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EC number: 218-145-5 | CAS number: 2052-25-7
- 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
Toxicity to reproduction
Administrative data
- Endpoint:
- extended one-generation reproductive toxicity - with developmental neurotoxicity (Cohorts 1A, 1B without extension, 2A and 2B)
- 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:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Reproductive and neurobehavioral effects of Allura Red AC administered to mice in the diet
- Author:
- Tanaka T
- Year:
- 1 994
- Bibliographic source:
- Toxicology, Volume 92, Issues 1–3, 6 September 1994, Pages 169-177
Materials and methods
- Principles of method if other than guideline:
- See attachment
- GLP compliance:
- not specified
- Limit test:
- no
- Justification for study design:
- The test substance was administered in diet to 60 mice (10/sex/group) at dietary levels of 0.42, 0.84, and 1.68 %. The control groups (20 mice, 10/sex) were given the basal diets (Nihon Clea, CE-2) for the corresponding period. Individual food intake of mice was measured during 5 divided periods; pre-conception (from 5 weeks of age to mating), mating (5 days), gestation (14 days), and lactation (from birth to weaning), and F 1 generation (4-9 weeks of age).
The animals from the F0 generation were 5 weeks of age at the start of the study.
At 9 weeks of age, each female was paired with one male from the same treatment group, for a period of 5 days. The males were removed from the females after 5 days, and the females were allowed to carry their litters to term, deliver and rear their offspring.
In the F 1 generation, litter size, litter weight and sex ratio (male/female) were measured on postnatal day (PND) 0 (at birth). The offspring were individually weighed on PNDs 0, 4, 7, 14 and 21 during the lactation period. The offspring were weaned when they were 4 weeks of age, and were randomly selected to continue treatment, one male and one female from each litter.
Neurobehavioral procedure
The functional and behavioral developmental parameters were measured and scored for individual offspring during the lactation period in the Fl generation (Tanaka, 1992), and were analysed on a whole-litter basis (Abbey and Howard, 1973). The measured parameters were as follows: surface righting on PNDs 4 and 7 (Fox, 1965; Pantaleoni et al., 1988), negative geotaxis on PNDs 4 and 7 (Fox, 1965; Altman and Sudarshan, 1975; Pantaleoni et al., 1988), cliff avoidance on PND 7 (Fox, 1965; Altman and Sudarshan, 1975; Pantaleoni et al., 1988), swimming behavior (direction, head angle, and limb movement) on PNDs 4 and 14 (Fox, 1965; Pantaleoni et al., 1988), and olfactory orientation on PND 14 (Altman and Sudarshan, 1975; Barlow et al., 1978; Meyer and Hansen, 1980).
Exploratory behavior of mice was measured in an animal movement analysing system ANIMATE AT-420 (Toyo Sangyo Co., Ltd, Toyama, Japan) at 3 and 8 weeks of age in the F1 generation. The system consisted of a doughnut-shaped cage with 36 detectors for measuring spontaneous motor activity (Matsumoto et al., 1990a, b).
The behavioral parameters were recorded for 5 min on one male and one female selected randomly from each litter at 3 weeks of age, and for 10 min on all animals at 8 weeks of age. The measurement parameters were number of movements, movement time (s), number of horizontal activities, total distance (cm), number of vertical activities, vertical time (s), number of turnings, average distance (cm), average speed (cm/s), and defecations.
The animals performed 3 trials in a multiple water T-maze of Biel's type adapted for mice at 7 weeks of age in the FI generation (Biel, 1940; Kitatani et al., 1988). The water temperature was maintained at 20 ± 1 °C. The time taken and number of errors were measured from the start to finish for a maximum 120 s. If the time taken was greater than 120 s, it was recorded as 120 s (Kitatani et al., 1988).
Test material
- Reference substance name:
- Disodium 6-hydroxy-5-[(2-methoxy-4-sulphonato-m-tolyl)azo]naphthalene-2-sulphonate
- EC Number:
- 247-368-0
- EC Name:
- Disodium 6-hydroxy-5-[(2-methoxy-4-sulphonato-m-tolyl)azo]naphthalene-2-sulphonate
- Cas Number:
- 25956-17-6
- Molecular formula:
- C18H16N2O8S2.2Na
- IUPAC Name:
- disodium 6-hydroxy-5-[(2-methoxy-3-methyl-4-sulfonatophenyl)diazenyl]naphthalene-2-sulfonate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- Name: Allura Red AC
Synonyms: FD&C Red No. 40, CI No. 16035
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- CD-1
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Male and female mice (Crj: CD-1, 4 weeks of age) were purchased from Charles River Japan Inc., Kanagawa, Japan.
They were individually housed in polycarbonate solid-floored cages with wood flakes, and kept in a temperature controlled room maintained at 24 +/- 1°C with a relative humidity of 55 +/- 5% and a 12-h light/dark cycle. They were given control or experimental diets (Nihon Clea, CE-2) and water ad libitum.
Administration / exposure
- Route of administration:
- oral: feed
- Details on exposure:
- Allura Red AC was administered in diet to 60 mice (10/sex/group) at dietary levels of 0.42, 0.84, and 1.68 %.
The control groups (20 mice, 10/sex) were given the basal diets (Nihon Clea, CE-2) for the corresponding period.
Individual food intake of mice was measured during 5 divided periods; pre-conception (from 5 weeks of age to mating), mating (5 days), gestation (14 days), and lactation (from birth to weaning), and F 1 generation (4-9 weeks of age). - Details on mating procedure:
- The animals from the F0 generation were 5 weeks of age at the start of the study.
At 9 weeks of age, each female was paired with one male from the same treatment group, for a period of 5 days.
The males were removed from the females after 5 days, and the females were allowed to carry their litters to term, deliver and rear their off
spring.
In the F1 generation, litter size, litter weight and sex ratio (male/female) were measured on postnatal day (PND) 0 (at birth). - Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- F0: from 5 weeks of age during mating (f+m), gestation and lactation (f)
pre-conception (from 5 weeks of age to mating), mating (5 days), gestation (14 days), and lactation (from birth to weaning), and
F1 generation: 4-9 weeks of age - Frequency of treatment:
- continuous
- Details on study schedule:
- The animals from the F0 generation were 5 weeks of age at the start of the study.
At 9 weeks of age, each female was paired with one male from the same treatment group, for a period of 5 days. The males were removed from the females after 5 days, and the females were allowed to carry their litters to term, deliver and rear their offspring.
In the F1 generation, litter size, litter weight and sex ratio (male/female) were measured on postnatal day (PND) 0 (at birth). The offspring were individually weighed on PNDs 0, 4, 7, 14 and 21 during the lactation period. The offspring were weaned when they were 4 weeks of age, and were randomly selected to continue treatment, one male and one female from each litter.
The functional and behavioral developmental parameters were measured and scored for individual offspring during the lactation period in the F1 generation (Tanaka, 1992), and were analysed on a whole-litter basis (Abbey and Howard, 1973). The measured parameters were as follows: surface righting on PNDs 4 and 7 (Fox, 1965; Pantaleoni et al., 1988), negative geotaxis on PNDs 4 and 7 (Fox, 1965; Altman and Sudarshan, 1975; Pantaleoni et al., 1988), cliff avoidance on PND 7 (Fox, 1965; Altman and Sudarshan, 1975; Pantaleoni et al., 1988), swimming behavior (direction, head angle, and limb movement) on PNDs 4 and 14 (Fox, 1965; Pantaleoni et al., 1988), and olfactory orientation on PND 14 (Altman and Sudarshan, 1975; Barlow et al., 1978; Meyer and Hansen, 1980).
Exploratory behavior of mice was measured in an animal movement analysing system ANIMATE AT-420 (Toyo Sangyo Co., Ltd, Toyama, Japan) at 3 and 8 weeks of age in the F1 generation. The system consisted of a doughnut-shaped cage with 36 detectors for measuring spontaneous motor activity (Matsumoto et al., 1990a, b).
The behavioral parameters were recorded for 5 min on one male and one female selected randomly from each litter at 3 weeks of age, and for 10 min on all animals at 8 weeks of age. The measurement parameters were number of movements, movement time (s), number of horizontal activities, total distance (cm), number of vertical activities, vertical time (s), number of turnings, average distance (cm), average speed (cm/s), and defecations.
The animals performed 3 trials in a multiple water T-maze of Biel's type adapted for mice at 7 weeks of age in the FI generation (Biel, 1940; Kitatani et al., 1988). The water temperature was maintained at 20 ± 1 °C. The time taken and number of errors were measured from the start to finish for a maximum 120 s. If the time taken was greater than 120 s, it was recorded as 120 s (Kitatani et al., 1988).
Doses / concentrationsopen allclose all
- Dose / conc.:
- 0.42 other: %
- Remarks:
- in diet
- Dose / conc.:
- 0.84 other: %
- Remarks:
- in diet
- Dose / conc.:
- 1.68 other: %
- Remarks:
- in diet
- Remarks:
- Doses / Concentrations:
700, 1420, 2928 mg/kg/day
Basis:
nominal in diet
males, pre-conception
- Remarks:
- Doses / Concentrations:
803, 1694, 3375 mg/kg/day
Basis:
nominal in diet
females, pre-conception
- Remarks:
- Doses / Concentrations:
620/598, 1242/1230, 2880/2550 mg/kg/day
Basis:
nominal in diet
females, mating/gestation
- Remarks:
- Doses / Concentrations:
2607, 5549, 10070 mg/kg/day
Basis:
nominal in diet
females, lactation
- No. of animals per sex per dose:
- 10
- Control animals:
- yes, plain diet
Examinations
- Parental animals: Observations and examinations:
- Food intake, clinical signs,
- Litter observations:
- Food intake, litter size, litter weight and the body weight of offspring
Sex ratio and survival index at PND 21
Functional and behavioral developmental parameters:
surface righting: PNDs 4 and 7
negative geotaxis: PNDs 4 and 7
cliff avoidance: PND 7
swimming behavior (direction, head angle, and limb movement): PNDs 4 and 14
olfactory orientation: PND 14
Exploratory behavior:
spontaneous motor activity: at 3 and 8 weeks of age
measurement parameters:number of movements, movement time (s), number of horizontal activities, total distance (cm), number of vertical activities, vertical time (s), number of turnings, average distance (cm), average speed (cm/s), and defecations
multiple water T-maze: at 7 weeks of age - Statistics:
- Food intake, litter size, litter weight and the body weight of offspring were assessed with Bonferroni's multiple comparison test after analysis of variance (ANOVA), or the Kruskal-Wallis test. Sex ratio and survival index at PND 21 were assessed with the x2-test (2 x 2 or 2 x 4). The behavioral developmental data and movement activity data were assessed with the Mann-Whitney U-test (Martin and Bateson, 1990). Multiple water T-maze performance data was assessed with the signed Wilcoxon test for trials and assessed with the Mann-Whitney U-test among each treatment group.
Results and discussion
Results: P0 (first parental generation)
General toxicity (P0)
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- increased food intake high dose
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Description (incidence and severity):
- increased food intake high dose
- Ophthalmological findings:
- not examined
- Haematological findings:
- not specified
- Clinical biochemistry findings:
- not specified
- Urinalysis findings:
- not specified
- Behaviour (functional findings):
- not examined
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- not specified
- Histopathological findings: non-neoplastic:
- not specified
- Other effects:
- effects observed, treatment-related
- Description (incidence and severity):
- Test substance intake: increased intake high dose
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- no effects observed
- Reproductive function: sperm measures:
- not specified
- Reproductive performance:
- no effects observed
Details on results (P0)
There were few adverse effects of Allura Red AC on the average food intake during each period with the exception of the mating period. During the mating period, the average food intake was significantly increased in high-dosed group.
Therefore, the chemical intake was consistently increased as dose-related during each period.
F0 generation
Several dams showed under-development of mammary glands in the first week of lactation; one each in the control, low- and middle-dosed groups. One dam died during the second week of lactation in the low-dosed group.
Effect levels (P0)
- Dose descriptor:
- NOAEL
- Effect level:
- >= 2 550 - <= 10 070 mg/kg bw/day
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- clinical signs
- mortality
- body weight and weight gain
- food consumption and compound intake
- reproductive performance
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Mortality / viability:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- increased at lowe dose during lactation
- Ophthalmological findings:
- not examined
- Haematological findings:
- not specified
- Clinical biochemistry findings:
- not specified
- Urinalysis findings:
- not specified
- Sexual maturation:
- no effects observed
- Organ weight findings including organ / body weight ratios:
- not specified
- Gross pathological findings:
- not specified
- Histopathological findings:
- not specified
Developmental neurotoxicity (F1)
- Behaviour (functional findings):
- no effects observed
Developmental immunotoxicity (F1)
- Developmental immunotoxicity:
- not examined
Details on results (F1)
No significant adverse effect was observed in either litter size or weight at birth. Sex ratio at birth was significantly reduced in the low-dosed group, while there were few adverse effects in other groups. The average body weight of offspring during the lactation period was significantly increased in the lower-dosed groups for each sex. Two litters died due to under-development of mammary glands of
their dams during the first week of lactation, one litter in the control and one in the low-dosed group, and one litter in the low-dosed group was destroyed humanely (to prevent them dying of starvation) in view of the death of their dam during the second week of lactation. The survival index at PND 21 showed no consistent adverse effect in treatment groups, while that for male offspring was significantly reduced in the low-dosed group and for female offspring was significantly increased in the high dose group.
As regards the neurobehavioral parameters, no adverse effect of Allura Red AC was found in the all parameters measured for behavioral development during the lactation period in each sex. Movement activity of exploratory behavior showed no adverse effect of Allura Red AC on pre-weaning period (at 3 weeks of age) for 5 min.
There were few adverse effects of Allura Red AC on multiple water T-maze performance in all treatment groups as compared with controls, while time taken was significantly reduced on the second trial in the low-dosed group of female and on the third trial in high-dosed group of both sexes as compared with the first trial. Movement activity of exploratory behavior showed no adverse effect of Allura Red AC on post-weaning period (at 8 weeks of age) for 10 min.
Effect levels (F1)
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- > 1.68 other: %
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- viability
- clinical signs
- mortality
- body weight and weight gain
- developmental neurotoxicity
Overall reproductive toxicity
- Reproductive effects observed:
- no
Applicant's summary and conclusion
- Conclusions:
- From the results, the dose levels of Allura Red AC in the present study, which were at least 86-times greater (during the mating period in the low-dosed group), and up to 1430-times greater (during the lactation period in the high-dosed group), than the human ADI of 7.0 mg/kg body weight, produced few adverse effects on the reproductive and neurobehavioral parameters measured in mice. These results suggest that Allura Red AC will not produce adverse effects on reproduction and behavior at typical human intake levels.
- Executive summary:
The color additive, Allura Red AC, was given in the diet to provide levels of 0.42, 0.84, and 1.68% (control, 0%), from 5 weeks of age of the F0 generation to 9 weeks of age of the F1 generation in mice, and selected reproductive and neurobehavioral parameters were measured. There were few adverse effects of Allura Red AC on either litter size or weight, and ratio of male to female was significantly reduced in the lowest dosed group. Average body weight of offspring during the lactation period was significantly increased in the lower dosed groups of each sex. As regards the neurobehavioral parameters, no adverse effect was observed in the behavioral development during lactation period. There were few adverse effects of Allura Red AC on either movement activity or maze learning in F1 generation mice, compared with controls in each sex. The dose levels of Allura Red AC in the present study (approximately 86–1430 times greater than human ADI) produced few adverse effects in reproductive and neurobehavioral parameters in mice.
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