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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 942-445-1 | 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 28 September 1998 to 02 October 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: OECD guideline N°405, GLP but substance analytical certificate not available (Substance identification: code name with information on test substance).
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:
- 1 998
- Report date:
- 1998
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- age of animals at study initiation was not reported
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- age of animals at study initiation was not reported
- Principles of method if other than guideline:
- Guideline study
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Hydrocarbons, C14-C18, n-alkanes, isoalkanes, cyclics, <2% aromatics
- IUPAC Name:
- Hydrocarbons, C14-C18, n-alkanes, isoalkanes, cyclics, <2% aromatics
- Reference substance name:
- DEV 98-25
- IUPAC Name:
- DEV 98-25
- Details on test material:
- - Name of test material (as cited in study report): DV 98-25
- Substance type: Petroleum product, UVCB
- Physical state: Bright and clear colourless liquid
- Analytical purity: 100% Commercial product
- Composition of test material, percentage of components: Hydrocarbons , C I 4-C 18, n-alkanes, isoalkanes, cyclics, < 2% aromatics
- Storage condition of test material: the test article kept at room temperature in the dark.
- Reception date of the test article: 09 September 1998
Constituent 1
Constituent 2
Test animals / tissue source
- Species:
- rabbit
- Strain:
- other: SPF albino rabbits of the stock Mol:Russian
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: M & B, Ejby, DK-4623 Lille Skensved, Denmark
- Age at study initiation: no data
- Weight at study initiation: 2.3 - 2.8 kg
- Housing: kept individually in PPO/HIPS cages (Noryl, floor area = 2576 cm²)
- Diet: pelleted complete rabbit diet "Altromin 2123" from Ch. Petersen ad libitum. Analysis for major nutritive components and relevant possible contaminations in the diet are performed regularly.
- Water: domestic quality drinking water acidified with hydrochloric acid to pH 2.5 ad libitum. Analyses for relevant possible contamination in the water are performed regularly.
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C +/- 3°C
- Humidity (%): 55% +/- 15%
- Air changes (per hr): 10
- Photoperiod :12 hrs dark /12 hrs light
IN-LIFE DATES: From: To:
Test system
- Vehicle:
- not specified
- Controls:
- other: the right eye of the treated animals was used as control
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied: 0.1 mL - Duration of treatment / exposure:
- 24 hours
- Observation period (in vivo):
- 1, 24, 48, 72 hours after application
- Number of animals or in vitro replicates:
- 3 females
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): with 20 mL 0.9% sodium chloride solution
- Time after start of exposure: 24 hrs
SCORING SYSTEM: grading according to OECD 405 recommendation
TOOL USED TO ASSESS SCORE: fluorescein, UV light
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- other: mean individual score for all animals
- Time point:
- other: 24h, 48h, 72h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: not applicable
- Remarks on result:
- other: See Table 1 for details
- Irritation parameter:
- iris score
- Basis:
- other: mean individual score for all animals
- Time point:
- other: 24h, 48h, 72h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- other: not applicable
- Remarks on result:
- other: See Table 1 for details
- Irritation parameter:
- chemosis score
- Basis:
- other: mean individual score for all animals
- Time point:
- other: 24h, 48h, 72h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- other: not applicable
- Remarks on result:
- other: See Table 1 for details
- Irritation parameter:
- conjunctivae score
- Basis:
- animal: #1 and #3 - Mean individual score
- Time point:
- other: 24h, 48h, 72h
- Score:
- 0
- Max. score:
- 3
- Reversibility:
- other: not applicable
- Remarks on result:
- other: See Table 1 for details
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Remarks:
- mean individual score
- Time point:
- other: 24h, 48h, 72h
- Score:
- 0.7
- Max. score:
- 3
- Reversibility:
- other: not applicable
- Remarks on result:
- other: See Table 1 for details
- Irritant / corrosive response data:
- Irritant effects on conjunctiva (redness) were minimal at 1 hour in all animals and were fully reversed at 72h in all animals. There were no effects on the cornea and the iris at any time point. Chemosis was not observed at any time point in all animals.
It can be concluded that DV 98-25 would not be classified as eye irritant. - Other effects:
- No data
Any other information on results incl. tables
Table 1: DV 98 -25 Acute eye irritation/corrosion study in the rabbit. Scores for ocular lesions.
Rabbit No / |
1 h |
24 hrs |
|
48 hrs |
72 hrs |
Individual mean score* |
||
weight (kg) |
F |
|||||||
3531 / 2.3 |
Cornea opacity, area |
0 |
0 |
0 |
0 |
0 |
|
|
Cornea opacity, degree |
0 |
0 |
0 |
0 |
0 |
0.0 |
||
Iris |
0 |
0 |
|
0 |
0 |
0.0 |
||
Conjunctiva |
Chemosis |
0 |
0 |
|
0 |
0 |
0.0 |
|
Redness |
1 |
0 |
|
0 |
0 |
0.0 |
||
Discharge |
3 |
0 |
|
0 |
0 |
|||
|
||||||||
3533 / 2.3 |
Cornea opacity, area |
0 |
0 |
0 |
0 |
0 |
|
|
Cornea opacity, degree |
0 |
0 |
0 |
0 |
0 |
0.0 |
||
Iris |
0 |
0 |
|
0 |
0 |
0.0 |
||
Conjunctiva |
Chemosis |
0 |
0 |
|
0 |
0 |
0.0 |
|
Redness |
1 |
1 |
|
1 |
0 |
0.7 |
||
Discharge |
3 |
0 |
|
0 |
0 |
|||
|
||||||||
3534 / 2.8 |
Cornea opacity, area |
0 |
0 |
0 |
0 |
0 |
|
|
Cornea opacity, degree |
0 |
0 |
0 |
0 |
0 |
0.0 |
||
Iris |
0 |
0 |
|
0 |
0 |
0.0 |
||
Conjunctiva |
Chemosis |
0 |
0 |
|
0 |
0 |
0.0 |
|
Redness |
1 |
0 |
|
0 |
0 |
0.0 |
||
Discharge |
3 |
0 |
|
0 |
0 |
0.0 |
F: Reading after instillation of oculoguttae fluoresceini.
* Only the scores from the 3 readings (24, 48 and 72 hours) are included in the calculation of the individual mean scores
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- under the test conditions, DV 98-25 is not classified as eye irritant according to the criteria of Annex VI of the Directive 67/548/EEC and the CLP Regulation 1272/2008.
- Executive summary:
The eye irritant effect of DV 98-25 was investigated according to the OECD Guideline No. 405 (1987) and EEC B.5 method (1992) and in compliance with Good Laboratory Practice.
Three female albino rabbits were exposed to 0.1 mL of the test article in the left eye. The eyes were examined and the changes were graded according to a numerical scale 1, 24, 48 and 72 hours after dosing.
Minimal conjunctival irritation (redness) was observed in the three rabbits 1 hour after dosing. During the rest of the observation period no abnormalities were observed for two animals while redness (score 1) was still observed up to 48 h in the third animal.
DV 98 -25 is not considered as irritating to the eyes according to Annex VI of the Directive 67/548/EEC and CLP Regulation 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.