NICKELOCENE
Synonym(s):Di(cyclopentadienyl)nickel(II);Nickelocene
- CAS NO.:1271-28-9
- Empirical Formula: C10H10Ni10*
- Molecular Weight: 188.88
- MDL number: MFCD00001441
- EINECS: 215-039-0
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-08-13 17:19:14
What is NICKELOCENE?
Chemical properties
GREEN TO DARK GREEN CRYSTALS OR CRYST. POWDER
Chemical properties
Nickelocene is a solid crystalline substance of dark green color, insoluble in water or carbon tetrachloride, slightly soluble in alcohol and liquid ammonia, and readily soluble in nonpolar organic solvents.
The Uses of NICKELOCENE
Nickelocene is obtained through reacting nickel halides with sodium cyclopentadienide. It is used as a catalyst or as a complexing agent.
The Uses of NICKELOCENE
Catalyst, complexing agent.
The Uses of NICKELOCENE
This metal alkyl may be used to synthesize hybrid organic-inorganic polymeric molecular layer deposition (MLD). Bis(cyclopentadienyl) nickel (Cp 2 Ni) may be used as a Ni precursor for the atomic layer deposition (ALD) of NiO/carbon nanotubes hybrids.
General Description
Dark liquid in an 8-10% solution in toluene. Insoluble in water.
Air & Water Reactions
Highly flammable. The neat material is sensitive to air. . Insoluble in water.
Reactivity Profile
Organometallics, such as NICKELOCENE, are reactive with many other groups. Incompatible with acids and bases. Organometallics are good reducing agents and therefore incompatible with oxidizing agents. Often reactive with water to generate toxic or flammable gases.
Hazard
Toxic by inhalation and skin contact, a carcinogen (OSHA).
Health Hazard
ACUTE/CHRONIC HAZARDS: NICKELOCENE can be absorbed through the skin.
Fire Hazard
NICKELOCENE is flammable.
Safety Profile
Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Poison by intraperitoneal and intramuscular routes. Moderately toxic by ingestion. When heated to decomposition it emits acrid smoke and irritating fumes. See also NICKEL COMPOUNDS.
Purification Methods
Dissolve the complex in Et2O, filter and evaporate in a vacuum. Purify it rapidly by recrystallisation from pet ether using a solid CO2/Me2CO bath, m 171-173o(in an evacuated tube). Also purify it by vacuum sublimation. [Wilkinson et al. J Am Chem Soc 76 1970 1954, Beilstein 16 IV 1831.]
Properties of NICKELOCENE
Melting point: | 171-173 °C(lit.) |
storage temp. | 2-8°C |
Water Solubility | Insoluble in water |
form | crystal |
color | dark green |
Sensitive | Air & Moisture Sensitive |
CAS DataBase Reference | 1271-28-9(CAS DataBase Reference) |
NIST Chemistry Reference | Nickelocene(1271-28-9) |
EPA Substance Registry System | Nickelocene (1271-28-9) |
Safety information for NICKELOCENE
Signal word | Danger |
Pictogram(s) |
Flame Flammables GHS02 Exclamation Mark Irritant GHS07 Health Hazard GHS08 |
GHS Hazard Statements |
H228:Flammable solids H302:Acute toxicity,oral H317:Sensitisation, Skin H350:Carcinogenicity |
Precautionary Statement Codes |
P201:Obtain special instructions before use. P210:Keep away from heat/sparks/open flames/hot surfaces. — No smoking. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of soap and water. P308+P313:IF exposed or concerned: Get medical advice/attention. |
Computed Descriptors for NICKELOCENE
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
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