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EC number: 308-766-0 | CAS number: 98283-67-1
- 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
Description of key information
Human Patch Test (24 h): not irritating
Additional information
There is additional data available on the skin irritating potential of D-Glucopyranose, oligomeric, undecyl glycoside in humans. In an in vivo occlusive patch test performed in compliance with GCP 11 female and 1 male Caucasian volunteers (18 to 27 years of age) were administered to the test material (10% a.i.) under occlusive conditions (patch test) for an exposure period of 24 h. The patch was applied to the left upper back which had not received any treatment before. A solution of 2% sodium lauryl sulfate was used as a positive control and was applied the same way on a different skin area. The second cup containing distilled water was used as negative control. Thirty minutes and 24 h after removal of the patch the skin area was observed for erythema, edema, dryness, vesicle, wrinkling and glazing. Slight to clear erythema formation was recorded in 11/12 volunteers (grade 1-2), whereas edema formation was only recorded in 4/12 volunteers (grade 1-2) 30 min after patch removal containing the positive control. Wrinkling (grade 1) was noted in 1/12 volunteers and neither glazing nor dryness was recorded in any volunteer. 1/12 volunteers did not show any skin reaction when treated with the positive control substance. 24 h after patch removal containing the positive control 11/12 volunteers showed erythema (grade 1-2), 2/12 edema (grade 1) and 7/12 wrinkling (grade 1-2). No vesicles, glazing and dryness were detected. Volunteers treated with the vehicle (distilled water) did not show edema, vesicles wrinkling, glazing and dryness, either 30 min or 24 h after patch removal. 1/12 volunteers showed slight erythema formation (grade 1) 24 h after application which was fully reversible within 24 h after patch removal. Due to their reaction to the application of controls, two volunteers were excluded from the study. 9/10 volunteers did not show any skin reaction when treated with the test material either 30 min or 24 h after patch removal. Slight erythema and wrinkling (grade 1) was present in only 1/10 volunteers 30 min after patch removal with the test material. The erythema was still present after 24 h after patch removal, whereas wrinkling was fully reversible at this time point.In summary, the test material is considered not to be irritating to human skin under the experimental conditions when applied as 18.2% (10% a.i.) formulation.
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