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EC number: 253-452-8 | CAS number: 37294-49-8
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 20 Oct 2014 - 21 Oct 2014
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study has been performed according to OECD and/or EC guidelines and according to GLP principles.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 014
- Report date:
- 2014
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 437 (Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants)
- Version / remarks:
- Adopted July 26, 2013
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU method B.47 (Bovine corneal opacity and permeability test method for identifying ocular corrosives and severe irritants)
- Version / remarks:
- EAmended by EC No. 1152/2010 No. L142, 09 December 2010
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: The Ocular Toxicity Working Group (OTWG) of the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) and the National Interagency Centre for the Evaluation of Alternative Toxicological Methods (NICEATM), March 2006
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: In Vitro Techniques in Toxicology Database (INVITTOX) protocol 127. Bovine Opacity and Permeability (BCOP) Assay, 2006
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Gautheron P., Dukic M., Alix D. and Sina J.F., Bovine corneal opacity and permeability test: An in vitro assay of ocular irritancy. Fundam Appl Toxicol 18:442-449, 1992
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Disodium C-isodecyl sulphonatosuccinate
- EC Number:
- 253-452-8
- EC Name:
- Disodium C-isodecyl sulphonatosuccinate
- Cas Number:
- 37294-49-8
- Molecular formula:
- C14H26O7S.2Na
- IUPAC Name:
- disodium 4-[(2-methylnonyl)oxy]-4-oxo-3-sulfonatobutanoate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): Disodium isodecyl sulfosuccinate
- Substance type: organic
- Physical state: White powder
- Storage condition of test material: At room temperature, in a well-sealed container
- pH: 5.7 (1% in water, indicative range)
Constituent 1
Test system
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: approx. 750 µl of 10% (w/v) dilution in physiological saline per cornea
- The stock solution was treated with ultrasonic waves until the test substance had completely dissolved
NEGATIVE CONTROL
- Amount applied: 750 µl of physiological saline per cornea
POSITIVE CONTROL
Amount applied: 750 µl per cornea
Concentration: 10% (w/v) benzalkonium chloride in physiological saline
- Duration of treatment / exposure:
- 10 minutes
- Details on study design:
- TEST SITE
- Isolated bovine cornea
REMOVAL OF TEST SUBSTANCE
- Washing: yes (with MEM with phenol red (Eagle’s Minimum Essential Medium, Invitrogen Corporation) and thereafter with cMEM)
- Time after start of exposure: 10 minutes
SCORING SYSTEM:
- After exposure the cornea is thoroughly rinsed to remove the test substance followed by incubation for 120 ± 10 minutes in cMEM. Then, corneas were incubated in sodium-fluorescein solution for 90 ± 5 minutes (both incubations at 32 ± 1°C).
- The mean opacity and mean permeability values (OD490) were used for each treatment group to calculate an in vitro score:
In vitro irritancy score (IVIS) = mean opacity value + (15 x mean OD490 value).
TOOL USED TO ASSESS SCORE:
- opacitymeter and microplate reader
DATA EVALUATION:
A test substance that induces an IVIS ≤ 3 is not classified for eye irritancy (UN GHS: no category);
A test substance that induces an IVIS > 55 is defined as a corrosive or severe irritan (UN GHS: category 1);
For a test substance that induces an IVIS >3 and ≥ 55, no prediction on irritant potency can be made (UN GHS: no prediction can be made)
Results and discussion
In vitro
Results
- Irritation parameter:
- in vitro irritation score
- Run / experiment:
- 10 minutes
- Value:
- >= 15.8 - <= 51.4
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: mean score 38.1
- Other effects / acceptance of results:
- The opacity value was 10 in all three corneas treated with disodium isodecyl sulfosuccinate and permeability values ranged from 0.406 to 2.785. The corneas were turbid with spots after the 10 minutes of treatment with disodium isodecyl sulfosuccinate. No pH effect of the test substance was observed on the rinsing medium. Hence, the in vitro irritancy scores ranged from 15.8 to 51.4 after 10 minutes of treatment with Disodium isodecyl sulfosuccinate.
Any other information on results incl. tables
The individual in vitro irritancy scores for the negative controls ranged from -0.4 to 0.7. The individual positive control in vitro irritancy scores ranged from 156 to 168 for benzalkonium chloride (mean IVIS = 161.6). The corneas treated with the positive control substance were turbid after the 10 minutes of treatment.
Applicant's summary and conclusion
- Interpretation of results:
- other: the outcome does not allow conclusion on classification
- Remarks:
- Criteria used for interpretation of results: other: UN GHS
- Conclusions:
- In a bovine corneal opacity and permeability (BCOP) test, performed according to OECD guideline and GLP principles, disodium isodecyl sulfosuccinate induced a mean IVIS of 38.1. Based on an IVIS > 3 and ≤ 55, no prediction on eye irritancy of the test substance can be made.
- Executive summary:
A bovine corneal opacity and permeability (BCOP) test was performed with disodium isodecyl sulfosuccinate according to OECD guideline and GLP principles. Reliable positive and negative controls were included. The corneas treated with disodium isodecyl sulfosuccinate were turbid with spots after the 10 minutes of treatment. Mean in vitro irritancy score was 38.1 after 10 minutes of treatment. The opacity value was 10 in all three corneas treated with disodium isodecyl sulfosuccinate and permeability values ranged from 0.406 to 2.785. based on an IVIS > 3 and ≤ 55, no conclusion on classification for eye irritancy can be drawn according to GHS UN.
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