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EC number: 265-044-7 | CAS number: 64741-44-2 A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of 205°C to 345°C (401°F to 653°F).
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1984-05-10 to 1984-05-24
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable with restrictions because although it was conducted similar to OECD guideline 404 and was GLP compliant, the exposure was 24 hours. The current recommended exposure duration is 4 hours.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1985
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- Skin was not evaluated 24 hours after patch removal because skin was occluded for 24 hours, not the recommended 4 hours.
- GLP compliance:
- yes
Test material
- Reference substance name:
- 64741-44-2
- Cas Number:
- 64741-44-2
- IUPAC Name:
- 64741-44-2
- Reference substance name:
- Straight run middle distillate
- IUPAC Name:
- Straight run middle distillate
- Test material form:
- other: liquid
- Details on test material:
- - Name of test material (as cited in study report): Straight run middle distillate (API 83-11)
- Name of test material (as cited in study report): API 83-11
- Molecular formula (if other than submission substance): Straight run middle distillate
- Clear, light yellow liquid
- CAS number: 64741-44-2
- Gravity API: 36.2
- Sulfur wt %:0.30
- Nitrogen ppm: 80
- Boiling range (ASTM D-86 equiv) 10%: 488 °F
- Initial Boiling Point 366 °F
- End Boiling Point 735 °F
- Viscosity at 40°C cSt: 4.16
- Aniline Point °F: 171
- Composition % by MS:
olefins 2.0
aromatics 21.0
saturates 77.0
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Hazelton Dutchland., Inc., Denver, Pennsylvania
- Age at study initiation: Approximately 16 weeks
- Weight at study initiation: 2.3 kilograms to 2.6 kilograms
- Housing: Individually in screen bottom cages
- Diet (e.g. ad libitum): Ad libitum
- Water (e.g. ad libitum): Ad libitum
- Acclimation period: At least 14 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 to 25
- Humidity (%): 58% to 65%
- Air changes (per hr): Not reported
- Photoperiod (hrs dark / hrs light): 12 hours dark/12 hours light
IN-LIFE DATES: From: 1984-05-10 To: 1984-05-24
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: shaved and shaved/abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 millilitres
- Duration of treatment / exposure:
- 24 hours
- Observation period:
- 14 days
- Number of animals:
- Six
- Details on study design:
- TEST SITE
- Area of exposure: Back and flanks
- % coverage: Not reported
- Type of wrap if used: Gauze overwrapped with Saran Wrap and Elastoplast tape
REMOVAL OF TEST SUBSTANCE
- Washing (if done): Wet disposable paper towels were used to wipe the test compound away from the area as much as possible, post exposure, without causing irritation.
- Time after start of exposure: 24 hours
SCORING SYSTEM: Draize
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Remarks on result:
- other: intact skin
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 48 h
- Remarks on result:
- not measured/tested
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 72 h
- Score:
- 1.7
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Remarks on result:
- other: intact skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24 h
- Score:
- 2.2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Remarks on result:
- other: intact skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 48 h
- Remarks on result:
- not measured/tested
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Remarks on result:
- other: intact skin
- Irritant / corrosive response data:
- Individual Dermal Irritation Scores
Erythmea Oedema
Intact Abraded Intact Abraded
24 hours 2, 1, 2, 2, 3, 2 2, 1, 2, 2, 3, 1 2, 1, 2, 2, 3, 2 2, 1, 2, 2, 3, 1
72 hours 2, 1, 2, 2, 2, 1 2, 1, 2, 1, 2, 1 1, 1, 1, 1, 1, 1 1, 1, 1, 0, 1, 0
96 hours 2, 1, 1, 1, 2, 1 1, 1, 1, 1, 1, 1 1, 1, 0, 0, 1, 0 1, 1, 0, 0, 1, 0
7 days 0, 1, 0, 1, 1, 1 0, 1, 0, 0, 1, 0 0, 0, 0, 0, 1, 0 1, 1, 0, 0, 1, 0
14 days 0, 0, 0, 0, 0, 0 0, 0, 0, 0, 0, 0 0, 0, 0, 0, 0, 0 0, 0, 0, 0, 0, 0 - Other effects:
- No other effects were noted.
Any other information on results incl. tables
Slight to moderate erythema and oedema were present at 24 hours (negligible difference in response between intact and abraded sites) and gradually resolved over 96 hours with barely perceptible reactions remaining at 7 days. Mean primary dermal irritation scores (that is, the sum of the irritation score for each site divided by the number of animals at each observation period) are presented below:
Time |
Erythema |
Oedema |
24 hours |
2.0-1.8 |
2.2-2.0 |
72 hours |
1.7-1.5 |
1.0-0.7 |
96 hours |
1.3-1.0 |
0.5 |
7 days |
0.7-0.3 |
0.2-0.5 |
14 days |
0-0 |
0-0 |
The primary dermal irritation index (representing the sum of 24 and 72 hour primary dermal irritation scores for intact and abraded skin, 8 values, divided by 4) was 3.2. Based on the severity of skin reactions present up to 72 hr, straight run middle distillate is condered moderately irritating to rabbit skin following 24 -hour occluded contact.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Exposure period was 24 hours not the recommended 4 hours Criteria used for interpretation of results: EU
- Conclusions:
- Based on the severity of skin reactions present up to 72 hr, straight run middle distillate is not irritating to rabbit skin following 24 hour occluded contact according to the study author.
- Executive summary:
A straight run middle distillate was tested for primary dermal irritancy in New Zealand White rabbits. The sample (0.5 mL) was applied to intact and abraded clipped skin on the back and flank of 6 rabbits, under occlusion for 24 hours. Dermal irritation was scored according to the method of Draize at 24, 72 and 96 hours, and 7 and 14 days after application of the test material. Slight to moderate erythema and oedema were present at 24 hours (negligible difference in response between intact and abraded sites) and gradually resolved over 96 hours with barely perceptible reactions remaining at 7 days. Mean primary dermal irritation scores (that is, the sum of the irritation score for each site divided by the number of animals at each observation period).
The primary dermal irritation index (representing the sum of 24 and 72 hour primary dermal irritation scores for intact and abraded skin (8 values) divided by 4) was 3.2. For intact skin, the mean erythema and oedema scores over 24 to 72 hours were 1.80 and 1.58, respectively. Although the test material is not classified under EU criteria because the exposure duration is 24 hours and not the recommended 4 hours, it appears to be not irritating based on the mean erythema and oedema scores. Additionally, since the exposure period was 24 hours, mean erythema and oedema scores are considered conservative.
This study received a Klimisch score of 2 and is classified as reliable with restrictions because although it was conducted similar to OECD guideline 404 and was GLP compliant, the exposure was 24 hours. The current recommended exposure duration is 4 hours.
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