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Trimethylgallium

An organic compound, C3H9Ga, 114.828 g/mol. Boiling point 55.7 °C @760 [mm Hg], melting point -15.9 °C, as published.

verified record, Organic compound, 3 measured properties

Identifiers

Molecular formula
C₃H₉Ga
Molecular weight
114.828 g/mol
Exact mass
113.995999 g/mol
IUPAC name
trimethylgallane
SMILES
C[Ga](C)C
InChI
InChI=1S/3CH3.Ga/h3*1H3;
InChIKey
XCZXGTMEAKBVPV-UHFFFAOYSA-N

Measured properties

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

Boiling Point
55.7 °C @760 [mm Hg]measured · PAC Chemical Database, U.S. Department of Energy
Melting Point
-15.9 °Cmeasured · PAC Chemical Database, U.S. Department of Energy
Vapor Pressure
223.0 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases

Calculated properties

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

Molecular weight
114.83 g/molcalculated · reference compound database
Average mass of one molecule, from reference compound database.
Exact mass
113.996 Dacalculated · reference compound database
Mass of the most common isotopic form.
Polar surface area
0 Ųcalculated · reference compound database
Polar surface area as computed by reference compound database.
Complexity
8calculated · 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
1.3706calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
0 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
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
23.346 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
1calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.4178calculated · 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
4
Total atoms, hydrogen included
13
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 Trimethylgallium yet.

Other names for it

The systematic name on this record is trimethylgallane.

The sources also call it trimethylgallane, Gallium, trimethyl-, Gallium trimethyl, EINECS 215-897-6, Trimethylgallium, elec.gr., Trimethylgallium, elec. gr., (CH3)3Ga, SCHEMBL26624, DTXSID2061696, AKOS015914830, NS00081434.

Structurally related

Nothing structurally close to Trimethylgallium has a page here yet.

Where these values came from

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.