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potassium acetate

C2H3KO2, 98.142 g/mol. Its structure, the values that were measured, the values that were calculated, and where each one came from.

verified recordOrganic compound3 measured properties

Drawn from the SMILES. It shows how the atoms are connected — not a photograph of a molecule, and not its shape in space.

Identifiers

Molecular formula
C₂H₃KO₂
Molecular weight
98.142 g/mol
Exact mass
97.977011 g/mol
IUPAC name
potassium acetate
SMILES
CC(=O)[O-].[K+]
InChI
InChI=1S/C2H4O2.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
InChIKey
SCVFZCLFOSHCOH-UHFFFAOYSA-M

Both are open without an account.

Measured properties

Values somebody obtained from a sample and published. Where two sources report the same property they are both shown, in the units each used — a disagreement between them is information, and averaging it away would be inventing a number neither one gave.

Melting Point
292 °Cmeasured · reference compound database
309 °Cmeasured · reference compound database
Solubility
Solubility in water, g/100ml at 20 °C: 256measured · reference compound database
Density
1.6 g/cm³measured · reference compound database
1.57 @25 °Cmeasured · reference compound database

Calculated properties

Derived from the structure rather than from a sample. These are reproducible and they are not measurements: a calculated partition coefficient and a measured one can differ by a long way, and where both exist they are listed apart on purpose.

Molecular weight
98.14 g/molcalculated · reference compound database
Average mass of one molecule, from reference compound database.
Exact mass
97.97701082 Dacalculated · reference compound database
Mass of the most common isotopic form.
Polar surface area
40.1 Ųcalculated · reference compound database
Polar surface area as computed by reference compound database.
Complexity
25calculated · reference compound database
A rough measure of how intricate the structure is.
H-bond donors
0calculated · reference compound database
H-bond acceptors
2calculated · reference compound database
logP
-4.2398calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
40.13 Ųcalculated · 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
2calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
0calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
10.681 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.5calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.2879calculated · chemistry engine
Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

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

Structure

Heavy atoms, hydrogen excluded
5
Total atoms, hydrogen included
8
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 potassium acetate yet.

Other names for it

The systematic name on this record is potassium acetate.

The sources also call it Diuretic salt, ACETIC ACID, POTASSIUM SALT, Potassium ethanoate, FEMA No. 2920, Octan draselny, Kali aceticum, Potassium acetates, Potassium acetate in plastic container, Acetate, Potassium, potassium;acetate, KOAc, Acetic acid potassium salt.

Structurally related

Nothing structurally close to potassium acetate has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as potassium acetate. 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.

Where these values came from

compound record.

What this page does not claim

The identifiers are what the source record holds, copied rather than recomputed. Measured values are reported as their source gave them, units and all; calculated values are marked as calculated and are not measurements. Where a field is absent the page says so, because a blank cell reads as a zero and a guessed value reads as a fact.

Nothing here is a hazard assessment, a purity statement or advice about handling a sample. A flash point quoted from a safety database is a number somebody published, not a judgement by us about whether this molecule is safe for what you intend.