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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Workers - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
0.05 mg/m³
Most sensitive endpoint:
developmental toxicity / teratogenicity
Route of original study:
By inhalation
DNEL related information
DNEL derivation method:
other: National OEL
Acute/short term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
104.4 mg/m³
Most sensitive endpoint:
acute toxicity
Route of original study:
By inhalation
DNEL related information
Overall assessment factor (AF):
7.5
Modified dose descriptor starting point:
other: HEC-NOAEC
Value:
783 mg/m³

Local effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
0.05 mg/m³
Most sensitive endpoint:
repeated dose toxicity
DNEL related information
DNEL derivation method:
other: national OEL
Acute/short term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
1.6 mg/m³
Most sensitive endpoint:
repeated dose toxicity
DNEL related information
Overall assessment factor (AF):
4.3
Dose descriptor starting point:
other: HEC-LOAEC

Workers - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
0.44 µg/cm²
Most sensitive endpoint:
sensitisation (skin)
DNEL related information
Overall assessment factor (AF):
1
Dose descriptor:
other: NOAEL
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified

Workers - Hazard for the eyes

Local effects

Hazard assessment conclusion:
medium hazard (no threshold derived)

Additional information - workers

Note 1. Exposures are always given in terms of mg nickel and NOT as mg substance


Note 2. All the values (including the dermal one) are provided in the table below.


Note 3. In cases where existing standards (OELs in case of workers, ambient air standards in case of general public) are used instead of DNEL/DMEL, the fields for Assessment factors and Dose descriptor Starting Points were left blank. Further information on the Standard derivation is contained in the documents referenced in the Table below.


 


Nickel sulphate hexahydrate DN(M)ELs for workers
































































































Exposure pattern



Route



Descriptor



DNEL / DMELa



AF



Corrected Dose descriptor



Most sensitive endpoint



Justification



Acute - systemic effects



Dermal



 



 



 



 



 



Not relevant, negligible absorption



Acute - systemic effects



Inhalation



DNEL (Derived No Effect Level)



104 mg Ni/m³


Inhalable Fractionb



7.5c



HEC-NOAEC: 783 mg Ni/m3


Inhalable Fractiond



acute toxicity (mortality)



 See footnotes



Acute - local effects



Dermal



 



 



 



 



 



No available data to derive DNEL. Not irritating <20% See footnote (f)



Acute - local effects



Inhalation



DNEL (Derived No Effect Level)



1.6 mg Ni/m³


Inhalable Fractionb



4.3e



HEC-LOAEC: 6.9 mg Ni/m3


Inhalable Fractionf



repeated dose toxicity


 (lung inflammation)



 See footnotes



Long-term - systemic effects



Dermal



 



 



 



 



 



Not relevant, negligible absorption



Long-term - systemic effects



Inhalation



DNEL (Derived No Effect Level)



0.05 mg Ni/m³


Inhalable fractiong



 



 



developmental toxicity



 See footnotes



Long-term - local effects



Dermal



DNEL (Derived No Effect Level)



0.00044 mg Ni/cm²h



1i



NOAEL:0.00044 mg Ni/cm2



sensitisation (skin)



 See footnotes



Long-term - local effects



Inhalation



DNEL (Derived No Effect Level)



0.05 mg Ni/m³


Inhalable fractiong



 



 



carcinogenicity and repeated toxicity (respiratory tract- inhalation)



 See footnotes



 
















Long-term - local effects



Inhalation



DNEL (Derived No Effect Level)



0.05 mg Ni/m³


Inhalable fractiong



 



 



carcinogenicity and repeated toxicity (respiratory tract- inhalation)



 See footnotes



a.       The approaches used in the derivation of DNELs are described in appendices C1 to C4 in the CSR for NiSO4, including more details on NOAEL identification and DNEL derivation.


 


b.       The derivation of the acute inhalation DNELs is described in detail in Appendix C3 (CSR NiSO4). Dosimetric modeling was used to calculate human equivalent air concentrations (HECs) for the points of departures based on effects associated with pulmonary deposited (systemic effects) or retained (local effects) nickel doses in rats. This modeling accounts for differences in pulmonary deposition of different particle sizes between rats and humans, and also allowed the incorporation of inhalable workplace particle size ranges in the calculations.


 


c.       Assessment Factor (AF) = 7.5. [AF interspecies differences in susceptibility (AS) = 1 for exposures expressed as concentrations mg/m3, and for lethal effects; AF interspecies remaining differences in susceptibility for respiratory tract = 2.5; AF intraspecies differences in susceptibility = 3 for substances that do not undergo metabolism, see Appendix C3 section C3.6 for more detailed justification; Overall AF = 2.5 x 3 =7.5].    


 


d.       The HEC-NOAEC of 783 mg Ni/m3 (inhalable fraction) was derived from the NOAEC of 120 mg Ni/m3 (MMAD=3µm) by applying a dosimetry adjustment as described in Appendix C3 (CSR NiSO4).


 


e.       AF = 4.3. [AF interspecies difference (AS) = 1 local respiratory effects. AF interspecies difference in susceptibility = 1 (for respiratory toxicity effects after inhalation of particles of nickel or most metal-containing substances in the respirable range, rats seem to be more susceptible to toxicity effects than mice, primates or humans; AF intraspecies differences in susceptibility=3 for substances that do not undergo metabolism. AF for conversion of LOAEC to NAEC=3 based on steep dose-response for nickel toxicity. An AF for exposure duration = 1/2.1 was applied to extrapolate from 16 day repeated exposures to a single exposure. Overall AF= 1 X 3 X 3 X 1/2.1 = 4.3]. See Appendix C3 (CSR NiSO4) for more detailed justification of AF selection.


 


f.        The HEC-LOAEC of 6.9 mg Ni/m3 (inhalable fraction) was derived from the LOAEC of 0.7 mg Ni/m3 (MMAD<4µm) by applying a dosimetry adjustment as described in Appendix C3 (CSR NiSO4).


 


g.       The justification for the use of an inhalable OEL of 0.05 mg Ni/m3 is provided in Appendix C2 of the CSR for NiSO4. This value is based on the SCOEL proposed inhalable OEL for nickel compounds of 0.01 mg Ni/m3 (June 2011) with further adjustments for differences in particle size distributions between animal experiments and workplace exposures and differences in sampling efficiency between workplace 37-mm and inhalable samplers. The SCOEL value was based on epidemiological data on cancer effects. The registrant-derived inhalable value of 0.05 mg Ni/m3 is based on carcinogenicity effects in the respiratory tract observed in human studies, as well as toxicity local effects observed in the lungs of rats after inhalation. Both registrant and SCOEL consider nickel compounds to be genotoxic carcinogens with a practical threshold. These values are also protective against possible reproductive effects. For detailed description of the DNEL derivation and selection of AF, see Appendices C1and C2 in CSR NiSO4.


 


h.       The DNEL for dermal sensitization/elicitation is based on a patch test study with Ni sulphate where exposure lasted for 48 h under occlusion. This value is likely to overestimate risk compared to workplace 8 h exposure without occlusion. This DNEL is protective of both acute and long-term dermal exposures. See Appendix B3 (CSR NiSO4).


 


i.        AF =1. Study done in humans, 48 hours under occlusion. Study was done with a susceptible population.


 


Appendix C1= Derivation of DNELs for 4 Reference Ni substances 


Appendix C2= Background Document in Support of Long-term Inhalable DNELs for Nickel Metal and Nickel Compounds


Appendix C3 = Background Document in Support of Acute DNELs and Guidance Values for Nickel Metal and Nickel Compounds


Appendix C4 = Excel table of DNEL derivations –nickel sulphate

General Population - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
60 ng/m³
Most sensitive endpoint:
developmental toxicity / teratogenicity
Route of original study:
By inhalation
DNEL related information
DNEL derivation method:
other:
Acute/short term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
8.8 mg/m³
Most sensitive endpoint:
acute toxicity
Route of original study:
By inhalation
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
12.5
Modified dose descriptor starting point:
other: HEC-NOAEC
Value:
109.6 mg/m³

Local effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
60 ng/m³
Most sensitive endpoint:
repeated dose toxicity
DNEL related information
DNEL derivation method:
other:
Acute/short term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
0.1 mg/m³
Most sensitive endpoint:
repeated dose toxicity
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
7.1
Dose descriptor starting point:
other: HEC-LOAEC

General Population - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
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:
DNEL (Derived No Effect Level)
Value:
0.011 mg/kg bw/day
Most sensitive endpoint:
developmental toxicity / teratogenicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
100
Modified dose descriptor starting point:
NOAEL
Value:
1.1 mg/kg bw/day
Acute/short term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
0.37 mg/kg bw/day
Most sensitive endpoint:
acute toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
100
Modified dose descriptor starting point:
NOAEL
Value:
36.6 mg/kg bw/day

General Population - Hazard for the eyes

Local effects

Hazard assessment conclusion:
medium hazard (no threshold derived)

Additional information - General Population

Note 1. Exposures are always given in terms of mg nickel and NOT as mg substance


Note 2. All the values (including the inhalation one) are provided in the table below:


Note 3. In cases where existing standards (OELs in case of workers, ambient air standards in case of general public) are used instead of DNEL/DMEL, the fields for Assessment factors and Dose descriptor Starting Points were left blank. Further information on the Standard derivation is contained in the documents referenced in the Table below.


 


Nickel sulphate hexahydrate DN(M)ELs for general population (MvE)


 




















































































































Exposure pattern



Route



Descriptor



DNEL / DMELa



AF



Corrected Dose descriptor



Most sensitive endpoint



Justification



Acute - systemic effects



Dermal



 



 



 



 



 



Not relevant, negligible absorption



 



Inhalation



DNEL (Derived No Effect Level)



8.8 mg Ni/m³b



12.5c



HEC-NOAEC: 109.6 mg Ni/m3 d



acute toxicity (mortality)



 See footnotes



 



Oral



DNEL (Derived No Effect Level)



0.37 mg Ni/kg/day



100e



NOAEL= 36.6 mg Ni/kg/day



acute toxicity (mortality)



See footnotes



Acute - local effects



Dermal



 



 



 



 



 



Not relevant, negligible dermal exposure



 



Inhalation



DNEL (Derived No Effect Level)



0.1 mg Ni/m³b



7.1f



HEC-LOAEC: 0.8 mg Ni/m3 g



repeated dose toxicity


(lung inflammation)



 See footnotes



Long-term - systemic effects



Dermal



 



 



 



 



 



Not relevant, negligible absorption



 



Inhalation



DNEL (Derived No Effect Level)



0.00006mg Ni/m3h



 



Calculated NAEC 0.11 mg Ni/m3



reproductive developmental toxicity



 See footnotes



 



Oral



 



0.011 mg Ni/kg/dayi



100j



NOAEL: 1.1 mg Ni/kg/day



reproductive developmental toxicity



See footnotes



Long-term - local effects



Dermal



 



 



 



 



 



Not relevant, negligible exposure



 



Inhalation



DNEL (Derived No Effect Level)



0.00006mg Ni/m3h



 



 Calculated NAEC 0.11 mg Ni/m3


 

repeated dose toxicity (lung inflammation)


carcinogenicity


 



 See footnotes



a.    The approaches used in the derivation of DNELs are described in appendices C1 to C4 in the CSR for NiSO4, including more details on NOAEL identification and DNEL derivation. 


b.       The derivation of the acute inhalation DNELs is described in appendix C3 (CSR NiSO4). Dosimetric modeling was used to calculate human equivalent air concentrations (HECs) for the points of departures based on effects associated with pulmonary deposited (systemic effects) or retained (local effects) nickel doses in rats. This modeling accounts for differences in pulmonary deposition of different particle sizes between rats and humans. HECs were calculated using particle size of animal aerosol that reasonably correspond to the PM10aerosol fraction of ambient air.


c.       Assessment Factor (AF) = 12.5. [AF interspecies differences in susceptibility (AS) = 1 for exposures expressed as concentrations mg/m3, and for lethal effects; AF interspecies remaining differences in susceptibility for respiratory tract = 2.5; AF intraspecies differences in susceptibility =5 for substances that do not undergo metabolism, seeAppendix C3section C3.6 for more detailed justification; Overall AF = 1 x 2.5 x 5 =12.5].            


d.       The HEC-NOAEC of 109.6 mg Ni/m3(ambient air) was derived from the NOAEC of 120 mg Ni/m3(MMAD=3µm) by applying a dosimetry adjustment as described in Appendix C3 to the CSR for NiSO4.




e.       AF= 100 [AF interspecies difference other =2.5; AF interspecies AS =4 (rat-human); AF intraspecies differences in susceptibility=10 for the general population according to ECHA Guidance Table R. 8-6 Default assessment factor;s AF to account for differences in exposure duration=1; Overall AF = 2.5 x 4 x 10 = 100.




f.        AF = 7.1 [AF interspecies difference (AS) = 1 local respiratory effects. AF interspecies difference in susceptibility = 1 (for respiratory toxicity effects after inhalation of particles of nickel or most metal-containing substances in the respirable range, rats seem to be more susceptible to toxicity effects than mice, primates or humans. AF intraspecies differences in susceptibility=5for substances that do not undergo metabolism. AF for conversion of LOAEC to NAEC=3, based on steep dose-response for nickel toxicity. An AF for exposure duration= 1/2.1 was applied to extrapolate from 16 day repeated exposures to a single exposure.See Appendix C3 to the CSR for NiSO4. for more detailed justification of AF. Overall AF= 1 X 5 X 3 X 1/2.1 = 7.1].


g.       The HEC-LOAEC of 0.8 mg Ni/m3(ambient air) was derived from the LOAEC of 0.7 mg Ni/m3(MMAD<4µm) by applying a dosimetry adjustment as described in Appendix C3 to the CSR for NiSO4


h.       An ambient air PM10 DNEL of 60 ng/m3was derived based on the dose descriptors reported by Oller et al., (2014) and the subsequent application of assessment factors described in Buekers et al. (2015) and described in Appendix C1 and Appendix D5 (CSR NiSO4). The DNEL value is applied to ‘total nickel’ (including all chemical forms of nickel) because information on the speciation of emitted Ni substances is not always available. The value is applicable to typical mixtures of Ni prevailing in ambient air, at the regional and local scale. This DNEL protects from possible respiratory toxicity and reproductive effects, as well as carcinogenicity by considering nickel compounds to be indirect genotoxic carcinogens with a practical threshold similar to the approach taken by SCOEL (2011) when deriving OELs for nickel compounds (see Appendix C1 and Appendix D5; CSR NiSO4).



i.         This DNEL value was derived byWHO (World Health Organization, 2007. Background document for development of WHO Guidelines for Drinking-water Quality. © World Health Organization, Geneva)as the Tolerable Daily Intake for nickel. In a well conducted two-generation study on rats, a NOAEL of 1.1 mg of nickel per kg of body weight per day was identified for all the end-points studied, including the variable of post-implantation/perinatal lethality (SLI, 2000). The application of an uncertainty factor of 100 (10 to account for interspecies variation and 10 to account for intraspecies variation) gives a TDI of 11 µg/kg of body weight.


j.    AF= 100 [AF interspecies difference other =2.5; AF interspecies AS =4 (rat-human); AF intraspecies differences in susceptibility=10 for the general population according to ECHA Guidance Table R. 8-6 Default assessment factor;s AF to account for differences in exposure duration=1; Overall AF = 2.5 x 4 x 10 = 100.; the inclusion of a factor of 2-3 for severity of effects is not justified since an exposure level corresponding to 2-fold the NOAEL in the second generation study with nickel sulphate was considered by some experts as the NOAEL for the observed effects.



 


Sensitive subpopulations. Sensitive subpopulations are not separately addressed as the oral DNEL values used for long term oral systemic exposure correspond to the TDI calculated by WHO for the general public. Although soluble nickel compounds carry a CLP classification as Resp. Sens. 1; H334, the occurrence of nickel-induced asthma among exposed workers is rare and there are only a few cases pointing to a workplace-related asthmatic disease. For this reason, deriving DNELs that protect workers or the general population from respiratory toxicity are considered to be protective of any possible sensitization effects as well. 


 


 


Appendix C1= VITO report: Derivation of DNELs for 4 Ni substances 


Appendix C2= Background Document in Support of Long-term Inhalable DNELs for Nickel Metal and Nickel


          Compounds


Appendix C3= Background Document in Support of Acute DNELs and Guidance Values for Nickel Metal and


          Nickel Compounds


Appendix C4= Excel table of DNEL derivations –nickel sulphate


Appendix D5= Man Via the Environment Risk Assessment