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EC number: 231-104-6 | CAS number: 7439-95-4
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Materials and methods well described; results presented adequately in text, tables and figures. A second observation (72 hours after beginning of the challenge) was not performed.
Data source
Reference
- Reference Type:
- publication
- Title:
- Evaluation of the skin sensitizing potential of biodegradable magnesium alloys
- Author:
- Witte, F. et al.
- Year:
- 2 007
- Bibliographic source:
- J. Biomed. Mater. Res. A. 86: 1041-1047.
- Report date:
- 2007
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- yes
- Remarks:
- see "rationale for reliability"
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- yes
- Remarks:
- see "rationale for reliability"
- Principles of method if other than guideline:
- The test animals are initially exposed to the test substance by intradermal injection (day 0) and topical induction (day 7). Following a rest period of 14 days (induction period), during which an immune response may develop, the animals are exposed to a challenge dose. The extent and degree of skin reaction to the challenge exposure (patch removal after 24h) in the test animals is compared with that demonstrated by control animals which undergo sham treatment during induction and receive the challenge exposure (48h after beginning of the challenge).
- GLP compliance:
- not specified
- Type of study:
- guinea pig maximisation test
Test material
- Reference substance name:
- see "details on test material"
- IUPAC Name:
- see "details on test material"
- Test material form:
- not specified
- Details on test material:
- Name of test material (as cited in study report):
4 different magnesium alloys:
(i) AZ31: MgAl(2.4 - 3.6%) Zn(0.5 - 1.5%) Mn(0.15 - 1%) Si 0.1% Cu 0.1% = Mg content between 96.8 - 93.7% (w/w)
(ii) AZ91: MgAl(8.1 - 9.3%) Zn(0.4 - 1%) Mn(0.17 - 0.35%) Si 0.2% = Mg content between 91.1% - 89.2% (w/w)
(iii) WE43: MgLi4Al(3.4 - 4.6%) rare earth(1.8 - 3%) Mn(min.0.25%) Zn (max0.22%) = Mg content between 94.3 - 92% (w/w)
(iv) LAE442: MgY(3.7 - 4.3%) rare earth(2.4 - 4.4%) Zr(0.4 - 1%) Li 0.2% Mn 0.15% = Mg content between 93.2 - 90% (w/w)
Numbers following the letters represent the percentage of the element content in the magnesium alloy displayed in % w/w
The test material AZ31 was achieve from Dead Sea Magnesium, Israel, the remaining alloys were purchased from Magnesium Elektron in UK.
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Harlan Winkelmann, Borchen, Germany
- Weight at study initiation: 400-550g
- Housing: in pairs in clean plastic cages (55 x 32.8 x 19 cm^3) on standard bedding
- Diet: ad libitum, standard pellets
- Water: ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature: 20 +/- 3°C
- Humidity: humidity of 30-70%
- Photoperiod: 2 hours dark/light cycle
No further details are given.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- other: see "concentration"
- Concentration / amount:
- 100%
All test items were tested both in a dissolved and in a solid state parallel to positive and negative control substances. Therefore, the magnesium alloys were dissolved by boiling in 2 mol/L HCl solution and buffered with 1 mol/L NaOH solution at pH 5.5. The supernatants were microfiltrated and the ion metal content was confirmed by ICP-AES.
Challengeopen allclose all
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- other: see "concentration"
- Concentration / amount:
- 100%
All test items were tested both in a dissolved and in a solid state parallel to positive and negative control substances. Therefore, the magnesium alloys were dissolved by boiling in 2 mol/L HCl solution and buffered with 1 mol/L NaOH solution at pH 5.5. The supernatants were microfiltrated and the ion metal content was confirmed by ICP-AES.
- No. of animals per dose:
- 20 animals for each test substance; 10 with the solid material and 10 with the dissolved material. 15 animals in the negative control group and 15 animals in the positive control group.
- Details on study design:
- An intradermal test and an epicutaneous patch test were performed. The skin reaction was interpreted by a qualitative grading of three independent observers immediately and 24 hours after patch removal. For grading of the skin reaction, the erythema classification according to Magnusson-Klingman test was used. A skin reaction graded greater than zero was defined as erythema.
The test site was clipped for intradermal injection. For topical application, the hair was clipped and closely shaved. Cellulose filters (2 x 4cm^2 and 2 x 2cm^2) were used as patches. Applied test patches were covered with overlapping pieces of impermeable plastic tape and fixed with 25cm long strips of elastic tape bandage which was secured by twp pieces of tape.
Cutaneous biopsies were harvested 24 hours after patch removal and analysed for histomorphological criteria. Epidermis and dermis were included in cell counting and histomorphological analysis. - Challenge controls:
- Negative control: sodium-lauryl-sulfate
Preliminary test performed with all test items with one animal each; non irritant concentration were determined - Positive control substance(s):
- yes
- Remarks:
- hydroxy-cinnamon-aldehyde
Results and discussion
- Positive control results:
- All guinea pigs exposed to the standard allergen showed persisting erythema for more than 24 hours after patch removal. One animal died during the challenge phase for reasons not related to the test and one skin biopsy was lost because of technical problems. The histological analysis showed in 12 (92.3%) of the remaining 13 biopsies all four criteria of allergy such as spongiosis, oedema, and diffuse as well as perivascular mononuclear infiltrates. The positive control biopsies contained a mean of 52.7 basophile cells/400 leukocyte cells. Furthermore, in biopsies of the positive control group, a significant higher number of basophile cells was found compared to the negative control group and all tested substances (p=0.001, ANOVA).
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: AZ91
- Dose level:
- dissolved test substance
- No. with + reactions:
- 3
- Total no. in group:
- 10
- Clinical observations:
- mild skin reactions after 24 hours
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: AZ91. Dose level: dissolved test substance. No with. + reactions: 3.0. Total no. in groups: 10.0. Clinical observations: mild skin reactions after 24 hours.
- Reading:
- 1st reading
- Hours after challenge:
- 0
- Group:
- other: AZ31
- Dose level:
- dissolved test substance
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Clinical observations:
- mild clinical skin response immediately after patch removal; 24h after the patch was removed, all erythema had faded.
- Remarks on result:
- other: see Remark
- Remarks:
- Reading: 1st reading. . Hours after challenge: 0.0. Group: other: AZ31. Dose level: dissolved test substance. No with. + reactions: 1.0. Total no. in groups: 10.0. Clinical observations: mild clinical skin response immediately after patch removal; 24h after the patch was removed, all erythema had faded..
- Reading:
- 2nd reading
- Hours after challenge:
- 24
- Group:
- other: AZ31
- Dose level:
- dissolved test substance
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 24.0. Group: other: AZ31. Dose level: dissolved test substance. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- No. with + reactions:
- 15
- Total no. in group:
- 15
- Clinical observations:
- persisting erythema
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: positive control. No with. + reactions: 15.0. Total no. in groups: 15.0. Clinical observations: persisting erythema.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- No. with + reactions:
- 0
- Total no. in group:
- 15
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: negative control. No with. + reactions: 0.0. Total no. in groups: 15.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: WE43 and LAE442
- Dose level:
- dissolved test substance
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- remarks: 10 per test substance (in total 20 animals)
- Remarks on result:
- other: see Remark
- Remarks:
- Reading: 1st reading. . Hours after challenge: 24.0. Group: other: WE43 and LAE442. Dose level: dissolved test substance. No with. + reactions: 0.0. Total no. in groups: 10.0. Clinical observations: remarks: 10 per test substance (in total 20 animals).
Any other information on results incl. tables
Test results for all substances used as received.
Between 90% (AZ31) and 100% (AZ91) of the tested skin areas displayed erythema immediately after patch removal. However, after 24 hours the erythema remained in 20% of the AZ91 group and 11% of the LAE442. To identify allergic erythema after 24 hours, dermal biopsies were taken. All biopsies exhibited significantly (p=0.001) less histomorphological criteria of allergenicity compared to the positive control group. In all biopsies no significant differences were found for basophile cells compared to the negative control. In the LAE442 group of the solid test substances, one animal died unrelated to the study conditions. Animals treated with AZ91and LAE442 which still had an erythema 24 hours after patch removal, showed no criteria of allergenicity in histomorphological analysis. No correlation was found between the cell count of eosinophiles and the concentration of aluminium in the test solutions (p>0.05).
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information
- Conclusions:
- The tested magnesium alloys (with a total magnesium content between 89.2 – 96.8%) provide no sensitising potential compared to the control groups.
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