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EC number: 200-431-6 | CAS number: 59-50-7
- 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
Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation
- Remarks:
- in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- other:
- Principles of method if other than guideline:
- The contact sensitivity caused by chlorocresol was studied in guinea pigs by the cumulative contact enhancement test
- GLP compliance:
- not specified
- Type of study:
- other: cumulative contact enhancement test (CCE T )
- Species:
- guinea pig
- Strain:
- other: Ssc:Al
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Statenes serum institute Copenhagen
- Age at study initiation: no data
- Weight at study initiation: 350-450 gm
- Housing: Plastic cages
- Diet (e.g. ad libitum): Rabbit pellet, Supperfos corn ad libitum
- Water (e.g. ad libitum): Vitamin C enriched water ad libitum
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-30 deg C
- Humidity (%): 45-75%
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12 hrs
IN-LIFE DATES: From: To: - Route:
- epicutaneous, occlusive
- Vehicle:
- other: 5 different vehicle were used -water containing Carbomer 941 as a gelling agent -water -olive oil / acetone (4:1) -propylene glycol -propylene glycol containing 0.1 5% Carbomer 941
- Concentration / amount:
- -5% PCMC partly dissolved , mainly suspended in water containing Carbomer 941 as a gelling agent
-a saturated aqueous solution of 0.3 8% PCMC, -5.0% PCMC in olive oil/acetone (4 /1) ,
-5.0% PCMC in propylene glycol
-5 .0% PCMC in propylene glycol containing 0 .1 5%Carbomer 941. - Route:
- epicutaneous, occlusive
- Vehicle:
- other: 5 different vehicle were used -water containing Carbomer 941 as a gelling agent -water -olive oil / acetone (4:1) -propylene glycol -propylene glycol containing 0.1 5% Carbomer 941
- Concentration / amount:
- -5% PCMC partly dissolved , mainly suspended in water containing Carbomer 941 as a gelling agent
-a saturated aqueous solution of 0.3 8% PCMC, -5.0% PCMC in olive oil/acetone (4 /1) ,
-5.0% PCMC in propylene glycol
-5 .0% PCMC in propylene glycol containing 0 .1 5%Carbomer 941. - No. of animals per dose:
- 0 , 3 , 7 , and 9 days
- Details on study design:
- RANGE FINDING TESTS:
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: four exposure
- Exposure period: 0 , 3 , 7 , and 9 days
- Test groups: yes
- Control group: yes
- Site: post nuchal region
- Frequency of applications: no data
- Duration: no data
- Concentrations: -5% PCMC partly dissolved , mainly suspended in water containing Carbomer 941 as a gelling agent
-a saturated aqueous solution of 0.3 8% PCMC,
-5.0% PCMC in olive oil/acetone (4 /1) ,
-5.0% PCMC in propylene glycol
-5 .0% PCMC in propylene glycol containing 0 .1 5%Carbomer 941.
B. CHALLENGE EXPOSURE
- No. of exposures: 1 exposure
- Day(s) of challenge: 21st day
- Exposure period: 1 day
- Test groups: yes
- Control group: yes
- Site: no data
- Concentrations: 0.1% and 1.0% PCMC in petrolatum
- Evaluation (hr after challenge): 48 and 72 hrs
OTHER: - Reading:
- 1st reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 0.1% and 1.0% PCMC in petrolatum
- Clinical observations:
- saturated PCMC aqueous solution had marked erythematous and edematous reactions at the patch - test site
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 72.0. Group: test group. Dose level: 0.1% and 1.0% PCMC in petrolatum. Clinical observations: saturated PCMC aqueous solution had marked erythematous and edematous reactions at the patch - test site.
- Interpretation of results:
- sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- A significant difference was observed between the sensitizing capacities of the preparations. The 5% PCMC suspensions in water and olive oil/acetone solution were the most sensitizing , with 12 of 19 and 11 of 20 animals reacting to 1% PCMC after 48 h , respectively ; the 5% PCMC in propylene glycol solution had the least sensitizing potential , with only 4 of 20 animals reacting o challenge with 1% after 48 h Carbomer 941 had no effect on the sensitization rate .
- Executive summary:
The contact sensitivity caused by chlorocresol was studied in guinea pigs by the cumulative contact enhancement test. Female albino guinea pigs were given the cumulative contact enhancement test using topical induction patches on days 0, 3, 7, and 9. Before the third induction patch test an emulsion of Freunds complete adjuvant was injected intradermally as an immune stimulant.
Challenge reactions were read 48 and 72 hours after the last application. A significant difference was observed between the sensitizing capacities of the preparations. The 5% PCMC suspensions in water and olive oil/acetone solution were the most sensitizing , with 12 of 19 and 11 of 20 animals reacting to 1% PCMC after 48 h , respectively ; the 5% PCMC in propylene glycol solution had the least sensitizing potential , with only 4 of 20 animals reacting o challenge with 1%after 48 h Carbomer 941 had no effect on the sensitization rate .
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
Based on studies of target substance CAS NO 59-50-7 reviewed for skin sensitization from reliable sources having Klimisch rating 2considering the weight of evidence approach.
The summary of the results are presented below
Sr. No
End point
effect
Species
Remark
1
Skin sensitization
sensitizing
guinea pig
Data is from publication for Target chemical
2
Skin sensitization
sensitizing
guinea pig
Data is from publication for Target chemical
3
Skin sensitization
not sensitizing
Humans
Data is from publication for Target chemical
Based on results summarized in above table for the target chemical CAS NO 59-50-7, it can be concluded that the substance is sensitizing to the skin of guinea pig but not humans.Thus Chlorocresol is considered to be sensitizing to skin as per the criteria of CLP regulation and will be classified as skin sen. category 1.
Migrated from Short description of key information:
The substance chlorocresol was found to be a potent skin sensitizers.
Justification for selection of skin sensitisation endpoint:
The contact sensitivity caused by chlorocresol was studied in guinea pigs by the cumulative contact enhancement test. Female albino guinea pigs were given the cumulative contact enhancement test using topical induction patches on days 0, 3, 7, and 9. Before the third induction patch test an emulsion of Freunds complete adjuvant was injected intradermally as an immune stimulant.
Challenge reactions were read 48 and 72 hours after the last application. A significant difference was observed between the sensitizing capacities of the preparations. The 5% PCMC suspensions in water and olive oil/acetone solution were the most sensitizing , with 12 of 19 and 11 of 20 animals reacting to 1% PCMC after 48 h , respectively ; the 5% PCMC in propylene glycol solution had the least sensitizing potential , with only 4 of 20 animals reacting o challenge with 1%after 48 h Carbomer 941 had no effect on the sensitization rate .
Justification for classification or non-classification
Based on the above studies it can be concluded that the substance chlorocresol was found to sensitizing to skin ans hence classified as Skin sen.1 category.
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