC, Differential blood count, Reticulocytes, Prothrombin time

CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood: At the end of the treatment period
- Animals fasted: Yes (20 hours before collection of blood)
- How many animals: 20 per sex and per group
- Following parameters were examined: Glucose, Urea, Total Protein, Creatinine, Albumine, Globuline, A/G ratio, Sodium, Potassium, Chloride, Calcium, Phosphorus inorganic, GPT, GOT, AP, Total Cholesterol

URINALYSIS: No

NEUROBEHAVIOURAL EXAMINATION: No

Postmortem examinations (parental animals):

GROSS PATHOLOGY: Yes
At the end of the test period all control and test animals were bled under ether anaesthesia and subjected to detailed autopsy. Liver,adrenals, brain, thymus, heart, kidneys and gonads were weighed. The following organs and tissues were preserved in 10% neutral formalin:
skin, mammary area, spleen, mesenteric lymph node, axillary lymph node, sternum with bone marrow, femur with joint, skeletal muscle, trachea, lung, heart, aorta, submandibular salivary gland, liver, pancreas, oesophagus, stomach, small intestine, large intestine, kidney, urinary bladder, prostate, seminal vesicle, testis, epididymis, uterus, ovary, pituitary gland, adrenal gland, thyroid with parathyroid gland, thymus, peripheral nerve, brain, spinal cord, eye with optic nerve, orbital gland, extraorbital lacrimal gland, organs and tissues showing macroscopical changes.
Complete autopsy with tissue preservation was performed also in all animals which died during the test period.

HISTOPATHOLOGY: Yes
After the fixation organ samples from each control and test rat were taken, embedded in paraplast, sectioned at 3-5 microns, stained with haematoxylin and eosin and subjected to microscopical examination.

Statistics:

For each time point and parameter a uni-variate statistical analysis was conducted. Due to the routine manner of the analysis system, parameter free methods were applied. Each treated group was compared to the control group in respect of dispersion and displacement (1). In addition a trend test (2) was applied considering all groups. Statistical analysis is performed to draw attention to distinct values. A statistically significant difference between two values does not necessarily imply biological relevance of that deviation and is not conclusive for a treatment related effect. Hence, the responsible scientist may not comment on statistically significant values lying within the physiological range and on the other hand may comment on statistically not significant values, which differ substantially from the expected normal values.
(1) Y. Lepage, Biometrika (1971) 58: pp. 213-217.
(2) H. R. Jonckheere, Biometrika (1954) 41: pp. 133-145

Results and discussion

Results: P0 (first parental generation)

General toxicity (P0)

Description (incidence and severity):

No clinical symptoms and no signs of local and/or systemic toxicity were observed.

Description (incidence):

No death which was related to the administration of the test compound occurred in the course of the study. One animal (male no 55, group 3) died during blood withdrawal at the end of the treatment period.

Description (incidence and severity):

The mean body weight gain of all treated male and female groups was similar to that of the respective control groups, except a marginally lower weight increase in treated male group 4 (10 000 ppm), which however was not significant and within a range of 10 % of the control value.

Description (incidence and severity):

The mean food consumption of all treated male and female groups was similar to that of the respective control groups. Specific food consumption in relation to body weight in treated animals was similar to that of the respective control groups.

Description (incidence and severity):

The mean water consumption of all treated male and female groups was similar to that of the respective control groups.

Description (incidence and severity):

Ophthalmic inspections and hearing examinations performed before and towards the end of the administration period revealed no evidence of a reaction to the treatment.

Description (incidence and severity):

Hematological investigations at week 14 showed a minimal increase in numbers of thrombocytes in females of group 4 (10000 ppm).

Description (incidence and severity):

Blood chemistry investigations revealed slightly lower sodium concentrations and higher concentrations of inorganic phosphorus in the females of group 4 (10000 ppm). The total protein concentration and the albumin concentration were noted to be marginally lower in the females of group 4 (10000 ppm). The globulin concentration of this group was slightly increased. The toxicological significance of these findings is doubtful.
Other parameters examined in hematology and blood chemistry achieving a level of statistical significance in their difference from control values were considered to have arisen fortuitously.

Description (incidence and severity):

Apart from an increasing incidence of nonspecific, minimal inflammatory cell infiltration in the liver in male animals of treated groups 3 and 4 (2000 and 10000 ppm) no microscopical changes were observed that were considered to be due to the administration of the test compound.

Effect levels (P0)

1

Dose descriptor:

NOAEL

Effect level:

624 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

male

Basis for effect level:

other: No adverse effects on gonads. Dose is corresponding to the highest dose tested.

2

Dose descriptor:

NOAEL

Effect level:

667 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

female

Basis for effect level:

other: No adverse effects on gonads. Dose is corresponding to the highest dose tested.

Overall reproductive toxicity

Reproductive effects observed:

not specified

Applicant's summary and conclusion

Conclusions:

In a 90-day repeated dose study according to OECD 408 the gonads of male and female animals were examined for abnormalities. No macroscopical or microscopical changes have been observed in the gonads of the animals. Overall, the test substance had no apparent effect on reproductive organs of either sex.