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EC number: 284-895-5 | CAS number: 84989-06-0 The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
- 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Remarks:
- Summary of available data used for the endpoint assessment of the target substance
- Adequacy of study:
- key study
- Justification for type of information:
- refer to analogue justification provided in IUCLID section 13
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: no information about strain used, no information on GLP, duration time not stated
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- 5 rabbits/dose, 4 doses, exposure time not mentioned, up to 14 day observation time, gross autopsy
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- no further data
- Vehicle:
- other: none
- Details on dermal exposure:
- no further data
- Duration of exposure:
- no data
- Doses:
- 215, 316, 464, 681 mg/kg bw
- No. of animals per sex per dose:
- 5 rabbits per dose
- Control animals:
- no
- Details on study design:
- no further data
- Statistics:
- yes, but method not mentioned
- Key result
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- ca. 301 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 213 - <= 426
- Mortality:
- 215 mg/kg bw: 1/5; 316 mg/kg bw: 3/5; 464 mg/Kg bw: 4/5; 681 mg/kg bw: 5/5
- Clinical signs:
- other: signs of intoxication from 4 - 12 hrs post appl.: tremor, salivation sedation, recovery occurred within 3 days post application
- Gross pathology:
- gross autopsy: survivors: no significant findings; decedents: inflammation of kidneys
- Other findings:
- dermal irritation: severe subdermal hemorrhaging, severe erythema
- Interpretation of results:
- other: CLP/EU GHS Category 3 (H311) according to Regulation (EC) No 1272/2008
- Conclusions:
- CLP: Acute tox 3, H 311
- Executive summary:
To determine LD-50 value, rabbits received dermal application of 215 - 681 mg/kg bw undiluted p-cresol and were observed for sclinical signs of toxicity and mortality for up to 14 days: LD50 was determined to be 301 mg/kg bw. As signs of intoxication tremor, salivation, sedation were noted; the treated skin showed severe erythema and severe subdermal hemorrhaging.
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: no information about strain used, statistical evaluation not given, no guideline followed
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- 5 rabbits/dose, 4 doses, exposure time not mentioned, up to 14 days post exposure observation time
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Limit test:
- no
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 2.29 - 2.67 kg - Type of coverage:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Details on dermal exposure:
- no further data
- Duration of exposure:
- no data
- Doses:
- 1000, 1470, 2150, 3160 mg/kg bw
- No. of animals per sex per dose:
- 5
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 days
- Necropsy of survivors and decedents performed: yes
- Other examinations performed: clinical signs - Statistics:
- yes, method not given
- Key result
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 2 050 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 1 590 - <= 2 650
- Mortality:
- 1000 mg/kg bw: 0/5
1470 mg/kg bw: 0/5
2150 mg/kg bw: 4/5
3160 mg/kg bw: 4/5 - Clinical signs:
- other: signs of intoxication from 4 hrs up to 12 hrs p.a.: lacrimation, salivation, hypersensitivity, convulsion, hypoactivity; dermal irritation: severely burned, severe oedema
- Gross pathology:
- survivors: no significant finding; gross necropsy-decedents: hyperemia of lungs and kidneys
- Other findings:
- no data
- Interpretation of results:
- other: CLP/EU GHS criteria are not met, no classification required according to Regulation (EC) No 1272/2008
- Conclusions:
- CLP: not classified
- Executive summary:
Application of test substance to the skin of rabbits and an exposure observation time for 14 days yielded a LD50 of 2050 mg/kg bw and severe irritational effects.
Table 1: Mortality and clinical symptoms
Dosage mg/kg bw |
onset of sympt 4-12 hrs |
mortality |
Mortality cumulative |
|
12-24 hrs |
day 3 |
|||
1000 |
0/5 |
|||
1470 |
0/5 |
|||
2150 |
S |
4/5 |
4/5 |
|
3160 |
S |
4/5 |
4/5 |
S = signs of intoxication from 4 hrs up to 12 hrs p.a.:
lacrimation,
salivation, hypersensitivity, convulsion, hypoactivity;
dermal irritation: severely burned, severe oedema; gross
necropsy-survivors: no significant finding, gross necropsy-decedents:
hyperemia of lungs and kidneys
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 402 (Acute Dermal Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- yes
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Dr. A. Ivanovas, Kisslegg/Allgäu/Germany
- Age at study initiation: no data
- Weight at study initiation: 210 - 235 g (male); 200 - 230 g (female)
- Fasting period before study: no
- Housing: 1 per cage
- Diet: ad libitum
- Water: ad libitum
ENVIRONMENTAL CONDITIONS
- Air-conditioned room
- Temperature (°C): 22 +- 1 °C
- Photoperiod (hrs dark / hrs light): 12/12 - Type of coverage:
- occlusive
- Vehicle:
- polyethylene glycol
- Details on dermal exposure:
- TEST SITE
- Area of exposure: 5 cm x 7.5 cm, shaved, intact skin
- Administration: Dosing in dissolved form by syringe (at elevated temperature to prevent precipitation)
- Type of wrap: thin aluminum foil covering the treated area and adhesive bandage ("Elastoplast") round the trunk
REMOVAL OF TEST SUBSTANCE
- Washing (if done): lukewarm water
- Time after start of exposure: 24 h
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 3 mL/kg bw of test solution (highest test volume technically achievable on the skin area)
- Concentration (if solution): 80% in PEG 300
- Constant volume or concentration used: yes
- For solid: dissolved in PEG at 50 °C, at lower temperature precipitation - Duration of exposure:
- 24 h
- Doses:
- 2400 mg/kg bw (3,5-xylenol)
[Note: In report 2.4 mL/kg is mentioned, but not conclusive as 80% solution of the solid test substance in PEG should relate to w/v. 3 mL solution/kg were applied => 80% (w/v) = 2.4 g/kg bw.] - No. of animals per sex per dose:
- 5
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: several-fold on the day of treatment, thereafter daily
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight - Statistics:
- not applicable
- Sex:
- male/female
- Dose descriptor:
- LD0
- Effect level:
- 2 400 mg/kg bw
- Based on:
- test mat.
- Key result
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 2 400 mg/kg bw
- Based on:
- test mat.
- Mortality:
- none
- Clinical signs:
- other: no particular observations
- Gross pathology:
- no skin reactions (effects scores = 0) ; no particular findings at organs
- Other findings:
- none
- Interpretation of results:
- other: CLP / GHS criteria not met, no classification required according to Regulation (EC) No 1272/2008.
- Conclusions:
- CLP: not classified
No clinical signs of toxicity reported up to 2400 mg/kg
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: individual animal data not shown, no information about strain used, statistical evaluation not given, no guideline followed
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- 5 rabbits/dose, exposure period not given, observation up to 14 days, gross autopsy
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- no further data
- Type of coverage:
- not specified
- Vehicle:
- other: undiluted
- Details on dermal exposure:
- no further data
- Duration of exposure:
- no data
- Doses:
- 681, 1000, 1470, 2150 mg/kg bw
- No. of animals per sex per dose:
- 5 rabbits/dose
- Control animals:
- not specified
- Details on study design:
- no further data
- Statistics:
- yes, but method not mentioned
- Key result
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 1 380 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 841 - <= 2 260
- Mortality:
- 681 mg/kg bw: 1/5
1000 mg/kg bw: 2/5
1470 mg/kg bw: 2/5
2150 mg/kg bw: 4/5 - Clinical signs:
- other: Hypoactivity salivation, tremors; dermal irritation: severe erythema
- Gross pathology:
- gross autopsy: survivors: no significant findings; decedents: hyperemia of the liver and lungs
- Other findings:
- no further details
- Interpretation of results:
- other: CLP/EU GHS Category 4 (H312) according to Regulation (EC) No 1272/2008
- Conclusions:
- CLP: Acute tox 4, H 312
- Executive summary:
Dermal application of the testsubstance to the skin of rabbits resulted in a LD50 value of 1380 mg/kg bw (Industrial Biotest Laboratories 1969).
Data source
Materials and methods
Test material
- Reference substance name:
- Tar acids, xylenol fraction
- EC Number:
- 284-895-5
- EC Name:
- Tar acids, xylenol fraction
- Cas Number:
- 84989-06-0
- Molecular formula:
- not applicable
- IUPAC Name:
- 2,3-dimethylphenol; 2,4-dimethylphenol; 2,5-dimethylphenol; 2,6-dimethylphenol; 3,4-dimethylphenol; 3,5-dimethylphenol
Constituent 1
Results and discussion
Effect levels
- Key result
- Sex:
- not specified
- Dose descriptor:
- LD50
- Remarks:
- rabbit
- Effect level:
- ca. 301 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 213 - <= 426
- Remarks on result:
- other: Source, CAS 106-44-5, p-cresol, IBTL, 1969
Any other information on results incl. tables
In the result table above the most critical value of the weight of evidence approach is given. In the following, the results are shown for the other source substances of this weight of evidence approach:
Source CAS 95 -48 -7: o-cresol: LD50 (sex unspecified, rabbit) = 1380 mg/kg bw (95% CL: >= 841 <= 2260); IBTL, 1969
Source CAS 108 -39 -4: m-cresol: LD50 (sex not specified, rabbit) > 2050 mg/kg bw; IBTL, 1969
Source CAS 108 -68 -9: 3,5-xylenols: LD50 (male/female, rat) >2400 mg/kg bw; Rütgers, 1981
Applicant's summary and conclusion
- Interpretation of results:
- other: CLP/EU GHS Category 3 (H311) according to Regulation (EC) No 1272/2008
- Conclusions:
- Based on all available information (weight-of-evidence), following an analogue read-across approach and in the absence of data regarding acute dermal toxicity of Tar acids, Xylenol fraction (CAS 84989-06-0), Tar acids, Xylenol fraction (CAS 84989-06-0) is classified for Acute dermal toxicity (Cat. 3, H311) as a worst case.
- Executive summary:
The acute dermal toxicty study on 3,5-xylenol resulted in a LD50 of > 2400 mg/kg bw for male and female rats. For the three cresol isomers the LD50 values were between 301 and 2050 mg/kg bw for rabbits. Thus, the cresol isomers seem to have a more toxic potential regarding acute dermal toxicity than 3,5-xylenol. However, as there are no acute dermal toxicity data available for Tar acids, Xylenol fraction (CAS 84989-06-0) a worst-case approach was conducted taking into account all available data on the source substances and Tar acids, Xylenol fraction (CAS 84989-06-0) was therefore classified in Cat. 3 (H311) for acute dermal toxicity according to Regulation (EC) No 1272/2008.
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