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EC number: 203-223-3 | CAS number: 104-65-4
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer-reviewed journal
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Fragrance material review on Cinnamyl formate
- Author:
- S.P. Bhatia, G.A. Wellington , J. Cocchiara , J. Lalko , C.S. Letizia , A.M. Api
- Year:
- 2 007
- Bibliographic source:
- Food and Chemical Toxicology 45 (2007) S70–S73
- Reference Type:
- publication
- Title:
- The FEMA GRAS assessment of cinnamyl derivatives used as flavor ingredients
- Author:
- Timothy B. Adamsa, Samuel M. Cohenb, John Daulle, Victor J. Ferond, Jay I. Goodmane, Lawrence J. Marnettf, Ian C. Munrog, Philip S. Portogheseh, Robert L. Smithi, William J. WaddeW, Bernard M. Wagnerk
- Year:
- 2 004
- Bibliographic source:
- Food and Chemical Toxicology 42 (2004) 157-185
- Reference Type:
- publication
- Title:
- Monographs on Fragrance Raw Materials: Cinnamyl formate
- Author:
- D. L. J. Opdyke
- Year:
- 1 976
- Bibliographic source:
- Food and Cosmetics Toxicology,Volume 14, Supplement, Pages 659-893 (1976)
- Reference Type:
- publication
- Title:
- Acute oral toxicity study of Cinnamyl formate (104-65-4) in Rat
- Author:
- U.S. National Library of Medicine
- Year:
- 2 017
- Bibliographic source:
- Chemidplus Database,U.S. National Library of Medicine ,2017
- Reference Type:
- publication
- Title:
- A toxicologic and dermatologic assessment of related esters and alcohols of cinnamic acid and cinnamyl alcohol when used as fragrance ingredients
- Author:
- D. Belsito, D. Bickers , M. Bruze , P. Calow , H. Greim ,J.M. Hanifin, A.E. Rogers , J.H. Saurat, I.G. Sipesi, H. Tagami
- Year:
- 2 007
- Bibliographic source:
- Food and Chemical Toxicology, 45, (2007) S1–S23
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: As mentioned below
- Principles of method if other than guideline:
- Acute Oral toxicity test was carried out to study the effects of Cinnamyl formate (104-65-4) on rats.
- GLP compliance:
- not specified
- Test type:
- other: No data available
- Limit test:
- yes
Test material
- Reference substance name:
- Cinnamyl formate
- EC Number:
- 203-223-3
- EC Name:
- Cinnamyl formate
- Cas Number:
- 104-65-4
- Molecular formula:
- C10H10O2
- IUPAC Name:
- cinnamyl formate
- Details on test material:
- - Name of test material (IUPAC name): Cinnamyl formate
- Common name: 3-Phenylallyl formate
- Molecular formula: C10H10O2
- Molecular weight: 162.187 g/mol
- Smiles notation: c1(\C=C\COC=O)ccccc1
- InChl: 1S/C10H10O2/c11-9-12-8-4-7-10-5-2-1-3-6-10/h1-7,9H,8H2/b7-4+
- Substance type: Organic
Constituent 1
- Specific details on test material used for the study:
- - Name of test material (as cited in study report):Cinnamyl formate
- Molecular formula :C10H10O2
- Molecular weight :162.187 g/mol
- Substance type:Organic
- Physical state:Colorless to slightly yellow liquid
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- No data available
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Details on oral exposure:
- No data available
- Doses:
- 2000, 2500, 3200, 4000 and 5000 mg/kg/bodyweight
- No. of animals per sex per dose:
- Total: 50 animals
2000 mg/kg/bw = 10 animals
2500 mg/kg/bw =10 animals
3200 mg/kg/bw =10 animals
4000 mg/kg/bw =10 animals
5000 mg/kg/bw =10 animals - Control animals:
- not specified
- Details on study design:
- Details on study design
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: No data available
- Necropsy of survivors performed: No data available
- Other examinations performed: Clinical signs - Statistics:
- No data available
Results and discussion
- Preliminary study:
- No data available
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 2 900 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- > 2 380 - < 3 540
- Remarks on result:
- other: 50% mortality was observed
- Mortality:
- At 2000 mg/kg bw - 1 rat died.
At 2500mg/kg bw - 4 rats died.
At 3200 mg/kg bw - 7 rats died.
At 4000 mg/kg bw - 9 rats died.
At 5000 mg/kg bw - 9 rats died. - Clinical signs:
- other: Clinical signs like ataxia and mucoid enteritis were observed
- Gross pathology:
- No data available
- Other findings:
- No data available
Applicant's summary and conclusion
- Interpretation of results:
- Category 5 based on GHS criteria
- Conclusions:
- The lethal concentration (LD50) value for acute oral toxicity test was considered to be 2900 mg/kg bw(95% C.I. 2380–3540 mg/kg) ,when 50 rats were treated with Cinnamyl formate (104-65-4) orally.
- Executive summary:
Acute Oral Toxicity study was performed in 50 rats using test material Cinnamyl formate (104-65-4). 50% Mortality was observed at dose 2900 mg/kg bw. A majority of the deaths occurred between days 1 and 2.Clinical signs like ataxia and mucoid enteritis were observed. Hence,LD50 value was considered to be 2900 mg/kg bw(95% C.I. 2380–3540 mg/kg),when rats were treated with Cinnamyl formate (104-65-4)orally.
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