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EC number: 200-680-0 | CAS number: 68-19-9
- 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: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: No guideline was followed. Only few data on test method reported.
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 950
Materials and methods
- Principles of method if other than guideline:
- 10 albino mice per group were given single peritoneal and subcutaneous injections of the test substance.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- Cyanocobalamin
- EC Number:
- 200-680-0
- EC Name:
- Cyanocobalamin
- Cas Number:
- 68-19-9
- Molecular formula:
- C63H88CoN14O14P
- IUPAC Name:
- cyanocobalamin
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): Vitamin B12.
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- other: albino mice.
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 11 g
Administration / exposure
- Route of administration:
- other: intraperitoneal and subcutaneous.
- Vehicle:
- unchanged (no vehicle)
- Doses:
- Intraperitoneal injections: 0.75 mg/kg (Group 1), 1.5 mg/kg (Group 2) and 3 mg/kg (Group 3).
Subcutaneous injections: 3 mg/kg (Group 4). - No. of animals per sex per dose:
- 10 animals/dose.
- Control animals:
- no
Results and discussion
Effect levelsopen allclose all
- Sex:
- not specified
- Dose descriptor:
- LD100
- Effect level:
- 3 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: (intraperitoneal route)
- Sex:
- not specified
- Dose descriptor:
- LD100
- Effect level:
- 3 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: (subcutaneous route)
- Mortality:
- No mortality was found in the 0.75 mg/kg dose group. Two out of 10 animals died after an intraperitoneal administration of 1.5 mg/kg of the test substance and the highest dose tested (3 mg/kg) was lethal for 100 per cent of the animals treated, both subcutaneously and intraperitoneally.
- Clinical signs:
- Excitation and convulsions were observed after administration of 1.5 mg/kg of Vitamin B12 intraperitoneally and 3 mg/kg, both subcutaneously and intraperitoneally. In the 3 mg/kg dose groups, the excitatory state ended in cardiac and respiratory failure.
- Body weight:
- No data.
- Gross pathology:
- At necropsy, only congestion and edema of the lungs and slight congestion of the visceral organs was observed.
- Other findings:
- - Histopathology: The lungs presented intense hyperemia. Histologic study of liver, kidney, adrenal gland, intestine, thymus, testicle and spleen did not show any pathologic change.
Any other information on results incl. tables
Table 1. Data Concerning Experimental Administration of Vitamin B12.
Group |
Animals treated |
Route of Injection |
Amount of Vitamin B12 (mg/kg) |
Signs of Toxicity |
Mortality Rate |
1 |
10 |
Intraperitoneal |
0.68 |
None |
None |
2 |
10 |
Intraperitoneal |
1.36 |
Excitatory state with convulsions |
2/10 |
3 |
10 |
Intraperitoneal |
2.73 |
Excitatory state with convulsions ending in cardiac and respiratory failure |
10/10 |
4 |
10 |
Subcutaneous |
2.73 |
Excitatory state with convulsions ending in cardiac and respiratory failure |
10/10 |
Applicant's summary and conclusion
- Conclusions:
- The intraperitoneal and subcutaneous LD100 of the test substance is determined to be 3 mg/kg.
- Executive summary:
Forty albino mice were given intraperitoneal injections of the test substance in doses of 0.75, 1.5 and 3 mg/kg and 3 mg/kg of the test substance subcutaneously.On the basis of the study findings, it can be stated that an intraperitoneal dose of 0.75 mg/kg is devoid of toxicity, while an intraperitoneal dose of 1.5 mg/kg is toxic, causing excitation and convulsions to the exposed animals. The highest dose tested (3 mg/kg) is lethal for 100 per cent of the animals treated, administered either intraperitoneally or subcutaneously. Mice that died after injection of Vitamin B12 showed no pathologic changes other than congestion of the lung. From these findings, the intraperitoneal and subcutaneous LD100 of the test substance is determined to be 3 mg/kg.
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