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Diss Factsheets
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EC number: 940-936-5 | CAS number: -
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- not reported
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: HaloSalt was evaluated with the Corrositex test method to determine its corrosive potential. The study was considered reliable and was conducted according to the guideline OECD 473 but not in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 003
- Report date:
- 2003
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 435 (In Vitro Membrane Barrier Test Method for Skin Corrosion)
- GLP compliance:
- no
Test material
- Reference substance name:
- Not applicable
- EC Number:
- 940-936-5
- Molecular formula:
- C4H12NCl.C4H12NOCl
- IUPAC Name:
- Not applicable
- Details on test material:
- - Name of test material (as cited in study report): XM-224
- Physical state: liquid
- Analytical purity: 100 %
- Lot/batch No.: C2618
- Other: pH 11.6
Constituent 1
Test animals
- Species:
- other: in vitro
Test system
- Details on study design:
- The Corrositex test was performed in three steps. First, a qualification test was done to insure that the test sample and the chemical detection system (CDS) reagent are compatible. This was achieved by placing either 150 ul of a liquid into an aliquot of the CDS reagent and observing it for the presence of any detectable change. If a physical or color change is observed, the sample is judged to be compatible with the detection solution and the remainder of the test is performed. The second step of the Corrositex test utilizes appropriate indicator solutions to permit categorization of the test sample as either a Category 1 or Category 2 material. Category 1 materials are typically strong acids/bases, while Category 2 materials are typically weak acids/bases. The third step in the test is performed by applying the test sample to the biobarrier. When the chemical permeates through or destroys the full thickness of this biobarrier, it comes into contact with the CDS which then undergoes a simple color change. This color change is visually observed and the time required for the color change to occur is recorded. The time required to destroy the biobarrier is recorded for four sample replicates and the mean of these replicates is utilized to designate the UN Packing Group classification as I (severe corrosivity), II (moderate corrosivity), III (mild corrosivity), or Noncorrosive (NC). Positive and negative controls were analyzed concurrently to confirm the test’s validity.
Results and discussion
In vitro
Resultsopen allclose all
- Irritation / corrosion parameter:
- other: other: Colour change in a chemical detection system
- Value:
- > 60
- Remarks on result:
- other:
- Remarks:
- Basis: other: Replicate 1. Remarks: The time required to colour change to occur (min). (migrated information)
- Irritation / corrosion parameter:
- other: other: Colour change in a chemical detection system
- Value:
- > 60
- Remarks on result:
- other:
- Remarks:
- Basis: other: Replicate 2. Remarks: The time required to colour change to occur (min). (migrated information)
- Irritation / corrosion parameter:
- other: other: Colour change in a chemical detection system
- Value:
- > 60
- Remarks on result:
- other:
- Remarks:
- Basis: other: Replicate 3. Remarks: The time required to colour change to occur (min). (migrated information)
- Irritation / corrosion parameter:
- other: other: Colour change in a chemical detection system
- Value:
- > 60
- Remarks on result:
- other:
- Remarks:
- Basis: other: Replicate 4. Remarks: Time required to colour change to occur (min9. (migrated information)
In vivo
- Other effects:
- The results of this study indicated that the sample was compatible with the Corrositex system and was classified as a Category 2 material.
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information Criteria used for interpretation of results: OECD GHS
- Conclusions:
- HaloSalt was analyzed by the Corrositex method to determine its corrosive potential. The result of this study demonstrated a mean time of > 60 minutes is required to destroy the synthetic biobarrier.
- Executive summary:
The original objective of the study was to analyze the corrosive potential of HaloSalt by the Corrositex method and to determine its packing group designation. The results obtained from the evaluation of four replicate samples were highly reproducible, demonstrating that a mean time of > 60 minutes required to destroy the synthetic biobarriers. These findings lead to the designation of this sample as a non-corrosive.
Corrositex method has been granted regulatory approval (OECD test guideline 435) and is used to rank chemicals with respect to their corrosive potential according to globally harmonised system of classification and labelling of chemicals (GHS). Based on the available study result (> 60 min), HaloSalt is classified as Corrosive category 1C according to GHS.
The study is considered as a key study in hazard assessment.
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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