Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 270-695-5 | CAS number: 68476-55-1
- 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

Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP, non-guideline, in-vitro and human experimental studies, published in peer reviewed literature, minor restrictions in design and reporting but otherwise acceptable for assessment.
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 996
Materials and methods
- Objective of study:
- toxicokinetics
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Toxicokinetic parameters for inhaled isoprene were determined in healthy human volunteers. These parameters were used to develop a physiological toxicokinetic model.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Isoprene
- EC Number:
- 201-143-3
- EC Name:
- Isoprene
- Cas Number:
- 78-79-5
- Molecular formula:
- C5H8
- IUPAC Name:
- 2-methylbuta-1,3-diene
- Reference substance name:
- 2-methyl-1,3-butadiene
- IUPAC Name:
- 2-methyl-1,3-butadiene
- Details on test material:
- in-vitro studies - Isoprene, 99% was supplied by Aldrich, Steinheim, Germany.
in-vivo animal studies - see Basic toxicokinetics, Supporting study, Peter et al, 1987.
Human study- Isoprene, 99.5% was supplied by Chemie AG, Buchs, Switzerland.
Constituent 1
Constituent 2
- Radiolabelling:
- no
Test animals
- Species:
- other: human, rat and mice
- Strain:
- other: healthy human volunteers, Sprague-Dawley rats and NMRI mice
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- In-vitro animal studies: male Sprague-Dawley rats and male NMRI were supplied by GSF, Neuherberg, Germany and Charles River, Sulzfeld, Germany respectively; blood and tissues were used for determination of partition coefficients.
In-vivo animal studies used male Wistar rats and male B6C3F1 mice; see Supporting study, Peter et. al., 1987 for details.
Human studies involving exposure by inhalation to isoprene: 4 male and 1 female healthy volunteers, 54-91kg body weight, 28-41 years.
Human studies involving measurement of endogenous production of isoprene: 3 male and 1 female healthy volunteers, 54-75kg body weight, 19-34 years.
Administration / exposure
- Route of administration:
- inhalation
- Vehicle:
- other: air
- Details on exposure:
- Human volunteers were exposed to isoprene using a modified spirometer system; the system was flushed and filled with synthetic air prior to exposures. Oxygen consumed during exposure was replaced.
- Duration and frequency of treatment / exposure:
- up to 2.5 hours
Doses / concentrations
- Remarks:
- Doses / Concentrations:
approximately 8 and 40 ppm
- Details on dosing and sampling:
- Isoprene concentrations in head space (in-vitro measurements) and inhaled atmospheres were determined by GC.
- Statistics:
- Toxicokinetic parameters were determined using Solvekin. A physiological toxicokinetic model for isoprene was developed using ACSL 9C1, Mitchell & Gauthier Associates, 1990, USA. The production of endogenous isoprene was determined using SimuSolv version 2.1, Dow Chemical Co., 1990, USA.
Results and discussion
- Preliminary studies:
- Tissue:air and tissue:blood partition coefficients for isoprene were determined in mouse, rat and human.
Toxicokinetic / pharmacokinetic studies
Toxicokinetic parametersopen allclose all
- Toxicokinetic parameters:
- other: Endogenous production of isoprene was 23.8 µmol/h for a 70kg man (0.34 µmol/h/kg).
- Toxicokinetic parameters:
- other: The rate of metabolism of endogenous isoprene in humans was 0.31 µmol/h/kg.
- Toxicokinetic parameters:
- other: Predicted blood concentration of isoprene in humans resulting from endogenous production are 9.5 nmol/L.
- Toxicokinetic parameters:
- other: Rates of metabolism of isoprene to the monoepoxides were approximately 14x faster in mice and 8x faster in rats than in humans.
- Toxicokinetic parameters:
- other: The AUC for isoprene in blood following exposure by inhalation to 10 ppm isoprene for 8 h is approximately 4 fold higher than the AUC resulting from 24h exposure to endogenous isoprene.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): no bioaccumulation potential based on study results
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.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.