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EC number: 201-740-9 | CAS number: 87-33-2
- 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
- Type of information:
- other: information from secondary source
- Adequacy of study:
- key study
- Study period:
- 2011
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- A reliable secondary source, summarising ISDN pharmaco-toxicological properties, was used. However, the primary sources were not revisited in order to verify their contents; for this reason reliability score 2 was used. The used secondary source has been updated on January, 2011; therefore it covers the most updated literature on the substance.
Data source
Referenceopen allclose all
- Reference Type:
- secondary source
- Title:
- No information
- Bibliographic source:
- Physicians' desk reference
- Reference Type:
- secondary source
- Title:
- No information
- Year:
- 2 011
- Bibliographic source:
- Drugdex Drug Evaluation: DRUGDEX® System. Thomson Reuters, Greenwood Village, Colorado.
Materials and methods
- Objective of study:
- other: assessment of pharmacokinetic parameters
Test guideline
- Qualifier:
- no guideline available
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Isosorbide dinitrate
- EC Number:
- 201-740-9
- EC Name:
- Isosorbide dinitrate
- Cas Number:
- 87-33-2
- Molecular formula:
- C6H8N2O8
- IUPAC Name:
- isosorbide dinitrate
Constituent 1
Results and discussion
Toxicokinetic / pharmacokinetic studies
Toxicokinetic parametersopen allclose all
- Test no.:
- #1
- Toxicokinetic parameters:
- half-life 1st: about 4 h for elimination
- Test no.:
- #2
- Toxicokinetic parameters:
- other: The distribution volume is 2-4 L/Kg
- Test no.:
- #3
- Toxicokinetic parameters:
- other: The clearance is 2-4 L/min
Metabolite characterisation studies
- Metabolites identified:
- yes
- Details on metabolites:
- There are two metabolites: isosorbide-2-mononitrate (half life is about 2 hours) and isosorbide-5-mononitrate (half life is about 5 hours).
Any other information on results incl. tables
After oral administration of both single and repeated doses (15, 30, 60 and 120 mg four times daily) of ISDN, peak serum levels are observed after 0.5 to 1 hours. Oral bioavailability ranges from 22% to 59%; it may be affected by food (reduced absorption); multiple-dose studies of ingested ISDN have shown progressive increases in bioavailability during chronic administration.
Protein binding is minimal. In humans the volume of distribution ranges from 48 to 473 liters (2 -4 L/kg). ISDN is metabolized to isosorbide-5-mononitrate and to isosorbide-2-mononitrate. The excretion is mainly renal (80% to 90% of the administered dose): the majority is excreted as conjugated metabolites within 24 hours . Total body clearance is 2 -4 liters/minute. During chronic administration, clearance decreased with increasing dose. The elimination half-life after oral administration is 4 hours.The daily dose-free interval is at least 14 hours due to the half-lives of ISDN and its active metabolites.
Applicant's summary and conclusion
- Executive summary:
After oral administration of both single and repeated doses (15, 30, 60 and 120 mg four times daily) of ISDN, peak serum levels are observed after 0.5 to 1 hours. Oral bioavailability ranges from 22% to 59%; it may be affected by food (reduced absorption); multiple-dose studies of ingested ISDN have shown progressive increases in bioavailability during chronic administration.
Protein binding is minimal. In humans the volume of distribution ranges from 48 to 473 liters (2 -4 L/kg). ISDN is metabolized to isosorbide-5-mononitrate and to isosorbide-2-mononitrate. The excretion is mainly renal (80% to 90% of the administered dose): the majority is excreted as conjugated metabolites within 24 hours . Total body clearance is 2 -4 liters/minute. During chronic administration, clearance decreased with increasing dose. The elimination half-life after oral administration is 4 hours.The daily dose-free interval is at least 14 hours due to the half-lives of ISDN and its active metabolites.
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