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Merck

656895

Nickel(II) sulfate

99.99% trace metals basis

Synonym(s):

Nickel(2+) sulfate, Nickelous sulfate

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About This Item

Linear Formula:
NiSO4
CAS Number:
7786-81-4
Molecular Weight:
154.76
NACRES:
NA.23
PubChem Substance ID:
329760092
UNSPSC Code:
12352302
EC Number:
232-104-9
MDL number:
MFCD00011146
Assay:
99.99% trace metals basis
Grade:
anhydrous
Form:
solid

Key Documents

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grade

anhydrous

Quality Level

100

assay

99.99% trace metals basis

form

solid

reaction suitability

core: nickel

impurities

≤150.0 ppm Trace Metal Analysis

SMILES string

[Ni++].[O-]S([O-])(=O)=O

InChI

1S/Ni.H2O4S/c;1-5(2,3)4/h;(H2,1,2,3,4)/q+2;/p-2

InChI key

LGQLOGILCSXPEA-UHFFFAOYSA-L

Related Categories

General description

Nickel(II) sulfate is an inorganic compound that exhibits high solubility in water. It is commonly used in electroplating, as a chemical intermediate in the preparation of other nickel salts, and as a source of nickel ions for various processes. Additionally, it has applications in the battery industry and as a catalyst in organic synthesis.
Properties of NiSO4:      
  • Highly soluble in water     
  • It can participate in redox reactions  
  • It can form complexes with various ligands

Application

Nickel(II) sulfate can be used as a precursor to synthesize:    
  • Nickel-based electrocatalysts for oxygen evolution.      
  • Ni-doped titanium dioxide nanoparticles for the photocatalytic degradation of organic pollutants such as methyl orange.     
  • Spherical silica particles coated with Ni, which find application in the field of ceramic industry and in catalysis.

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Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 1 - Carc. 1A Inhalation - Muta. 2 - Repr. 1B - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Inhalation

target_organs

respiratory tract irritation

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Specified Class I Designated Chemical Substances

prtr

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

656895-25G:4548173294933 + 656895-100G:4548173294902 + 656895-VAR: + 656895-50G-PW: + 656895-50G:4548173294940 + 656895-BULK: + 656895-250G:4548173294926 + 656895-10G-PW: + 656895-10G:4548173294919

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Certificates of Analysis (COA)

Lot/Batch Number
05798LJ
31999MJ
11590TH
09488KH
09588KH

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L Curto et al.
Journal of the European Academy of Dermatology and Venereology : JEADV, 28(10), 1356-1362 (2014-03-13)
Topical corticosteroids (TC) consistently show effectiveness against itch, a paradigmatic symptom, in various eczemas. Rapid itch relief is a therapeutic goal. The early response of itch to TC has not been adequately studied. To assess the effect on itch of
Fenxia Hou et al.
ALTEX, 37(3), 451-468 (2020-04-24)
There are currently no skin sensitization assays based on T cell activation. We built a novel in vitro model to assess T cell activation and test its performance to discriminate skin sensitizers from non-sensitizers using 52 reference chemicals. Jurkat Clone
Hsiao-Chi Chuang et al.
Toxicology and applied pharmacology, 266(2), 298-306 (2012-11-21)
Heart rate variability (HRV) has been reported to be a putative marker of cardiac autonomic imbalance caused by exposure to ambient particulate matter (PM). Our objective in this study was to determine the effects on HRV from exposure to nickel
K Amudha et al.
Chemico-biological interactions, 193(1), 57-64 (2011-05-24)
This study was conducted to investigate the beneficial role of naringin on nickel induced nephrotoxicity. Nickel (Ni) (20mg/kg body weight (b.w.) was administered intraperitoneally (i.p.) for 20 days. Naringin was administered orally (20, 40 and 80 mg/kg b.w.) with i.p.
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