Amphetamine

An aromatic primary amine, C9H13N, 135.21 g/mol. Boiling point 392 to 397 °F at 760 mmHg, melting point 25 °C, as published.

verified recordOrganic — aromatic primary amine8 measured properties

Identifiers

Molecular formula: C₉H₁₃N
Molecular weight: 135.21 g/mol
Exact mass: 135.104799 g/mol
IUPAC name: 1-phenylpropan-2-amine
SMILES: CC(N)Cc1ccccc1
InChI: InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3
InChIKey: KWTSXDURSIMDCE-UHFFFAOYSA-N

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Measured properties

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

Boiling Point: 392 to 397 °F at 760 mmHg (EPA, 1998)measured · CAMEO Chemicals; 64.7 ºC at 760 mm Hgmeasured · DrugBank
Melting Point: -98 ºCmeasured · DrugBank; 25 °Cmeasured · Human Metabolome Database (HMDB)
Density: 0.913 at 77 °F (EPA, 1998) - Less dense than water; will floatmeasured · CAMEO Chemicals; 0.936 g/cu cm at 25 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Solubility: Moderate solubilitymeasured · DrugBank; Sparingly soluble in water (1:50)measured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure: 0.24 Torr /mm Hg/ at 20 °Cmeasured · Hazardous Substances Data Bank (HSDB)
LogP: 1.76measured · DrugBank; log Kow = 1.76measured · Hazardous Substances Data Bank (HSDB)
Flash Point: 80 °F (EPA, 1998)measured · CAMEO Chemicals; </= 100 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Refractive Index: Index of refraction: 1.518 at 26 °C/Dmeasured · Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-456

Calculated properties

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

Molecular weight: 135.21 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 135.104799419 Dacalculated · reference compound database; Mass of the most common isotopic form.
XLogP3: 1.8calculated · reference compound database; Estimated oil/water partition, computed by reference compound database.
Polar surface area: 26 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 84calculated · reference compound database; A rough measure of how intricate the structure is.
H-bond donors: 1calculated · reference compound database
H-bond acceptors: 1calculated · reference compound database
logP: 1.5763calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 26.02 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 1calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 1calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 2calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 43.7954 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.3333calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.6542calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon9 atoms · 79.9% by mass
N Nitrogen1 atom · 10.4% by mass
H Hydrogen13 atoms · 9.7% 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: 10
Total atoms, hydrogen included: 23
Rings: 1
Aromatic rings: 1
Stereocentres: 1
Formal charge: 0

Functional groups

Primary amine
Nitrogen bonded to one carbon and two hydrogens.
Aromatic ring
A flat six-membered ring with delocalised electrons.

Matched by structural pattern, not by a measurement.

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 Amphetamine yet.

Other names for it

The systematic name on this record is 1-phenylpropan-2-amine.

The sources also call it Amfetamine, 1-phenylpropan-2-amine, dl-Amphetamine, 1-Phenyl-2-aminopropane, Desoxynorephedrine, Norephedrane, Elastonon, Fenopromin, Phenedrine, beta-Aminopropylbenzene, Propisamine.

Structurally related

Molecules sharing this formula, or whose fingerprint is at least 40% similar to this one. Similarity is Tanimoto on Morgan fingerprints over this library only — it is a measure of structural overlap, not of how alike they behave.

1,2-Diphenylethylamine

C14H15N

(+-)-p-Methoxyamphetamine

C10H15NO

Where these values came from

reference compound database3007
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.