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EC number: 273-234-6 | CAS number: 68953-96-8 This substance is identified by SDA Substance Name: C11-C13 branched alkyl benzene sulfonic acid calcium salt and SDA Reporting Number: 25-097-06.
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP laboratory study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Test already existing perior to the preparation of this dossier
Test material
- Reference substance name:
- Branched CaDDBS
- IUPAC Name:
- Branched CaDDBS
- Details on test material:
- Calcium bis(tetrapropylenebenzenesulphonate); CAS No. 11117-11-6
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Pirbright-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Hoeschst AG, Kastengrund, SPF breeding colony
- Age at study initiation: Not stated
- Weight at study initiation: Mean = 334 g
- Housing: Makrolon Type 4 cages on soft wood granulate in fullyl air-conditioned rooms in groups of 5 animals
- Diet (e.g. ad libitum): ad libitum, Altromin 3112 diet for guinea pigs and rabbits
- Water (e.g. ad libitum): ad libitum, tap water in plastic bottles
- Acclimation period: at least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 3 C
- Humidity (%): 55 +/- 20%
- Air changes (per hr): Not stated
- Photoperiod (hrs dark / hrs light): 12:12 dark:light
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal
- Vehicle:
- other: semi-liquid paraffin
- Concentration / amount:
- Intradermal induction was performed using 0.2% Phenylsulfonat CA in semi-liquid paraffin. Dermal induction were carreid out with 3% Phenylsulfonat CA in petrolatum. 0.1% Phenylsulfonat CA in petrolatum was selected for challenge treatment.
Challengeopen allclose all
- Route:
- epicutaneous, open
- Vehicle:
- other: semi-liquid paraffin
- Concentration / amount:
- Intradermal induction was performed using 0.2% Phenylsulfonat CA in semi-liquid paraffin. Dermal induction were carreid out with 3% Phenylsulfonat CA in petrolatum. 0.1% Phenylsulfonat CA in petrolatum was selected for challenge treatment.
- No. of animals per dose:
- 10 animals in the treatment group and 5 animals in the control group were used.
- Details on study design:
- Chronlogical description of the test procedure indicating the day at which the procedure was carried out:
Day 0: The body weights of the animals were determined. Guinea pigs were shaved mechanically over a dorsal area of 4x6 cm in the vicinity of the shoulders.
Day 1: Intradermal induction treatment: Two intradermal injections per animal of the following preparations. Injection sites 1, 2 and 3 were all within the dorsal area of 2 x 4 cm and were left uncovered.
Treated group:
Site 1: 2 x 0.1 mL of 50% Freund's adjuvant
Site 2: 2 x 0.1 mL of 0.2% solution of test substance in semi-liquid paraffin
Site 3: 2 x 0.1 mL of 0.2% solution of test substance in 50% Freund's adjuvant
Control and escort groups:
Site 1: 2 x 0.1 mL of 50% Freund's adjuvant
Site 2: 2 x 0.1 mL of semi-liquid paraffin
Site 3: 2 x 0.1 mL of 50% Freund's adjuvant
Days 1-7: The application area was examined for local tolerance. Any systemic toxic effects were recorded.
Day 8: Dermal induction treatment: 0.5 g of test substance preparation or the vehicle was applied to a 2 x 4 cm cellulose patch, which covered the area where intradermal injection had been made. The application area was kept for 48 hours under an occlusive bandage with an impermeable film and an elastic bandage.
Treatment group: 3% test substance in petrolatum
Control and escort group: petrolatum
Day 10: Occlusive bandage removed and irritant effects recorded.
Days 11-21: No treatment of control or treated group. Test animals kept under observation.
Days 15-18: Challenge treatment of escort group carried out in same way as that of control and treated groups (see days 22-25). Escort group (left flank): 1% Phenylsulfonat CA in petrolatum
Day 22: Dermal challenge treatment: One area of approximately 5 x 5 cm on the left flank was shaved mechanically. 0.5 g of the test substance preparation was applied to a 2 x 2 cm cellulose patch. The application area was then kept for 24 hours under an occlusive bandage with an impermeable film and an elastic bandage. Treated and control groups (left flank): 0.1% Phenylsulfonat CA in petrolatum.
Day 23: Occlusive bandage removed.
Day 24: Skin examined.
Day 25: Skin examined and body weights of test animals determined. - Challenge controls:
- See details of study design.
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- other: not available
- Group:
- test chemical
- Dose level:
- 0.2% induction in semi-liquid paraffin
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- No signs of irritation at 24 or 48 hours after removal of the occlusive bandage
- Remarks on result:
- other: Reading: other:. Clinical observations: No signs of irritation at 24 or 48 hours after removal of the occlusive bandage.
- Reading:
- other: not available
- Group:
- negative control
- Remarks on result:
- other: Data on the negative control is not available
- Reading:
- other: not available
- Group:
- positive control
- Remarks on result:
- other: Data on the positive control is not available
Any other information on results incl. tables
No signs of irritation were observed in the control and treatment groups 24 and 48 hours after removal of the occlusive bandage. No adverse effects on body weight gains were observed. The treated animals showed no clinical signs of intoxication throughout the study.
The intradermal injections with Freund's adjuvant (with and without test substance) casused severe erythema and oedema, indurations and encrustations. The application sites treated with the test substance showed very slight to well-defined erythema and very slight to slight oedema. Injections of the vehicle alone did not cause any sign of irritation. Due to these strong irritation reactions of the skin, 10% sodium dodecylsulfate was not applied at day 7.
After the removal of the patch at day 10, erythema and oedema, indurated adn encrusted skin as well as necrosis were observed at the application sites treated with Freund's adjuvant (with and without test substance). Additionally, the sites treated with test substance in Fruend's adjuvant exhibited open wounds in some cases. Very slight to well-defined erythema occurred at the application sites treated with the test substance in the vehicle.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The test substance showed no evidence of sensitisation.
- Executive summary:
Testing for sensitising properties of Phenylsulfonat CA was performed in female Guinea pigs according to OECD Guideline 406 methods (Guinea pig maximization test). Intradermal induction was performed using 0.2% Phenylsulfonat CA in semi-liquid paraffin. Dermal induction was carried out with 3% Phenylsulfonat CA in petrolatum. 0.1% Phenylsulfonat CA in petrolatum was selected for the challenge treatment. Results show no evidence for sensitisation. Phenylsulfonat CA is therefore not a dermal sensitiser.
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