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EC number: 470-470-3 | CAS number: 9022-75-7
- 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
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
Additional information
There is no reliable and relevant information source in which the toxicokinetic properties (absorption, distribution, metabolism, elimination) of CHIMEXANE NV were investigated. The expected toxicokinetic behaviour is derived from the physicochemical properties and the results from the available toxicological data following the guide given in the REACH guidance document R.7c.
CHIMEXANE NV is a substance composed of constituents having a molecular weight of 260, 334 and 409. It is a pasty solid with an estimated water solubility of 16 mg/L. Vapour pressure was determined to be about 227 Pa at 25 °C and it has lipophilic properties (for the 2 main constituents, log Kow 1 = 3.78 and Log Kow 2 = 4.25). The surface tension is 26.6 mN/m. Detailed information can be found in section 4 of CHIMEXANE NV IUCLID dossier.
Absorption:
In acute toxicity studies, either by oral or dermal route, no systemic toxic effects were observed. Only local effects such as necrosis associated with severe oedema, showing the corrosive properties of the substance, were identified. In a reproduction /developmental toxicity screening test and in a 4-week repeated dose toxicity study by oral route, the main effects elicited by the substance were transient reduced body weight gain and food consumption, particularly in the males, excessive salivation, loud breathing and half-closed eyes in both sexes. These observations indicate partial bioavailability of CHIMEXANE NV via oral route.
Although no signs of toxicity were observed in an acute dermal toxicity study, CHIMEXANE NV has a molecular weight < 500 and is a lipophilic substance (for the 2 main constituents log Kow is around 4) therefore dermal absorption is expected. However, due to its low water solubility, dermal absorption is expected to be low or moderate. But, as the substance has also corrosive properties, damage to the skin surface may enhance penetration.
Thus, indications of oral and dermal uptake of CHIMEXANE NV are given. Therefore the bioavailability of CHIMEXANE NV can be considered to be existent but maybe limited.
Distribution:
The physico-chemical information (low molecular weight, lipophilicity and low water solubility) indicates that CHIMEXANE NV could be distributed to many tissues and, due to its lipophilicity, may have a particular affinity for fatty tissues.
Metabolism:
No data are available but, in in vitro genotoxicity studies (particularly in MLA test), differences in cytotoxicity were observed with and without metabolic activation. This indicates that CHIMEXANE NV may be metabolised by hepatic microsomal fractions.
Excretion:
As no toxic effects were observed in kidneys in repeated toxicity studies, it is difficult to determine if CHIMEXANE NV is excreted in urine. However, based on the physico-chemical information (low molecular weight and low water solubility), renal excretion of CHIMEXANE NV and/or its metabolites cannot be excluded.
Accumulative potential:
Based on the physico-chemical information (log Pow and low water solubility), it is concluded that the potential for bioaccumulation is low.
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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