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Diss Factsheets
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EC number: 201-550-6 | CAS number: 84-66-2
- 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:
- 1978
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Well conducted study performed in accordance with recognised test methods
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: FHSA
- Principles of method if other than guideline:
- Method used was Draize as described in "Appraisal of the safety of chemicals in food, drugs and cosmetics" as published by the Association of Food and Drug Officials of the United States.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Diethyl phthalate
- EC Number:
- 201-550-6
- EC Name:
- Diethyl phthalate
- Cas Number:
- 84-66-2
- Molecular formula:
- C12H14O4
- IUPAC Name:
- .
- Details on test material:
- - Name of test material (as cited in study report): Diethyl phthalate
- Analytical purity: 100%
- Lot/batch No.: ARG-01-3379
- Storage condition of test material: Not reported
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- not specified
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Not reported
- Age at study initiation:
- Weight at study initiation:
- Housing: Not reported
- Diet (e.g. ad libitum): Not reported
- Water (e.g. ad libitum): Not reported
- Acclimation period: Not reported
ENVIRONMENTAL CONDITIONS
- Temperature (°C): Not reported
- Humidity (%): Not reported
- Air changes (per hr): Not reported
- Photoperiod (hrs dark / hrs light): Not reported
IN-LIFE DATES: From: To: Not reported
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: Shaved and abraded sites on each rabbit
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.5 ml of DEP as supplied was applied to a 2X2 cm area of shaved and intact or abraded skin.
- Duration of treatment / exposure:
- The exposure period was 24 hours.
- Observation period:
- The observation period was 72 hours with evaluations of skin reaction performed at the end of the 24h contact period and again 48 hours later (72 h after application).
- Number of animals:
- 3
- Details on study design:
- Three healthy, normal, albino rabbits were used. On the day before the study began 10% of the total body surface was carefully clipped free of hair. On the posterior of the clipped area several minor abraisions were made so as to penetrate the stratum corneum but not disturb the derma in order to prevent bleeding.
0.5 ml of DEP was applied to the unscarified area and an additional 0.5 ml was applied to the scarified area. Each 2X2 cm application area was covered with Webril patches and the entire experimental area sealed with Blenderm surgical tape.
The animals were imobilised in racks for 24 hours. At the end of this contact period and 48 hours later the treated skin was evaluated using the Draize method, as described in "Appraisal of the safety of chemicals in food, drugs and cosmetics" as published by the Association of Food and Drug Officials of the United States.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
- Remarks on result:
- other: No response on intact or abraded skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: Not applicable
- Remarks on result:
- other: No response on intact or abraded skin
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: Not applicable
- Remarks on result:
- other: No response on intact or abraded skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: Not applicable
- Remarks on result:
- other: No response on intact or abraded skin
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24 - 72 hours
- Score:
- 0
- Max. score:
- 0
- Irritant / corrosive response data:
- No evidence of irritation or corrosive effects. Score of 0 throughout for all 3 rabbits
- Other effects:
- None reported
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- In this study when DEP was applied as solution to the intact or abraded skin of the rabbit for 24 hours under occlusive conditions. No reaction was observed on either type of skin.
- Executive summary:
Primary skin irritation has been investigated according to FHSA test methods with 24 hours exposure to intact and abraded skin. The substance was not irritating to the skin of the albino rabbit.
Exposure was for a 24 hour period in contrast with 4 hours required by current OECD/EU test methods. However, the information obtained clearly demonstrate the substance to be not irritating and classification as a skin irritant would not be required under the EU/GHS classification scheme.
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