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EC number: 216-721-0 | CAS number: 1653-19-6
- 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:
- key study
- Study period:
- 1974
- Reliability:
- 2 (reliable with restrictions)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 974
- Report date:
- 1974
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Six male albino rats with initial body weights of 248-289 grams were exposed to an atmosphere containing the test material for a single four-hour period. All surviving animals were weighed and observed daily for 14 days post-exposure. Selected animals were sacrificed at one, two, seven and fourteen days post exposure for histopathological examination.
- GLP compliance:
- no
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Reference substance name:
- Butadiene, 2,3-dichloro-
- IUPAC Name:
- Butadiene, 2,3-dichloro-
- Reference substance name:
- 8798
- IUPAC Name:
- 8798
- Reference substance name:
- LRT-218
- IUPAC Name:
- LRT-218
- Reference substance name:
- 1,3 Butadiene, 2-chloro
- IUPAC Name:
- 1,3 Butadiene, 2-chloro
- Reference substance name:
- 8849
- IUPAC Name:
- 8849
- Reference substance name:
- LRT-220
- IUPAC Name:
- LRT-220
- Details on test material:
- No further details.
Constituent 1
Constituent 2
Constituent 3
Constituent 4
Constituent 5
Constituent 6
Test animals
- Species:
- rat
- Strain:
- other: ChR-CD
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Six male albino ChR-CD rats with initial body weights of 248-289 grams were used in the study.
Administration / exposure
- Route of administration:
- inhalation: gas
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: The test material was metered along with nitrogen in a delivery tube in order to carry the test material into the 20-litre glass exposure chamber
- Details on inhalation exposure:
- The test material was metered using a syringe infusion pump, into a 1/4-inch stainless steel delivery tube. The tube was heated to 40 °C for H-8798 and was maintained at room temperature for H-8849. Nitrogen was also metered into the delivery tube to carry the test material to the 20-litre glass exposure chamber. At the port of entry into the chamber, oxygen was added in order to produce a 20% oxygen atmosphere.
- Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- Known volumes of the atmosphere were drawn through two midget impingers in series, each containing 15 milliliters of methanol and analysed directly by gas chromatography. Time-weighted concentrations were calculated.
- Duration of exposure:
- 4 h
- Concentrations:
- 8798 was tested at concentrations of 1.02, 1.13, 1.15, 1.71, 1.84, 1.98 and 3.05 mg/litre.
8849 was tested at concentrations of 1.95, 6.24, 8.42, 13.04, 13.30 and 19.58 mg/litre. - No. of animals per sex per dose:
- 6 rats in total were used for each substance at each dose level (8798 and 8849).
- Control animals:
- no
- Details on study design:
- Groups of six male albino rats with initial body weights of 248-289 grams were exposed to atmosphere containing the test material for a single four-hour period. All surviving animals were weighed and observed daily for 14 days post-exposure. Selected animals were sacrificed at one, two, seven and fourteen days post exposure for histopathological examination.
- Statistics:
- Probit analysis (1964) was undertaken.
Results and discussion
- Preliminary study:
- Not performed.
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 2.08 mg/L air
- Based on:
- test mat.
- Mortality:
- 8798 (LRT-218)
1.02 mg/L = 0/6 mortality
1.13 mg/L = (this group was used for serial sacrifice)
1.15 mg/L = 1/6 mortality
1.71 mg/L = 1/6 mortality
1.84 mg/L = 1/6 mortality
1.98 mg/L = 3/6 mortality
3.05 mg/L = 6/6 mortality
8849 (LRT-220)
1.95 mg/L = 0/6 mortality
6.24 mg/L = 0/6 mortality
8.42 mg/L = 1/6 mortality
13.04 mg/L = 2/6 mortality
13.30 mg/L = 2/6 mortality
19.58 mg/L = (this group was used for serial sacrifice) - Clinical signs:
- other: 8798 (LRT-218) None reported during exposure. Post exposure - severe initial weight losses and rapid respiration. Deaths occurred from one to nine days. Delayed deaths were preceded by weight gains at three to four days and then continued losses. 8849
- Body weight:
- No bodyweight data post exposure was included in the study report.
- Gross pathology:
- H-8798 (Pathology report No. 79-74)
Both rats that died on one day post exposure at 3.05 mg/litre demonstrated necrosis of: bronchiolar epithelium, centrilobular to midzonal hepatocytes, renal tubular epithelium and germinal cells of the testes; pulmonary oedema and haemorrhage were also observed. Rats exposed to 1.13 mg/litre showed basically similar lesions as those described above at one day post-exposure. A reparative process was observed in rats sacrificed at two, seven and fourteen days.
H-8849 (Pathology report No. 80-74)
One rat that died two days post exposure demonstrated haemorrhagic infarctions in the lungs. Rats that were sacrificed at one and two days showed, in addition to the above, desquamation and degeneration of the bronchial and bronchiolar epithelium and pulmonary oedema. The tissue changes in the lungs and liver seen at seven and fourteen days were due to regeneration and healing processes of acutely damaged tissue. - Other findings:
- No additional information provided.
Any other information on results incl. tables
No additional information provided.
Applicant's summary and conclusion
- Interpretation of results:
- harmful
- Remarks:
- Migrated information 2,3 -Dichlorobutadiene had an LC50 of 2.08 mg/L requiring classification as harmful by inhalation and R20 labelling in respectof the risk phrase Criteria used for interpretation of results: EU
- Conclusions:
- H-8798 (LRT-218)
The median lethal concentration (LC50) for young adult male rats exposed to 2,3 -Dichlorobutadiene for four hours was 2.08 mg/litre with 95% confidence limits of 1.79 and 2.68. This compound caused no obvious clinical signs during exposure, but severe weight losses and rapid respiration were observed during the early recovery period. Deaths, both early and delayed were preceded only by severe weight losses. Histopathologically this compound produced necrosis in the bronchiolar epithelium, liver, kidney and testes. The survivors demonstrated partial recovery from these injuries at the end of the 14 -day recovery period. 2,3 -Dichlorobutadiene should be considered moderately toxic by inhalation exposure.
H-8849 (LRT-220)
The approximate lethal concentration (ALC) for young adult male rats exposed to 2 -chloro-1, 3 -butadiene for four hours was 8.42 mg/litre. On the basis of the available data, a median lethal concentration could not be determined for this compound. Laboured respiration and pallor were observed during exposures and severe weight losses and deaths, often delayed, were observed in concentrations of 8.42 mg/L and above. Histopathologically this compound caused severe damage in the lungs and liver which was partially healed by 14 days post-exposure. 2 -chloro-1, 3 -butadiene is classified as a slightly toxic compound by inhalation exposure. - Executive summary:
Six male albino ChR-CD rats were exposed to atmospheres containing the test material for a single 4 -hour period. All surviving animals were weighed and observed daily for 14 days post-exposure. Selected animals were sacrificed at 1, 2, 7 and 14 days post-exposure for histopathological examination. The LC50 was 2.08 mg/L. The test substance caused no obvious clinical signs during exposure, but severe weight losses and rapid respiration were observed during the early recovery period. Deaths, both early and delayed, were preceded only by severe weight losses. Histopathologically, the test substance produced necrosis in the bronchiolar epithelium, liver, kidney, and testes. The survivors demonstrated partial recovery from these injuries at the end of the 14 -day recovery period.
2,3 -Dichlorobutadiene (LRT-218) should be considered moderately toxic by inhalation exposure and 2 -chloro-1, 3 -butadiene is classified as a slightly toxic compound by inhalation exposure (LRT-220). Under REACH Classification the material is harmful by inhalation, R20.
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