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EC number: 248-093-9 | CAS number: 26896-20-8
- 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 – 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
![](https://echa.europa.eu./o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Description of key information
Dose level selection was based on a three month study on rat dietary levels of 500, 1500, 5000, and 15000 ppm neodecanoic acid. No compound effect was noted in regard to physical appearance and behavior of the test rats at the levels of 500 and 1500 ppm. All high level males and females (15000 ppm) appeared thin and hunched; the majority of the rats had a pale appearance. Growth for the high level males and females throughout the study, and for the 5000 ppm test rats (both sexes) during the first week only was significantly lower than that for the corresponding controls. The growth rate for the 5000 ppm test rats was lower than the controls for the remainder of the study, but not significantly different. Food consumption for the high level test rats of either sex and for the 5000 ppm females was significantly lower compared with the control values. Survival for the male and female high level test rats was significantly lower than the controls. Hence, 1500 ppm was selected as the high dose for the modified three-generation reproductive toxicity study.
Link to relevant study records
- Endpoint:
- three-generation reproductive toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1968
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented study report which meets basic scientific principles: pre-GLP
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 416 (Two-Generation Reproduction Toxicity Study)
- Deviations:
- yes
- Remarks:
- 3 generations used, dietary administration
- GLP compliance:
- no
- Limit test:
- no
- Justification for study design:
- This study was conducted to evaluate the effects of long-term ingestion of the test substance on reproduction in rats. The test material
at dietary levels of 100, 500, and 1500 ppm was fed to the rats through two parental and two two-litter filial generations. Following nine weeks of
dietary administration to the F2B weanlings designated as the third parental generation, the study was terminated. - Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River
- Age at study initiation: (P) young
- Weight at study initiation: (P) Males: 108-164 g; Females: 101-144 g;
- Diet (e.g. ad libitum): prepared, ad libitum
- Water (e.g. ad libitum): ad libitum - Route of administration:
- oral: feed
- Vehicle:
- other:
- Remarks:
- Basal Diet
- Details on exposure:
- DIET PREPARATION
- Rate of preparation of diet (frequency): Fresh diets were prepared every 2 weeks or weekly as needed.
- Mixing appropriate amounts with (Type of food): Purina Laboratory Chow
- Storage temperature of food: Room temperature
Control rats were fed a basal diet of Purina Laboratory Chow. The test material was incorporated into the basal diet on a weight-perweight basis and thoroughly mixed in a Hobart blender to provide the desired dietary level for each test group. Fresh diets were prepared every two weeks or weekly as needed, and the appropriate diets and water were available to the animals at all times. - Details on mating procedure:
- - M/F ratio per cage: 1/2
- Length of cohabitation: week
- After successful mating each pregnant female was caged (how): individually - Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- Premating exposure period (males): P1: 9 weeks
Premating exposure period (females): P1: 9 weeks
Duration of test: 3 generations - Frequency of treatment:
- Continuous
- Details on study schedule:
- P1 GENERATION
Prior to initiation of the first and second breeding phases, the parental generation animals were maintained in individual cages and fed the appropriate diets until they reached maturity, 9 weeks. At the end of the ninth week, two females and one male within each group were mated. Males were rotated for 3 weeks.
F1A GENERATION
Twenty-four hours after birth, the F1A litters were arbitrarily reduced to a maximum of eight pups for nursing. After 21 days, representative pups from each litter were sacrificed and gross necropsies were performed. All other weanlings were discarded.
F1B GENERATION
One week after weaning the last F1A litter, the P1 parents were re-mated are previously described to produced the F1B generation. After a 21-day nursing period, 20 female and 10 male weanlings were designated as the P2 generation. One third of the remaining weanlings were gross necropsied, the remaining were discarded.
P2 GENERATION
The P2 animals were individually hosed until they reached 100 days of age. Mating occurred as described previously.
F2A GENERATION
As described previously – F1A
F2B GENERATION
As described previously – F1B - Remarks:
- Doses / Concentrations:
0, 100, 500, 1500 ppm in diet
Basis:
nominal in diet
approximately 5, 25 and 75 mg/kg/day, respectively - No. of animals per sex per dose:
- 20 Females, 10 Males per dose group
- Control animals:
- yes
- Details on study design:
- Rationale for Dose Selection: A preliminary three-month subacute toxicity study (i.e., mortality, body weight, food consumption, physical appearance, behavioral signs, gross examination, organ weight, histopathology, clinical biochemistry) in rats fed daily dietary dose levels of ~500, 1500, 5000, and 15000 ppm neodecanoic acid was performed (15 rats/sex/group) to select doses for a three-generation reproductive toxicity study. No compound effects were noted in regard to physical appearance and behavior of the test rats at the dose levels of 500 ppm and 1500 ppm. However, in the 15,000 ppm group, there was mortality (73% survival: 4 males/5 females) and all rats exhibited clinical signs of thin and hunched; the majority of the rats also had a pale appearance. In the 5,000 ppm and 15,000 ppm dose groups, there was significantly decreased mean body weight gain in male/female rats at the end of the study (10%/14% and 73%/57% below control, respectively). Also, food consumption for the 5,000 ppm females and 15,000 ppm male and female rats was significantly lower compared with control values (7% and 42% below control, respectively. Also, there were gross examination findings in liver and kidneys. Hepatotoxic changes were seen in the male and female rats at 15,000 and 5,000 ppm. There were renal changes affecting the tubules of both the male and female rats who were
dosed with 15,000, 5,000 and 1500 ppm of neodecanoic acid. Therefore, based on mortality, clinical signs, decreased body weight gain and decreased food consumption at 5000 ppm and 15,000 ppm, 1,500 ppm was selected as the high dose for the definitive three-generation reproductive toxicity study. - Parental animals: Observations and examinations:
- Observations were made at 5 and 9 weeks
- Oestrous cyclicity (parental animals):
- No data
- Sperm parameters (parental animals):
- No data
- Litter observations:
- Immediately after birth
- Postmortem examinations (parental animals):
- All parent animals
Necropsies were performed on all parent animals which died during the study, gross observations were recorded, and tissues taken from these
animals were preserved in 10% neutral buffered formalin. - Postmortem examinations (offspring):
- All offspring
Litter size, mortality, pup body weights, clinical signs - Statistics:
- N/A
- Reproductive indices:
- The reproductive indices were derived as follows: fertility index, number of pregnancies divided by the number of matings; gestation index, number of litters born divided by the number of pregnancies observed; live birth index, number of pups born alive divided by the number of pups born; lactation index, number of pups weaned divided by the number of pups nursed.
- Offspring viability indices:
- Fertility, gestation, live birth, lactation.
- Clinical signs:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related clinical observations in any dose group of the parental generation. The appearance and behavior of the rats in the test groups were generally comparable with that of the controls.
- Mortality:
- mortality observed, non-treatment-related
- Description (incidence):
- One control P1 female was found dead following the second mating period (F1B). The right adrenal was enlarged and dark red in color, and the lungs were dark red in color. The observation was not considered treatment-related.
- Body weight and weight changes:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related body weight changes in any dose group of the parental generation. Body weight gain changes of the test animals were similar to the controls. See information panel for tables.
- Food consumption and compound intake (if feeding study):
- no effects observed
- Description (incidence and severity):
- There were no test substance-related food consumption in any dose group of the parental generation. Food consumption changes of the test animals were similar to the controls. See information panel for tables.
- Food efficiency:
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Behaviour (functional findings):
- no effects observed
- Description (incidence and severity):
- There were no behavioral findings in any dose group.
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related neuropathological findings in any dose group.
- Histopathological findings: non-neoplastic:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related histopathologic changes in any dose group of the parental generation. The variations in histopathological findings w comparable with that of the controls, were observed in a single animals and/or were common findings in this species.
- Histopathological findings: neoplastic:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related histopathologic changes in any dose group of the parental generation. The variations in histopathological findings w comparable with that of the controls, were observed in a single animals and/or were common findings in this species.
- Reproductive function: oestrous cycle:
- not examined
- Reproductive function: sperm measures:
- not examined
- Reproductive performance:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related effects on reproductive performance in any group. For the first reproduction phase, the various Indices, litter size, and pup body weights were comparable among the control and test groups for both cycles. The appearance and behavior of the newborn and of the F1A and F1B pups during lactation were comparable to controls. See information panel for tables.
P0 to F1A:
Dose Level (ppm)
0 100 500 1500
No. of Matings 20 20 20 20
No. of Pregnancies 20 20 20 20
Fertility Index % 100 100 100 100
No. of Litters Born 20 20 20 20
Gestation Index 100 100 100 100
Live Birth Index% 98.8 99.2 98.7 96.6
P0 to F1B:
No. of Matings 20 20 20 20
No. of Pregnancies 19 19 19 20
Fertility Index % 95 95 95 100
No. of Litters Born 18 19 19 20
Gestation Index 94.7 100 100 100
Live Birth Index% 99.6 99.2 99.6 99.6
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no adverse general toxicity, reproductive toxicity and fertility effects observed in P0 males or females at any dose level during the premating, mating or weaning phases. This study was conducted prior to GLP guidelines.
- Clinical signs:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related clinical observations in any dose group of the parental generation. The appearance and behavior of the rats in the test groups were generally comparable with that of the controls.
- Mortality:
- mortality observed, non-treatment-related
- Description (incidence):
- Two intermediate dose P1 males were found dead following the first (F2A) mating period. The gastrointestinal tract of both animals was filled with gas, the lungs of one were dark gray in color, and the lungs of the other were distended and dark red with grayish areas. One control P1 female was found dead following weaning of the F2B litter. Necropsy findings included advanced autolysis; pituitary and thymus dark red consolidated and abscessed areas on lungs; liver and kidneys dark red with dark black areas; poor differentiation between cortex and medulla of kidneys; pyloric portion of stomach red; and intestinal tract red and contained blackish red, semithick material. The observations were not considered treatment-related.
- Body weight and weight changes:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related body weight changes in any dose group of the parental generation. Body weight gain changes of the test animals were similar to the controls. See information panel for tables.
- Food consumption and compound intake (if feeding study):
- no effects observed
- Description (incidence and severity):
- There were no test substance-related food consumption in any dose group of the parental generation. Food consumption changes of the test animals were similar to the controls. See information panel for tables.
- Food efficiency:
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- no effects observed
- Description (incidence and severity):
- There were no behavioral findings in any dose group.
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related changes in organ weights in any dose group.
- Gross pathological findings:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related gross examination findings in any dose group.
- Neuropathological findings:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related neuropathological findings observed in any dose level.
- Histopathological findings: non-neoplastic:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related histopathology findings observed in any dose level.
Histopathological evaluation was performed on sections of the above listed tissues from five female and five male animals in the control (0 ppm) and high level (1500 ppm) groups. In addition, sections of thyroid, lung, liver, kidney, adrenal, and trachea from five female and five male animals in the low level (100 ppm) and intermediate level (500 ppm) groups were examined microscopically. - Histopathological findings: neoplastic:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related histopathology findings observed in any dose level.
- Other effects:
- no effects observed
- Reproductive function: oestrous cycle:
- not examined
- Reproductive function: sperm measures:
- not examined
- Reproductive performance:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related effects on reproductive performance in any group. For the first reproduction phase, the various Indices, litter size, and pup body weights were comparable among the control and test groups for both cycles. The appearance and behavior of the newborn and of the F2A and F2B pups during lactation were comparable to controls. See information panel for tables.
Dose Level (ppm)
0 100 500 1500
No. of Matings 20 20 20 20
No. of Pregnancies 20 20 20 20
Fertility Index % 100 100 100 100
No. of Litters Born 20 20 20 20
Gestation Index 100 100 100 100
Live Birth Index% 100 99.6 98.2 99.6
P1 to F2B:
Dose Level (ppm)
0 100 500 1500
No. of Matings 20 20 20 20
No. of Pregnancies 20 20 20 19
Fertility Index % 100 100 100 95
No. of Litters Born 20 20 20 19
Gestation Index 100 100 100 100
Live Birth Index% 100 99.2 99.6 98.4 - Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no adverse general toxicity, reproductive toxicity and fertility effects observed in P1 males or females at any dose level during the premating, mating or weaning phases. This study was conducted prior to GLP guidelines.
- Clinical signs:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related clinical observations in any dose group of the parental generation. The appearance and behavior of the rats in the test groups were generally comparable with that of the controls.
- Mortality / viability:
- mortality observed, non-treatment-related
- Description (incidence and severity):
- Mutilation of pups found dead at birth was noted in one control and two high level F1 litters. The observation was not considered treatment-related.
- Body weight and weight changes:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related body weight changes in any dose group of the F1 generation. Body weight gain changes of the test animals were similar to the controls. See information panel for tables.
- Food consumption and compound intake (if feeding study):
- no effects observed
- Description (incidence and severity):
There were no test substance-related food consumption in any dose group of the F1generation. Food consumption changes of the test animals were similar to the controls. See information panel for tables.- Food efficiency:
- not examined
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Sexual maturation:
- not examined
- Anogenital distance (AGD):
- not examined
- Nipple retention in male pups:
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Description (incidence and severity):
There were no test substance-related changes in organ weights in any dose group.- Gross pathological findings:
- no effects observed
- Description (incidence and severity):
There were no test substance-related gross examination findings in any dose group.- Histopathological findings:
- no effects observed
- Description (incidence and severity):
There were no test substance-related histopathologic changes in any dose group of the F1 generation. The variations in histopathological findings w comparable with that of the controls, were observed in a single animals and/or were common findings in this species.- Other effects:
- no effects observed
- Behaviour (functional findings):
- not examined
- Developmental immunotoxicity:
- not examined
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F1a
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no adverse general and reproductive toxicity effects observed in F1a males or females at any dose level. This study was conducted prior to GLP guidelines.
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F1b
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no adverse general and reproductive toxicity observed in F1b males or females at any dose level. This study was conducted prior to GLP guidelines.
- Clinical signs:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related clinical observations in any dose group of the F2 generation. The appearance and behavior of the rats in the test groups were generally comparable with that of the controls.
- Mortality / viability:
- mortality observed, non-treatment-related
- Description (incidence and severity):
- Mutilation of pups found dead at birth or during the nursing period was noted in one control F2 litter and in one low level litter in the F2A and F2B cycles each. The observation was not considered treatment-related.
- Body weight and weight changes:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related body weight changes in any dose group of the F2 generation. Body weight gain changes of the test animals were similar to the controls.
- Food consumption and compound intake (if feeding study):
- no effects observed
- Description (incidence and severity):
There were no test substance-related food consumption in any dose group of the F2 generation. Food consumption changes of the test animals were similar to the controls.- Food efficiency:
- not examined
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Sexual maturation:
- not examined
- Anogenital distance (AGD):
- not examined
- Nipple retention in male pups:
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Description (incidence and severity):
There were no test substance-related changes in organ weights in any dose group.- Gross pathological findings:
- no effects observed
- Description (incidence and severity):
- There were no test substance-related gross examination findings in any dose group.
- Histopathological findings:
- no effects observed
- Description (incidence and severity):
There were no test substance-related histopathologic changes in any dose group of the F2 generation. The variations in histopathological findings w comparable with that of the controls, were observed in a single animals and/or were common findings in this species.- Behaviour (functional findings):
- not examined
- Developmental immunotoxicity:
- not examined
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F2a
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no test substance-related adverse effects on F2a generation pups.
- Key result
- Dose descriptor:
- NOAEL
- Generation:
- F2b
- Effect level:
- 1 500 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no test substance-related adverse effects on F2b generation pups.
- Key result
- Reproductive effects observed:
- no
- Lowest effective dose / conc.:
- 1 500 ppm
- Conclusions:
- No adverse effects on general toxicology, reproduction or development were noted.
- Executive summary:
These studies were conducted in 1968, prior to the GLP guidance.
A dose range-finding three-month subacute toxicity study in rats fed daily dietary dose levels of ~500, 1500, 5000, and 15000 ppm neodecanoic acid was performed (15 rats/sex/group) to select doses for a three-generation reproductive toxicity study. The following parameters were examined: mortality, body weight, food consumption, physical appearance, behavioral signs, gross examination, organ weight, histopathology, clinical biochemistry.
In the 15,000 ppm group, there was mortality (73% survival: 4 males/5 females) and all rats exhibited clinical signs of thin and hunched; the majority of the rats also had a pale appearance. In the 5,000 ppm and 15,000 ppm dose groups, there was significantly decreased mean body weight gain in male/female rats at 13 weeks, end of the study (10%/14% and 73%/57% below control, respectively). Also, food consumption for the 5,000 ppm females and 15,000 ppm male and female rats was significantly lower compared with control values (7% and 42% below control, respectively. Also, there were gross examination findings in liver and kidneys. Hepatotoxic changes were seen in the male and female rats at 5,000 and 15,000 ppm dose groups. There were renal changes affecting the tubules of both the male and female rats who were dosed with 1500, 5,000 and 15,000 ppm of neodecanoic acid. No test substance effects were noted in regard to physical appearance and behavior of the test rats at the dose levels of 500 ppm and 1500 ppm. Therefore, based on mortality, clinical signs, decreased body weight gain, decreased food consumption, and gross / histopathologic examination changes at 5000 ppm and 15,000 ppm, 1,500 ppm was selected as the high dose for the definitive three-generation reproductive toxicity study.
A definitive modified three-generation reproductive toxicity study was performed to evaluate the effects of long-term ingestion of neodecanoic acid on reproduction in albino rats. Neodecanoic acid was administered in the diet at levels of 100, 500, and 1500 ppm fed to the rats through two parental and to two-litter filial generations. Following nine weeks of dietary administration to the F2B weanlings designated as the third parental generation, the study was terminated. There was no evidence at any test level of an adverse effect on the survival, appearance, behavior, body weight gain, and food consumption of the parental generations; on the reproductive performance of the parents reflected by the various indices; or on the growth, appearance, and behavior of the offspring. Gross and macroscopic pathological findings revealed no evidence of a compound-related effect at any of the dietary levels.
Reference
BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS)
No effects noted
TEST SUBSTANCE INTAKE (PARENTAL ANIMALS)
No effects noted
REPRODUCTIVE FUNCTION: ESTROUS CYCLE (PARENTAL ANIMALS)
No effects noted
REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)
No effects noted
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
No effects noted
ORGAN WEIGHTS (PARENTAL ANIMALS)
No effects noted
GROSS PATHOLOGY (PARENTAL ANIMALS)
No effects noted
HISTOPATHOLOGY (PARENTAL ANIMALS)
No effects noted
OTHER FINDINGS (PARENTAL ANIMALS)
No effects noted
F2A and F2B – The various indices, litter size, pup body weights, appearance, and behavior of the newborn and of the pups during lactation were comparable among the control and test groups for both cycles. At birth, two pups from one high level F2A litter were found cold to the touch. Minor incidental findings were also noted.
Effect on fertility: via oral route
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 75 mg/kg bw/day
- Study duration:
- subchronic
- Experimental exposure time per week (hours/week):
- 168
- Species:
- rat
- Quality of whole database:
- The data is reliable and consistent based on study design, size, quality, biological plausibility, dose. However, the study was performed prior to the introduction of GLPs.
Additional information
In a modified three-generation reproductive toxicity study, male and female Sprague-Dawley rats were administered neodecnoic acid at 0, 100, 500 and 1500 ppm (approximately 0, 5, 25 and 75 mg/kg-bw/day, respectively) in the diet. No adverse effects were observed on survival, appearance, behavior, body-weight gain and food consumption in the parental, F1 or F2 generations. The reproductive performance of the parents was not affected. No treatment-related gross or microscopic pathological findings were observed at any of the dietary levels.
Effects on developmental toxicity
Effect on developmental toxicity: via oral route
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- NOAEL
- 250 mg/kg bw/day
- Study duration:
- subacute
- Experimental exposure time per week (hours/week):
- 168
- Species:
- rat
- Quality of whole database:
- The data for C6-C8 neoacids is reliable and consistent based on study design, size, quality, biological plausibility, dose-rsponse.
Additional information
In developmental toxicity study, pregnant rats, n=22 per dose, were treated by oral gavage to 50, 250, 600 or 800 mg/kg/day neoheptanoic acid, a substance similar in structure to neodecanoic acid, during gestation days 6-15. On gestation day 21, the dams were euthanized and the pups were examined for signs of developmental toxicity. Under the conditions of the experimental methods, the test material produced maternal toxicity at dose levels of 600 and 800 mg/kg with maternal lethality at 800 mg/kg. The test material was severely embryotoxic at 800 mg/kg with less than 20% of embryos surviving. Offspring of the 800 mg/kg group had reduced body weight, reduced crown-rump distance, displayed variations signifying delayed development, and a significant percentage (25%) were malformed. In the 600 mg/kg group, there was an increase number of dams with 3 or more resorptions. Offspring of the 600 mg/kg group displayed significant incidences of major (hydrocephalus) and minor (knobby or angular ribs, extra lumbar vertebrae) malformations but showed few signs of delayed development and were not runted. There was no statistically significant evidence of maternal toxicity at dose levels of 50 or 250 mg/kg. There was a slight, but not statistically significant, increase in embryonic resorption noted for the 250 mg/kg group. There was no statistically significant evidence of developmental toxicity at doses for 50 or 250 mg/kg. The NOAEL for maternal toxicity is 250 mg/kg and the NOAEL for developmental toxicity is 250 mg/kg.
Justification for classification or non-classification
No classification for reproductive or developmental toxicity is indicated according to the general classification and labeling requirements for dangerous substances and preparations (Directive 67-548-EEC) or the classification, labeling and packaging (CLP) regulation (EC) No 1272/2008.
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.
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