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EC number: 214-275-1 | CAS number: 1119-34-2
- 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
Endpoint summary
Administrative data
Description of key information
Acute oral toxicity: Key study. Test method similar to OECD 401. The LD50 of L-argine-HCl was determined to be 12400 mg/kg b.w. in a toxicity study with rats.
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1973
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- - Principle of test:
Determination of acute toxicity by Seventy-Two-Hour LD50 calculation. The number dead at 72 hr. was counted and analyzed by the method of Litchfield and Wilcoxon (J. T. Litchfield, Jr., and F. Wilcoxon, J. Pharmacol. Exp Ther., 96, 99(1949))
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: 2 months
- Weight at study initiation: 125-150 g
- Fasting period before study: 24 h
- Housing: no data
- Diet (e.g. ad libitum): Ad libitum.
- Water (e.g. ad libitum): Ad libitum.
- Acclimation period: 1 week
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Remarks:
- (distilled water)
- Details on oral exposure:
- VEHICLE
- Amount of vehicle (if gavage): 6 ml
- Concentration in vehicle: 10 and 20 % (w/v)
- Justification for choice of vehicle: Destilled water has no impact on its own
MAXIMUM DOSE VOLUME APPLIED: 6 ml - Doses:
- 10 and 20 % (w/v) in vehicle
- No. of animals per sex per dose:
- 5
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 72 hours
- Frequency of observations and weighing: mortality at 72 h.
- Other examinations performed: ataxia and sleeping time. - Key result
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 12 400 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: 12.40 ± 0.61 (calculated by the method of Litchfield and Wilcoxon)
- Mortality:
- Not specified.
- Clinical signs:
- Some signs of toxicity did appear such as ataxia, dyspnea, decreased muscle tonus, and loss of righting reflex. Toxicity signs were first observed 11 g/kg bw.
- Body weight:
- Not specified.
- Gross pathology:
- not specified.
- Interpretation of results:
- other: No category (CLP Regulation EC no. 1272/2008)
- Conclusions:
- LD50 of L-argine-HCl was determined to be 12400 mg/kg b.w. in a toxicity study with rats.
- Executive summary:
The acute oral toxicity of L-argine-HCl was investigated with Sprague-Dawley rats. Test item was administered at two dose levels of 10 and 20% (w/v) in distilled water (five males and five females per group). After 72 hours, neurological parameters like ataxia or sleeping time were observed and the number of dead was counted and analyzed by the method of Litchfield and Wilcoxon.Some signs of toxicity were reported such as ataxia, dyspnea, decreased muscle tonus, and loss of righting reflex. Toxicity signs were first observed 11 g/kg bw. LD50 of L-argine-HCl was determined to be 12400 mg/kg b.w.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 12 400 mg/kg bw
- Quality of whole database:
- Key study with Klimisch score = 2
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Acute oral toxicity: Key study: The acute oral toxicity of L-argine-HCl was investigated with Sprague-Dawley rats. Test item was administered at two dose levels of 10 and 20% (w/v) in distilled water (five males and five females per group). After 72 hours, neurological parameters like ataxia or sleeping time were observed and the number of dead was counted and analyzed by the method of Litchfield and Wilcoxon.Some signs of toxicity were reported such as ataxia, dyspnea, decreased muscle tonus, and loss of righting reflex. Toxicity signs were first observed 11 g/kg bw. LD50 of L-argine-HCl was determined to be 12400 mg/kg b.w.
Justification for classification or non-classification
Based on the available data, the substance does not need to classify for acute toxicity according to CLP Regulation (EC) no. 1272/2008.
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