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It is also one of many [[List of additives in cigarettes|additives in cigarettes.]]
It is also one of many [[List of additives in cigarettes|additives in cigarettes.]]



Heptanoic acid can be used to synthesize pure hexane, which is the main chemical component of gasoline.<ref>Charles D. Allison, A Chemist</ref>
Concentrated hydrochloric acid can be used to catalyze the decarboxylation reaction:

C7H14O2 + HCl + (Heat) -> C6H14 + CO2 + HCl

OR:

H3C-CH2-CH2-CH2-CH2-CH2-COOH + HCl(aq) + (Heat) -> H3C-CH2-CH2-CH2-CH2-CH3 + CO2 + HCl

Heptanoic acid is known to exist in [[Acacia_dealbata|Mimosa]].

Finding plant sources that contain high levels of this fatty acid and Hexanoic acid would be helpful in solving energy/fuel crisis problems.
Hexanoic acid and Heptanoic acid can be used to synthesize pentane and hexane, both of which have lower boiling points than Octane and Heptane. Because of their low boiling points, they burn cleaner in combustion engines and give better mileage than high octane fuels.<ref>Charles D. Allison, a chemist</ref>


==References==
==References==

Revision as of 16:41, 10 April 2012

Heptanoic acid[1]
Heptanoic acid
Names
IUPAC name
Heptanoic acid
Other names
Enanthic acid; Oenanthic acid; n-Heptylic acid; n-Heptoic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.490 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C7H14O2/c1-2-3-4-5-6-7(8)9/h2-6H2,1H3,(H,8,9) checkY
    Key: MNWFXJYAOYHMED-UHFFFAOYSA-N checkY
  • InChI=1/C7H14O2/c1-2-3-4-5-6-7(8)9/h2-6H2,1H3,(H,8,9)
    Key: MNWFXJYAOYHMED-UHFFFAOYAP
  • O=C(O)CCCCCC
Properties
C7H14O2
Molar mass 130.187 g·mol−1
Appearance Oily liquid
Density 0.9181 g/cm3 (20 °C)
Melting point −7.5 °C (18.5 °F; 265.6 K)
Boiling point 223 °C (433 °F; 496 K)
0.2419 g/100 mL (15 °C)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Heptanoic acid, also called enanthic acid, is an organic compound composed of a seven-carbon chain terminating in a carboxylic acid. It is an oily liquid with an unpleasant, rancid odor.[1] It contributes to the odor of some rancid oils. It is slightly soluble in water, but very soluble in ethanol and ether.

Heptanoic acid is used in the preparation of esters, such as ethyl heptanoate, which are used in fragrances and as artificial flavors.

It is also one of many additives in cigarettes.


Heptanoic acid can be used to synthesize pure hexane, which is the main chemical component of gasoline.[2] Concentrated hydrochloric acid can be used to catalyze the decarboxylation reaction:

C7H14O2 + HCl + (Heat) -> C6H14 + CO2 + HCl

OR:

H3C-CH2-CH2-CH2-CH2-CH2-COOH + HCl(aq) + (Heat) -> H3C-CH2-CH2-CH2-CH2-CH3 + CO2 + HCl

Heptanoic acid is known to exist in Mimosa.

Finding plant sources that contain high levels of this fatty acid and Hexanoic acid would be helpful in solving energy/fuel crisis problems. Hexanoic acid and Heptanoic acid can be used to synthesize pentane and hexane, both of which have lower boiling points than Octane and Heptane. Because of their low boiling points, they burn cleaner in combustion engines and give better mileage than high octane fuels.[3]

References

  1. ^ a b Merck Index, 11th Edition, 4581
  2. ^ Charles D. Allison, A Chemist
  3. ^ Charles D. Allison, a chemist