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EC number: 420-920-1 | CAS number: 128446-35-5
- 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

Particle size distribution (Granulometry)
Administrative data
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
- Report date:
- 1997
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 110 (Particle Size Distribution / Fibre Length and Diameter Distributions)
- GLP compliance:
- yes
- Type of method:
- sieving
- Type of distribution:
- mass based distribution
Test material
- Reference substance name:
- .beta.-Cyclodextrin, 2-hydroxypropyl cycloheptaamylose
- IUPAC Name:
- .beta.-Cyclodextrin, 2-hydroxypropyl cycloheptaamylose
- Reference substance name:
- -
- EC Number:
- 420-920-1
- EC Name:
- -
- Cas Number:
- 128446-35-5
- Molecular formula:
- Hill formula: (C42H70-nO35)(C3H7O)n; n(mittel)=5,25
- IUPAC Name:
- 5,10,15,25-tetrakis(hydroxymethyl)-40,44,47,49-tetrakis(2-hydroxypropoxy)-20,30,35-tris[(2-hydroxypropoxy)methyl]-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.2³,⁶.2⁸,¹¹.2¹³,¹⁶.2¹⁸,²¹.2²³,²⁶.2²⁸,³¹]nonatetracontane-36,37,38,39,41,42,43,45,46,48-decol
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- Physical Appearance: white powder
Batch No.: 01 (DRD#: SIETS 96.010)
Purity: 89.16%
Water Solubility: >=180 g/L at 20 °C (SLI Report #97 -1 0-7113)
Density: 991 kg/m³ (0.991 g/cm³) at 24.9 °C (SLI Report #97-4-6948)
Storage conditions: room temperature in a dark, ventilated cabinet
Constituent 1
Constituent 2
Results and discussion
Particle size
- Key result
- Percentile:
- D50
- Remarks on result:
- other: 0.0745 ± 0.0486 mm (length) by 0.0462 ± 0.0331 mm (width)(migrated from fields under 'Mass median diameter' as D50 percentile. No source field for Standard deviation.)
Particle size distribution at different passagesopen allclose all
- No.:
- #1
- Size:
- 2 mm
- Distribution:
- > 0 %
- Remarks on result:
- other: Representative Particle Size Range: >2.0 mm
- No.:
- #2
- Size:
- 1 mm
- Distribution:
- < 0.1 %
- Remarks on result:
- other: Representative Particle Size Range: 1.0-2.0 mm
- No.:
- #3
- Size:
- 0.5 mm
- Distribution:
- 0.4 %
- Remarks on result:
- other: Representative Particle Size Range: 0.500-1.0mm
- No.:
- #4
- Size:
- 0.212 mm
- Distribution:
- 10.7 %
- Remarks on result:
- other: Representative Particle Size Range: 0.212-0.500mm
- No.:
- #5
- Size:
- 0.125 mm
- Distribution:
- 23.7 %
- Remarks on result:
- other: Representative Particle Size Range: 0.125-0.212mm
- No.:
- #6
- Size:
- 0.075 mm
- Distribution:
- 25.3 %
- Remarks on result:
- other: Representative Particle Size Range: 0.075-0.125 mm
- No.:
- #7
- Size:
- 0.063 mm
- Distribution:
- 9.37 %
- Remarks on result:
- other: Representative Particle Size Range: 0.063-0.075 mm
- No.:
- #8
- Size:
- 0.045 mm
- Distribution:
- 11.7 %
- Remarks on result:
- other: Representative Particle Size Range: 0.045-0.063 mm
- No.:
- #9
- Size:
- other: basin
- Distribution:
- 18.5 %
- Remarks on result:
- other: Representative Particle Size Range: fines
Any other information on results incl. tables
Microscopic Analysis:
A portion of the test substance was examined under a light microscopic using 40X magnification. The test substance appeared to be a fine, loose powder with no clumping. The test substance was observed to be white with a generally elongated shape. Using a graduated ocular lens, the length and width of 24 particles were measured. The mean ocular length, width and standard deviation (in millimeters) were calculated. The average particle size was calculated to be 0.0745 ± 0.0486 mm (length) by 0.0462 ± 0.0331 mm (width).
Sieve Analysis
Based on the particle size observed in the microscopic analysis, sieve sizes ranging from 2.0 to 0.045 mm were selected.
No hydroxypropylated .beta.-cyclodextrin was retained on the 2.0 -mm sieve. It is recommended in CIPAC Miscellaneous Technique (MT) 58 that personal protective equipment be worn when working with substances with a particle size distribution of this type.
Applicant's summary and conclusion
- Executive summary:
This report describes the determination of the particle size of hydroxypropylated .beta.-cyclodextrinusing the dry sieve technique. Particle size between 2.0 to 0.045 mm was measured, and results are reported as the percent of particle retained on each sieve.
Information on the particle size distribution of a chemical in the environment is needed to assess its transport. Test substances with small particle sizes may easily penetrate through soils, whereas large particle sizes may affect the availability of the test substance to terrestrial and aquatic populations as well as affecting the potential biotic and abiotic degradation of the test substance.
The study was initiated on 7 April1997, the day the Study Director signed the protocol, and terminated on the day the Study Director signed the final report. The experimental phase of this study was conducted on 28 April1997 at Springborn Laboratories, Inc. (SLI), located in Wareham, Massachusetts. All original raw data and the final report produced during this study are stored in Springborn's archives at the above location.
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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