Propionate

Propionate
Names
IUPAC name
Propionate
Other names
Propanoate, Propanoic acid, ion(1-)
Identifiers
3D model (JSmol)
ChemSpider
Properties
C3H5O2
Appearance Colorless, oily liquid
Density 0.993 g/mL at 20°C[1]
Melting point −21.5 °C (−6.7 °F; 251.7 K)[1]
Boiling point 141.1 °C (286.0 °F; 414.2 K)[1]
Hazards
Main hazards Flammable, Corrosive
Flash point 52 °C (126 °F; 325 K)[1]
465 °C (869 °F; 738 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

The propionate, or propanoate ion, is C2H5COO (the conjugate base of propionic acid).

A propionic, or propanoic, compound is a small salt or ester of propionic acid. In these compounds, propionate is often written in shorthand, as CH3CH2CO2 or simply EtCO2.

Propionates should not be confused with propenoates (commonly known as acrylates), the ions/salts/esters of propenoic acid (also known as 2-propenoic acid or acrylic acid).

Propionate is observed to be among the most common short-chain fatty acids produced by human gut microbiota in response to indigestible carbohydrates (fiber) in the diet.[2] A study in mice suggests that propionate is produced by the bacteria of the genus Bacteroides in the gut, and that it offers some protection against Salmonella there.[3]

Examples

References

  1. 1 2 3 4 5 "propionate | C3H5O2- - PubChem". PubChem.
  2. How gut microbes talk to organs: The role of endocrine and nervous routes. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004142 | Section 2.1, paragraph 2: The microbial fermentation of carbohydrates in the gut typically produces acetate, propionate, butyrate, and lactate, which are specific SCFAs.
  3. http://med.stanford.edu/news/all-news/2018/07/gut-bacteria-byproduct-protects-against-salmonella.html


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