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EC number: 939-648-2 | CAS number: 75081-73-1
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2013
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- An in vitro/ex vivo eye irritation study (according to HET-CAM protocol) was performed before the conduct of the present in vivo study. Since the result of this study was not conclusive regarding classification and labelling purposes, a fully valid in vivo eye irritation was performed.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 013
- Report date:
- 2013
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- adopted October 02, 2012
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Version / remarks:
- Commision Regulation (EC) No. 440/2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- tetrasodium 4-{2-[(Z)-(1-oxidododecylidene)amino]ethoxy}-4-oxo-2-sulfobutanoate 4-{2-[(Z)-(1-oxidododecylidene)amino]ethoxy}-4-oxo-3-sulfobutanoate
- EC Number:
- 939-648-2
- Cas Number:
- 75081-73-1
- Molecular formula:
- C18H31NNa2O8S
- IUPAC Name:
- tetrasodium 4-{2-[(Z)-(1-oxidododecylidene)amino]ethoxy}-4-oxo-2-sulfobutanoate 4-{2-[(Z)-(1-oxidododecylidene)amino]ethoxy}-4-oxo-3-sulfobutanoate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- Himalayan
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: LPT Laboratory of Pharmacology and Toxiclogy GmbH & Co. KG, Branch Löhndorf, 24601 Löhndorf/Post Wankendorf, Germany
- Age at dosing: Approx. 4.5 – 7.5 months
- Weight at dosing: Animal no. 1,2 and 3 : 2.7 kg each
- Housing: For 8 hours following test item application, the animals were kept singly in restrainers which allowed free movement of the head but prevented a complete body turn, wiping of the eyes with the paws and excluded irritation of the eye by excrements and urine. During the acclimatisation period and after the 8-hour period in restrainers, the animals were kept singly in cages with dimensions of 380 mm x 425 mm x 600mm (manufacturer: Dipl.Ing. W. EHRET GmbH, 16352 Schönwalde, Germany).
- Diet (e.g. ad libitum): Commercial diet , ssniff®K-H, ssniff Spezialdiäten GmbH, 59494 Soest, Germany, ad libitum
- Water (e.g. ad libitum): Tap water ad libitum
- Acclimation period: At least 20 adaptation days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C ± 3°C (maximum range)
- Humidity (%): 30% - 70% (maximum range)
- Air changes (per hr): Not provided
- Photoperiod (hrs dark / hrs light): 12/12 (about 150 lux at approx. 1.50 m room height)
IN-LIFE DATES: From: February 4, 2013 To: February 22, 2013
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: The left eye, which remained untreated, served as a control.
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1mL
- Concentration (if solution): undiluted (39.90% solid content) - Duration of treatment / exposure:
- Single instillation into the conjunctival sac
- Observation period (in vivo):
- Observations were performed at 1 hour, 24, 48, 72 hours, 7, 14, and 21 days
- Number of animals or in vitro replicates:
- 3 males and 3 females
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): Yes, with physiol. saline
- Time after start of exposure: 24 h
SCORING SYSTEM:
The grades of ocular reaction (conjunctivae, cornea and iris) were recorded at each examination according to the following scheme:
Cornea
Opacity: degree of density (Readings taken from most dense area. The area of corneal opacity will be noted)
No ulceration or opacity: 0
Scattered or diffuse areas of opacity (other than slight dulling of normal lustre), details of iris clearly visible: 1
Easily discernible translucent area, details of iris slightly obscured: 2
Nacreous area, no details of iris visible, size of pupil barely discernible: 3
Opaque cornea, iris not discernible through the opacity: 4
Iris
Normal: 0
Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperaemia, or injection, iris reacting to light (a sluggish reaction is considered to be an effect): 1
Haemorrhage, gross destruction, or no reaction to light: 2
Conjunctivae
Redness: (refers to palpebral and bulbar conjuntivae, excluding cornea and iris)
Normal: 0
Some blood vessels hyperaemic (injected): 1
Diffuse, crimson colour, individual vessels not easily discernible: 2
Diffuse beefy red: 3
Chemosis
Swelling (refers to lids and/or nictating membranes)
Normal: 0
Some swelling above normal: 1
Obvious swelling, with partial eversion of lids: 2
Swelling with lids about half closed: 3
Swelling, with lids more than half closed: 4
TOOL USED TO ASSESS SCORE:
slit lamp: prior to the administration and 1 hour, 24, 48 and 72 hours after the instillation
fluorescein: 24 hours after administration the eyes were treated additionally with fluorescein before being examined to aid evaluation of the cornea for possible lesions
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.11
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.56
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 h
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.22
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 48 h
- Irritant / corrosive response data:
- Under the present test conditions, a single instillation of 0.1 mL Butanedioic acid, 2(or 3)-sulfo-, 4-[2-[(1-oxododecyl)amino]ethyl]ester, disodium salt per animal into the conjunctival sac of the right eye of three rabbits caused following changes:
Corneal opacity (grade 1) was observed in animal no. one 24 hours after instillation.
Conjunctival redness was observed in all animals:
animal no. 1: 24 and 48 hours (grade 1) after instillation;
animal no. 2: 48 hours (grade 1) after instillation;
animal no. 3: 60 minutes (grade 2) and 24 and 48 hours (grade 1) after instillation.
Chemosis was observed in all animals:
animal no. 1: 60 minutes (grade 3) after instillation;
animal no. 2: 60 minutes (grade 2) and 24 hours (grade 1) after instillation;
animal no. 3: 24 hours (grade 1) after instillation.
The irises were not affected by instillation of the test item.
There were no systemic intolerance reactions.
Any other information on results incl. tables
Table 1. Examination of the treated eye
Animal no.: 1/2/3 |
||||
Time after administration |
Cornea opacity |
Iris |
Conjunctivae |
|
Redness# |
Chemosis## |
|||
Before dosing |
0/0/0 |
0/0/0 |
0/0/0 |
0/0/0 |
60 minutes |
0/0/0 |
0/0/0 |
0/0/2 |
3/2/0 |
24 hours |
1/0/0 |
0/0/0 |
1/0/1 |
0/1/1 |
48 hours |
0/0/0 |
0/0/0 |
1/1/1 |
0/0/0 |
72 hours |
0/0/0 |
0/0/0 |
0/0/0 |
0/0/0 |
# refers to palpebral and bulbar conjunctivae; excluding cornea and iris
##swelling: refers to lids and/or nictating membrane
24 hours fluorescein test: all animals: no pathological findings
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Not irritating
- Executive summary:
Under the present test conditions, a single instillation of 0.1 mL test item, containing 39.90% active ingredient, per animal into the conjunctival sac of the right eye of three rabbits caused following changes: corneal opacity (grade 1) in on animal 24 hours after instillation, conjunctival redness (grade 1) in all animals, chemosis in all animals up to 24 hours after instillation (grade 1 -3). The irises were not affected by instillation of the test item. Mean 24-72h scores were 0.11/4, 0.55/3 and 0.22/4 for cornea opacity, conjuctivae redness and chemosis, respectively.
All scores were reversible within 72 hours and fell below classification criteria, therefore the test item was not irritant for the eyes.
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