Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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: - | CAS number: -
- 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:
- calculation (if not (Q)SAR)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- accepted calculation method
Data source
Reference
- Reference Type:
- other: Guidance
- Title:
- Guidance on the Application of the CLP Criteria - Guidance to Regulation (EC) No 1272/2008 on classification, labelling and packaging (CLP) of substances and mixtures
- Author:
- ECHA
- Year:
- 2 017
- Bibliographic source:
- ECHA-17-G-21-EN
Materials and methods
- Principles of method if other than guideline:
- Classification based on calculation rules for mixtures of the CLP Regulation
Test material
- Reference substance name:
- litsea cubeba (fruit) extract – terpenes fraction
- Molecular formula:
- not applicable
- IUPAC Name:
- litsea cubeba (fruit) extract – terpenes fraction
- Test material form:
- liquid
Constituent 1
Results and discussion
Effect levels
- Key result
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 2 687 mg/kg bw
- Based on:
- test mat.
Any other information on results incl. tables
The NCS is composed of several identified constituents and in that, it can be considered as a mixture according to the definition of the CLP Regulation.
The decision logic for classification of mixtures from the ECHA Guidance on the Application of the CLP Criteria (2017) was used to determine the acute oral toxicity hazard of the registered substance.
An oral DL50 or an ATE estimate can be derived based on the current classification for a part of these constituents.
Data on constituents:
Constituent | CAS# | Range | Typical concentration | Oral DL50/ ATE estimates | Sources |
l-limonene | 5989-54-8 | 45-60 | 51 | LD50 > 5000 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/10807/7/3/1 |
Eucalyptol | 470-82-6 | 1-10 | 5,50 | LD50 = 4500 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/13231/7/3/1 |
Beta-myrcene | 123-35-3 | 1-10 | 5,30 | LD50 > 5000 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/14795/7/3/1 |
(Z)-3,7-dimethylocta-2,6-denial | 106-26-3 | 1-10 | 5,00 | LD50 = 6800 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/6329/7/3/1 |
6-methylhept-5-en-2-one | 110-93-0 | 1-10 | 5,00 | LD50 = 3570 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/12205/7/3/1 |
(1S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-2-ene (alpha pinene) | 7785-26-4 | 1-10 | 5,00 | Oral LD50 cut-off value = 500 mg/kg Acute Tox. 4 | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/14528/7/3/1 |
Beta-pinene | 127-91-3 | 1-10 | 4,10 | Not classified | C&L Inventory: https://echa.europa.eu/fr/information-on-chemicals/cl-inventory-database/-/discli/details/36440 |
(R)-3,7-dimethyl-1,6-octadien-3-ol (l-linalool) | 126-91-0 | 1-10 | 3,00 | LD50 ≥ 2000 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/27524/7/3/2 |
Sabinen | 3387-41-5 | 1-10 | 2,80 | Oral LD50 cut-off value = 2000 mg/kg Acute Tox. 4 | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/26637/7/3/1 |
(R)-3,7-dimethyloct-6-enal (R-citronellal) | 2385-77-5 | 1-10 | 2,70 | LD50 = 2423 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/22664/7/3/1 |
Geranial | 141-27-5 | 0-5 | 2,50 | LD50 = 6800 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/17552/7/3/2 |
Camphene | 79-92-5 | 0-5 | 1,50 | LD50 > 2000 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/14290/7/3/1 |
Isogeranial | 72203-98-6 | 0-5 | 1,00 | LD50 = 3220 mg/kg bw Not classified | IFRA Labelling Manual 2019 |
Isoneral | 72203-97-5 | 0-1 | 0,40 | LD50 = 3220 mg/kg bw Not classified | IFRA Labelling Manual 2019 |
p-mentha-1,4(8)-diene | 586-62-9 | 0-1 | 0,30 | LD50 = 3740 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/10412/7/3/1 |
2,3-Dehydro 1,8-cineol | 92760-25-3 | 0-2 | 0,25 | No data | / |
Alpha phellandrene | 99-83-2 | 0-2 | 0,25 | Acute tox 4 or Not classified Precautionary approach: ATE = 500 | C&L Inventory: https://echa.europa.eu/fr/information-on-chemicals/cl-inventory-database/-/discli/details/22821 |
6-Methyl hept-5-en-2-ol | 1569-60-4 | 0-1 | 0,20 | Not classified | C&L Inventory : https://echa.europa.eu/fr/information-on-chemicals/cl-inventory-database/-/discli/details/84179 |
Gamma-terpinene | 99-85-4 | 0-1 | 0,20 | LD50 > 2000 mg/kg bw Not classified | https://echa.europa.eu/fr/registration-dossier/-/registered-dossier/26624/7/3/2 |
Minor constituents not contributing to the C&L | / | 0-10 | 0,75 | / | / |
For substances not classified or with an oral LD50 > 2000 mg/kg bw, an ATE estimates of 2001 has been considered according to the CLP Regulation.
For substances with an oral LD50 > 5000 mg/kg bw, an ATE estimates of 5001 has been considered according to the CLP Regulation.
See full study report on attached background material for detailled calculation.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based on existing data on constituents (additivity principles), the registered substance has an oral ATE mixture estimated at 2687 mg/kg bw and should not be classified for acute oral toxicity hazard according to the rules for classification of mixtures of Regulation (EC) No 1272/2008.
- Executive summary:
The NCS is composed of several identified constituents and in that, it can be considered as a mixture according to the definition of the CLP Regulation.
The decision logic for classification of mixtures from the ECHA Guidance on the Application of the CLP Criteria (2017) was used to determine the acute oral toxicity hazard of the registered substance. An oral DL50 or an ATE estimate can be derived based on the current classification for a part of these constituents.Based on existing data on constituents (additivity principles), the ATE of the Essential oil of Litsea cubeba (Lauraceae) obtained from the fruits by distillation, terpenes fraction is the following:
Oral ATE(mix) = 2687 mg/kg bw
As the oral DL50/ATE of the substance is calculated to be higher than 2000 mg/kg bw, therefore, the Essential oil of Litsea cubeba (Lauraceae) obtained from the fruits by distillation, terpenes fraction is not classified for acute oral toxicity.
In conclusion, the decision not to classify the substance was taken on the basis of existing data on constituents (additivity principles): the registered substance has an oral ATE mixture estimated at 2687 mg/kg bw and should not be classified for acute oral toxicity hazard according to the rules for classification of mixtures of Regulation (EC) No 1272/2008.
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.