Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 429-270-1 | CAS number: 136210-30-5
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates ā in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Link to relevant study records
- Endpoint:
- two-generation reproductive toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- GLP guideline study with deviations: This study was originally planned as a one-generation study and later enhanced to a two-generation study. As deviation to the guidelines of a two-generation study histopathology of F1 parental rats was done only in liver and kidneys.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 416 (Two-Generation Reproduction Toxicity Study)
- Version / remarks:
- (2001)
- Deviations:
- yes
- Remarks:
- , histopathology of F1 parental rats was done only in liver and kidneys.
- Principles of method if other than guideline:
- This study was originally planned as a one-generation study and later enhanced to a two-generation study. As deviation to the guidelines of a two-generation study histopathology of F1 parental rats was done only in liver and kidneys.
- GLP compliance:
- yes (incl. QA statement)
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Strain: SPF-bred rats of the strain Wistar Crl: (Wi)WU BR
- Source: Charles River GmbH, Sulzfeld, Germany
- Age at study initiation: Animal age at delivery (F0): 4-5 weeks
- Weight at study initiation: (F0) Males: 110 (86-128) g; Females: 94 (79-113) g; the scatter of the animal weights (except one male) was less than 20% around the mean for each sex.
- Housing: singly, except when co-housed for matings or with litters in Makrolon cages Type IIIh. The animal room was accommodated within a special building domain, separated from other areas by a barrier system. The air pressure in the animal room was about 20 Pa above the normal pressure.
- Diet and water: ad libitum
- Acclimation period: 6 days
ENVIRONMENTAL CONDITIONS
- Temperature (Ā°C): 23 +/- 2Ā°C
- Humidity (%): 55 +/- 5%
- Air changes (per hr): >/= 10 passages per hour
- Photoperiod (hrs dark / hrs light): 12 hours rythm
IN-LIFE DATES: From: July 28, 2008 To: May 4, 2009 (281 days) - Route of administration:
- oral: gavage
- Type of inhalation exposure (if applicable):
- other: not applicable
- Vehicle:
- polyethylene glycol
- Details on exposure:
- Administration volume: 5 ml/kg bw
PREPARATION of Formulation(s). as needed, mostly once weekly
VEHICLE
Polyethylene glycol 400
- Justification for use and choice of vehicle (if other than water): The formulation was a clear liquid and and stability of it had been confirmed. - Details on mating procedure:
- In general, the first adult F0 male was caged over night with the first F0 female from the same test group, whereas the third F1 female was mated with the first male of the corresponding dose group, and so on. Mating occurred at a maximum of 12 times during the three-week mating period until sperm cells in vaginal smears taken the next morning or a vaginal plug were observed. Inseminated females were not further co-housed with the below mentioned exception. Generally, if a male had to be necropsied prior to co-housing the previous or next male was co-housed with two females.
Rematings:
Remating with the same male
F0 and/or F1 females found sperm-positive after the first mating day but not shown to be pregnant (lack of weight gain within 14 days following insemination) were co-housed again over one week with the same male without checking insemination or food intake during possible further gestation. According to our experience occurrence of sperms after the first co-housing day without a following gestation can happen, if an inexperienced male, co-housed with a female for the first time, inseminated the female outside the estrus. Two pregnant F0 females of the control group were remated because a gestation could not be established by sperm positive vaginal smear, a vaginal plug or body weight gain.
Remating with another (fertile) male
F0 females, which presented no vaginal plug or sperm cells in the vaginal smears from the males appointed or did not show body weight gain indicating pregnancy, were co-housed additionally for two weeks with another male of the same group, which had been shown to be fertile. These additional co-housings were done to investigate the cause of lack of pregnancy of these females.
Three pregnant females [one of the 40 mg/kg group and two of the 200 mg/kg group] were remated with other males because a gestation could not be established by sperm positive vaginal smear, a vaginal plug or body weight gain.
One female of the control group and 3 females of the high dose group were mated with fertile males of the same dose group.
Remating occurred at a maximum of 11 times during the two-week remating period until sperm cells in vaginal smears taken the next morning or a vaginal plug were observed. Vaginal smears were also used for measurement of estrus cycling. Inseminated females were not further co-housed. Afterwards the females were kept individually until littering. During gestation clinical observations were made, body weights and food intake were measured as described for regular mating. During lactation food weight was taken on day 0 and 4 p.p. from one of three dams, body weights and clinical observations daily until necropsy from all dams. Body weights and clinical observations of pups were taken on day 0 and 4 p.p. The litters were nursed at least up to day 4 p.p. and then necropsied together with the dams. - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- For analytical verification a liquid chromatographic method was developed (HPLC on reversed phase (C18) with MSD-detection (MSD; SIM-Ions = 292.5 and 583.5). Content checks revealed that the formulations used were properly performed (checked at begin and near termination of the study and four times in between).
- Duration of treatment / exposure:
- Total duration of in-Life Phase: 281 days (day 1 = first day of administration). The test substance or vehicle was administered to the animals from the first day of the study (F0) or from Day 29 after birth (F1) until spontaneous death, moribund sacrifice or until scheduled necropsy
- Frequency of treatment:
- once daily
- Details on study schedule:
- The F0 animals were pretreated with the test substance for about 10 weeks up to the cohabitation period. Within the weeks 8-10 of the premating period examinations on estrus cycle were performed. Then the mating period of 3 weeks followed.
After a gestation period of about 22 days litters were born and the dams were allowed to rear them. If necessary, four days after birth the F1 litters were reduced (=culled) to eight pups. If possible, four male and four female pups remained per litter. Pups found in a moribund state on Day 4 were excluded from lactation. This was done to investigate possible malformations and to prevent cannibalism during the further rearing period. The remaining F1 pups were reared to an age of four weeks and then necropsied when not used as weanlings for further treatment. F0 females were killed and necropsied when about 28 days old F1 pups had been weaned. F0 males were killed after the mating period partly in the course of spermatological investigation.
25 male and 25 female F1 rats per group were selected for further treatment and to breed the F2 generation. This was done by randomly selecting one male and one female as far as possible from each litter. The weaned F1 offspring was treated further with the substance for at least 10 weeks premating period and then co-housed for mating. During the last three weeks of the premating period estrus cycle determinations were performed. The procedures during the mating, gestation and lactation period of F1 rats were the same as described for F0 rats. The F1 parental animals were killed as scheduled after their F2 litters had been weaned at about Day 28 p.p. as described for F0 rats.
Weaning of Pups: All pups were weaned on Day 28 p.p. The necropsy of weanlings and dams could be postponed up to three days later in case that Day 28 was a Saturday, Sunday or public holiday. However, selection of weanlings for the next generation was done exactly on Day 28 p.p.
Selection of Weaned F1 Pups for Further Treatment: One F1 male and one F1 female per litter were selected to appoint them to the study groups for further treatment. This was done by random selection (prepared on a HP 3000 computer system using a random-number generator) of one male and one female as far as possible from each litter. The selected F1 male out of the first litter of a group was appointed as the first F1 male of the dose group where it came from. The selected F1 female of the same litter was appointed as the first F1 female within its dose group. And so on. In cases where this procedure was not possible (severe clinical findings, missing pups or if pup weight differed extremely from the group mean) another pup or pups of other litters were chosen.
Selection Procedure for F1 co-Housings: As far as possible the first F1 male was co-housed group internally with a female taken from a litter with a different number. Using this procedure sibling matings among the F1 generation were excluded. - Remarks:
- Doses / Concentrations:
40, 200 and 1000 mg/kg bw/day
Basis:
actual ingested - No. of animals per sex per dose:
- 25
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Dose selection rationale: Dose selection was based on the results of a subacute gavage study in rats (21908, 1992; see chapter 7.5.1).
- As Pilot Study for this Two-Generation Study an Orientating Subacute Toxicity Study in Wistar Rats was conducted, with the test substance administrated via diet for 4 weeks (Bayer Health Care/Bayer Schering Pharma, AT 05474, study No. T4079062, Eiben, 2009-09-03). In this study duodenum and jejunum of male and female animals receiving 10000 or 15000 ppm test substance (corresponding to actual doses of 1176 and 1827 mg/kg bw in males and 1583 and 2319 mg/kg bw in females, respectively) exhibited a changed content (white mucous) at necropsy. Histopathology of the duodenum and jejunum revealed a certain change in villus epithelium (marked vacuolation) in all dose groups (beginning at 5000 ppm), indicating impaired resorption, which was presumably the reason for the increase in food and water intake without changes in body weight gain within this study. As such alteration was not seen in a previous study, where the test substance was administered by gavage (cf chapter 7.5.1 report no. 2190A, 2009) the effect on the intestine was considered to be most probably promoted by or related to administrationof the test substance in the diet. Therefore, the observations are not regarded to be directly related to test substance toxicity but promoted by the administration type and no NOAEL for administration of the test subtsance via diet could be established. - Parental animals: Observations and examinations:
- Observations on F0/F1 Parental Animals: Yes
- Time schedule: Inspections on mortality and morbidity of the animals were done twice daily (once daily on weekends and public holidays). Clinical findings were recorded individually daily. General clinical examinations were made daily about 30-60 minutes after the last animal was administered (cage-side observation). All signs of illness or clinical reactions to treatment (especially during littering) were recorded daily. All further clinical symptoms were also recorded. This investigation included the observation of the general state of health, behavior, condition of the fur, and the orifices as well as excretory products. Any further findings e.g. prolonged parturition were recorded as well.
A detailed clinical examination was done prior to the first administration of the test substance and then weekly as a rule, except females, which were investigated daily starting at mating period.
BODY WEIGHT: Yes
- Time schedule for examinations: Body weights were recorded directly prior to the first administration and thereafter daily including the day of necropsy.
FOOD CONSUMPTION:
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
The individual food consumption was measured (by weighing the quantity of food provided and back-weighing the amount, which remained unconsumed) as follows: - Males: Weekly from week 1 up to necropsy (except during mating period).
- Females: Weekly from week 1 up to mating (During gestation Day 0-7, 7-14 and 14-20 p.c., During lactation Day 0-4 and 4-7 p.p.)
WATER CONSUMPTION: No data
OTHER: Determination of Insemination
During the mating periods vaginal smears were taken in the morning after rats had been co-housed over night to determine time to insemination and gestation length. The vaginal smears were obtained using a flame-sterilized platinum loop and plated out on slides. Smears were stained for about 1 minute with MAY GRĆNWALDĀ“S Eosine-methylene blue solution modified for microscopy.
The date on which a vaginal plug was noted or sperms were found microscopically was taken as gestation Day 0 for calculating the gestation length. Females which exhibited marked weight gains although insemination had not been established were not further co-housed. No duration of gestation could be determined for these animals. - Oestrous cyclicity (parental animals):
- Estrus cycle length determination was done by evaluation of vaginal smears received daily over 19 consecutive days about 3 weeks prior to the mating period and during remating with a fertile male until the vaginal smear was sperm positive or a vaginal plug was found. The smears were examined microscopically for large serrated cells indicating that estrus had occurred. These data were used to determine the estrus cycle length and whether females were cycling properly.
- Sperm parameters (parental animals):
- Spermatological investigation was performed in all surviving F0 and F1 males of the 0 and 1000 mg/kg group on the day of necropsy.
- Determination of spermatozoa motility and viability: Just after testes and epididymides had been dissected sperm samples were collected from the right cauda epididymis and suspended in HAM`s F10 tissue culture medium (38Ā°C). A sample of about 20 Āµl of the culture medium was placed on a 38Ā°C warmed and siliconated slide and then covered with a warmed cover glass. Then sperm motility was recorded on 100 spermatozoa during minute 1 and minute 5 after preparation of the sample using semi-dark field microscope. The microscope stage was warmed up at 37Ā°C. Spermatozoa showing a forward swimming movement were given a positive score.
Furthermore, the difference between motility recorded during the first minute and that measured during the fifth minute was calculated.
- Determination of spermatozoa morphology: Spermatozoa morphology was evaluated in a formalin citrate fixed and Eosin G stained sperm sample collected from the right cauda epididymis. Morphological changes of the head, upper and middle tail were evaluated on 200 spermatozoa using the microscope as mentioned above.
- Determination of spermatozoa in epididymis: Determination of spermatozoa density was performed in a suspension (0.9% NaCl) of minced cauda epididymis tissue by counting of spermatozoa in a hemocytometer and calculation of spermatozoa density per mg epididymis. The samples used for counting had been heated shortly. Each sample was counted in 5 tertiary squares of two secondary squares. All 10 values were averaged and taken for calculating spermatozoa density per mg epididymis.
- Determination of homogenization resistant spermatid heads in the testis: Determination of spermatid head density was performed in a suspension (0.9% NaCl plus Triton x-100) of homogenized testis tissue by counting of spermatid heads in a hemocytometer. Each sample was counted in 5 tertiary squares of two secondary squares. All 10 values were averaged and taken for calculating spermatid head density per mg testis. - Litter observations:
- STANDARDISATION OF LITTERS
- Performed on day 4 postpartum: yes
- If yes, maximum of 8 pups/litter (4/sex/litter as nearly as possible); excess pups were killed and discarded.
PARAMETERS EXAMINED:
Number of live pups, Pup weight, External alterations (=clinical and necropsy observation), Number of dead pups, Sex of each pup (M/F).
Developmental Milestones in F1 Weanlings were recorded: In all F1 weanlings selected for further treatment the age and body weight when balano-preputial separation or vaginal opening occurred were recorded. This was done by investigating daily the preputium (from Day 38 p.p. onwards) and vagina (from Day 28 p.p. onwards) up to the time point when the balano-preputial separation or vaginal opening occurred. Time of vaginal opening and balano-preputial separation of F1 weanlings was recorded together with actual body weight. Absolute and body weight related data were calculated per group.
GROSS EXAMINATION OF DEAD PUPS: yes, for external and internal abnormalities. - Postmortem examinations (parental animals):
- SACRIFICE
For males and non pregnant females: When no longer needed for matings, for females with pups: At weaning of at least 28 days old pups.
GROSS NECROPSY
Macroscopical investigation was done on all rats. Animals were subjected to detailed post-mortem examinations as follows. Gross necropsy consisted of external and internal examinations including the cervical, thoracic, and abdominal viscera.
Implantation sites were counted after staining the uterus with 10% aqueous ammonium sulfide. In cases where implausible discrepancies existed between the number of observed implantation sites and the number of pups delivered (more pups than implantation sites) the number of pups was used as number of implantation sites. In case of autolytic rats or rats killed pre-scheduled the number of pups was taken as the number of implantation sites.
Vaginal smears were performed and evaluated at scheduled necropsy as precaution but not reported.
Rats found dead or which had to be killed in moribund condition were necropsied as early as possible in the same way.
The following tissues of adult F0 and F1 rats were generally fixed in 10% formalin with the exception of ovaries, the left and two thirds of the right kidney and testes, which were fixed in Davidsonās solution: Abnormalities (if any), Adrenals, Brain, Epididymides unilateral, Esophagus, Kidneys, Liver, Ovaries and oviducts, Pituitary gland, Prostate, Physical identifier, Seminal vesicles and coagulating glands, Skin in mammary region, Spleen, Testes unilateral, Thyroid/Parathyroids, Trachea, Uterus (incl. cervix), Vagina, Head with scull cap.
HISTOPATHOLOGY / ORGAN WEIGHTS
The following organs were weighed: Adrenals, Brain, Epididymides unilateral, Kidneys, Liver, Ovaries and oviducts, Pituitary gland, Prostate, Seminal vesicles and coagulating glands, Spleen, Testes unilateral, Thyroid/Parathyroids, Uterus (incl. cervix).
The following organs were evaluated histopathologically (F0) at least in control and high dose animals: Adrenals, Epididymides unilateral, Esophagus, Kidneys, Liver, Ovaries and oviducts, Pituitary gland, Prostate, Seminal vesicles and coagulating glands, Testes unilateral, Thyroid/Parathyroids, Trachea, Uterus (incl. cervix), Vagina. Kidneys were evaluated in all dose groups.
The following organs were evaluated histopathologically (F1) at least in control and high dose animals: Kidneys, Liver. Kidneys were evaluated in all dose groups. - Postmortem examinations (offspring):
- SACRIFICE
All F1 weanlings not selected for further treatment were killed when they were at least 4 weeks old and examined macroscopically.
All F2 weanlings were killed after a 4 week lactation period and examined macroscopically.
GROSS NECROPSY
All pups culled for standardization of litter size, found dead or which had to be killed moribund during lactation were necropsied and investigated macroscopically with particular attention to the organs of reproduction except for cases of autolysis or cannibalism.
This included also visible skeletal abnormalities as far as possible.
A lung flotation in water was performed during the necropsy of pups found dead on the day of the first litter inspection to determine whether pups had breathed at birth (live birth) or not.
Grossly abnormal tissues if any were fixed in all pups/weanlings. In F1 and F2 weanlings brain, spleen, thymus and uterus of one male and one female out of the firstly necropsied 5 litters per group were fixed in 10% formalin.
ORGAN WEIGTHS
The brain, spleen, thymus and uterus of one male and one female per F1/F2 litter were trimmed and weighed as soon as possible after dissection. The ratio of organ weights to body weights was calculated. Therefore, all these weanlings were weighed at day of necropsy. - Statistics:
- Statistical evaluation was performed on an Alpha 800 5/500 computer (TASC-system) using the following methods:
a) Analysis of Variance (ANOVA) and in case of significant results Dunnettās test as post hoc test for:
ā¢ Body weights and body weight gains of the male and female animals
ā¢ Food consumption of the male and female animals
ā¢ Number of implantation sites per female
ā¢ Number of viable pups per female
ā¢ Organ weights at necropsy
ā¢ Number of estruses
ā¢ Time to insemination
ā¢ Life birth, viability and lactation rate
ā¢ Determination of estrous length
b) 2 by N CHI2 test; in case of significant differences Fisher's exact test with Bonferroni correction for:
ā¢ Number of viable pups per group based on the number of implantations
ā¢ Insemination, fertility, gestation and rearing rate
c) Kruskall-Wallis test and in case of significant differences Dunnett's test for:
ā¢ Number of prenatal loss per litter
The sperm and spermatid count data were not evaluated statistically, because no meaningful differences occurred between the high dose and control groups.
Generally, differences between the control group and groups treated with the test substance groups were considered as statistically significant when p ā¤ 0.05. Significant differences from the control are indicated with * for p ā¤ 0.05 and ** for p ā¤ 0.01. - Reproductive indices:
- The following reproductive indices were calculated: Insemination index (%), Fertility index (%), Gestation index (%), Rearing index (%).
- Offspring viability indices:
- The following viability indices were calculated from lactation records of litters in the study (index calculation from litter means): Live birth index (%), Viability index (%), Lactation index (%).
- Dose descriptor:
- NOAEL
- Effect level:
- 200 mg/kg bw/day (actual dose received)
- Sex:
- male/female
- Basis for effect level:
- other: General toxicity: Mild kidney effects (basophilic tubules, focal tubular dilation/hyaline casts) in F0 male rats combined with elevated absolute and/or relative kidney weights in F0 males and females and F1 rats at next higher dose group (1000 mg/kg)
- Remarks on result:
- other: Generation: P (F0 and F1) (migrated information)
- Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day (actual dose received)
- Sex:
- male/female
- Basis for effect level:
- other: Reproduction toxicity: no changes in reproductive performance up to the highest dose tested (1000 mg/kg)
- Remarks on result:
- other: Generation: P (F0 and F1) (migrated information)
- Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day (actual dose received)
- Sex:
- male/female
- Basis for effect level:
- other: Developmental toxicity: no indications for developmental toxicity up to the highest dose tested (1000 mg/kg)
- Remarks on result:
- other: Generation: F1 and F2 (migrated information)
- Reproductive effects observed:
- not specified
- Executive summary:
A two-generation reproduction study (OECD 416) was performed with the structural analogue aspartic acid, N,N'-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester administered to 25 male and 25 females F0 and F1 rats at doses of 0 (vehicle control; polyethylene glycol), 40, 200 and 1000 mg/kg bw via gavage. Parental F0 animals received the test substance for a period of about 10 weeks and a subsequent mating period of up to 3 weeks. F1 offspring were nursed up to an age of four weeks. Some of them were selected for further treatment and for breeding a F2 generation. Generally, the test substance was administered to each parental animal up to its necropsy.
The study was originally planned as a one-generation study and later enhanced to a two-generation study, therefore as deviation to the guideline histopathology of F1 parental rats was done only in liver and kidneys.There was no change in survival and clinical appearance up to 1000 mg/kg in parental rats.At 1000 mg/kg body weights and body weight gain were decreased in F0 males during the premating phase. The food intake was not influenced up to 1000 mg/kg in F0 and F1 rats.
Kidney histopathology revealed an increase in severity of basophilic tubules and in frequency of focal tubular dilation/casts at 1000 mg/kg in F0 males considered as adverse. Slight non-adverse tubular change of inner renal cortex was noted slightly more frequent in 1000 mg/kg F0 females. These findings correlated with elevated absolute and/or relative kidney weights, which were seen in 1000 mg/kg F0 males and females as well as in 1000 mg/kg F1 rats, where, however, kidney histopathology was inconspicuous. Taken together, there were signs of kidney damage in 1000 mg/kg F0 males and indications of changes in kidney function in 1000 mg/kg F0 females and F1 rats based on increase of kidney weights and/or tubular change. Necropsy and histopathology of the remaining organs revealed no treatment-related changes.
Investigations of estrus cycling and sperm analyses revealed no substance-related effects.The parameters of the reproductive performance such as insemination, fertility and gestation indices as well as gestation length and the number of litters born were not influenced by the test substance up to 1000 mg/kg.
The litter data such as mean number of implantations, prenatal loss, live birth index, sex distribution, numbers of pups born and litter sizes at birth were not affected by the test substance at levels of up to 1000 mg/kg. The rearing and lactation indices were reduced in F0 generation at 1000 mg/kg. As these changes were minor and not seen in F1 females, a reprotoxic effect is not assumed. The viability index was not test substance-relatedly reduced up to 1000 mg/kg.There were no clinical and necropsy findings in F1 and F2 pups up to 1000 mg/kg. In F1 pups body and litter weights were unaffected up to 1000 mg/kg. In F2 pups body and litter weights were test substance-related depressed at 1000 mg/kg. Concerning the marginal lower pup weights of 200 mg/kg F2 pups a test substance-related effect is unlikely. The occurrence of sexual maturation in F1 post-weanlings revealed no test substance-related effect up to 1000 mg/kg.
Overall in this study there was no indication of effects on reproductive performance up to 1000 mg/kg. Test substance-related effects on offspring were limited to a decrease in F2 pup weight gain starting at lactation day 14 without any other obvious effect on F2 pups at 1000 mg/kg.
Thus, under the conditions described, the NOAEL is established at 200 mg/kg bw for kidney histopathology in F0 males and indications of changes in kidney function in F0 females and F1 rats.
Reference
There were no changes in survival and clinical appearance up to 1000 mg/kg in parental rats.
In both generation rats died sporadically in each dose group (dose groups 0-40-200-1000 mg/kg: F0 males 0-0-1-2 and females 1-0-1-2; F1 males 0-0-0-1 and females 0-1-0-0). No test substance-specific death causes including signs of administration error were seen in these rats. According to our experience during long term administration normally some rats die because of administration errors, if animals defend themselves or when rats try to regurgitate administration formulation.
Therefore, survival of parental rats was not influenced by the treatment with the test substance up to 1000 mg/kg in F0 and F1 rats.
No toxicologically relevant changes in clinical appearance and behavior of parental rats were observed during daily in-cage or detailed clinical observations up to 1000 mg/kg (F0 and F1 in both sexes).
BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS)
At the end of the premating periods no adverse effect on body weights and body weight gain was noted up to 200 mg/kg in F0 males and up to 1000 mg/kg in F0 females and F1 rats. At 1000 mg/kg F0 males exhibited statistically significant lower body weights and body weight gain than corresponding control rats.
The food consumption was comparable with that of controls up to 1000 mg/kg in both sexes and generations.
No toxicologically relevant body weight depression and changes in food consumption were noted in pregnant or lactating F0 or F1 females up to 1000 mg/kg.
REPRODUCTIVE FUNCTION: ESTROUS CYCLE (PARENTAL ANIMALS)
Results from the evaluation of vaginal smears performed at the end of the premating periods indicate that there were no toxicologically relevant effects on the estrus cycle up to 1000 mg/kg neither in F0 nor in F1 rats.
REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)
No biologically relevant effects on sperm parameters (epididymal sperm counts, sperm motility and morphology and testicular spermatids counts) were detected neither in F0 nor in F1 rats at 1000 mg/kg.
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
Concerning the indices for the insemination, fertility and gestation as well as the mating behavior (co-housings until sperm positive findings) no relevant difference between treated and control rats occurred. The gestation length was not changed by the treatment up to 1000 mg/kg in either generation. At 1000 mg/kg a relatively low rearing index was calculated for F0 rats, which was outside the reference range of historical controls.
ORGAN WEIGHTS (PARENTAL ANIMALS)
F0 rats: Organ weight measurements revealed increased (p=0.01) absolute and relative kidney weights (both by 13%) in F0 females at 1000 mg/kg. Relative kidney weights were slightly (by 7%) but statistically significantly increased (p=0.01) in F0 males at 1000 mg/kg. A statistically significantly (p=0.05) increased mean for the absolute kidney weights in 40 mg/kg females does not reflect a toxic effect, because this mean is based on one value of a female with hydronephrosis.
Absolute liver weights were not dose-dependently changed in F0 rats, whereas relative liver weights were statistically significantly increased in F0 rats at 1000 mg/kg (8%). The statistical significance of absolute liver weights in 40 and 1000 mg/kg F0 females, which were above the control value, is considered to be incidental as a dose correlation is missing.
The mean relative brain weight of 1000 mg/kg F0 males was statistically significantly higher than at 0 mg/kg due to the lower body weight in this group.
Statistically significantly reduced means for the weights of adrenals at 40 and 200 mg/kg in F0 males do not reflect a toxic effect, because a dose-dependence is missing. The absolute (by 16%) and relative (by 17%) adrenal weights of F0 females were increased (p=0.01) at 1000 mg/kg.
F1 rats: There was a dose-dependent and partly statistically significant increase in absolute and/or relative kidney weights beginning at 40 mg/kg in F1 males and females up to 10%.
Absolute and relative liver weights were not dose-dependently changed up to 200 mg/kg but increased in 1000 mg/kg F1 males (13%).
The relative adrenal weights were statistically significantly increased in F1 females at 1000 mg/kg (9%). Decreased absolute and relative adrenal weights of males at 40 and 200 mg/kg, marked as statistically significant, do not reflect a toxic effect, because a dose-dependence is missing.
Other statistical significancies among absolute or relative weights are considered incidental, because a clear dose correlation is missing (left epididymides of F1 males at 40 mg/kg) or the statistical significance is based on relatively wide spreading of absolute individual values without correlation to relative weights (pituitary of F1 females).
GROSS PATHOLOGY (PARENTAL ANIMALS)
At necropsy no macroscopical findings due to the treatment were observed up to 1000 mg/kg in F0 and F1 rats.
HISTOPATHOLOGY (PARENTAL ANIMALS)
F0 generation: In males of the F0 generation basophilic tubules in the kidneys were slightly increased by severity and focal tubular dilation/casts were slightly more frequent at 1000 mg/kg, which is considered as an adverse effect.
In F0 females a slight tubular change of the inner renal cortex was observed mainly at 1000 mg/kg. The morphology of this finding did not indicate any adverse impact and might, therefore, result from functional changes.
The remaining organs investigated were morphologically inconspicuous. Reproduction organs of the few F0 breeding pairs lacking offspring did not demonstrate any test substance-related changes.
F1 generation: The kidneys and liver of treated F1 rats showed no treatment-related alterations.
The live birth and viability indices, the mean litter size at birth, the percentage of males born, the number of born pups and the number of implantation sites including prenatal loss were not changed toxicologically relevantly up to 1000 mg/kg in both generations.
The lactation index of F1 pups was slightly but statistically significantly (p=0.05) reduced at 1000 mg/kg (data were out of the range of historical controls), but not in F2 pups.
CLINICAL SIGNS (OFFSPRING)
Clinical observations on pups revealed no remarkable increase in clinical symptoms up to 1000 mg/kg in F1 and F2 pups. Some incidences of F1 and F2 pups being thin, relatively small and/or lacking milk spots were comparable with historical controls.
BODY WEIGHT (OFFSPRING)
Offspring body or litter weights were not toxicologically relevantly reduced up to 1000 mg/kg in F1 generation and up to 40 mg/kg in F2 generation. At 200 and 1000 mg/kg body weights and weight gain of F2 pups were statistically significantly lower from day 14 p.p. onwards, if compared with concurrent controls.
However, because the mean weights of 200 mg/kg pups were mostly not remarkably different from the means calculated for 0 mg/kg F1 pups at the same age, a test substance-related effect on the reproduction and pup development is unlikely. This interpretation was supported by the fact that the appearance of pups was inconspicuous up to 1000 mg/kg and F2 litter weights were roughly comparable with those of F1 and/or F2 controls up to 200 mg/kg.
At 1000 mg/kg F2 pup/litter weights were reduced test substance-relatedly.
SEXUAL MATURATION (OFFSPRING)
The mean age of vaginal opening was unchanged in F1 females up to 1000 mg/kg and that of balano-preputial separation was unchanged in F1 males up to 1000 mg/kg.
ORGAN WEIGHTS (OFFSPRING)
No statistically significant changes in absolute or relative organ weights were observed in male and female F1 or F2 weanlings up to 200 mg/kg.
There were slightly but partly statistically significantly increased relative brain weights in F1 and F2 female weanlings at 1000 mg/kg. These deviations are considered most likely to differences in body weights.
Slightly but statistically significantly (p=0.05) decreased absolute spleen weights of F2 male weanlings at 200 and 1000 mg/kg do not correlate with the corresponding relative weights and are within the range of historical controls.
GROSS PATHOLOGY (OFFSPRING)
No remarkable changes in incidences of macroscopical findings were found at pup or weanling necropsies up to 1000 mg/kg.
HISTOPATHOLOGY (OFFSPRING)
Not performed, cause no findings were apparent at gross pathology.
Study was performed with Aspartic acid, N,N'-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester which is a structural analogue to Aspartic acid, N,N'-(methylenedi-4,1-cyclohexanediyl)bis-, 1,1',4,4'-tetraethyl ester. Both substances are diethyl esters of aspartic acid linked to a dicyclohexylmethyldiamine moiety. The difference between these two substances is merely the presence of two methyl groups connected to the cyclohexane rings. This structural analogy was confirmed by the responsible for the notification of both substances under the NONS regulation. They decided that test results obtained for one substance can be transferred to the other substance and that testing of both substances is usually not required. This decision is in accordance with the grouping of substances and read-across approach in Annex XI, 1.5 of the REACH Regulation.
Effect on fertility: via oral route
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
- Study duration:
- subchronic
- Species:
- rat
Effect on fertility: via inhalation route
- Endpoint conclusion:
- no study available
Effect on fertility: via dermal route
- Endpoint conclusion:
- no study available
Additional information
A two-generation reproduction study according to OECD TG 416 is available for the structural analogue aspartic acid, N,N'-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester. In this study doses of 0 (vehicle control), 40, 200 and 1000 mg/kg bw were administered daily via gavage to groups of male and female Wistar rats. Parental F0 animals received the test substance for a period of about 10 weeks and a subsequent mating period of up to 3 weeks. For female F0 rats test substance administration was continued for a gestation period of about 22 days and a weaning period of about 28 days. Then females were killed and necropsied. Some of the weaned F1 offspring was selected for breeding a F2 generation and further treated with the substance for at least a 10 weeks premating period. The procedures during the mating, gestation and lactation period of F1 rats were the same as described for F0 rats. Generally, the test substance was administered to each parental animal up to its necropsy.
The study revealed no change in survival and clinical appearance up to 1000 mg/kg bw in parental rats. At 1000 mg/kg bw body weights and body weight gain were decreased in F0 males during the premating phase. The food intake was not influenced up to 1000 mg/kg bw in F0 and F1 rats.
Summarizing the results on necropsy/histopathology, the study revealed signs of kidney damage in 1000 mg/kg bw F0 males and indications of changes in kidney function in 1000 mg/kg bw F0 females and F1 rats. This was based on increase of kidney weights and/or tubular change. Necropsy and histopathology of the remaining organs revealed no treatment-related changes.
With respect to reproductive performance no indication of effects were found up to 1000 mg/kg bw. Test substance-related effects on offspring were limited to a decrease in F2 pup weight gain starting at lactation day 14 without any other obvious effect on F2 pups at 1000 mg/kg.
Thus, the NOAELs of the study were set 200 mg/kg bw for general toxicity (effects on kidney), and 1000 mg/kg bw for both reproduction toxicity/fertility and developmental toxicity.
The study was performed with aspartic acid, N,Nā-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester which is a structural analogue to aspartic acid, N,Nā-(methylenedi-4,1-cyclohexanediyl)bis-, 1,1',4,4'-tetraethyl ester. Both substances are diethyl esters of aspartic acid linked to a dicyclohexylmethyldiamine moiety. The difference between these two substances is merely the presence of two methyl groups connected to the cyclohexane rings. This structural analogy was confirmed by the Member State responsible for the notification of both substances under the NONS regulation. The Member State decided that test results obtained for one substance can be transferred to the other substance and that testing of both substances is usually not required. This decision is in accordance with the grouping of substances and read-across approach in Annex XI, 1.5 of the REACH Regulation.
Justification for selection of Effect on fertility via oral route:
Only one study available
Effects on developmental toxicity
Link to relevant study records
- Endpoint:
- developmental toxicity
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 414 (Prenatal Developmental Toxicity Study)
- Version / remarks:
- (2001)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.31 (Prenatal Developmental Toxicity Study)
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.3700 (Prenatal Developmental Toxicity Study)
- Qualifier:
- according to guideline
- Guideline:
- other: Japanese MAFF guidelines: Guideline on the Compiling of Test Results on Toxicity āTeratology Studyā, 12-Nousan No. 8147 of November 24, 2000, amended June 26, 2001
- GLP compliance:
- yes (incl. QA statement)
- Limit test:
- no
- Species:
- rat
- Strain:
- Wistar
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Harlan Nederlands, 5960 AD Horst, The Netherlands
- Age at study initiation: 12 - 19 weeks
- Weight at study initiation: males 397 - 586 g, females 225 - 276 g
- Housing: Starting from gestation day 0 individually in Type IIIh Makrolon cages on low-dust wood shavings.
- Diet and water: ad libitum
- Acclimation period: at least 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (Ā°C): 22 Ā± 2Ā°C
- Humidity (%): approximately 55 %
- Air changes (per hr): > 10 per hour
- Photoperiod (hrs dark / hrs light): 12/12 - Route of administration:
- oral: gavage
- Type of inhalation exposure (if applicable):
- other: not applicable
- Vehicle:
- polyethylene glycol
- Details on exposure:
- Administration volume: 5 mL/kg bw
VEHICLE
Polyethylene glycol 400
- Justification for use and choice of vehicle (if other than water): The vehicle was suitable as analytical investigations revealed that the test substance was stable in the vehicle for at least 8 days. - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- The results of the homogeneity tests and content checks in samples with concentrations of 20, 60 (content checks, only), and 200 mg/mL during the study showed no meaningful deviation of the active ingredient content from the nominal value, except for the 20 mg/kg sample of August 23, 2011, which was therefore not used for administration.
- Details on mating procedure:
- The animals were mated by placing one female overnight into a Type IIIh cage together with one male rat. If sperm was detected in the vaginal smear taken on the morning following mating, this day was regarded as day 0 of gestation.
- Duration of treatment / exposure:
- Day 6 - 20 p. c.
- Frequency of treatment:
- once daily (between 06:00 and 12:00 CET)
- Duration of test:
- From experimental starting to end of in-life-Phase 22 days.
- Remarks:
- Doses / Concentrations:
100, 300 and 1000 mg/kg bw
Basis:
actual ingested - No. of animals per sex per dose:
- 25 female rats
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Dose selection rationale: The dose levels were selected based on the results of a previous pilot prenatal developmental toxicity study in rats with the test substance (T2081689).
- Maternal examinations:
- CLINICAL EXAMINATIONS: Yes
- Time schedule: The females were inspected once daily from day 0 to 21 p.c. (once daily only on weekends, on public holidays, and on day 21 p.c.), and all findings were recorded. Attention was paid to disturbances in the general condition of the rats (appearance, behavior), and any alterations concerning their excretory products.
BODY WEIGHT: Yes
- Time schedule for examinations: The body weights of the females were determined on day 0 p.c. and daily from days 6 to 21 p.c. Corrected body weight gain was determined by subtracting the uterus weight on day 21 p.c. from the body weight gain from days 0 to 21 p.c.
FOOD AND WATER CONSUMPTION: Yes
- The food intake of the animals was determined from the difference in weight between the food offered and the food not consumed for the following days of gestation: Days 0 - 3, 3 - 6, 6 - 9, 9 - 12, 12 - 15, 15 - 18, and 18 -21.
Water intake was assessed daily by visual estimation of the quantities left over and reported together with clinical findings.
POST-MORTEM EXAMINATIONS: Yes
- The females were subjected to gross pathological evaluation at cesarean section on day 21 p.c. Necropsy was performed without knowledge of treatment groups. - Ovaries and uterine content:
- The ovaries and uterine content was examined after termination: Yes
Necropsies/cesarean sections were performed on day 21 p.c. without knowledge of treatment groups.
Examinations included:
- Gravid uterus weight: Yes
- Number of corpora lutea: Yes
- Number of implantations: Yes
- Number of early resorptions: Yes
- Number of late resorptions: Yes
- Number of dead and live fetuses: Yes
- Other: individual weight and appearance of the placentas - Fetal examinations:
- - Sex of live fetuses
- Individual weights of live fetuses
- External examinations: Yes, findings in alive and dead fetuses are included
- Soft tissue and head examinations: Yes, evaluation of about half of alive fetuses per litter
- Skeletal and cartilage abnormalities: Yes, evaluation in about half of alive fetuses per litter - Statistics:
- Differences between the control and test item treated groups were considered to be significant when p < 0.05. Significant differences from the control group are indicated with * for p < 0.05 and ** for p < 0.01.
Statistical evaluation was performed on an Alpha 800 5/500 computer using the following methods:
- Analysis of Variance (ANOVA); in case of significance Dunnett's test for feed intakes, body weights, body weight gains, and corrected body weight gains, uterine weights, number of corpora lutea per female, number of implantations per female, number of live fetuses per female and as percentage of implantations per female, placental weights per female, fetal weights per female.
- 2 by N CHI2 test; in case of significant differences Fisher's exact test with Bonferroni correction for fertility rate, gestation rate, number of implantations per group, number of preimplantation losses per group, number of postimplantation losses, early resorptions, late resorptions or dead fetuses per group, number of live fetuses per group as percentage of implantations per group, number of male or female fetuses or fetuses with indeterminable sex per group, number of placentas with findings or litters with placental findings per group, number of fetuses or litters with external, visceral or skeletal findings, with malformations or with external or visceral deviations per group.
- Kruskal-Wallis test and in case of significant differences Dunn's test for number of preimplantation losses per female, number of postimplantation losses, early resorptions, late resorptions or dead fetuses per female, number of male or female fetuses or fetuses with indeterminable sex per female, number of placentas with findings per female, number of fetuses with external or visceral findings, with malformations or with external or visceral deviations per female.
- CHI2 test (correction according to yates) for number of fetuses or litters with cartilaginous tissue observations. - Indices:
- gestation rate
- Details on maternal toxic effects:
- Maternal toxic effects:no effects
Details on maternal toxic effects:
Salivation after administration occurred in all dose groups, which is most likely related to the bad taste of the test item and considered as not adverse. One female of the 100 mg/kg group revealed piloerection for a single day, for which a treatment related effect is excluded due to a lacking dose dependency and because of the single occurrence.
Thus, appearance, behavior, mortality, absolute and corrected body weight gains, food intake, water intake, and fecal and urinary excretions were unaffected at dose levels up to 1000 mg/kg.
No treatment related gross pathological findings occurred at dose levels up to 1000 mg/kg.
Fertility rate (percentage of inseminated females with implantations), the mean numbers of corpora lutea, preimplantation losses, and implantation sites in the dose groups did not differ to a meaningful extent from the control group values indicating a homogeneous distribution regarding these parameters. - Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day (actual dose received)
- Basis for effect level:
- other: maternal toxicity
- Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day (actual dose received)
- Basis for effect level:
- other: developmental toxicity
- Details on embryotoxic / teratogenic effects:
- Embryotoxic / teratogenic effects:no effects
Details on embryotoxic / teratogenic effects:
The gestation rate, appearance and weights of placentas, postimplantation loss and correspondingly the number of fetuses, fetal sex distribution, and fetal weights were unaffected by treatment at dose levels up to 1000 mg/kg.
A treatment related effect on malformations, external, visceral, and skeletal (including cartilage) deviations was not evident at dose levels up to 1000 mg/kg.
The overall incidences of fetuses or litters with malformations lay within the range of historical control data, revealed no statistical significance, and were thus unaffected by treatment at dose levels up to 1000 mg/kg. The types of malformations observed in this study are generally a representative sample of spontaneous malformations in the rat strain used (e.g. microphthalmia, dilation of lateral brain ventricles missing thyroid gland, ventricular septal defect of the heart, vertebral malformations with pelvis shift, malformation of ribs, supernumerary vertebrae) and comparable with spontaneous findings in the current control group and/or historical control groups. Malformations of the eyes (eye ball reduced in size) occurred in all dose groups and the control group in comparable incidences of affected fetuses and litters without a dose dependency and were thus unaffected by treatment at dose levels up to 1000 mg/kg. At the 1000 mg/kg level, one fetus revealed a hairline ventricular septal defect of the heart, for which a treatment related effect is not assumed due to its single occurrence, and since this finding lay well within the range of historical control data of the rat strain used. Furthermore, each one fetus of the 1000 mg/kg and 300 mg/kg groups showed a multiple malformation of cervical vertebrae with/without fusion of ribs, which is comparable with spontaneous findings in the rat strain used. Therefore, a treatment related effect is not assumed for these findings. All remaining findings were isolated findings, revealed no dose dependency and were thus also considered as incidental. Thus, a treatment related effect on malformations (incidence or type) was not evident at dose levels up to 1000 mg/kg.
The overall incidences of fetuses or litters with external and visceral deviations were unaffected at dose levels up to 1000 mg/kg and revealed the highest value on a fetal basis in the control group. The external and visceral deviations observed in this study were of a common type and comparable with spontaneous findings in the current control group and/or historical control groups and represented the normal range of scattering in the rat strain used. Histopathological evaluation of additional circumscribed hard whitish tissue in the nasopharynx was performed in a prenatal developmental toxicity study with the same rat strain (T0076746) and revealed calcium concrements without connection to the underlying tissue in the affected localizations. Calcium might have been dissolved from the fetal bones by the Wilson fixative and precipitated in the nasopharyngeal duct so that these findings were regarded as artifacts. Thus, a treatment related effect on external and visceral deviations was not evident at dose levels up to 1000 mg/kg.
At the 1000 mg/kg level, fetal examinations for skeletal retardations and variations revealed statistically significantly progressed ossification of a few localizations (1st, 4th-5th distal phalanges of toes left, 2nd-3rd 3rd distal phalanges of toes bilateral), when calculation was done on a fetal basis and partially also on a litter basis, for which a treatment related effect is not assumed, since this is caused by the incidentally higher incidence of retarded ossification in the current control group. At the 300 mg/kg level, fetal examinations for skeletal retardations and variations revealed statistically significantly progressed ossification of several localizations ((2nd, 4th-5th proximal phalanges of digits bilateral, 3rd proximal phalanges of digits left, 4thdistal phalanges of toes left, 4th proximal phalanges of toes left), when calculation was done on a fetal basis, for which a treatment related effect is not assumed, since this is caused by the incidentally higher incidence of retarded ossification in the current control group. At the 100 mg/kg level, fetal examinations for skeletal retardations and variations revealed statistically significantly progressed ossification of two localizations (1st distal phalanges of toes left, 7th caudal vertebral bodies, parietal bones bilateral), when calculation was done on a fetal basis and litter basis (1st distal phalanges of toes, only), for which a treatment related effect is not assumed, since this is caused by the incidentally higher incidence of retarded ossification in the current control group, and because a dose dependency was lacking. Evaluation of fetal cartilaginous tissue revealed no treatment related findings at dose levels up to 1000 mg/kg. Thus, a treatment related effect on skeletal deviations (retardations, variations, including cartilaginous tissue findings) was not evident at dose levels up to 1000 mg/kg. - Abnormalities:
- not specified
- Developmental effects observed:
- not specified
- Executive summary:
A developmental toxicity study according to OECD TG 414 was performed with the structural analogue Aspartic acid, N,N'-[methylenebis(2 -methyl-4,1 -cyclohexanediyl)]bis-,1,1',4,4'-tetraethyl ester. Twenty-five inseminated female Wistar rats were treated daily orally by gavage with doses of 0 (vehicle control), 100, 300 and 1000 mg/kg bw from day 6 to day 20 p.c. The fetuses were delivered by cesarean section on day 21 of gestation. Investigation was performed on general tolerance of the test substance by the females as well as on its effect on intrauterine development.
Appearance, behavior, mortality, absolute and corrected body weight gains, food intake, water intake, and fecal and urinary excretions were unaffected at dose levels up to 1000 mg/kg bw.
No treatment related gross pathological findings occurred at dose levels up to 1000 mg/kg.
The gestation rate, appearance and weights of placentas, postimplantation loss and correspondingly the number of fetuses, fetal sex distribution, and fetal weights were unaffected by treatment at dose levels up to 1000 mg/kg.
A treatment related effect on malformations, external, visceral, and skeletal (including cartilage) deviations was not evident at dose levels up to 1000 mg/kg.
Summarizing and evaluating all data investigated the NOAELs were determined to be 1000 mg/kg bw for maternal toxicity and 1000 mg/kg bw for developmental toxicity.
Reference
Study was performed with Aspartic acid, N,N'-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester which is a structural analogue to Aspartic acid, N,N'-(methylenedi-4,1-cyclohexanediyl)bis-, 1,1',4,4'-tetraethyl ester. Both substances are diethyl esters of aspartic acid linked to a dicyclohexylmethyldiamine moiety. The difference between these two substances is merely the presence of two methyl groups connected to the cyclohexane rings. This structural analogy was confirmed by the responsible for the notification of both substances under the NONS regulation. They decided that test results obtained for one substance can be transferred to the other substance and that testing of both substances is usually not required. This decision is in accordance with the grouping of substances and read-across approach in Annex XI, 1.5 of the REACH Regulation.
Study key results in tabular form:
General Reproduction Data:
Dose (mg/kg b.w./day) |
0 |
100 |
300 |
1000 |
inseminated females |
25 |
25 |
25 |
25 |
inseminated females evaluated |
25 |
25 |
25 |
25 |
females with implantations |
23 |
22 |
22 |
22 |
in % of those inseminated |
92.0 |
88.0 |
88.0 |
88.0 |
mean values per female with implantation sites |
||||
corpora lutea |
14.4 |
15.0 |
15.8 |
14.5 |
preimplantation loss |
0.9 |
0.9 |
2.0 |
1.1 |
implantations |
13.5 |
14.2 |
13.8 |
13.4 |
A treatment related effect for the slightly increased preimplantation loss at the 300 mg/kg level is not assumed due to a lacking dose dependency, and because this value lay within the range of historical control data of the rat strain used.
Gestation Rate:
Dose |
Females with |
||
|
viable fetuses on day 21 p.c. |
total resorption |
|
mg/kg b.w./day |
n |
in % of females with implantations |
n |
0 |
23 |
100.0 |
0 |
100 |
22 |
100.0 |
0 |
300 |
22 |
100.0 |
0 |
1000 |
22 |
100.0 |
0 |
Mean Values of the Prameters of Intrauterine Development:
Dose (mg/kg b.w./day) |
0 |
100 |
300 |
1000 |
number of females |
||||
with implantations (a) |
23 |
22 |
22 |
22 |
with viable fetuses (b) |
23 |
22 |
22 |
22 |
mean values per female |
||||
placental weight in gb |
0.60 |
0.58 |
0.61 |
0.62 |
number of fetusesb |
12.6 |
13.1 |
13.2 |
12.9 |
postimplantation lossa, b |
1.0, 1.0 |
1.1, 1.1 |
0.6, 0.6 |
0.5, 0.5 |
males in %b |
49.9 |
46.9 |
53.8 |
44.4 |
fetal weight in gb |
4.92 |
4.94 |
4.90 |
4.90 |
Fetal Malformations:
Malformation |
Dose (mg/kg b.w./day) |
|||
|
0 |
100 |
300 |
1000 |
eyeball reduced in size right |
- |
- |
1 |
- |
dilation of lateral brain ventricles bilateral |
- |
- |
1 |
- |
thyroid gland missing |
- |
1 |
- |
- |
hairline ventricular septal defect of the heart |
- |
- |
- |
1 |
multiple malformation of thoracic vertebrae and ribs |
- |
1 |
- |
- |
multiple malformation of cervical vertebrae with/without fusion of ribs |
- |
- |
1 |
1 |
head of 1strib missing right |
1 |
- |
- |
- |
1stsacral vertebral arch has the shape of a lumbar vertebral arch right, pelvis shift to caudal right |
1 |
- |
- |
- |
one supernumerary lumbar vertebra |
- |
- |
1 |
- |
number of fetuses per group |
289 |
288 |
290 |
283 |
number of fetuses with malformations |
2 |
2 |
4 |
2 |
malformed fetuses per group (%) |
0.7 |
0.7 |
1.4 |
0.7 |
number of litters per group |
23 |
22 |
22 |
22 |
number of litters with malformations |
2 |
2 |
4 |
2 |
malformed litters per group (%) |
8.7 |
9.1 |
13.6 |
9.1 |
() number of litters affected |
Fetal External and Visceral Deviations:
Deviation |
Dose (mg/kg b.w./day) |
|||
|
0 |
100 |
300 |
1000 |
circumscribed hard whitish area at nasal cavities |
3 (3) |
2 (1) |
2 (2) |
- |
slight dilation of lateral brain ventricle(s) |
- |
- |
2 (2) |
- |
thyroid gland reduced in size |
1 |
1 |
1 |
- |
thymus extended cranially |
10 (8) |
9 (6) |
9 (7) |
7 (6) |
thoracic cavity filled with brown mass |
- |
- |
- |
1 |
abdominal cavity filled with brown mass |
9 (8) |
7 (5) |
5 (4) |
4 (3) |
brown spot(s) in the liver |
12 (8) |
6 (6) |
12 (9) |
4 (4) |
slight dilation of renal pelvis |
4 (4) |
5 (5) |
2 (1) |
5 (5) |
dilation of renal pelvis |
- |
1 |
- |
- |
slight dilation of ureter |
- |
3 (3) |
2 (1) |
1 |
dilation of ureter |
- |
- |
- |
1 |
testi(e)s lying on bladder |
4 (4) |
3 (3) |
3 (2) |
3 (2) |
testi(e)s lying slightly more cranially |
3 (3) |
1 |
6 (6) |
5 (5) |
brown spot(s) at the throat under the skin |
1 |
- |
- |
- |
number of fetuses per group |
289 |
288 |
290 |
283 |
number of fetuses with deviations |
36 |
28 |
35 |
27 |
fetuses with deviat. per group (%) |
12.5 |
9.7 |
12.1 |
9.5 |
number of litters per group |
23 |
22 |
22 |
22 |
number of litters with deviations |
15 |
16 |
19 |
13 |
litters with deviat. per group (%) |
65.2 |
72.7 |
86.4 |
59.1 |
() number of litters affected |
Effect on developmental toxicity: via oral route
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
- Study duration:
- subacute
- Species:
- rat
Effect on developmental toxicity: via inhalation route
- Endpoint conclusion:
- no study available
Effect on developmental toxicity: via dermal route
- Endpoint conclusion:
- no study available
Additional information
A developmental toxicity study according to OECD TG 414 was performed with the structural analogue aspartic acid, N,N'-[methylenebis(2 -methyl-4,1 -cyclohexanediyl)]bis-,1,1',4,4'-tetraethyl ester. Twenty-five inseminated female Wistar rats were treated daily orally by gavage with doses of 0 (vehicle control), 100, 300 and 1000 mg/kg bw from day 6 to day 20 p.c. The fetuses were delivered by cesarean section on day 21 of gestation. Investigation was performed on general tolerance of the test substance by the females as well as on its effect on intrauterine development.
Appearance, behavior, mortality, absolute and corrected body weight gains, food intake, water intake, and fecal and urinary excretions were unaffected at dose levels up to 1000 mg/kg bw.
No treatment related gross pathological findings occurred at dose levels up to 1000 mg/kg.
The gestation rate, appearance and weights of placentas, postimplantation loss and correspondingly the number of fetuses, fetal sex distribution, and fetal weights were unaffected by treatment at dose levels up to 1000 mg/kg.
A treatment related effect on malformations, external, visceral, andskeletal (including cartilage) deviations was not evident at dose levels up to 1000 mg/kg.
Summarizing and evaluating all data investigated the NOAELs were determined to be 1000 mg/kg bw for maternal toxicity and 1000 mg/kg bw for developmental toxicity.
The study was performed with aspartic acid, N,Nā-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethyl ester which is a structural analogue to aspartic acid, N,Nā-(methylenedi-4,1-cyclohexanediyl)bis-, 1,1',4,4'-tetraethyl ester. Both substances are diethyl esters of aspartic acid linked to a dicyclohexylmethyldiamine moiety. The difference between these two substances is merely the presence of two methyl groups connected to the cyclohexane rings. This structural analogy was confirmed by the Member State responsible for the notification of both substances under the NONS regulation. The Member State decided that test results obtained for one substance can be transferred to the other substance and that testing of both substances is usually not required. This decision is in accordance with the grouping of substances and read-across approach in Annex XI, 1.5 of the REACH Regulation.
Justification for selection of Effect on developmental toxicity: via oral route:
Only one study available
Justification for classification or non-classification
Additional information
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.