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EC number: 270-348-8 | CAS number: 68425-34-3
- 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, other
- Remarks:
- in vivo study, since in vitro studies were not available at that time
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 2007-11-26 to 2007-12-06
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restriction because it is a well-documented study report that followed OECD Guideline 405.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Paraffin Wax (CAS # 848301-87-1) (For Petrolatum (Non-carcinogenic Feed-stock))
- IUPAC Name:
- Paraffin Wax (CAS # 848301-87-1) (For Petrolatum (Non-carcinogenic Feed-stock))
- Details on test material:
- Read Across to Paraffin and Hydrocarbon Wax
- Name of test material (as cited in study report): Paraffin waxes (Fischer - Tropsch), full range, C15-50- branched and linear
- Substance type: Paraffin wax and Hydrocarbon Wax
- Physical state: turbid colourless liquid
- Storage condition of test material: room temperature in the dark under nitrogen
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Harlan UK Limited, Oxon, UK
- Age at study initiation: 12 to 20 weeks old
- Weight at study initiation: 2.0 to 3.5 kg
- Housing: individually housed in suspended cages
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17 to 23°C
- Humidity (%): 30 to 70%
- Air changes (per hr): at least 15 air changes pe rhour
- Photoperiod (hrs dark / hrs light): 12 hours light/12 hours dark
IN-LIFE DATES: From: 2007-11-26 to 2007-12-06
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- 0.1 mL
- Duration of treatment / exposure:
- single dose followed by observation period of 72 hours
- Observation period (in vivo):
- 72 hours
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): none
- Time after start of exposure: none
SCORING SYSTEM:
Eyes were scored at 1, 24, 48, and 72 hours using an initial pain reaction scale and then the modified Kay and Calandra system.
Score for conjunctivae = (A + B + C) x 2, maximum score = 20
Score for iris = D x 5, maximum score = 10
Score for cornea = (E x F) x 5, maximum score = 80
where A = redness, B = chemosis, C = discharge, D= iris involvement, E = degree of opacity, F = area of cornea involved
TOOL USED TO ASSESS SCORE: standard ophthalmoscope
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24 to 72 hours
- Score:
- 0
- Max. score:
- 80
- Remarks on result:
- other: Unwashed eyes
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24 to 72 hours
- Score:
- 0
- Max. score:
- 10
- Remarks on result:
- other: Unwashed eyes
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 24 to 72 hours
- Score:
- 2
- Max. score:
- 20
- Reversibility:
- fully reversible within: 24 hours
- Irritant / corrosive response data:
- No corneal or iridial effects were observed. Slight conjunctival irritation was noted in all treated eyes at one and 24 hours after treatment. All eyes appeared normal at the 24-hour observation.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Paraffin wax is considered not irritating. Slight conjunctival irritation was observed at 1 and 24 hours after treatment and fully reversible after the 24 hour timepoint.
- Executive summary:
Read across justification
No eye irritation studies have been reported for petrolatum (non-carcinogenic feed-stock), but data has been reported for paraffin and hydrocarbon waxes, materials similar to petrolatum (non-carcinogenic feed-stock).
In a primary eye irritation study, 0.1 millilitres of paraffin wax was instilled into the conjunctival sac of three male New Zealand White rabbits whose eyes were unwashed. Animals then were observed for 72 hours. Irritation was scored by the method of Draize and a modified Kay and Calandra interpretation of the eye irritation test. Results are presented in the Draize method of scoring.
Slight conjunctival irritation was observed at 1 and 24 hours after treatment and fully reversible after the 24 hour timepoint.In this study, paraffin wax is not an eye irritant based on minimal conjunctival irritation (maximum score of 2 based on redness in each animal) at 24 hours which was fully reversible after the 24 -hour observation.
This study received a Klimisch score of 1 and is classified as reliable without restriction because it closely followed OECD Guideline 405.
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