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Nickel(II) Chloride Hydrate

Catalog Number
ACM69098153-1
Product Name
Nickel(II) Chloride Hydrate
CAS
69098-15-3
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Synonyms
Nickel(II) chloride
IUPAC Name
Dichloronickel;hydrate
Molecular Weight
147.61
Molecular Formula
Cl2H2NiO
Canonical SMILES
O.Cl[Ni]Cl
InChI
InChI=1S/2ClH.Ni.H₂O/h2*1H;1H2/q;+2;/p-2
InChI Key
HGGYAQHDNDUIIQ-UHFFFAOYSA-L
Melting Point
1001 °C
Purity
99%+
Solubility
Freely soluble in water
Appearance
Green crystalline aggregates
Complexity
2.8
Covalently-Bonded Unit Count
2
EC Number
231-743-0
Exact Mass
145.883612
Formal Charge
0
H-Bond Acceptor
1
H-Bond Donor
1
Heavy Atom Count
4
MDL Number
MFCD00149808
MeSH Entry Terms
nickel chloride;nickel chloride dihydrate;nickel chloride hemihydrate;nickel chloride heptahydrate;nickel chloride hexahydrate;nickel chloride hydrate;nickel chloride monohydrate;nickel chloride monohydroxide;nickel chloride tetrahydrate;nickel chloride trihydroxide
Monoisotopic Mass
145.883612
Physical State
Green crystals
Rotatable Bond Count
0
Topological Polar Surface Area
1 Ų
Application
Nickel(II) Chloride Hydrate serves multiple purposes across various chemical processes, primarily functioning as a catalyst and a precursor in organic chemistry. It plays a vital role in electroplating and is utilized as a catalyst in organic conversions, such as the chemo-selective thioacetalization of aldehydes. When combined with lithium aluminum hydride, it acts as an effective reducing agent for alkenes, alkynes, and organic halides, while also having the capability to cleave N-O bonds and open epoxides. This compound is a key precursor to various nickel-phosphine complexes like bis(triphenylphosphine)nickel(II) chloride, which are instrumental in reactions such as alkyne trimerizations, carbonylations, and Suzuki-Miyaura cross-coupling reactions, offering an alternative to palladium(0) catalysts. Additionally, it provides the foundation for the acetylacetonate complex of nickel, essential for producing the 1,5-cyclooctadiene complex, a significant reagent in organonickel chemistry. Furthermore, Nickel(II) Chloride Hydrate is crucial for preparing the sandwich compound nickelocene through the dimethoxyethane complex of nickel chloride.
February 14, 2025

Essential Catalyst for Advanced Organic Conversions

Nickel(II) Chloride Hydrate from Alfa Chemistry is indispensable in my lab work. It's effective for electroplating and vital as a catalyst in chemo-selective thioacetalization processes. It enhances our organic synthesis efficiencies significantly.

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