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Diss Factsheets
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EC number: 482-430-2 | 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
pH
Administrative data
- Endpoint:
- pH
- Type of information:
- experimental study
- Adequacy of study:
- key study
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: CIPAC MT75
- Qualifier:
- according to guideline
- Guideline:
- CIPAC MT 75 (Determination of pH Values)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Test material form:
- other: Liquid
Constituent 1
Results and discussion
pH value
- pH value:
- 9.4
- Temp.:
- 20 °C
- Concentration:
- other: Undiluted
Applicant's summary and conclusion
- Conclusions:
- The pH of undiluted Inhibitor AHM P500 was pH 9.4.
- Executive summary:
A GLP guideline study was performed to determine the physical-chemical properties of Inhibitor AHM P500.
The following properties were determined; appearance, boiling point, relative density, solubility in water, octanol/water partition coefficient, pH, flash point.
The appearance of the test substance was determined in accordance with OPPTS 830.6302, 830.6303 and 830.6304. The test substance is a liquid of low non distinctive odour. The colour, as described using the Munsell colour system, was 10R 3/6 Dark Red.
The boiling point was determined in duplicate using the Siwoloboff method as described in EEC Method A2. The test substance decomposed before boiling therefore no definitive value was determined.
The relative density was determined at 20±1°C using a glass hydrometer, in accordance with EEC Method A3. The mean value of duplicate determinations was 0.935.
The water solubility was determined in accordance with OECD guideline 105 using the flask method. Determination of the test substance in the aqueous phase was by HPLC with UV detection. The analytical method for the determination of Inhibitor AHM P500 solubility in water was validated for linearity, accuracy, precision and selectivity. The method validation met the criteria specified in the study plan and was considered acceptable for use.
The water solubility of the test substance was 2.22 g/L at 20±1°C.
The octanol/water partition coefficient was determined in accordance with OECD guideline 117 using HPLC with UV detection. A Log Pow value of 3.24 was determined.
The pH of undiluted test material was measured at 20±1°C using a calibrated pH meter and glass electrode in accordance with CIPAC Method 75. The mean of duplicate determinations was 9.4. The pH of 1% solution in water was not determined due to the lack of water solubility of the test substance in water. The pH of a saturated aqueous solution, as measured during the water solubility determination, was pH 10.7.
The flash point was determined using the closed cup method in accordance with EU method A9. The mean result of duplicate determinations was 124°C.
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.
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