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Diss Factsheets
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EC number: 200-834-7 | CAS number: 75-04-7
- 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
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
Additional information
In a study conducted in 1940, not according to current guidelines, a human test person who received an oral dose of 2 g of the hydrochlorid form of the test substance (the dose was well tolerated by the person) excreted 32 % (after correction for the normal concentration of N) unchanged test substance in the day urine. The remaining 68% are excreted as urea in the urine and C02 in the expiration air.
However, no valid data are available for the determination of toxicokinetics (absorption, distribution, metabolism, and excretion).
Therefore, this evaluation is based on the physico-chemical properties of the substance.
Absorption
Toxic effects have been observed after oral, dermal and inhalative exposure to the test substance. Therefore, an absorption via all three routes is likely. Furthermore, the test substance has a low molecular weight of 45,08 g/mol which supports this assumption. Due to the moderate log Pow value (-0,27), the test substance is favourable for absorption by passive diffusion by oral and inhalative route.
The boiling temperature of the test substance has been determined to be 16,6°C. Therefore the physical state at room temperature is gaseous. Moreover, the high vapour pressure (139700 Pa at 25°C) indicates that the test substance is highly volatile.
Distribution
Due to the low molecular weight of 45,08 g/mol and the miscibility in water, the test substance is expected to have a wide distribution and to diffuse through aqueous channels and pores. The test substance is not lipophilic (log Pow = -0,27) and is therefore not likely to distribute into cells.
Metabolism
The test substance includes an amino group (-NH2). This functional group in general tend to undergo Phase II conjugation reactions.
Excretion
The low molecular weight as well as the miscibility in water are indicators for renal excretion. Furthermore, gases are in general likely to be excreted in exhaled air. The substance is not expected to accumulate in the human body.
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.