Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 205-117-2 | CAS number: 133-66-4
- 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
PBT assessment
Administrative data
PBT assessment: overall result
- PBT status:
- the substance is not PBT / vPvB
- Justification:
P criteria
The substance is not readily biodegradable according to both the estimated value with EPYSUITE 4.1 and the read across with the available data for the substance 16470-24-9 that achieves 1,2% in 28 days.
According to the hydrolysis available data for the substance 16090 -02 -1 (read across), the substance 133-66-4 can be considered stable in the environment at a pH between 4 and 9 for more than 1 year.
Therefore it is assumed that the substance CAS 133-66-4 is stable in water as well.
The substance is then considered to be persistent in the environment were exposure to occur based on the known lack of biodegradability.
B criteria
The bioconcentration factor (BCF) has been calculated as 10 L/kg wet-wt. using QSAR estimation based upon the SMILES code of the molecular structure Arnot-Gobas BCF & BAF Methods by structural fragmentation of the EPI Suite v4.1.
The bioaccumulation potential was also tested with a close structural analogue (read across with 16090-02-1) on fish, and after 70 days of exposition to the substance no detectable or very close to the method sensitivity threshold bioconcentration values were found.
The partition coefficient of the substance has been calculated using QSAR estimation based upon the SMILES code of the molecular structure US EPA KOWWIN v1.68 of the EPI Suite v4.1. Based upon structural fragmentation drawn from a database of >40,000 substance, the log Pow is estimated to be 8.96. High log Pow is likely to be due in part to the hydrophobic nature of the molecule.
Furthermore, assessment of the Toxicokinetic activity of the substance 16090-02-1 (read across) conducted with a radioisotope demonstrates that a rapid and complete excretion of radioactive material was observed: more than 95% of the administered radioactive material was excreted by faeces within 48 hrs.
Based on these data the substance is considered to be non-bioaccumulating.
T criteria
Eco-toxicity studies:
The toxicological examination on a close structural analogue (read across with 16090-02-1) on fish, daphnia and algae provided an EC50 >100 mg/L.
The toxicological examination of the chronic toxicity to aquatic invertebrates on a close structural analogue (read across with 16090-02-1) provided a NOEC= 1 mg/L.
Mammalian toxicity studies:
Also in this case the toxicological examination on a close structural analogue (read across with 16090-02-1) for genetic toxicity demonstrated a lack of mutagenic response.
Mutagenicity in bacterial reverse mutation assays (Ames test) investigated on a close structural analogue (read across with 16090-02-1), provided negative results with and without metabolic activation.
Also the induction of micronuclei in vivo investigated on mice, which were orally treated with a close structural analogue (read across with 16090-02-1), at doses of 5000 mg/kg/bw, provided no increase in the number of micronuclei. No toxic effects were observed
The Prenatal Developmental Toxicity, on a close structural analogue (read across with 16470-24-9), produced a NOAEL =1000 mg/kg bw/day.
Considering all the available toxicological information the substance can be assessed as not toxic.
The substance may pose a persistence (P) hazard but as the results produced no bioaccumulation (B) or toxicity (T) properties the substance cannot be considered as a PBT/vPvBT.
Since the criteria for B and T are not fulfilled, the substance is not PBT or vPvB
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.