NICKEL(II) CHLORIDE
NICKEL(II) CHLORIDE Basic information
- Product Name:
- NICKEL(II) CHLORIDE
- Synonyms:
-
- NICKEL(II) CHLORIDE HYDRATE
- NICKEL(II) CHLORIDE HYDRATE, 99.95%
- Puratronic99.995%(metalsbasis)
- nickel(ii) chloride hydrate, puratronic
- Nickel(II) chloride hydrate, Puratronic(R), 99.995% (metals basis)
- Nickel(II) chloride hydrate, Puratronic, 99.995% (metals basis)
- Nickel(II) chloride hydrate 99.95% trace metals basis
- CAS:
- 69098-15-3
- MF:
- Cl2H2NiO
- MW:
- 147.61
- EINECS:
- 677-901-6
- Product Categories:
-
- Catalysis and Inorganic Chemistry
- Chemical Synthesis
- Nickel Salts
- NickelMetal and Ceramic Science
- Salts
- Mol File:
- 69098-15-3.mol
NICKEL(II) CHLORIDE Chemical Properties
- Melting point:
- 1001 °C
- vapor pressure
- 1 mm Hg ( 671 °C)
- form
- Crystalline Aggregates
- color
- Green
- Water Solubility
- Freely soluble in water. Soluble in ethylene glycol, ethanol, and ammonium hydroxide.
- Sensitive
- Hygroscopic
- Merck
- 14,6505
- Exposure limits
- NIOSH: IDLH 10 mg/m3; TWA 0.015 mg/m3
Safety Information
- Hazard Codes
- T,N
- Risk Statements
- 45-23/24/25-36/37/38-42/43-68-50/53-48/23-38-23/25-61-49
- Safety Statements
- 53-26-27-28-36/37/39-45-61-60
- RIDADR
- UN 3288 6.1/PG 3
- WGK Germany
- 3
- RTECS
- QR6480000
- TSCA
- Yes
- HazardClass
- 6.1
- PackingGroup
- III
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
NICKEL(II) CHLORIDE Usage And Synthesis
Uses
It is used in electroplating and as a catalyst for organic conversions, for example in chemo-selective thioacetalization of aldehydes. In combination with lithium aluminum hydride, it serves as a reducing agent for alkenes, alkynes, and organic halides; it can cleave N-O bond and open epoxides. It is a precursor to several nickel-phosphine complexes, such as bis(triphenylphosphine)nickel(II) chloride, which are used in alkyne trimerizations, carbonylations, and as catalysts in organic reactions such as Suzuki-Miyaura cross coupling reactions as an alternative to palladium(0) catalysts. It is the precursor to acetylacetonate complex of Ni, used for producing 1,5-cyclooctadiene complex, an important reagent in organonickel chemistry. It can be used to prepare the sandwich compound nickelocene through dimethoxyethane complex of nickel chloride.
Purification Methods
It crystallises from dilute HCl to form the green hexahydrate. At 70o this dehydrates to the tetrahydrate, and at higher temperatures it forms the anhydrous salt. It sublimes in yellow hexagonal scales in a stream of HCl. Store it in a desiccator as it is deliquescent. [Hart & Partington J Chem Soc 104 1943.]
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