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Diss Factsheets
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EC number: 287-494-3 | CAS number: 85536-14-7
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- disregarded due to major methodological deficiencies
- Study period:
- 9/13/1983-12/02/1983
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: Test substance identity is uncertain and not representative of LAS; study lacks proper analytical information.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1984
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Water control not included. Groups of six male 8-week old rats were restrained in perforated, stainless steel cylinders with conical nose pieces. Exposure was nose-only to an aerosol atmosphere for 4 hours. After exposure, rats were returned to their cages and observed for clinical signs for 14 days.
- GLP compliance:
- no
- Test type:
- other: Approximate lethal concentration (ALC)
- Limit test:
- yes
Test material
- Reference substance name:
- Benzenesulfonic acid, dodecyl, sodium salt
- IUPAC Name:
- Benzenesulfonic acid, dodecyl, sodium salt
- Reference substance name:
- Sodium dodecylbenzenesulfonate
- EC Number:
- 246-680-4
- EC Name:
- Sodium dodecylbenzenesulfonate
- Cas Number:
- 25155-30-0
- IUPAC Name:
- sodium 2-dodecylbenzenesulfonate
- Test material form:
- aerosol dispenser: not specified
- Details on test material:
- - Name of test material (as cited in study report): Sodium Dodecylbenzene Sulfonate
- Physical state: liquid
- Analytical purity: 98%
- Impurities (identity and concentrations): 1% sodium xylene sulfonate, 0.5% sodium sulfate, 0.5% free oil
- Composition of test material, percentage of components: 26.8% Sodium dodecylbenzenesulfonate, 70% water
- Stability under test conditions: stable
- Other: Industry has used the term “sodium dodecylbenzenesulfonate” for everything from pure C12 LAS (homologue) to the normal detergent range substance (LAS) to even (at least in the literature) branched alkylbenzene sulfonate (ABS). The terms “Slurry 1260” or Sulfonium 1260” are not found either in the 2008 LAS SIDS dossier or in an internet search of synonyms for LAS. The test substance is noted to contain sodium xylene sulfonate (SXS), which is not formed in the production of LAS and thus must have been added to the sample. This is further evidence that the sample is not representative of LAS.
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- other: CD (SD) BR
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Breeding Laboratories, Kingston, NY
- Age at study initiation: 8 weeks
- Weight at study initiation: 222-273 g
- Housing: Singly in 5" x 11" x 7" steel-mesh cages
- Diet (e.g. ad libitum): Purina Certified Rodent Chow #5002 ad libitum
- Water (e.g. ad libitum): ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 25-26 degrees C
- Humidity (%): 29-54%
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Route of administration:
- inhalation: aerosol
- Type of inhalation exposure:
- nose only
- Vehicle:
- air
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: conical nose pieces
- Method of holding animals in test chamber: perforated stainless steel cylinders
- System of generating particulates/aerosols: Test material was pumped into a nebulizer. The aerosol stream went through a cyclone elutriator.
TEST ATMOSPHERE
- Brief description of analytical method used: Particle concentrations was taken about every 30 min, by drawing atmosphere through pre-weighed glass fiber filters. Atmospheric concentration was deterimined by weighing the filters after sampling. MMAD was determined by a Sierra Cascade Impactor.
VEHICLE
- Composition of vehicle (if applicable): distilled water
- Concentration of test material in vehicle (if applicable): 1.5-12% active ingredient
TEST ATMOSPHERE (if not tabulated)
- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): 2.5 microns - Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 4 h
- Concentrations:
- 65, 120, 260, and 310 mg/m3
- No. of animals per sex per dose:
- 6
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- other: Acute Lethal Concentration
- Effect level:
- 310 mg/m³ air
- Based on:
- not specified
- Exp. duration:
- 4 h
- Mortality:
- At 310 mg/m3, one rat died during exposure and 2 rats died one day post exposure.
- Clinical signs:
- other: Clear to red nasal discharge in all rats. Rats showed a diminishing response to having their cages tapped in the 260 and 310 mg/m3 groups. 1 rat in the 310 mg/m3 group had red nasal discharge 2 days post exposure.
- Body weight:
- Slight to severe weight loss 1 day post exposure.
Any other information on results incl. tables
An assumption that the test article aerosolized (a mix of water and the test substance and other components) was a homologous mixture and that this mixture was stable for the entire dosing period. Typically one would conduct analytical measurements of the active material from the sampled air from the test chamber (and not rely on a calculated value). Instead the study assumes that the particles samples from the test chamber contained the active ingredient based on the mathematical calculation from dilution in water. If for some reason the particles were not a homologous mix, then one could be over or under estimating the air concentration of active material.
Applicant's summary and conclusion
- Interpretation of results:
- moderately toxic
- Remarks:
- Migrated information Criteria used for interpretation of results: other: Approximate lethal concentration (ALC)
- Conclusions:
- No mortality occurred at concentrations up to 260 mg/m3. At 310 mg/m3, one rat died during exposure and 2 rats died one day post exposure. The test material is considered moderately toxic by inhalation. However, it is important to note that this laboratory exposure is not representative of the possible LAS exposure during actual use. Given this lack of relevance to real-world exposure potential, the use of this study for risk assessment purposes is limited.
- Executive summary:
The ALC is defined as the lowest atmospheric concentration generated that caused death in 1 or more rats either on the day of exposure or within 14 days post exposure. No mortality occurred at concentrations up to 260 mg/m3. At 310 mg/m3, one rat died during exposure and 2 rats died one day post exposure. The test material is considered moderately toxic by inhalation. However, it is important to note that this laboratory exposure is not representative of the possible LAS exposure during actual use. In this study, animals were given high exposures to respirable-sized particles (MMAD at 310mg/m3= 2.5 microns). Spray products containing LAS are designed to produce large particle sizes. These large particles are needed for efficient delivery of the spray to the surface being cleaned. This results in particle sizes that are much larger than the respirable particle sizes used in testing and therefore would not be able to reach far into the lungs where effects could occur. Given this lack of relevance to real-world exposure potential, the use of this study for risk assessment purposes is limited.
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.
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