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EC number: 203-529-7 | CAS number: 107-88-0
- 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

Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- n/a
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: control and 1000 mg/L at test start and after 48 h of exposure
- Sampling method: 1.5 mL taken from each test vessel
- Sample storage conditions before analysis: analysis performed on day of sampling - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: addition of an aqueous solution of the test substance (10.0 wt.%) to dilution water
- Differential loading: limit test
- Controls: negative control: dilution water
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): not used
- Concentration of vehicle in test medium (stock solution and final test solution): not used
- Evidence of undissolved material (e.g. precipitate, surface film, etc): no - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: waterflea
- Source: laboratory culture, original source: National Environmental Research Centre
- Age at study initiation (mean and range, SD): < 24 h
- Feeding during test: no - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Test temperature:
- 20.4 to 20.5 °C
- pH:
- 7.4 to 8.0
- Dissolved oxygen:
- 8.06 to 9.61 mg/L
- Nominal and measured concentrations:
- Nominal: 1000 mg/L
Measured recovery after 48 h: > 80 % - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): open
- Material, size, headspace, fill volume: 100mL-capacity glass beaker
- Renewal rate of test solution (frequency/flow rate): yes, but no data on intervals (probably once after 24 h)
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: OECD M4 medium
- Culture medium different from test medium: no data
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 hours light, 8 hours dark
- Light intensity: room light
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : immobilisation (48 h)
TEST CONCENTRATIONS
- Spacing factor for test concentrations: not applicable
- Justification for using less concentrations than requested by guideline: limit test - Reference substance (positive control):
- not specified
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- mobility
- Details on results:
- - Behavioural abnormalities: no
- Mortality of control: 0%
- Abnormal responses: no
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: no
- Effect concentrations exceeding solubility of substance in test medium: no - Validity criteria fulfilled:
- yes
- Conclusions:
- The 48-h EC50 for acute effects of 1,4-butanediol to Daphnia magna is > 1000 mg/L.
- Executive summary:
The acute toxicity of 1,4 -butanediol was tested under static conditions in a 48-h toxicity study on the waterflea (Daphnia magna) following OECD TG 202. Analytical verification of the test substance concentrations revealed recovery rates of > 80 % after 48 h. Based on nominal concentrations, the 48 -h EC50 was determined to be > 1000 mg/L.
Reference
Mortality/immobilisation: no dead or immobile animals observed
Analytical monitoring:
Test concentration |
|||||
nominal [mg/L] |
measured [mg/L] |
[% of nominal] |
|||
|
0 h |
48 h |
Mean |
0 h |
48 h |
0 (control) |
< 20 |
< 20 |
--- |
--- |
--- |
1000 |
884 |
1016 |
947 |
88.4 |
102 |
Description of key information
48-h EC50 (Daphnia magna, immobility) > 1000 mg/L (OECD 202, Env. Angency of Japan, 1997)
Key value for chemical safety assessment
Additional information
Read-across approach: butane-1,4 -diol (source), butane-1,3 -diol (target) (see also Read-across justification in IUCLID section 13)
In the available key study, acute toxicity of the source compound 1,4 -butanediol was tested under static conditions in a 48 -h toxicity study on the water flea (Daphnia magna) following OECD TG 202 (RL1). Analytical verification of the test substance concentrations revealed recovery rates of > 80 % after 48 h. Based on nominal concentrations, the 48 -h EC50 was determined to be > 1000 mg/L for source and target substance ( no conversion factor applied as source and target compound have the same molecular weight).
A calculated result is available for 1,3 -butanediol, indicating that the acute toxicity to aquatic invertebrates is beyond 1000 mg/L (Daly, 2000, RL4). Regarding the other studies, the original reports are not available (RL 4), but the results are published under reviewed programmes and by reliable organisations like ECB (see summary of results below).
Test substance |
Species |
EC50 |
Reliability |
Remark |
Reference |
1,4-butanediol (C4) |
Daphnia magna |
> 1000 (48 h) |
1 |
key study; measured; analytical monitoring |
Environmental Agency of Japan, 1997 |
1,4-butanediol (C4) |
Daphnia magna |
813 (48 h) |
4 |
measured; analytical monitoring |
ECB, 2000 |
1,3 -butanediol (C4) | Daphnia sp. | 8702 (48 h) | 4 | calculated | Daly, 2000 |
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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