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Diss Factsheets
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EC number: 212-454-9 | CAS number: 818-61-1
- 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
Direct observations: clinical cases, poisoning incidents and other
Administrative data
- Endpoint:
- direct observations: clinical cases, poisoning incidents and other
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Remarks:
- Basic data given: acceptable study report
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 970
- Report date:
- 1970
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 970
- Report date:
- 1970
Materials and methods
- Study type:
- study with volunteers
- Endpoint addressed:
- respiratory irritation
- Principles of method if other than guideline:
- The experimental procedures consisted of generating and analysing HEA experimental atmosphere in a glass dynamic exposure chamber of 160 liter volume. The chamber was built as such that a subject could protrude his head into the chamber through a rubber diaphragm. Six male volunteers took part in the exposure studies. Each subject would expose himself for three minutes and report his experience to an observer during the exposure.
- GLP compliance:
- no
- Remarks:
- (Study was conducted prior to the advent of GLP regulations)
Test material
- Reference substance name:
- 2-hydroxyethyl acrylate
- EC Number:
- 212-454-9
- EC Name:
- 2-hydroxyethyl acrylate
- Cas Number:
- 818-61-1
- Molecular formula:
- C5H8O3
- IUPAC Name:
- 2-hydroxyethyl acrylate
- Test material form:
- not specified
- Details on test material:
- not specified
Constituent 1
Method
- Type of population:
- occupational
- Subjects:
- - Number of subjects exposed: 6
- Sex: male
- Profession: Of the six subjects, four were industrial hygiene personnel who were frequently exposed to various chemical plant atmospheres. The remaining two were technical personnel of the Inhalation Toxicology Laboratory who were also frequently exposed to airborne chemical pollutants. One of the subjects had hay fever at the time of experimentation. Otherwise, all subjects could be considered healthy. - Route of exposure:
- inhalation
- Reason of exposure:
- intentional
- Exposure assessment:
- measured
- Details on exposure:
- HEA experimental atmosphere was generated and analyzed in a glass dynamic exposure chamber of 160 L volume. The chamber was built as such that a subject could protrude his head into the chamber through a rubber diaphragm. Six male volunteers were took part in the exposure studies. Each subject would expose himself for 3 minutes and report his experience to an observer during the exposure.
- Examinations:
- no data
Results and discussion
- Clinical signs:
- Irritation of eyes and nose was observed at exposure concentrations of 3 ppm (nominal) and higher.
The severity of irritation increased with concentration and could be tolerated for several minutes at 10 ppm. - Outcome of incidence:
- HEA vapour could be detected at concentrations as low as 3 ppm (nominal concentration) and could be tolerated at concentrations as high as 10 ppm. Clinical signs: Irritation of eyes and nose was observed at exposure concentrations of 3 ppm (nominal) and higher. The severity of irritation increased with concentration and could be tolerated for several minutes at 10 ppm.
Any other information on results incl. tables
The results of the human exposure studies are summarized in the table below. It could be seen that HEA could be detected at concentrations as low as 3 -4 ppm, but could be tolerated at concentrations as high as 10 ppm.
Subjects |
HEA concentrations [ppm] |
||||||||
nominal 3 ppm (anal. 4.6 ppm) |
nominal 6 ppm (anal. 7.1 ppm) |
nominal 10 ppm (anal. 10.x* ppm) |
|||||||
|
Eye |
Nose |
Throat |
Eye |
Nose |
Throat |
Eye |
Nose |
Throat |
A |
- |
+ |
- |
/ |
/ |
/ |
- |
+ |
- |
B |
- |
- |
- |
- |
+ |
- |
- |
+ |
- |
C |
- |
+ |
- |
± |
+ |
- |
+ |
+ |
- |
D |
- |
+ |
- |
- |
+ |
- |
/ |
/ |
/ |
E |
- |
+ |
- |
/ |
/ |
/ |
/ |
/ |
/ |
F |
- |
- |
- |
- |
+ |
- |
± |
+ |
- |
- no irritation
± practically no irritation
+ definite irritation, but tolerable
/ unwilling to take part in further studies
* original value not readable on TSCAT copy of the report
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.