Registration Dossier
Registration Dossier
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: 282-490-8 | CAS number: 84238-29-9 Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Vetiveria zizanioides, Gramineae.
- 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

Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 18/02/1980 - 03/03/1980
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Test was not conducted according to OECD guideline, but under GLP Standards, 1978. Acceptable basic data.
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
- Report date:
- 1980
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The method was based on the procedure originally suggested by Draize, H.J. "Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics", Assoc. of Food and Drug Officials of the U.S., Austin, Texas (1959). The test substance was instilled in one eye of six rabbits, the other eye served as control. The results were scored for up to 15 days. The scoring system and conclusion were based on the Draize system.
- GLP compliance:
- yes
- Remarks:
- Federal Register, Vol. 43, No. 247, December 22, 1978
Test material
- Reference substance name:
- VETIVERT OIL HAÏTI
- IUPAC Name:
- VETIVERT OIL HAÏTI
- Details on test material:
- - Name of test material (as cited in study report): VETIVERT OIL HAÏTI
- Physical state: liquid
- Lot/batch No.: confidential
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: no data
- Age at study initiation: no data
- Weight at study initiation: 2.0 to 3.5 kg
- Housing: singly under standard laboratory conditions. Housing criteria specified in the 'Guide for the Care and Use of Laboratory Animals' (DHEW Publication No. (NIH) 78-23, Revised 1978).
- Diet: Purina rabbit chow (100g) supplemented with oats daily
- Water: ad libitum
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS: "STANDARD LABORATORY CONDITIONS". Housing and maintenance criteria specified in the 'Guide for the Care and Use of Laboratory Animals' (DHEW Publication No. (NIH) 78-23, Revised 1978).
IN-LIFE DATES: no data
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the other (left) eye served as control (not treated)
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 ml
- Concentration (if solution): 100% - Duration of treatment / exposure:
- One instillation of 0.1 ml of test material 100%, no washout, 10 days observation.
- Observation period (in vivo):
- 24, 48, and 72 hours, and day 4 and 7 (and day 10 if persistent changes observed at day 7)
- Number of animals or in vitro replicates:
- 6 rabbits (unspecified sex)
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): no removal of test substance
SCORING SYSTEM:
The scoring was performed according to the method of Draize. Classification of irritancy was according to the following scheme: non-irritating (0.0 to 0.5); practically non-irritating (0.6 to 10.0); mildly irritating (10.0 to 25.0); moderately irritating (25.1 to 50.0); extremely irritating (50.1 to 110)
TOOL USED TO ASSESS SCORE: hand held ophtalmoscope and fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 19
- Max. score:
- 110
- Reversibility:
- fully reversible within: day 10
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 12.33
- Max. score:
- 110
- Reversibility:
- fully reversible within: day 10
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 11.5
- Max. score:
- 110
- Reversibility:
- fully reversible within: day 10
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 4 days
- Score:
- 3.67
- Max. score:
- 110
- Reversibility:
- fully reversible within: day 10
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 7 days
- Score:
- 0.83
- Max. score:
- 110
- Reversibility:
- fully reversible within: day 10
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 10 days
- Score:
- 0
- Max. score:
- 110
- Reversibility:
- fully reversible
- Irritant / corrosive response data:
- 24 hours: 5 of the 6 rabbits have slight opacity, one rabbit has iritis
72 hours: a second rabbit found with iritis
day 4: both iritis have subsided, 3 of the 6 rabbits still have a slight opacity (the other 3 rabbits' eyes back to normal)
day 7: one rabbit only has a small area with slight opacity
day 10: the eyes of all 6 rabbits are back to normal. - Other effects:
- Not relevant
Any other information on results incl. tables
Not relevant
Applicant's summary and conclusion
- Interpretation of results:
- irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Vetivert oil Haïti has a mildly irritating effect on rabbit's eyes. This effect is totally reversible within 10 days after exposure, under the conditions of the study. Based on the results in this study and according to the EC criteria for classification and labelling requirements for dangerous substances and preparations (Guidelines in Commission Directive 93/21/EEC), Vetivert oil Haiti is classified as irritating to eyes.
- Executive summary:
0.1 ml of Vetivert oil was instilled into the right eye of 6 young albino type rabbits. The untreated left eye served as a control. Draize scoring of both eyes was conducted at 24, 48, and 72 hours and at days 4 and 7. Fluorescein staining was conducted at 24 hours and day 7 on both eyes. Any persistent changes observed on Day 7 were re-evaluated on Day 10 using a hand held ophthalmoscope and the fluorescein method. Classification of the relative irritancy was made according to the following scale, utilizing the highest reading obtained at 24, 48 or 72 hours after instillation of the test material. Reactions were considered as non-irritating with scores of 0.0 to 0.5; practically non-irritating at 0.6 to 10.0; mildly irritating at 10.0 to 25.0; moderately irritating at 25.1 to 50.0; and extremely irritating at score of 50.1 to 110.
Under the conditions of the study, 0.1 ml of 100% test material instilled into the right eye of each of six animals was mildly irritating, causing slight iritis and corneal opacity. The mean ocular irritation score was 19.0/110 at 24 hours.
Based on these results and according to the EC criteria for classification and labelling requirements for dangerous substances and preparations (Guidelines in Commission Directive 93/21/EEC), Vetivert oil Haiti is classified as irritating to eyes.
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.
