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Names | |
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Preferred IUPAC name
2,3-Dimethylpentane | |
Identifiers | |
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3D model (
JSmol)
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ChEBI |
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ChemSpider | |
ECHA InfoCard | 100.008.437 |
EC Number |
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PubChem
CID
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UNII |
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UN number | 1206 |
CompTox Dashboard (
EPA)
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Properties | |
C7H16 | |
Molar mass | 100.205 g·mol−1 |
Appearance | Colourless liquid |
Density | 0.7076 g/mL (25 °C), 0.6413 (80 °C), 0.7380 (25 °C, 45 MPa), 0.6891 (80 °C, 45 MPa) (racemic) [1] |
Boiling point | 89.7 °C (racemic) [2] [3] [4] |
Vapor pressure | 2.35 psi (37.7 °C) [5] |
Viscosity | 0.356 mPa s (30 °C), 0.232 (80 °C), 0.624 (30 °C, 60 MPa) (racemic) [1] |
Thermochemistry | |
Heat capacity (C)
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34.308 cal/K/mol (−189 °C), 51.647 (20 °C), 58.735 (86.6 °C) (racemic) [6] |
Std molar
entropy (S⦵298) |
71.02 cal/K/mol (25 °C) (racemic) [6] |
Hazards | |
GHS labelling: | |
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Danger | |
H225, H304, H315, H335, H336, H410 | |
P210, P233, P240, P241, P242, P243, P261, P264, P271, P273, P280, P301+P310, P302+P352, P303+P361+P353, P304+P340, P312, P321, P331, P332+P313, P362, P370+P378, P391, P403+P233, P403+P235, P405, P501 | |
Flash point | −7 °C (19 °F; 266 K) [5] |
337 °C (639 °F; 610 K) [5] | |
Related compounds | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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2,3-Dimethylpentane is an
organic compound of
carbon and
hydrogen with formula C
7H
16, more precisely CH
3–CH(CH
3)–CH(CH
3)–CH
2–CH
3: a molecule of
pentane with
methyl groups –CH
3 replacing hydrogen atoms on carbon atoms 2 and 3. It is an
alkane ("paraffin" in older nomenclature), a
fully saturated
hydrocarbon; specifically, one of the isomers of
heptane.
Like typical alkanes, it is a colorless flammable compound; under common ambient conditions, it is a mobile liquid, less dense than water. [1]
2,3-Dimethylpentane is notable for being one of the two simplest alkanes with
optical (enantiomeric) isomerism. The
optical center is the middle carbon of the pentane backbone, which is connected to one hydrogen atom, one methyl group, one
ethyl group –C
2H
5, and one
isopropyl group –CH(CH
3)
2. The two enantiomers are denoted (3R)-2,3-dimethylpentane and (3S)-2,3-dimethylpentane. (The other simplest chiral alkane is its
structural isomer
3-methylhexane.)
Most properties listed in the literature refer to the racemic compound (an equimolar mixture of the two optical isomers).
The boiling point of 89.7 °C is 0.3 °C higher than the value of 89.4 °C predicted by Wiener's formula, based on the structure of the molecule and the boiling point of n-heptane. [2] [3]
The speed of sound at 3 MHz is 1149.5 m/s at 20 °C and 889.5 m/s at 80 °C. [7] [8] [9]
The racemic mixture has a glass transition temperature of about 123 K (−150 °C), but reportedly it does not crystallize—a fact that has been claimed to be a characteristic of high-purity optically active alkanes. [4] [6] [10]
2,3-Dimethylpentane is practically absent in the synthetic fuel produced from hydrogen and carbon monoxide by the Fischer–Tropsch process. [11]
The pure compound can be prepared by reacting the
Grignard reagent
sec-butyl magnesium bromide C
4H
9–MgBr with
acetone to form
2,3-dimethyl-2-pentanol, then dehydrating this
alcohol to form
2,3-dimethyl-2-pentene, and
hydrogenating this product.
[4]
The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture being the isomer 2,2,3-trimethylbutane, obtained at almost 50% yield). [12]