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: 221-070-0 | CAS number: 2997-92-4
- 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: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Remarks:
- 2,2’-Azobis(2-amidinopropane) dihydrochloride is expected not to be acute dermal toxic because the analogue 2,2’-Azobis(2-amidinopropane) sulfate has not shown acute dermal toxicity properties in a well performed study. The source chemical 2,2’-Azobis(2-amidinopropane) sulfate is sufficiently similar to read-across towards 2,2’-Azobis(2-amidinopropane) dihydrochloride.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
- Report date:
- 1980
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 402 (Acute Dermal Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- 2,2'-Azobis(2-amidinopropane) sulfate
- IUPAC Name:
- 2,2'-Azobis(2-amidinopropane) sulfate
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): 2,2'-Azobis (2-amidinopropane) sulfate
- Molecular formula (if other than submission substance): C8H20N6O4S
- Molecular weight (if other than submission substance): 296,347 g/mol
- Smiles notation (if other than submission substance): OS(O)(=O)=O.CC(C)(\N=N\C(C)(C)C(N)=N)C(N)=N
- InChl (if other than submission substance): InChI=1S/C8H18N6.H2O4S/c1-7(2,5(9)10)13-14-8(3,4)6(11)12;1-5(2,3)4/h1-4H3,(H3,9,10)(H3,11,12);(H2,1,2,3,4)
- Structural formula attached as image file (if other than submission substance):
- Substance type: organic
- Physical state: solid
Purity/impurities
The impurities in the target substance do not indicate toxicological relevence to this endpoint. The impurities are all below 1 %.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 207 to 300 g
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- other: aquesous methylcellulose 1%
- Details on dermal exposure:
- TEST SITE
- Area of exposure: dorso-lumbar region
- % coverage: 10 %
- Type of wrap if used: aluminium foil, held in place with impermeable dressing
REMOVAL OF TEST SUBSTANCE
- Washing: with warm water
- Time after start of exposure: 24 h
TEST MATERIAL
- suspended in vehicle
- Amount(s) applied (volume or weight with unit): 6.3 ml/kg bw
- Concentration (if solution): 60 % w/v suspension
- Constant volume or concentration used: yes
VEHICLE
- Amount(s) applied (volume or weight with unit): 6.3 ml/kg bw
- Concentration (if solution): 60 % w/v suspension - Duration of exposure:
- 24 hours
- Doses:
- 3.78 g /kg bw
- No. of animals per sex per dose:
- 5
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations: daily
- Frequency of weighing: weekly
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight - Statistics:
- No statistics necessary
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 3 780 mg/kg bw
- Based on:
- test mat.
- Mortality:
- No mortality observed
- Clinical signs:
- other: Local dermal reactions at the site of application included slight to well-defined erythemaof a focal nature in nine animals between one and four days after treatment. This was accompanied by slight oedema in six animals between one and four days after tre
- Gross pathology:
- Terminal autopsy findings were normal
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
For 2,2’-Azobis(2-amidinopropane) sulfate an in vivo study is available showing no dermal toxicity up to the dose of 3780 mg/kg bw.- Executive summary:
For 2,2’-Azobis(2-amidinopropane) sulfate an in vivo study is available showing no dermal toxicity up to the dose of 3780 mg/kg bw.
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.