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EC number: 210-036-0 | CAS number: 603-35-0
- 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
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: screening test: discrepancy between documented test parameters and standard methods, but scientifically acceptable
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 971
- Report date:
- 1971
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- - detection of skin irritation according to BASF-internal standards
- Principle of test: The test substance was applied to the back (A) or ear skin (B) of rabbits. Signs of local irritation and intoxication were recorded 24 hours and 8 days after application.
A) Back skin: The test substance was administered as a 2.5 x 2.5 cm patch loaded with a 50% alcoholic suspension (quanitity not specified) to the shaved skin of 2 rabbits for defined time intervals of either 1 min, 5 min, 15 min or 20 h. After the short exposure times of 1 - 15 min the skin was washed, no washing was conducted after the 20 hour exposure.
B) Ear: Cotton-wool soaked with approx. 2 g of the 50% alcoholic suspension (equivalent to 1g test substance) were applied to the pinna and held in place gauze bandages for 20 h. - GLP compliance:
- no
Test material
- Reference substance name:
- Triphenylphosphine
- EC Number:
- 210-036-0
- EC Name:
- Triphenylphosphine
- Cas Number:
- 603-35-0
- Molecular formula:
- C18H15P
- IUPAC Name:
- triphenylphosphine
- Test material form:
- solid: crystalline
Constituent 1
- Specific details on test material used for the study:
- - Purity: 99%.
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: preparation of a 50% alcoholic suspension
FORM AS APPLIED IN THE TEST (if different from that of starting material): suspension
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: purchased freely.
- Weight at study initiation: 3.1 kg.
- Diet: ad libitum.
- Water: ad libitum.
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- other: alcoholic suspension
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): not specified for apllication on back skin; 2g 50% alcoholic preparation on rabbit ear. - Duration of treatment / exposure:
- A) Back skin: 1 min, 5 min, 15 min or 20 hours
B) Ear: 20 hours - Observation period:
- 8 days
- Number of animals:
- 2
- Details on study design:
- A) Back Skin:
TEST SITE
- Area of exposure: 2.5 x 2.5 cm.
- Type of wrap if used: patch loaded with the suspension.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): Skin was washed with undiluted Lutrol and 50% Lutrol/Water solution.
- Time after start of exposure: Washing conducted after 1, 5, 15 min exposure but not after 20 h exposure.
OBSERVATION TIME POINTS
(indicate if minutes, hours or days): Text indicates readings 0, 1, 2, and 7 days after removal, however, results are given for 1 and 8 days.
SCORING SYSTEM:
- Method of calculation: grading system for reddening and edema (no effect, slight, marked).
---------------------------------------------------------
A) Ear:
TEST SITE
- Area of exposure: soaked Cotton-wool (no further details).
- Type of wrap if used: gauze bandages to hold cotton wool in place.
OBSERVATION TIME POINTS
(indicate if minutes, hours or days): Text indicates readings 0, 1, 2, and 7 days after removal, however, results are given for 1 and 8 days.
SCORING SYSTEM:
- Method of calculation: grading system for reddening and edema (no effect, slight, marked).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Remarks:
- Back skin
- Basis:
- other: 1 of 2 animals
- Time point:
- 24 h
- Score:
- 2
- Reversibility:
- fully reversible within: 8 days
- Remarks on result:
- other:
- Remarks:
- slight reddening (R+)
- Irritation parameter:
- erythema score
- Remarks:
- Ear
- Basis:
- other: 1 of 2 animals
- Time point:
- 24 h
- Score:
- 2
- Reversibility:
- fully reversible within: 8 days
- Remarks on result:
- other:
- Remarks:
- slight reddening (R+)
- Irritant / corrosive response data:
- A) Back skin: After exposures of up to 15 min, no skin reactions were observed. 20-h exposure caused slight reddening at the application site in 1/2 animals 24 h after removal of the patch, which was fully reversible within 8 days.
B) Ear: 20-h exposure caused slight reddening at the application site in 1/2 animals 24 h after removal of the bandage, which was fully reversible within 8 days. - Other effects:
- No systemic clinical effects were observed.
Any other information on results incl. tables
Table 1: Local irritation
Application |
Application |
Number and Sex |
findings |
|
after 24 hours |
after 8 days |
|||
Back Skin |
1 min |
1 female |
- |
- |
5 min |
1 female |
- |
- |
|
15 min |
1 female |
- |
- |
|
20 h |
1 female |
- |
- |
|
Ear |
20 h |
1 female |
- |
- |
R+ = slight reddening
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- A 20-hour application of an 50% alcoholic TS prepration induced a slight reddening of the back skin and ears of 1/2 rabbits, which was fully reversible within 8 days. Therefore, the TS is considered to be not irritating.
- Executive summary:
The irritation/corrosion potential of the test substance was tested according to BASF-internal standards.
A 50% alcoholic preparation of the test substance was applied occluded to the back (1 min, 5 min, 15 min and 20 hours) and ear skin (20 hours) of two rabbits. Signs of local irritation and intoxication were recorded 24 hours and 8 days after application.
A exposure of rabbit back skin for up to 15 min produced no evidence of skin irritation. A 20-hour application induced a slight reddening of the back and ear skin of 1/2 rabbits (male), which was fully reversible within 8 days.
Therefore, the test substance is considered to be not irritating.
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