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EC number: 290-475-2 | CAS number: 90170-42-6
- 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
A 28 day oral toxicity study performed according to OECD Guideline 407 and under GLP with Sodium N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6 is available, with reliability rating 1. Based on the absence of functional or morphological disturbances supporting the changes noted in the study, a NOAEL of > 1000 mg/kg was established.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- 1 000 mg/kg bw/day
- Study duration:
- subacute
- Species:
- rat
- Quality of whole database:
- Read across from sodium salt, sodium β-Alanine, N-C8-18-alkyl derivs. EC 305-318-6
The study is performed according to OECD 407 guideline and under GLP and has reliability rating 1. It is sufficient to cover the information requirements in Annex VIII.
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
A 28-day
oral toxicity study according to OECD 407 has been performed on Sodium
N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6. The
dose levels tested were 1000 mg/kg/day, 300 mg/kd/day and 50 mg/kg/day.
This study was performed according to the current OECD 407 and EU method
B7 protocols, with full GLP compliance and a well-defined test
substance. No adverse effects were found in the study. The
histopathology showed that the statistically higher thymus weight seen
in females at 1000 mg/kg were minor, non-adverse, treatment-related
lymphocytolysis. Since lymphocytolysis is a common background finding
and based on the incidence, degree and lack of clear dose-relation seen
in this study, this finding was not considered to be an adverse effect
of the test item.
The minimal lymphoid hyperplasia in the mesenteric lymph nodes of the
males and the remaining microscopic findings recorded were within the
normal range of background pathology encountered in Wistar(Han) rats of
this age and strain. No adverse toxicity findings were observed up to
the highest dose level tested, and a NOAEL value could therefore not be
defined. The highest dose tested is therefore reported as NOAEL value
for these this endpoint, since the use of ">" is not possible in the
IUCLID filed specified for effect level.
The data from the 28 day oral toxicity study is therefore used to determine the DNEL values for oral, inhalation and dermal exposure following the ECHA guidance document for deriving DNEL values. As appropriate DNEL values can be calculated using the oral dosing study data, and due to the low vapour pressure of the substance, it is not justified on animal welfare grounds to perform repeat dose dermal or inhalation toxicity studies.
Justification for selection of repeated dose toxicity via oral route - systemic effects endpoint:
The only available 28-day oral toxicity study on Sodium N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6, is performed according to OECD 407 guideline under GLP conditions and has reliability rating 1. No adverse effects were seen in any of the selected doses in the study, and a NOAEL value could therefore not be defined. The highest dose tested is therefore reported as NOAEL value for this endpoint and used for DNEL derivation, since the use of ">" is not possible in the IUCLID filed specified for effect level below.
Justification for selection of repeated dose toxicity dermal - systemic effects endpoint:
There is no repeat dose dermal study Sodium N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6, but a 28 day oral toxicity study according to OECD 407 is available. Based on the physicochemical properties of the substance, it is considered very unlikely that dermal absorption would exceed oral absorption, so it would be expected than the oral NOAEL would be lower than a corresponding value from a dermal study. Results from the two acute toxicity tests available on the substance show no differences in toxicological profile, LD50 is > 2000 mg/kg bw for both exposure routes. Data from the repeat dose oral study can be used in the setting of DNELs in accordance with the REACH guidelines. As appropriate DNEL values can be calculated using the oral dosing study data, it is not justified on animal welfare grounds to perform a repeat dose dermal toxicity study.
Justification for selection of repeated dose toxicity dermal - local effects endpoint:
There is no repeat dose dermal study Sodium N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6, but all three acute skin irritation / corrosion studies and the one acute dermal toxicity study in combination with the 28 day oral toxicity study indicates low toxicity of the substance. This does not justify the requirement for an additional dermal animal study to establish a local NOAEL for dermal exposure.
Justification for classification or non-classification
The EU CLP (GHS) criteria for classification for Specific Target Organ Toxicity (STOT) are based on data from a 90 day study, for Category 2 the range for such effects is 10-<100 mg/kg/day. Where the data are from a 28 day study these levels are multiplied by three. However there were no indications of any specific systemic toxic effects such as serious organ damage in any of the dose groups of Sodium N-(2-carboxyethyl)-N-(2-ethylhexyl)-β-alaninate, CAS No 94441-92-6. Based on the lack of findings from the available 28 day oral toxicity study, there is no evidence of relevant specific target organ toxicity in the rats dosed at up to the highest dose level of 1000 mg/kg/day. Therefore it does not have to be classified and has no obligatory labelling requirement according to the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations (2011), nor the Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures.
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.
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