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Diss Factsheets
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EC number: 212-079-0 | CAS number: 760-23-6
- 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:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Adopted according to OECD SIDS (public available peer reviewed source). The original source is not available and has not been reviewed.
Data source
Referenceopen allclose all
- Reference Type:
- secondary source
- Title:
- SIDS Initial Assessment Report for 11th SIAM, UNEP Publications
- Author:
- OECD SIDS
- Year:
- 2 003
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 967
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- An acute single dose inhalation toxicity test was performed on 6 male rats in order to determine the LC50.
- GLP compliance:
- no
- Remarks:
- GLP was not mandatory at the time of the study
- Test type:
- other: Single Dose Inhalation Toxicity Test
Test material
- Reference substance name:
- 3,4-dichlorobut-1-ene
- EC Number:
- 212-079-0
- EC Name:
- 3,4-dichlorobut-1-ene
- Cas Number:
- 760-23-6
- Molecular formula:
- C4H6Cl2
- IUPAC Name:
- 3,4-dichlorobut-1-ene
- Details on test material:
- - Name of test material (as cited in study report): 3,4-Dichlorobut-1-ene
- Analytical purity: 98%
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: ChR;CD (SD)
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 246-295 g bw
Administration / exposure
- Route of administration:
- inhalation: vapour
- Vehicle:
- not specified
- Details on inhalation exposure:
- The test material was metered by a syringe drive into a stainless steel T tube where it was vaporized at 120-150°C. The resulting vapours were carried by a stream of air into a 16 liter exposure chamber.
- Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- The chamber atmosphere was analyzed at least once every hour by a gas chromatographic method.
- Duration of exposure:
- 4 h
- Concentrations:
- 1000, 2250, 3000 ppm
- No. of animals per sex per dose:
- 6 (only male animals were tested)
- Control animals:
- other: not necessary
- Details on study design:
- - Necropsy of survivors performed: yes
- Organs examined at necropsy: kidney, liver, trachea, lung, brain, testes, bone marrow, spleen, thymus, gastro intestinal tract were examined.
- Other examinations performed: clinical signs, histopathology. - Statistics:
- Statistical analysis by metod of Litchfield, J. T., Jr., and F. Wilcoxon, J. Pharmacol. And Exper. Ther., 96, 99 (1949).
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- 10.89 mg/L air
- Based on:
- test mat.
- Exp. duration:
- 4 h
- Mortality:
- Deaths occurred 2-6 days post-exposure.
- Clinical signs:
- other: Clinical signs of irregular breathing, incoordination, unresponsiveness and lacrimation (only at the beginning of the exposure) were observed.
- Body weight:
- No data
- Gross pathology:
- No data
- Other findings:
- Inhalation at both high and low dosage levels was followed by degenerative lesions of the livers and/or kidneys of rats which died or killed within two days of exposure. Observable lesions were not present in the tissues examined from rats killed at seven days following low level exposure or fourteen days following medium level exposure.
Any other information on results incl. tables
On the basis of the results, 3,4 -dichlorobut-1 -ene is to be classified as Xn, R20 (Harmful by inhalation), according to the DSD classification criteria and Acute Tox. 4 (Harmful by inhalation) according to CLP classification criteria.
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.