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EC number: 933-779-9 | 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
Endpoint summary
Administrative data
Description of key information
Acute Oral LD50 (Rat) > 2000 mg/kg bw (OECD 423)
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2018-07-10 to 2018-07-25
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
- Version / remarks:
- 17 December 2001
- Deviations:
- yes
- Remarks:
- Deviations have no presumed impact on the outcome or integrity of the study.
- GLP compliance:
- yes (incl. QA statement)
- Test type:
- acute toxic class method
- Limit test:
- yes
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: Emerald Kalama Chemical Ltd. (United Kingdom); Lot No. A170524D
- Expiration date of the lot/batch: 2019-06-06
- Purity test date: 2018-02-07
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature (15-25oC, ≤70 RH%), under inert gas, protected from humidity (tight closed container)
- Stability under test conditions: Not specified
- Solubility and stability of the test substance in the solvent/vehicle: Not specified
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: The test item was freshly formulated at a concentration of 200 mg/mL in the vehicle, in the Pharmacy of Citoxlab Hungary Ltd. on the day of administration. The formulation container was stirred continuously up to finishing the treatment.
FORM AS APPLIED IN THE TEST (if different from that of starting material) : Colorless liquid - Species:
- rat
- Strain:
- Wistar
- Remarks:
- CRL:(WI)
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories, Research Models and Services (Germany GmbH, Sandhofer Weg 7, D-97633 Sulzfeld)
- Females (if applicable) nulliparous and non-pregnant: yes
- Age at study initiation: Young healthy adult rats, 8 weeks old
- Weight at study initiation: 175 – 197 g
- Fasting period before study: On the night before treatment, the animals were fasted. The food but not water was withheld during an overnight period.
- Housing: 3 animals / cage (Type II polypropylene/polycarbonate)
- Diet (e.g. ad libitum): ssniff®SM R/M "Autoclavable complete diet for rats and mice – breeding and maintenance" (ssniff Spezialdiäten GmbH, D-59494 Soest, Germany (Batch no.: 883 29966, expiry date: 31 October 2018)) ad libitum
- Water (e.g. ad libitum): tap water from the municipal supply, as for human consumption from 500 ml bottles, ad libitum.
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20.6 – 24.7°C
- Humidity (%): 33 – 80%
- Air changes (per hr): 15 – 20 air exchanges/hour
- Photoperiod (hrs dark / hrs light): 12 hours daily, from 6.00 am to 6.00 pm
IN-LIFE DATES: From: 2018-07-05 To: 2018-07-25 - Route of administration:
- oral: gavage
- Vehicle:
- propylene glycol
- Remarks:
- Propylene glycol with 1% polysorbate 80
- Details on oral exposure:
- VEHICLE
- Concentration in vehicle: 200 mg/mL
- Amount of vehicle (if gavage): 10 mL/kg bw
- Justification for choice of vehicle:The selection of the vehicle was made during trial formulations with the test material. On the basis of the trial formulations with the test material, and considering the use of the vehicle in the ensuing repeated dose studies, the vehicle used was propylene glycol with 1% polysorbate 80.
- Lot/batch no. (if required): a) Propylene glycol (1,2-Propanediol), Batch no: K49089078; b) Polysorbate 80, Batch no: BCBV5152
- Purity: Not specified
MAXIMUM DOSE VOLUME APPLIED: 10 mL/kg bw
DOSAGE PREPARATION: The test material was freshly formulated at a concentration of 200 mg/mL in the vehicle, in the Pharmacy of Citoxlab Hungary Ltd. on the day of administration. The formulation container was stirred continuously up to finishing the treatment.
CLASS METHOD (if applicable)
- Rationale for the selection of the starting dose: Initially, three females (assigned to Group 1) were treated at a dose level of 2000 mg/kg body weight (bw). The test material did not cause mortality in this group therefore a confirmatory group (Group 2) was treated at the same dose level. The test material did not cause mortality in the confirmatory group, so no further testing was required according to OECD 423 and Commission Regulation (EC) No 440/2008 of 30 May 2008, B.1.tris. - Doses:
- Single oral gavage dose of 2000 mg/Kg bw
- No. of animals per sex per dose:
- 6
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Clinical observations were performed at 30 minutes, 1, 2, 3, 4 and 6 hours after dosing and daily for 14 days thereafter. Body weight was measured on Days -1, 0 and 7 and Day 14.
- Necropsy of survivors performed: yes, All animals were subjected to a necropsy and a macroscopic examination.
- Other examinations performed: clinical signs (Individual observations were performed on the skin, fur, eyes, mucous membranes, respiratory, circulatory, autonomic and central nervous system, somatomotor activity and behaviour pattern. Particular attention was directed to observation of tremors, convulsions, salivation, diarrhoea, lethargy, sleep and coma.), body weight - Statistics:
- The method used was not intended to allow the calculation of a precise LD50 value.
The test material was ranked into categories of Globally Harmonized Classification System (GHS (rev. 7) 2017).
Clinical signs, body weight, body weight gain and gross macroscopic data were tabulated. - Preliminary study:
- Initially, three females (assigned to Group 1) were treated at a dose level of 2000 mg/kg body weight (bw). The test material did not cause mortality in this group therefore
a confirmatory group (Group 2) was treated at the same dose level. - Key result
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- The test material did not cause mortality at the dose level of 2000 mg/Kg bw.
- Clinical signs:
- other: No clinical signs of toxicity were observed susbsequent to oral exposure to the test material at 2000 mg/Kg bw.
- Gross pathology:
- Focal thickness of the non-glandular stomach mucosa was observed in 3 out of 6 animalsexposed to 2000 mg/Kg bw of the test material.
- Interpretation of results:
- Category 5 based on GHS criteria
- Conclusions:
- Under the conditions of this study, the acute oral LD50 value for the test material was determined to be >2000 mg/Kg bw in female Crl:WI rats.
According to the GHS criteria, the test material (Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene]) can be ranked as "Category 5" or “Unclassified” for acute
oral exposure. - Executive summary:
In a key study, the single-dose oral toxicity of the test material (Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene) was evaluated in Crl:WI rats according to the acute toxic class method (OECD Guideline 423).
Initially, three females (assigned to Group 1) were treated at a dose level of 2000 mg/Kg bw. The test material did not cause mortality in this group, therefore a confirmatory group (Group 2) was treated at the same dose level. The test material did not cause mortality in the confirmatory group, so no further testing was required as per Guideline recommendations.
A single oral treatment was carried out by gavage for each animal after an overnight food withdrawal. Food was made available again 3 hours after the treatment. The test material was administered formulated in propylene glycol with 1% polysorbate 80 at a concentration of 200 mg/mL at a dose volume of 10 mL/kg bw.
Clinical observations were performed at 30 minutes, 1, 2, 3, 4 and 6 hours after dosing anddaily for 14 days thereafter. Body weight was measured on Days -1, 0 and 7 and Day 14. All animals were subjected to a necropsy and a macroscopic examination.
No mortality was observed through the study period and there was no evidence of clinical toxicity subsequent to treatment at 2000 mg/Kg bw. Normal body weight gain was observed in the observation period. However, one animal exhibited slight body weight loss between Day 7 and Day 14. As normal body weight changes were observed from Day 0 up to Day 7, and no other animal showed a similar trend between Day 7 up to Day 14, this change was considered incidental and minimal and not treatment-related.Focal thickness of the non-glandular stomach mucosa was observed in 3 out of 6 animals exposed to the test material.
Under the conditions of this study, the acute oral LD50value for the test material was determined to be >2000 mg/Kg bw in female Crl:WI rats.
According to the GHS criteria, the test material (Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene]) can be ranked as "Category 5" or “Unclassified” for acute oral exposure.
Reference
Table 1. Clinical Observations |
||||||||||||||||
Cage No. |
Animal Number |
Observations |
Observation days |
Frequency |
||||||||||||
0 |
1 |
2 |
3 |
2 |
5 |
6 |
7-14 |
|||||||||
30’ |
1h |
2h |
3h |
4h |
6h |
|||||||||||
1 |
4174 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
4175 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
|
4176 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
|
2 |
4177 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
4178 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
|
4179 |
Symptom Free |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
20/20 |
+ = present
' = minute
h = hour (s)
Frequency of observation = number of occurrence of observation / total number of observations
Table 2. Body Weight Data |
|||||||||
Cage No. |
Animal Number |
Body weight (g) Days |
Body Weight Gain (g) |
||||||
-1 |
0 |
7 |
14 |
-1-0 |
0-7 |
7-14 |
-1-14 |
||
1 |
4174 |
205 |
197 |
228 |
248 |
-8 |
31 |
20 |
43 |
4175 |
201 |
186 |
225 |
236 |
-15 |
39 |
11 |
35 |
|
4176 |
202 |
187 |
223 |
229 |
-15 |
36 |
6 |
27 |
|
2 |
4177 |
199 |
190 |
229 |
249 |
-9 |
39 |
20 |
50 |
4178 |
186 |
175 |
212 |
207 |
-11 |
37 |
-5 |
21 |
|
4179 |
194 |
185 |
200 |
228 |
-9 |
15 |
28 |
34 |
|
Mean |
197.8 |
186.7 |
219.5 |
232.8 |
-11.2 |
32.8 |
13.3 |
35.0 |
|
Standard Deviation |
6.9 |
7.2 |
11.3 |
15.5 |
3.1 |
9.2 |
11.8 |
10.5 |
Table 3. Necropsy Findings |
|||||
Cage No. |
Animal Number |
Necropsy Date/ Necropsy Day |
External Observations |
Internal Observations |
Organ/Tissue |
1 |
4174 |
24 July 2018 Day 14 |
No external observations recorded |
No internal observations recorded |
Not Applicable |
4175 |
24 July 2018 Day 14 |
No external observations recorded |
No internal observations recorded |
Not Applicable |
|
4176 |
24 July 2018 Day 14 |
No external observations recorded |
No internal observations recorded |
Not Applicable |
|
2 |
4177 |
25 July 2018 Day 14 |
No external observations recorded |
Thickness, focal, non-glandular mucosa |
Stomach |
4178 |
25 July 2018 Day 14 |
No external observations recorded |
Thickness, focal, non-glandular mucosa |
Stomach |
|
4179 |
25 July 2018 Day 14 |
No external observations recorded |
Thickness, focal, non-glandular mucosa |
Stomach |
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- > 2 000 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Acute Oral Toxicity
In a key OECD Guideline 423 study, the single-dose oral toxicity of the test material (Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene) was evaluated in Crl:WI rats according to the acute toxic class method.
Initially, three females (assigned to Group 1) were treated at a dose level of 2000 mg/Kg bw. The test material did not cause mortality in this group, therefore a confirmatory group (Group 2) was treated at the same dose level. The test material did not cause mortality in the confirmatory group, so no further testing was required as per Guideline recommendations.
A single oral treatment was carried out by gavage for each animal after an overnight food withdrawal. Food was made available again 3 hours after the treatment. The test material was administered formulated in propylene glycol with 1% polysorbate 80 at a concentration of 200 mg/mL at a dose volume of 10 mL/kg bw.
Clinical observations were performed at 30 minutes, 1, 2, 3, 4 and 6 hours after dosing and daily for 14 days thereafter. Body weight was measured on Days -1, 0 and 7 and Day 14. All animals were subjected to a necropsy and a macroscopic examination.
No mortality was observed through the study period and there was no evidence of clinical toxicity subsequent to treatment at 2000 mg/Kg bw. Normal body weight gain was observed in the observation period. However, one animal exhibited slight body weight loss between Day 7 and Day 14. As normal body weight changes were observed from Day 0 up to Day 7, and no other animal showed a similar trend between Day 7 up to Day 14, this change was considered incidental and minimal and not treatment-related.Focal thickness of the non-glandular stomach mucosa was observed in 3 out of 6 animals exposed to the test material.
Under the conditions of this study, the acute oral LD50 value for the test material was determined to be >2000 mg/Kg bw in female Crl:WI rats.
According to the GHS criteria, the test material (Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene]) can be ranked as "Category 5" or “Unclassified” for acute oral exposure.
Justification for classification or non-classification
Reaction mass of dipentene and (Z)-3,7-dimethylocta-1,3,6,-triene does not meet the criteria to be classified for acute oral toxicity under EU Regulation (EC) No 1272/2008 (CLP). However, according to the GHS criteria, based on an oral LD50 of >2000 mg/kg bw, the test material can be classified as "Category 5" or “Unclassified” for acute oral exposure.
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