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EC number: 283-659-9 | CAS number: 84696-55-9 Substance resulting from the use and production of tin and its alloys obtained from primary and secondary sources and including recycled plant intermediates. Composed primarily of tin compounds and may contain other residual nonferrous metals and their compounds.
- 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
Toxicological Summary
- Administrative data
- Workers - Hazard via inhalation route
- Workers - Hazard via dermal route
- Workers - Hazard for the eyes
- Additional information - workers
- General Population - Hazard via inhalation route
- General Population - Hazard via dermal route
- General Population - Hazard via oral route
- General Population - Hazard for the eyes
- Additional information - General Population
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- high hazard (no threshold derived)
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- high hazard (no threshold derived)
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - workers
5.0. Introduction
The hazard assessment of inorganic UVCBs for the purpose of classification and derivation of threshold values (i.e. DNELs) is a complex process. Due to the variability of the composition of an UVCB, it is not possible to select a sample that would be representative for the hazard profile of the UVCB and could subsequently be used for toxicity testing. Instead of testing, a precautionary approach is followed in which the UVCB nature of a complex metal containing substance having a number of constituents (metals and their compounds or other inorganic compounds) is acknowledged. The hazard profile of each individual constituent is used for deriving the classification of the UVCB (using the mixture rules) and for the derivation of the DNELs of the constituent. Using the unmodified DNEL values of all individual constituents addresses the varying composition of an UVCB on a pre-cautionary basis as it implicitly assumes that the UVCB entirely consists of the specific constituent, i.e. that each constituent would be present to 100% in the UVCB. Thus, this hazard assessment can be considered a conservative approach. The identificationof constituents which are hazardousfor human health also defines the scope of the exposure assessment and risk characterisation (Chapters 9&10).
The hazard profile of the inorganic UVCB and the individual constituents is dependent on their chemical speciation.Depending on the level of knowledge, the following situations can be distinguished:
· If chemical speciation of the constituent in the UVCB is known, this is used for classification.
· If chemical speciation of the constituent as present in the workplace is known, this is used for risk characterisation.
· When information on chemical speciation is not complete, the worst-case speciation for the purpose of risk characterisation and classificationis assumed, i.e. the speciation that would lead to the most severe classification or to the lowest DNEL.It is noted that different chemical species could be relevant (see below).
Selection of toxicological information for classification
The UVCB classification is calculated by applying the CLP mixture rules based on the classification of the known or worst-case speciation of each constituent and worst-case constituent concentration in the UVCB (i.e. the maximum value of the typical concentration reported by the individual legal entities), using the MeClas tool.
Selection of toxicological information for risk assessment
For the purpose of the human health risk assessment for the UVCB,the hazards of each constituent will be assessed and DNEL values for constituentsfor which a hazard has been identifiedare compiled. As indicated above, workers may be exposed to different chemical species compared to those present in the UVCB. Hence, the information onthe intrinsic properties of the UVCB constituents relevant for classification can be refined if it is known which chemical species is present in the workplace. If speciation is unknown, the chemical species of an individual constituent is considered having the lowest DNEL which could be different when compared to the species used for classification.
For the sake of readability of the CSR and the IUCLID, the below sections therefore outlinetoxicity effects derived for the UVCB itself. Information on hazards linked to speciation occurring in case individual constituing species of the UVCB (see CSR 3.0 Introduction to Classification) are released during production/use of the UVCB and are reported in a separate annex of this CSR, if deemed relevant for the risk assessment.
Hazard conclusions for the purpose of classification
The UVCB is treated as a complex metal containing substance with a number of discrete constituting compounds (mainly metals). The hazard classifications of each compound are then factored into a combined classification of the UVCB as a whole. For health endpoints, UVCB classifications are based on the combined hazards of the compounds whereby additivity or key cut off levels, specified in look-up tables are used, depending on the endpoint and amount of information available for the constituting compounds. The classification was derived using Meclas (MEtals CLASsification tool - see www.meclas.eu), a calculation tool that follows classification guidance and implementation in accordance to legal rules and technical guidance from ECHA and CLP see IUCLID section 13 attachment for MeClas Classification conclusions.
Table34:Summary of the information on toxicological information for the purpose of classification
UVCB constituent |
Variabiliy of elemental composition |
Classification according each relevant endpoint |
|
Element |
Speciation* taken forward for Tier 1 human health classification |
|
|
Sn |
Sn metallic |
Maximum |
Self classification of the speciation, see MECLAS report in CSR Annex I |
Ag |
Ag massive |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
C |
inorganic C and C compounds |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
Cd |
Cd metallic |
Maximum |
Harmonised classification of the speciation, see MECLAS report in CSR Annex I |
Cu |
Cu massive |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
Fe |
Fe/Fe compounds |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
Pb |
Pb massive |
Maximum |
Self- classification of the speciation, see MECLAS report in CSR Annex I |
Sb |
Sb |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
Zn |
Zn massive |
Maximum |
Not classified, see MECLAS report in CSR Annex I |
Minors: As, Ni |
Metallic (massive) |
Maximum |
Below 0.1% and/or the speciation not impacting classification, see MECLAS report in CSR Annex I |
* see IUCLID/CSR section 1.2 composition and IUCLID 4.23 additional Physico-chemical Information
Selection of the DNEL(s) for the purpose of risk assessment
The UVCB is an intermediate, with a very limited life cycle (manufacturing and industrial uses only).Testing the UVCB is difficult because of the large uncertainty involved when selecting representative samples due to the variable elemental concentrations in the composition of the UVCB.Derivation of a DNEL for the UVCB as such is therefore difficult to interpret and to extrapolateresults of testing to the entirety of variations of the UVCB because of the uncertainty related to the representativeness of the testing. Also, exposure to the UVCB cannot be measured or modelled because of the multi-constituent character of the UVCB. For these reasons, the UVCB toxicological assessment is driven by the assessment of the individual UVCB constituents.
The human health assessment is based on all hazardous constituents for human health of the UVCB. Different speciation is relevant to consider. In some cases, human health toxicity is driven by free metal ion. In other cases, human health toxicity is different per species and since the speciation of the exposure is not always known, the species with the worst-case DNEL was further considered for the assessment. Toxicological information on the individual UVCB constituents is reported in each constituent summary for which a quantitative exposure and risk assessment was conducted (the information is taken from the respective constituent IUCLID dossiers).
The relevant copper speciations for occupational exposure are Cu2+ion, Cu2O and CuO. There is no difference between the DNEL values of these speciations (apart from the molecular weight conversion). The DNEL values are therefore based on the soluble form. There is no separate DNEL derived for powder form. The common DNEL values are taken forward to risk characterisation.
The relevant lead speciations for occupational exposure are lead metal and lead oxide. All DNELs are based upon systemic biomarkers of exposure and not on external exposure. The DNEL values used for occupational exposure assessment are therefore based on internal concentration of soluble lead concentrations.
Workers can be exposed to arsenic under different speciations i.e. arsenic metal, arsenic sulfide and diarsenic trioxide. Only DNEL values are available for diarsenic trioxide. It is assumed that the arsenic ion is the driver for toxicity. The DNEL for arsenic can therefore be calculated based on the DNEL of arsenic oxide using the molecular weight conversion. These recalculated DNEL values are used for the risk assessment of arsenic. The same rationale holds for antimony.
The relevant nickel speciations are Ni metal, Ni sulfide and Ni oxide. There are differences in DNEL values between these speciations for a few type of effects. The DNEL values of the worst-case speciation form are therefore taken forward to risk characterisation. Ni sulfide has a DNEL of 0.47 mg/m3for the local acute inhalation effects (range 0.47-4 mg Ni/m3). The local long-term dermal DNEL of 0.00044 mg Ni/cm2/day (range 0.00044 -0.07 mg Ni/cm2/day) is taken forward to risk characterisation.
Zn substances are divided in 2 solubility groups: “soluble” substances or “slightly soluble”/“insoluble” substances. The “soluble” DNEL values are selected since these have the lowest (worst-case) DNEL values.
Carbon is speciated as charcoal. There are no other relevant speciations to consider.
The scope of the exposure assessment and type of risk characterization required for workers for each constituent is described in section 9 of this CSR.
Table35:Summary of the information on toxicological information for the purpose of risk assessment
UVCB constituent |
Variability in chemical composition |
DNELs for systemic and local effects, inhalation and dermal route, short term and long term. |
|
Element |
Speciation used for occupational exposure assessment |
||
Sn |
Sn metal considered |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Cu |
Cu ion is toxic driver |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Fe |
Fe ion is toxic driver |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Pb |
Pb ion is toxic driver |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Ag |
Ag compounds |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Cd |
Cd ion is toxic driver |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
As |
Arsenic ion is the driver for toxicity |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Ni |
Difference between Ni metal, Ni sulphide, Ni oxide |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Zn |
2 solubility groups: 1) "soluble" substances 2) "slightly soluble" and 'insoluble" substances |
Hazard assumed as if UVCB consists of 100% worst-case speciation |
See respective DNEL summary in IUCLID or table below |
Table36: Human health hazard conclusions taken forward to CSA
Route |
Type of effect |
Cu |
Pb |
As |
Ni |
Cd |
Zn |
||||||||
Ni metal |
|
NiS |
NiO |
|
|
||||||||||
Assessment rationale for different speciation |
Conservative read-across from Cu2+ |
Lead cation is the primary mediator of lead toxicity |
Arsenic ion is the driver for toxicity |
Difference between Ni metal, Ni sulphide, Ni oxide |
Cd and Cd compounds effect assessment based on Cd |
2 solubility groups: 1) "soluble" substances 2) "slightly soluble" and 'insoluble" substances |
|||||||||
Inhalation |
Systemic Long Term |
See internal DNEL |
See internal DNEL |
1.9mg As/m3(read across from As2O3: 5mg/m3) |
0.05 mg/m3 (inhalable) |
|
0.05 mg/m3 (inhalable) |
0.05 mg/m3 (inhalable) |
0.004 mg/m3(respirable fraction) |
1.25 mg/m3(soluble) 5 mg/m3(insoluble) |
|||||
Systemic Acute |
20.0 mg/m3 |
DNEL not relevant (Pb is not acutely toxic) |
DNEL not relevant |
680 mg/m3 |
|
16.8 mg/m3 |
520 mg/m3 |
No threshold effect and/or no dose-response information available |
No threshold effect and/or no dose-response information available |
||||||
Local Long Term |
OEL 1 mg/m3 |
DNEL not relevant |
DNEL not relevant |
0.05 mg/m3 |
|
0.05 mg/m3 |
0.05 mg/m3 |
No threshold effect and/or no dose-response information available |
No threshold effect and/or no dose-response information available |
||||||
Local Acute |
OEL 1 mg/m3 |
DNEL not relevant (Pb is not acutely toxic) |
DNEL not relevant |
4 mg/m3 |
|
0.47 mg/m3 |
3.9 mg/m3 |
No threshold effect and/or no dose-response information available |
No threshold effect and/or no dose-response information available |
||||||
OEL (Long Term) |
1 mg/m3 (Inhalable) 0.1-0.2 mg/m3(respirable) |
0.05-0.15 mg/m3(Inhalable) |
0.01 -0.05 mg/m3(Inhalable) |
0.05-1mg/m3 (Inhalable) |
0.01 – 0.15 mg/m3(inhalable) 0.002-0.01 mg/m3(respirable) |
ZnO fume: 4-5 mg/m3 ZnO dust: 3-15 mg/m3 ZnCl: 0.5-5 mg/m3 |
|||||||||
Dermal |
Systemic Long Term |
137 mg/kg bw/day |
See internal DNEL |
As2O3: 112μg/kg bw/day As acid: 85 μg/kg bw/d |
Negligible absorption |
|
Negligible absorption |
Negligible absorption |
Exposure based waiving |
83.3 mg/kg bw/day |
|||||
Systemic Acute |
273 mg/kg bw/day |
DNEL not relevant (Pb is not acutely toxic) |
DNEL not relevant |
Not relevant (negligible absorption) |
|
Not relevant (negligible absorption) |
Not relevant (negligible absorption) |
Exposure based waiving |
No threshold effect and/or no dose-response information available |
||||||
Local Long Term |
Exposure based waiving |
DNEL not relevant |
DNEL not relevant |
0.07 mg/cm2/day |
|
0.0048 mg/cm2 |
0.024 mg/cm2/day |
Exposure based waiving |
No threshold effect and/or no dose-response information available |
||||||
Local Acute |
Exposure based waiving |
DNEL not relevant (Pb is not acutely toxic) |
DNEL not relevant |
Not applicable |
|
Not applicable |
Not applicable |
Exposure based waiving |
No threshold effect and/or no dose-response information available |
||||||
Internal |
Systemic Long Term |
Internal DNEL (using MPPD model) 0.04075 mg/kg/day |
DNEL: Male: 40 μg/dL blood Female: 30 μg/dLblood Female of reproductive capacity: 10 μg/dL blood |
BLV 0.9739 μg/dL blood, 30 μg/g creatinine in urine |
Notassessed (indicative 1μg/dL blood) |
European Commission BLV: 2 μg/g creatinine in urine, 0.5 μg/dL blood |
/ |
||||||||
Eye |
Not to be assessed since safety goggle are used where needed. |
*PTWI: Provisional Tolerable Weekly Intake (FAO/WHO)
**Arsenic drinking water:http://www.who.int/water_sanitation_health/dwq/chemicals/nitratenitritesum.pdf
Route |
Type of effect |
Sn |
Sb |
C |
Fe |
Al |
Assessment rationale for different speciation |
Not in multimetallic database |
Read across from antimony trioxide (Data are for Sb) |
Not in multimetallic database,Charcoal speciation most relevant |
Metallic speciation |
Toxicological effects can be attributed to the aluminium ion, Al3+ |
|
Inhalation |
Systemic Long Term |
11.75 mg/m3 |
/ |
10 mg/m3 |
No DNEL needs to be derived |
No-threshold effect available |
Systemic Acute |
11.75 mg/m3 |
No acute effects |
No-threshold effect available |
No DNEL needs to be derived |
No-threshold effect available |
|
Local Long Term |
No hazard identified |
0.5 mg/m3 |
10 mg/m3 |
No DNEL needs to be derived |
3.72 mg/m3 |
|
Local Acute |
No hazard identified |
No acute local effects |
No-threshold effect available |
No DNEL needs to be derived |
No-threshold effect available |
|
OEL (Long Term) |
|
0.5mg/m3 |
14.3 mg/kg bw/d |
|
|
|
Dermal |
Systemic Long Term |
133.3 mg/kg bw/day
|
234.7 mg/kg bw/day 281 for Sb2O3 |
No-threshold effect available |
No DNEL needs to be derived
|
No-threshold effect available |
Systemic Acute |
133.33 mg/kg bw/day |
No acute effects |
No-threshold effect available |
No DNEL needs to be derived |
No-threshold effect available |
|
Local Long Term |
No hazard identified |
No local long term effects expected |
No-threshold effect available |
No DNEL needs to be derived |
No-threshold effect available |
|
Local Acute |
No hazard identified |
No acute local effects |
|
|
|
Eye |
Not to be assessed since safety goggle are used where needed. |
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- high hazard (no threshold derived)
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- high hazard (no threshold derived)
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- high hazard (no threshold derived)
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - General Population
DNELs for the general population are currently not included because an assessment of exposure of man via the environment is not reported but instead considered to be already included in the dossiers of the constituents. However, DNELs for the general population and the assessment of exposure of man via the environment might be amended by further analysis (please refer to Chapter 9.0.2.3. for further details).
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.