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Diss Factsheets
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EC number: 295-374-7 | CAS number: 92044-94-5
- 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
Sensitisation data (human)
Administrative data
- Endpoint:
- sensitisation data (humans)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in accordance with generally accepted scientific principles, possibly with incomplete reporting or methodological deficiencies, which do not affect the quality of the relevant results. The information does not come from a test report, and the minimum fields required cannot be filled in.
Data source
Reference
- Reference Type:
- publication
- Title:
- Reproducibility of patch test results: a concurrent right-versus-left study using TRUE Test™
- Author:
- Ale IS & Maibach IH
- Year:
- 2 004
- Bibliographic source:
- Contact Dermatitis, 2004, 50, 304-312
Materials and methods
- Type of sensitisation studied:
- skin
- Study type:
- study with volunteers
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- This study is not focused on skin sensitization potential of Lanolin but rather a study of patch test reproducibility where Lanolin alcohol was included in the panel of substances tested. The reproducibility of the TRUE Test™ was tested in 500 volunteers (58% women, 42% men, mean age 42.4 years) with suspected contact dermatitis (based on history and clinical examination) but with no active dermatitis. Each volunteer was administered a TRUE Test™ panel (strips) on the left and right side of the upper back. After 48 hours the panels were removed and the reaction was assessed. The test area was read after 96 hours in the majority of volunteers.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Lanolin Alcohols
- IUPAC Name:
- Lanolin Alcohols
Constituent 1
Method
- Type of population:
- other: Volunteers (58% women, 42% men, mean age 42.4 years) with suspected contact dermatitis (based on history and clinical examination) but with no active dermatitis.
- Ethical approval:
- other: The study was approved by the Ethics Committee of the University Hospital, Montevideo, Uruguay.
- Subjects:
- - Number of subjects exposed: 500
- Sex: 58% women & 42% men
- Age: mean age 42.4 years
- Race: Not reported
- Demographic information: Uruguay
- Other:
Criteria for inclusion in the study were:
-Contact dermatitis suspected from history and clinical examination
-Over 15 years old
-No active dermatitis (except from mild localized dermatitis)
-No active dermatitis of any degree on or around the test area
-No systemic corticosteroid or immunosuppressive treatment during the previous 30 days
-No topical treatment with corticosteroids during the previous 15 days on or around the test area
-Not pregnant (by history) - Clinical history:
- - History of allergy or casuistics for study subject or populations:
Deatils of present dermatitis
- Exposure history: Occupational and non-occupational exposures, including hobbies, topical and systemic therapies, personal skin care, etc.
- Family history: personal & family atopy
- Medical history (for respiratory hypersensitivity): histiry of previous dermatitis - Controls:
- Not reported
- Route of administration:
- dermal
- Details on study design:
- TYPE OF TEST(S) USED: patch test (epicutaneous test)
ADMINISTRATION
- Type of application: occlusive
- Description of patch: TRUE Test™ panel (strips)
- Testing/scoring schedule:
The test area was read after 96 hours in the majority of volunteers.
- Removal of test substance:
After 48 hours the panels were removed and the reaction was assessed
EXAMINATIONS
- Statistical analysis: The X2 -test and the two-sided Student's t-test were used for statistical comparisons between different subgroups of patients. A P-value of 0.05 or less was considered to indicate statistical significance.
- Other:
Results and discussion
- Results of examinations:
- Lanolin alcohol was positive concordant (reaction observed on both application areas) in 7 volunteers and positive discordant (reaction observed in only one application area) in 3 volunteers.
Applicant's summary and conclusion
- Conclusions:
- There was a relatively large degree of discordant observations with Lanolin alcohols
- Executive summary:
This study is not focused on skin sensitization potential of Lanolin but rather a study of patch test reproducibility where Lanolin alcohol was included in the panel of substances tested. The reproducibility of theTRUE Test™was tested in 500 volunteers (58% women, 42% men, mean age 42.4 years) with suspected contact dermatitis (based on history and clinical examination) but with no active dermatitis. Each volunteer was administered a TRUE Test™ panel (strips) on the left and right side of the upper back. After 48 hours the panels were removed and the reaction was assessed. The test area was read after 96 hours in the majority of volunteers. Lanolin alcohol was positive concordant (reaction observed on both application areas) in 7 volunteers and positive discordant (reaction observed in only one application area) in 3 volunteers.
There was a relatively large degree of discordant observations with Lanolin alcohols
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