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Diss Factsheets
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EC number: 267-051-0 | CAS number: 67774-74-7
- 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
Long-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- long-term toxicity to fish, other
- Remarks:
- Prolonged acute fish toxicity test
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 10 Feb 2000 to 2 Mar 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Guideline 203
- Deviations:
- yes
- Remarks:
- Study was extended to 21 days
- GLP compliance:
- not specified
- Remarks:
- Not stated, but appears to be conducted similar to GLP studies
- Analytical monitoring:
- yes
- Details on sampling:
- - Sample storage conditions before analysis: samples were analyzed immediately and processed within 2 hrs, analytical standards were kept in acetonitrile at 0 - 4°C.
- Vehicle:
- yes
- Remarks:
- acetone
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: 40 µL of test compound was dissolved in 22 mL of acetone. After that, 356 mL of MilliQ water was added. The solution was pumped into a premix flask. Fresh stock solution was prepared daily.
- Concentration of vehicle in test medium (stock solution and final test solution(s) including control(s)): < 100 mg/L - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: zebra fish
- Source: Agrojardin, Avda. Cantabria 4, San Sebastian de los Reyes, 28050 Madrid, Spain
- Length at study initiation: 2 ± 1 cm
FEEDING DURING TEST
- Food type: Nutrafin
- Amount: 2% mean bodyweight
- Frequency: once every three days
ACCLIMATION
- Acclimation period: 14 days
- Acclimation conditions (same as test or not): water temperature, photoperiod and feed were similar to those in test
- Type and amount of food: Nutrafin, 10% of bodyweight
- Feeding frequency: once a day every working day
- Health during acclimation (any mortality observed): no mortality observed - Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 21 d
- Hardness:
- 49.52 - 60.95 mg/L as CaCO3
- Test temperature:
- 20 ± 1°C
- pH:
- 6.33 - 7.41
- Dissolved oxygen:
- 44 - 85.8% of saturation
- Nominal and measured concentrations:
- Measured: 57.78 ± 31.85 ng/mL (equivalent to 57.78 µg/L)
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Aquaria
- Material, size, fill volume: Glass, 40 cm x 25 cm x 20 cm, 15 L
- Aeration: Dilution water tank was aerated with oil-free air; exposure tanks were not aerated
- Type of flow-through (e.g. peristaltic or proportional diluter): peristaltic
- Flow rate: 1.32 L/hr
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 10
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Madrid tap water, dechlorinated using sodium thiosulphate, purified with charcoal
- Nitrites: 0.003-0.070 mg NO2-
- Conductivity: 142.6 - 213 µS/cm
- Intervals of water quality measurement: every 3 - 4 days (hardness, pH and dissolved oxygen were determined twice weekly and temperature was determinded daily)
OTHER TEST CONDITIONS
- Photoperiod: 12 hrs light/12 hrs dark
EFFECT PARAMETERS MEASURED: Mortality, behaviour and toxic symptoms
TEST CONCENTRATIONS
- Test concentrations: Acetone was used as a vehicle to obtain a testing concentration above the water solubility (37.2 ± 11.7 ng/mL) of LAB. Note that all concentrations in the study were reported in units of ng/mL, which is equivalent to µg/L. The standard unit for aquatic toxicity data is µg/L and so this unit was used to report the results in this summary. - Reference substance (positive control):
- no
- Key result
- Duration:
- 21 d
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 57.78 µg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- other: behaviour, toxic symptoms, mortality
- Remarks on result:
- other: no toxic effects observed
- Duration:
- 21 d
- Dose descriptor:
- other: LC0
- Remarks on result:
- other: above water solubility limit
- Details on results:
- No mortality was observed in the test substance aquarium. One incidental non-treatment related mortality was observed in the control group. Another fish was removed from the control group due to attack by other fish. No toxic symptoms were observed in any of the test aquaria. Note that individual homologues were also tested. Phenyl C10, C12 and C18 also resulted in no toxic symptoms for the duration of the study.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the findings, the 21-day NOEC zebra fish exposed to LAB was determinded to be ≥ 57.78 µg/L, and the LC0 was above the water solubility limit.
- Executive summary:
The effects of LAB on zebra fish (Danio rerio) was studied in a flow-through toxicity test. The study was conducted according to OECD TG 203. It was not compliance with GLP but appears to be conducted similar to GLP studies. Two groups of ten zebra fish were exposed in an extended acute test to a test solution of LAB for 21 days. This high exposure was obtained by using acetone as a vehicle. The measured test concentration was 57.78 µg/L, which was above the water solubility of 37.2 µg/L (determined in a water solubility test conducted concurrently). No mortality, behavioural changes, or toxic symptoms were noted in the exposure groups.
Based on the findings, the 21 -day NOEC for zebra fish was determined to be ≥ 57.78 µg/L, the LC0 was above the water solubility limit of LAB.
Reference
Description of key information
A 21-day long-term toxicity test of the test subtsance to freshwater fish (Danio rerio) was conducted according to OECD guideline No.203. The NOEC based on behaviour, toxic symptoms and mortality was determinded to be > 57.78 µg/L.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 57.78 µg/L
Additional information
An OECD 203 study with zebra fish (Danio rerio) was conducted in which the exposure period was extended to 21 days. Fish were exposed to LAB in a flow-through system at a limit concentration of 58 µg/L using acetone as a solvent. Fish were fed with Nutrafin once every three days during the test. No mortality was observed in the treatment solutions during the study. No toxic symptoms were observed. The 21-day NOEC is therefore greater than the limit dose of 58 µg/L.
The lack of fish toxicity is
consistent with expectations. Overall, LAB has very low water solubility
and in a 14-day study with fish there were no effects at the limits of
water solubility. In fact, in short-term tests conducted by Gledhill et
al. (1991), fish were unaffected even at nominal concentrations of 1000
mg/L and with LAB visibly floating on the surface of the test vessels.
Furthermore, short-term studies conducted with aquatic invertebrates and
algae indicated no doseresponsive effects at the water solubility limit.
Finally, a 21-day long-term study in Daphnia was conducted and resulted
in a LOAEC of 0.015 mg/L (15 µg/L). Based on the generally greater
sensitivity of Daphnia than fish, the lack of bioaccumulation potential,
the available fish, invertebrate and algae data, and in accordance with
Annex IX, Section 9, column 2 of the REACH regulation, a long-term
toxicity study in fish is not deemed necessary.
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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