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EC number: 203-093-8 | CAS number: 103-26-4
- 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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- chronic toxicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 2004
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Expert panel report, published by a reliable scientific institution, contributing to the assessment. Both, Cinnamaldehyde as well as methylcinnamate are metabolised through cinnamic acid as primary metabolite, as shown in the metabolism diagram (see attached background material), and thus fulfill the criterion for read-across as indicated in Annex XI, 1.5(2). An equivalent category approach was used by WHO when assessing dietary uptake on cinnamyl derivates via food and by the European Food Safety Authority in their "Scientific Opinion on Flavouring Group Evaluation 15, Revision 2 (FGE.15Rev2) on Aryl-substituted saturated and unsaturated primary alcohol/aldehyde/ester derivatives from chemical group 22". Thus, the study conducted with cinnamaldheyde is acceptable to be used for read-across to methyl cinnamate as both do metabolise via cinnamic acid.
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 453 (Combined Chronic Toxicity / Carcinogenicity Studies)
- Deviations:
- yes
- Remarks:
- all animals were exposed through entire life span (2 years)
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- 14371-10-9
- EC Number:
- 604-377-8
- Cas Number:
- 14371-10-9
- IUPAC Name:
- 14371-10-9
- Reference substance name:
- trans-CINNAMALDEHYDE
- IUPAC Name:
- trans-CINNAMALDEHYDE
- Test material form:
- other: a pale yellow liquid
- Details on test material:
- Smiles code: O=CC=Cc1ccccc1
Mol. Formula: C9H8O
Mol. Weight: 132.16
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Male and female F344/N rats were obtained from Taconic Laboratory Animals and Services (Germantown, NY). On receipt, the rats were 5 to 6 weeks old. Rats were quarantined for 11 (males) or 12 (females) days; rats were approximately 6 weeks old on the first day of the studies. Before the studies began, five male and five female rats were randomly selected for parasite evaluation and gross observation for evidence of disease. Serologic analyses were performed on five male and five female sentinel rats 4 weeks after the study began and on five male and five female untreated control rats at study termination using the protocols of the NTP Sentinel Animal Program.
Animal identification by tail tattoo. Diet and water was available ad libitum.
Cages
Polycarbonate (Lab Products, Inc., Maywood, NJ) changed twice weekly (rats and female mice) or once weekly (male mice)
Bedding
Sani-Chips® (P.J. Murphy Forest Products Corp., Montville, NJ), changed twice weekly (rats and female mice) or once weekly (male mice)
Cage Filters
Dupont 2024 spun-bonded polyester (Snow Filtration Co., Cincinnati, OH), changed every 2 weeks
Racks
Stainless steel (Lab Products, Inc., Maywood, NJ), changed and rotated every 2 weeks
Animal Room Environment
Temperature: 72° ± 3° F
Relative humidity: 50% ± 15%
Room fluorescent light: 12 hours/day
Room air changes: 10/hour
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- other: empty starch microcapsules
- Details on oral exposure:
- The dose formulations were prepared at least every 3 weeks by mixing microencapsulated trans-cinnamaldehyde with nonirradiated NTP-2000 feed during the 3-month studies. Placebo and/or loaded microcapsules were combined with feed to a concentration of 10% (3-month studies) in the diet.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Periodic analyses of the dose formulations used during the 2-year studies were conducted by the study laboratory using HPLC. During the 2-year studies, the dose formulations were analyzed approximately every 9 to 12 weeks; animal room samples of these dose formulations were also analyzed.
During the 3-month and 2-year studies, problems with animal room samples were encountered due to the animals’ ability to eat around the microcapsules (causing high animal room sample analyses results) and due to contamination of the feed with urine and feces which softened the microcapsules (causing low results). Both problems were more prevalent in the 3-month studies because the animals were younger and smaller and because of the higher concentrations of cinnamaldehyde in the feed. - Duration of treatment / exposure:
- 104 to 105 (males) weeks or 105 to 106 (females) weeks
- Frequency of treatment:
- once daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0, 1000, 2100, 4100 ppm microencapsulated trans-cinnamaldehyde (equivalent to average daily doses of approximately 0, 50, 100 and 200 mg trans-cinnamaldehyde/kg body weight to males and females).
Basis:
nominal in diet
- No. of animals per sex per dose:
- 50
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- Groups of 50 male and 50 female core study rats were fed diets containing 1000, 2100 and 4100 ppm microencapsulated trans-cinnamaldehyde for2 years. Additional groups of 50 male and 50 female core study rats received untreated feed (untreated controls) or feed containing placebo microcapsules (vehicle controls).
Feed and water were available ad libitum. Rats were housed five per cage. Observations were made twice daily; animals were weighed initially, on day 8, every 4 weeks thereafter, and at the end of the study.
Clinical findings were recorded on day 36, every 4 weeks thereafter, and at the end of the studies. Feed consumption was recorded by cage for a 1-week period approximately every 4 weeks.
Examinations
- Observations and examinations performed and frequency:
- Observed twice daily; animals were weighed initially, weekly, and at the end of the studies; clinical findings were recorded on day 8 and every 4 weeks thereafter. Feed consumption was recorded by cage for a 1-week period approximately every 4 weeks.
- Sacrifice and pathology:
- Method of Sacrifice
Carbon dioxide asphyxiation
Necropsy
Necropsies were performed on all core study animals. Organs weighed were heart, right kidney, liver, lung, right testis, and thymus.
Histopathology
Complete histopathology was performed on all rats. In addition to gross lesions and tissue masses, the following tissues were examined: adrenal gland, bone with marrow, brain, clitoral gland, esophagus, heart with aorta, large intestine (cecum, colon, rectum), small intestine (duodenum, jejunum, ileum), kidney, liver, lung, lymph nodes (mandibular and/or mesenteric), mammary gland, nose, ovary, pancreas, parathyroid gland, pituitary gland, preputial gland, prostate gland, salivary gland, skin, spleen, stomach (forestomach and glandular), testis with epididymis and seminal vesicle, thymus, thyroid gland, trachea, urinary bladder, and uterus.
Hippuric Acid – Biomarker of Exposure
Urine was collected during a 24-hour period from 10 male and 10 female rats from each group at 2 weeks and 3, 12, and 18 months. Parameters evaluated included creatinine and hippuric acid concentrations and volume. - Statistics:
- Survival Analyses:
The probability of survival was estimated by the product-limit procedure of Kaplan and Meier (1958) and is presented in the form of graphs. Animals found dead of other than natural causes or missing were censored from the survival analyses; animals dying from natural causes were not censored. Statistical analyses for possible dose-related effects on survival used Cox’s (1972) method for testing two groups for equality and Tarone’s (1975) life table test to identify dose-related trends. All reported P values for the survival analyses are two sided.
Calculation of Incidence
The incidences of neoplasms or nonneoplastic lesions were presented as numbers of animals bearing such lesions at a specific anatomic site and the numbers of animals with that site examined microscopically. For calculation of statistical significance, the incidences of most neoplasms and all non neoplastic
lesions are given as the numbers of animals affected at each site examined microscopically.
Analysis of Neoplasm
Tests of significance included pairwise comparisons of each exposed group with controls and a test for an overall exposure-related trend. Continuity-corrected Poly-3 tests were used in the analysis of lesion incidence, and reported P values are one sided. The significance of lower incidences or decreasing trends in lesions is represented as 1-P with the letter N added (e.g., P=0.99 is presented as P=0.01N).
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- slightly reduced body weights at 2100 and 4100 ppm in males and at 4100 ppm in females.
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Description (incidence and severity):
- slight effects at 2100 and 4100 ppm n males and 4100 ppm in females
- Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- not examined
- Ophthalmological findings:
- not examined
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- no effects observed
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Gross pathological findings:
- not examined
- Histopathological findings: non-neoplastic:
- no effects observed
- Histopathological findings: neoplastic:
- no effects observed
- Details on results:
- Survival of 4,100 ppm males was greater than that of the vehicle control group; survival of other exposed groups of males and of exposed females was similar to that of the vehicle control groups.
Mean body weights of 4,100 ppm males were less than those of the vehicle controls throughout the study, mean body weights of 2,100 ppm males were less after week 94, and mean body weights of 4,100 ppm females were less after week 18 (Figure 3; Tables 6 and 7). Feed consumption by 2,100 and 4,100 ppm males and 4,100 ppm females was less than that by the vehicle controls at the beginning and end of the study. Dietary concentrations of 1,000, 2,100, or 4,100 ppm delivered average daily doses of approximately 50, 100, or 200 mg/kg body weight to males and females. There were no clinical findings related to trans-cinnamaldehyde exposure.
Hippuric acid excretion in urine expressed as the hippuric acid to creatinine ratio was proportional to dose, indicating that neither absorption, metabolism, nor excretion was saturated in either male or female rats exposed to dosed feed containing 1,000 to 4,100 ppm trans-cinnamaldehyde.
Preputial and Prostate Glands:
The incidences of adenoma of the preputial gland (vehicle control, 5/50; 1,000 ppm, 1/49; 2,100 ppm, 2/50; 4,100 ppm, 0/50) and prostate gland (4/50, 0/49, 0/49, 0/50) in 4,100 ppm males were significantly decreased compared to those in the vehicle controls. The incidences of preputial gland adenoma in the exposed and vehicle control groups were within the historical range in controls (all routes) given NTP-2000 diet [45/907 (4.2% ± 3.5%), range 0%-13%]. Similarly, the incidences of carcinoma of the preputial gland (1/50, 2/49, 3/50, 1/50) were within the historical range in controls given NTP-2000 diet [27/907 (3.3% ± 3.0%), range 0%-10%]. The incidence of prostate gland adenoma in the vehicle controls (4/50) exceeded the historical control range [13/906 (1.4% ± 1.7%), range 0%-4%] (Suwa et al., 2001). The incidences of preputial and prostate gland adenomas likely represent biologic variation unrelated to exposure to trans-cinnamaldehyde.
Mononuclear Cell Leukemia: The incidence of mononuclear cell leukemia in 4,100 ppm males was significantly decreased (18/50, 15/50, 21/50, 9/50), was
considered unrelated to trans-cinnamaldehyde exposure, and may have contributed to the increased survival in this group. The historical control incidence for vehicle controls given NTP-2000 diet is 401/909 (44.1% ± 11.8%) with a range of 22% to 68%. Mononuclear cell leukemia is one of the most common
neoplasms of F344/N rats in 2-year studies.
Effect levels
open allclose all
- Dose descriptor:
- NOAEL
- Effect level:
- 4 100 ppm
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no clinical findings related to trans-cinnamaldehyde exposure at all doses up to 4100 ppm (200 mg/kg bw/d males and females) and thus the high dose may be seen as NOAEL in this study with rats.
- Dose descriptor:
- NOAEL
- Effect level:
- 200 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: There were no clinical findings related to trans-cinnamaldehyde exposure at all doses up to 4100 ppm (200 mg/kg bw/d males and females) and thus the high dose may be seen as NOAEL in this study with rats.
Target system / organ toxicity
- Critical effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- Based on the available data it was concluded that trans-cinnamaldheyde did not cause adverse effects to rats at concentrations of 50, 100 and 200 mg/kg bw/d compared with untreated control group. The NOAEL may be set to 4100 ppm (200 mg/kg bw/d males and females).
- Executive summary:
Groups of 50 male and 50 female F344/N rats were fed diets containing 1,000, 2,100, or 4,100 ppm microencapsulated trans-cinnamaldehyde for 2 years. Additional groups of 50 male and 50 female rats received untreated feed (untreated controls) or feed containing placebo microcapsules (vehicle controls). Dietary concentrations of 1,000, 2,100, or 4,100 ppm delivered average daily doses of approximately 50, 100, or 200 mg/kg to males and females. Survival of 4,100 ppm males was greater than that of the vehicle controls. Mean body weights of 4,100 ppm males and females were generally less than those of the vehicle controls throughout the study (91% males and 92% females at end of study, compared to control). Feed consumption by 2,100 and 4,100 ppm males and 4,100 ppm females was less than that by the vehicle controls at the beginning and end of the study, whereas survival in the highest dose group was s higher, particularly for male rats. There were no neoplasms or nonneoplastic lesions that were attributed to exposure to trans-cinnamaldehyde at all dose groups. The incidence of mononuclear cell leukemia in 4,100 ppm males was significantly decreased (18/50, 15/50, 21/50, 9/50), was considered unrelated to trans-cinnamaldehyde exposure, and may have contributed to the increased survival in this group. Thus, the NOAEL for repeated dose toxicity is set to 4100 ppm (i.e. 200 mg/kg bw/d) in this study.
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