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Potassium benzoate

Potassium benzoate
Potassium benzoate.png
Potassium benzoate ball-and-stick.png
Potassium benzoate.jpg
Names
IUPAC name
Potassium benzoate
Identifiers
582-25-2 YesY
3D model (Jmol) Interactive image
ChemSpider 10921 YesY
ECHA InfoCard 100.008.621
EC Number 209-481-3
E number E212 (preservatives)
PubChem 23661960
UNII 763YQN2K7K YesY
Properties
C7H5KO2
Molar mass 160.21 g·mol−1
Appearance White hygroscopic solid
Odor Odorless
Density 1.5 g/cm3
Melting point >300 °C (572 °F; 573 K)
69.87 g/100 mL (17.5 °C)
73.83 g/100 mL (25 °C)
79 g/100 mL (33.3 °C)
88.33 g/100 mL (50 °C)
Solubility in other solvents Soluble in ethanol
Slightly soluble in methanol
Insoluble in ether
Vapor pressure 1.6 Pa
Hazards
S-phrases S22-S24/25
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 111.4 °C (232.5 °F; 384.5 K)
950 °C (1,740 °F; 1,220 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Potassium benzoate (E212), the potassium salt of benzoic acid, is a food preservative that inhibits the growth of mold, yeast and some bacteria. It works best in low-pH products, below 4.5, where it exists as benzoic acid.

Acidic foods and beverages such as fruit juice (citric acid), sparkling drinks (carbonic acid), soft drinks (phosphoric acid), and pickles (vinegar) may be preserved with potassium benzoate. It is approved for use in most countries including Canada, the U.S., and the EU, where it is designated by the E number E212.

Potassium benzoate is also used in the whistle in many fireworks.

One very common way to make potassium benzoate is by oxidizing toluene to benzoic acid followed by a neutralization with potassium hydroxide. Another way to synthesize potassium benzoate in the lab setting is by hydrolyzing methyl benzoate with potassium hydroxide.

The mechanism of food preservation begins with the absorption of benzoic acid into the cell. If the intracellular pH changes to 5 or lower, the anaerobic fermentation of glucose through phosphofructokinase is decreased by 95%.


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Wikipedia

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