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: 211-063-0 | CAS number: 628-96-6
- 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

Long-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- long-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Proposed ASTM method for 3-brood renewal toxicity test (Draft 3).
- Deviations:
- not specified
- GLP compliance:
- no
- Remarks:
- Study is based on a standard national protocol with no variations or quality control issues and is very well-documented. Note that it is unlikely that the laboratory was operating according to all GLP principles at the time of the testing.
Test material
- Reference substance name:
- Glycerol trinitrate
- EC Number:
- 200-240-8
- EC Name:
- Glycerol trinitrate
- Cas Number:
- 55-63-0
- Molecular formula:
- C3H5N3O9
- IUPAC Name:
- propane-1,2,3-triyl trinitrate
Constituent 1
- Specific details on test material used for the study:
- NG dissolved in JHU/APL well water at 1g/L was obtained from the US Naval Ordnance Section, Indian Head, MD.
Reverse phase HPLC determined that no impurities were present during testing.
Stability of stock solution was checked periodically during the study period.
Test solutions
- Vehicle:
- no
Test organisms
- Test organisms (species):
- Ceriodaphnia dubia
- Details on test organisms:
- Test species was Ceriodaphnia dubia cultured at 25 °C and fed a diet of Cerophyl and green algae. Starter cultures were obtained from Center for Lake Superior Environmental Studies, University of Wisconsin.
1 daphnid neonate was randomly assigned to each control or treatment replicate.
Test organisms were fed diet described above before the test, at test initiation and at each 24 h renewal time.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 7 d
Test conditions
- Details on test conditions:
- Acute test with static renewal system with renewal at 24 hrs.
The negative control with 10 replicates was run concurrently.
Photoperiod, temperature, DO, pH, alkalinity, conductivity and total hardness were monitored and reported.
Photoperiod was 16:8 light:dark.
Mean and range of temperature and water quality parameters fell within ranges specified in study guideline.
10 replicates were used per treatment.
Exposure period was 7 days
Exposure pathway was aqueous
Geometric dilution series of 5 concentrations was tested.
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 7 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.23 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 7 d
- Dose descriptor:
- LOEC
- Effect conc.:
- 5.48 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- Endpoint = 7-d LOEC = 5.48 mg/L; 7-d NOEC = 3.23 mg/L
Effect = reproduction
Significant mortality of adults observed in treatment with 16.05 mg/L NG - Reported statistics and error estimates:
- Statistical analysis of concentration data and organism response was based on mean measured concentrations of NG.
Neonate production data were not normally distributed (Chi-square test for normality p<0.05) and therefore, Steel’s Many-One Rank Test (non-parametric) test was conducted to determine which dilutions were significantly different from the control (alpha = 0.05).
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
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.