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EC number: 816-146-0 | CAS number: 1016788-34-3
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- March 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: HET-CAM, in accordance with the protocol proposed in the Official Journal of the Republic of France (#300) dated 26 December 1996
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 3-[(2-acetamidoacetyl)amino]propanoic acid
- EC Number:
- 816-146-0
- Cas Number:
- 1016788-34-3
- Molecular formula:
- C7H12N2O4
- IUPAC Name:
- 3-[(2-acetamidoacetyl)amino]propanoic acid
- Test material form:
- solid: particulate/powder
Constituent 1
Test animals / tissue source
- Strain:
- other: Hen's eegs (White Leghorn)
- Details on test animals or tissues and environmental conditions:
- Temperature: 37 ºC
Test system
- Vehicle:
- physiological saline
- Controls:
- yes, concurrent positive control
- yes, concurrent negative control
- Amount / concentration applied:
- Test system:
Fertilized hen egg (White Leghorn strain) weight from 50 to 65 g at receipt.
Reference items:
-Negative control: Lauryl Sulfo BetaYne (LSB) - CAS number: 14933-08-5 solution at 0.05 % in physiological serum
- Positive control: Lauryl Sulfo BetaYne (LSB) - CAS number: 14933-08-5 solution at 3.2 and 0.4 % in physiological serum
Series definition:
The test item diluted at 5 % is tested on four eggs (300 microL per egg). The reference items are tested in each analysis on two eggs (300 microL). - Duration of treatment / exposure:
- 300 microL of the warmed test item (undiluted or diluted) are carefully placed on the CAM with a pipette and the time clock is started. After contact for 20 seconds the membrane is rinsed with 5 ml of physiological saline at 37°C avoiding any violent splashing. The rinse liquid is removed by tilting the egg.
- Duration of post- treatment incubation (in vitro):
- Any irritant effects are observed for 5 minutes. The time interval when each effect appears (hyperaemia, haemorrhage, coagulation) is recorded by the all or nothing law. The presence and not the severity of the effect is recorded.
- Number of animals or in vitro replicates:
- Test item tested on four eggs, the reference items are tested in each analysis on two eggs.
- Details on study design:
- The principle of the method is based on the observation of the irritant effects (hyperaemia, haemorrhage, coagulation) which may occur within five minutes after placing a test item onto the chorio-allantoic
membrane (CAM) of an embryonic hen egg on the tenth day of incubation.
A score is established from the presence (or absence) of these effects and the time when they appear.
The mean score obtained from four eggs is used to classify the substance into four categories of irritant potential.
Test protocol:
The different stages are performed rapidly under suffic ient lighting not emitting heat. Drying of the CAM must be avoided (if drying occurs maintain the humidity level by spraying).
The egg is placed veltically on a SUppOlt (air pocket upwards).
The shell is cracked at the level of the air pocket and then removed to the level of the shell membrane.
Eggs which do not have a live hen embryo are removed.
The released surface is moistened with physiological saline solution warmed to 37°C and the solution is removed by tilting the egg.
The shell membrane is delicately detached with tweezers and then removed in order to uncover the underlying CAM. Any egg with a defective CAM or traces of haemorrhage is removed. The MCA
integrity is recorded for every egg on scores sheet at the time of the test.
300 !ll of the warmed test item (undiluted or diluted) are carefully placed on the CAM with a pipette and the time clock is started. After contact for 20 seconds the membrane is rinsed with 5 ml of
physiological saline at 37°C avoiding any violent splashing. The rinse liquid is removed by tilting the egg.
At the end of the test, eggs receive a lethal injection of 0.2 ml20 mglml pentobarbital.
Reading procedure:
Any irritant effects are observed for 5 minutes. The time interval when each effect appears (hyperaemia, haemorrhage, coagulation) is recorded by the all or nothing law. The presence and not
the severity of the effect is recorded.
Hyperaemia or injection: Capillaries which were invis ible before adding the substance become visible whereas capillaries which were already visible dilate and become redder. This phenomenon
may affect large diameter vessels.
Haemorrhage: Release of blood escaping from the vessels and or capillaries may take on different appearances, particularly « cauliflower» patches, diffuse sheet, or punctate (the blood escapes
intermittently at di fferent places in the membrane).
It must be noted that:
Haemorrhage may take on a transient appearance: this must nevertheless by counted.
Masked hyperaemia must be counted if massive haemorrhage occurs during the first 30 seconds.
Coagulation, opacity andlor thrombosis:
Opacity: opalescent sheet or direct opacification of part or all of the membrane (take care that this effect is not due to the physico-chemical properties of the substance in aqueous medium, formation of a colloid or precipitate etc.).
Thrombosis: discontinuation of blood flow producing a segmented appearance of the vessels (alternating areas of strangulation more or less dark turgescent areas). Changes occurring in the capillaries are not counted.
Results and discussion
In vitro
Results
- Irritation parameter:
- other: evaluation score
- Run / experiment:
- Mean score
- Value:
- ca. 0
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Other effects / acceptance of results:
- Same results found for each egg (total number of eggs: 4), details:
Hyperanemia: Notation: 0 , Score: 0
Haemorrhage: Notation: 0, Score:0
Opacity: Notation 0 , Score 0
Subsequently, Score for each egg is 0, and Mean score (4 eggs) is 0.
Control: Lauryl sulfobetaïne
At 3.2% (positive control), score on 2 eggs: 17 (Irritant)
At 0.4% (positive control), score on 2 eggs: 10 (Moderately irritant or Irritant)
At 0.05% (negative control), score on 2 eggs: 0 (Practically non-irritant or Slightly irritant)
Results found for the reference items allow to validate the test.
Any other information on results incl. tables
An evaluation score is assigned to each phenomenon according to its occurrence time:
Scores according to the time:
Time
Effect T < 30s 30s<T<2min 2<1'<5min
Hyperaemia 5 3 1
Haemorrhage 7 5 3
Coagulation, opacity and/or thrombosis 9 7 5
The score for each egg is the sum of each phenomenon scores. The test item rating is the arithmetic mean, rounded to two decimal points, of the scores obtained for all eggs (maximum rating 21).
The test item irritation potential (pure or dilute) is given by the following scale:
Rating (N) Classification
N < 1 Practically non irritant
1 =< N<5 Slightly irritant
5 =< N <9 Moderately irritant
N >9 Irritant
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Under the retained experimental conditions, the irritant potential of the test item Acetylglycyl-beta-alanine tested diluted at 5 %, may be classified as practically non irritant according to the adopted scale.
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