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dodecane

File:DodecaneFull.png · Wikimedia Commons · See Wikimedia Commons

EntityQ150744· pop 39· linked from 69 articles

Also known as n-dodecane, CH3-[CH2]10-CH3, Bihexyl, Dihexyl, Duodecane, Adakane 12

Dodecane (also known as dihexyl, bihexyl, adakane 12, or duodecane) is an oily liquid n-alkane hydrocarbon with the chemical formula C12H26 (which has 355 isomers).

OverviewAI-generated

Dodecane is a chemical compound with the formula C₁₂H₂₆ and a mass of 170.203. Its canonical SMILES notation is CCCCCCCCCCCC. The substance has a density of 0.75 and a refractive index of 1.4216. It exhibits a boiling point of 216.32 and a flash point of 74. Melting points are recorded as -9.6 and -10, while its dynamic viscosity is 1.34.

According to PubChem data, dodecane has a weight of 170.33 and an xlogp value of 6.1. It possesses a topological polar surface area of 0, with no hydrogen bond donors or acceptors, and carries a charge of 0. The compound is referenced by 69 other encyclopedia articles and has 2365 associated PubMed entries.

Synthesized by Vinony from 24 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C12H26
Molecular weight
170.33 g/mol
IUPAC name
dodecane
SMILES
CCCCCCCCCCCC
InChIKey
SNRUBQQJIBEYMU-UHFFFAOYSA-N
XLogP
6.1
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Research

2,365 papers

via PubMed

~1 min read

Encyclopedic overview

5 sections
Contents
  • Combustion reaction
  • Jet fuel surrogate
  • See also
  • References
  • External links

Dodecane (also known as dihexyl, bihexyl, adakane 12, or duodecane) is an oily liquid n-alkane hydrocarbon with the chemical formula C12H26 (which has 355 isomers).

It is used as a solvent, distillation chaser, and scintillator component. It is used as a diluent for tributyl phosphate (TBP) in nuclear reprocessing plants.

Excerpted from Wikipedia’s “dodecane” article, available under the CC BY-SA 4.0 licence.

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