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EC number: 905-287-4 | CAS number: 1638758-52-7
- 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
Acute oral toxicity:
Key study -mixed ethylphenols. York, 2005. KL.1. LD50 980.62mg/kg; NOEL 175mg/kg;
Supporting study: mixed xylenols. York, 2005. KL.1 LD50 980.62mg/kg; NOEL 175mg/kg;
Supporting study: m-cresol. IBTL, 1969. KL.3. NOEL not identified. LOAEL 147mg/kg;
Supporting study: o-cresol. IBTL, 1969. KL.3. NOEL not identified. LD50 121mg/kg; LOAEL 68mg/kg;
Supporting study: p-cresol. IBTL, 1969. KL.3. NOEL not identified. LD50 207mg/kg; LOAEL 100mg/kg;
Acute inhalation toxicity:
No key or supporting studies identified;
Acute dermal toxicity:
No key or supporting studies identified;
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- discriminating dose
- Value:
- 175 mg/kg bw
Additional information
Acute oral toxicity
The key study on ethyl phenols and the supporting study on xylenols both confirm the LD50 at 980.62 mg/kg and the NOEL at 175 mg/kg. These studies performed were available to review and the robustness of the NOEL confirmed.
For all three cresol isomers the data summaried was already provided and therefore reports were not available to enable complete evaluation and suitability for the LD50 / LOAEL values set. These studies are in excess of 40 years old and consequently not conducted to any guideline, with data absent. The LOAEL determined have been dictated by the dose levels set, with clinical signs of toxicity observed at the LOAEL similar to that observed at higher doses in both the guideline compliant studies on ethylphenols and xylenols. It is likely that the true NOEL for the cresols if conducted to modern day guideline compliant protocol would be similar to that observed for the xylenols and ethylphenols.
Furthermore, it is important to note that Cresols will only constitute <25% of xylenol / ethylphenol mixture and so would only affect NOAEL / NOEL of mixtures in which they were present if they were significantly more toxic than xylenol /ethylphenol isomers.
Acute dermal toxicity
The key study available on 3,5 xylenol confirms an LD50 value in excess of 2400 mg/kg for a study conducted nearly 30 years ago. This value is reinforced by similar LD50 vaules ranging from 2000 to 2325 mg/kg for the 2,4 and 2,6 isomers. Whilst the cresols data reports are in excess of 40 years old, the LD50 values reported for m and p cresol (2050 and 138 mg/kg, respectively) reinforce the data obtained for the xylenols. Based on structural similarities, one would assume that the ethyl phenols would give similar values. It should be noted that the LD50 value for o-cresol was 301 mg/kg. As o-cresol is only a very small component of the mixture (if present) is unlikely to affect the overall NOAEL.
Effects reported (with the exclusion of 3,5 xylenol where no clinical signs of toxicity or skin reactions were noted) clinical signs were attributed to local irritant effects. With transient signs of increased salivation and hypoactivity.
The available acute dermal toxicity data is limited, but consistently shows that local irritant effects are the endpoint of concern which persisted without resolution.
Currently under EU Directive 67/548 EEC both xylenols and cresols are classified as corrosive, with the R phrases of R24 'toxic in contact with skin and R34 'cause burns' applied. Therefore in accordance with REACH R7.A guidance no further testing is warranted. DNEL setting for the dermal route will be extrapolated form the oral route. The dermal studies reported are limited in respect of the data available; therefore route to route extrapolation has been undertaken from the oral data inorder to derive a acute dermal systemic DNEL.
Acute inhalation toxicity
No key or supporting studies were identified. What information is available reports LC50 values 0.29 mg/L through to 30 mg/m3 where no mortality was observed. The exposure duration is either 1 hour or unknown and therefore not compliant with the required 4hr exposure.
Justification for classification or non-classification
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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