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Naphthalene

An aromatic hydrocarbon, C10H8, 128.174 g/mol. Boiling point 424 °F at 760 mmHg, melting point 80.2 °C, as published.

verified record, Organic — aromatic hydrocarbon, 9 measured properties

Identifiers

Molecular formula
C₁₀H₈
Molecular weight
128.174 g/mol
Exact mass
128.0626 g/mol
IUPAC name
naphthalene
SMILES
c1ccc2ccccc2c1
InChI
InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H
InChIKey
UFWIBTONFRDIAS-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
424 °F at 760 mmHg (NTP, 1992)measured · CAMEO Chemicals
217.9 deg Cmeasured · Hazardous Substances Data Bank (HSDB)
Melting Point
176.4 °F (NTP, 1992)measured · CAMEO Chemicals
80.2 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Density
1.15 (NIOSH, 2024) - Denser than water; will sinkmeasured · CAMEO Chemicals
1.162 at 20 °C/4 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Solubility
less than 1 mg/mL at 72 °F (NTP, 1992)measured · CAMEO Chemicals
In water, 31 mg/L at 25 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure
0.05 mmHg at 68 °F ; 1 mmHg at 126.7 °F (NTP, 1992)measured · CAMEO Chemicals
0.08 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
LogP
log Kow = 3.30measured · Hazardous Substances Data Bank (HSDB)
3.30measured · Human Metabolome Database (HMDB)
Flash Point
190 °F (NTP, 1992)measured · CAMEO Chemicals
174 °F (NFPA, 2010)measured · CAMEO Chemicals
Viscosity
0.754 cP at 20 °Cmeasured · Mason RT; Naphthalene. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2014). New York, NY: John Wiley & Sons. Online Posting Date: 25 Jan 2002
Refractive Index
Index of refraction: 1.58212 at 100 °C/Dmeasured · O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1187
Index of refraction: 1.4003 at 24 °C/Dmeasured · Lide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V4: 3467

Calculated properties

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

Molecular weight
128.17 g/molcalculated · reference compound database
Average mass of one molecule, from reference compound database.
Exact mass
128.062600255 Dacalculated · reference compound database
Mass of the most common isotopic form.
XLogP3
3.3calculated · reference compound database
Estimated oil/water partition, computed by reference compound database.
Polar surface area
0 Ųcalculated · reference compound database
Polar surface area as computed by reference compound database.
Complexity
80calculated · 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
2.8398calculated · 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
43.948 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
0.5114calculated · 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
10
Total atoms, hydrogen included
18
Rings
2
Aromatic rings
2
Stereocentres
0
Formal charge
0

Functional groups

  • 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 Naphthalene yet.

Other names for it

The systematic name on this record is naphthalene.

The sources also call it Naphthalin, Tar camphor, White tar, Albocarbon, Naphthene, Camphor tar, naphtalene, Naphthaline, Moth balls, Moth flakes, Dezodorator.

Structurally related

Nothing structurally close to Naphthalene 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.