Nickel

An element / simple molecule, Ni, 58.693 g/mol. Boiling point 5139 °F at 760 mmHg, melting point 2831 °F, as published.

verified recordElement / simple molecule5 measured properties

Identifiers

Molecular formula: Ni
Molecular weight: 58.693 g/mol
Exact mass: 57.935343 g/mol
IUPAC name: nickel
SMILES: [Ni]
InChI: InChI=1S/Ni
InChIKey: PXHVJJICTQNCMI-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Measured properties

Published measurements, each with its source. Two readings of one property are both shown, in the units each used.

Boiling Point: 5139 °F at 760 mmHg (NIOSH, 2024)measured · CAMEO Chemicals; 4946 °F at 760 mmHg (NTP, 1992)measured · CAMEO Chemicals
Melting Point: 2831 °F (NIOSH, 2024)measured · CAMEO Chemicals; 2651 °F (NTP, 1992)measured · CAMEO Chemicals
Density: 8.9 (Metal) (NIOSH, 2024) - Denser than water; will sinkmeasured · CAMEO Chemicals; 8.908 (NTP, 1992) - Denser than water; will sinkmeasured · CAMEO Chemicals
Solubility: Insoluble (NIOSH, 2024)measured · CAMEO Chemicals; Insoluble (NTP, 1992)measured · CAMEO Chemicals
Vapor Pressure: 0 mmHg (approx) (NIOSH, 2024)measured · CAMEO Chemicals; 1 mmHg at 3290 °F (NTP, 1992)measured · CAMEO Chemicals

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

Molecular weight: 58.693 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 57.935342 Dacalculated · reference compound database; Mass of the most common isotopic form.
Polar surface area: 0 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 0calculated · reference compound database; A rough measure of how intricate the structure is.
H-bond donors: 0calculated · reference compound database
H-bond acceptors: 0calculated · reference compound database
logP: -0.0025calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 0 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 0calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 0calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 0calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 0 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.3441calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

Ni Nickel1 atom · 100.0% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 1
Total atoms, hydrogen included: 1
Rings: 0
Aromatic rings: 0
Stereocentres: 0
Formal charge: 0

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Nickel yet.

Other names for it

The systematic name on this record is nickel.

The sources also call it Metallic nickel, Fibrex, Nickel particles, Fibrex P, Niccolum metallicum, Nickel 200, Nickel 201, Nickel 205, Nickel 207, Nickel 270, Alcan 756.

Structurally related

Nothing structurally close to Nickel has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Nickel. This says nothing about structure: most of them are the bases, solvents, ligands and catalysts the chemistry needed, and they are here because somebody put them in the same flask.

1,3-Butadiene

used as a reactant

C₄H₆, 54.092 g/mol.

1,2,3,4-Tetrahydrocyclopent[b]indol-3-amine

formed as a product

C₁₁H₁₂N₂, 172.231 g/mol.

Where these values came from

reference compound database935
compound record
chemistry engine
structure perception

compound record.

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.