Difference between revisions of "Sodium benzoate"

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[[File:Sodium_benzoate.jpg|thumb|300px|Sodium benzoate.]]
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{{Chembox
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| Name = Sodium benzoate
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| Reference =
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| IUPACName = Sodium benzoate
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| PIN =
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| SystematicName =
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| OtherNames = Antimol<br>Benzoate of soda<br>E211<br>Sobenate
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| ImageFile = Sodium_benzoate.jpg
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| ImageCaption = Sodium benzoate from the store.
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| Section1 = {{Chembox Identifiers
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| 3DMet =
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| Abbreviations =
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| Section2 = {{Chembox Properties
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| AtmosphericOHRateConstant =
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| Appearance = White solid
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| BoilingPt =
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| BoilingPtC =
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| BoilingPt_ref =
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| BoilingPt_notes = Decomposes
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| Density = 1.497 g/cm<sup>3</sup>
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| Formula = C<sub>7</sub>H<sub>5</sub>O<sub>2</sub>Na<br>C<sub>6</sub>H<sub>5</sub>COONa
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| HenryConstant =
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| LogP = -2.27
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| MolarMass = 144.10 g/mol
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| MeltingPt =
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| MeltingPtC = 410
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| MeltingPt_notes = (decomposes)
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| Odor = Odorless
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| pKa =
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| pKb =
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| Solubility = 62.69 g/100 ml (0 °C)<br>62.78 g/100 ml (15 °C)<br>62.81 g/100 ml (20 °C)<br>62.87 g/100 ml (30 °C)<br>71.11 g/100 ml (100 °C)
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| SolubleOther = Soluble in liq. [[ammonia]], [[pyridine]]
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| Solubility1 = 0.0000818 g/100 g (25 °C)
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| Solvent1 = 1,4-Dioxane
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| Solubility2 = 2.3 g/100 g (25 °C)<br>8.3 g/100 g (78 °C)
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| Solvent2 = ethanol
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| Solubility3 = 8.22 g/100 g (15 °C)<br>7.55 g/100 g (66.2 °C)
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| Solvent3 = methanol
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| VaporPressure = 2.9·10<sup>-12</sup> mmHg (25 °C)
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| AutoignitionPt = 500 °C (932 °F; 773 K)
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| ExploLimits =
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| ExternalMSDS = [https://www.docdroid.net/apfiI6z/sodium-benzoate-sa.pdf.html Sigma-Aldrich]
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| FlashPt = 100 °C (212 °F; 373 K)
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| LD50 = 4,100 mg/kg (rat, oral)
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| LC50 =
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| MainHazards = Irritant
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| OtherCompounds = [[Benzoic acid]]
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'''Sodium benzoate''' is an organic chemical compound, used as a food preservative.
 
'''Sodium benzoate''' is an organic chemical compound, used as a food preservative.
  
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Sodium benzoate will react with [[sodium hydroxide]] to produce [[benzene]]:
 
Sodium benzoate will react with [[sodium hydroxide]] to produce [[benzene]]:
  
:C<sub>6</sub>H<sub>5</sub>OONa + NaOH → C<sub>6</sub>H<sub>6</sub> + Na<sub>2</sub>CO<sub>3</sub>
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:C<sub>6</sub>H<sub>5</sub>COONa + NaOH → C<sub>6</sub>H<sub>6</sub> + Na<sub>2</sub>CO<sub>3</sub>
  
[[Ascorbic acid]] will also reduce the salt to benzene.
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Small amounts of biphenyl and [[benzophenone]] will also be produced as side products.
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[[Ascorbic acid]] will also reduce the salt to benzene under certain conditions.
  
 
===Physical===
 
===Physical===
Sodium benzoate is a white hygroscopic compound, with a characteristic smell. It has a solubility in water of 62.7 g/100 mL at standard conditions. Sodium benzoate is also soluble in liquid ammonia and pyridine. It is poorly soluble in [[methanol]] and [[ethanol]].
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Sodium benzoate is a white hygroscopic compound, with a characteristic smell. It has a solubility in water of 62.7 g/100 ml at standard conditions. Sodium benzoate is also soluble in liquid ammonia and pyridine. It is poorly soluble in most alcohols, like [[methanol]] and [[ethanol]].
  
 
==Availability==
 
==Availability==
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==Projects==
 
==Projects==
 
*[[Benzene]] synthesis
 
*[[Benzene]] synthesis
*Whistle mix
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*Make benzoic acid
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*Make benzoic acid esters
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*[[Whistle mix]]
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*Food preservative
  
 
==Handling==
 
==Handling==
 
===Safety===
 
===Safety===
 
Sodium benzoate has low toxicity to humans, and recent studies have shown to have some beneficial effects, in preventing Alzheimer and Parkinson's, though the results aren't conclusive so far. Cats however, have a significantly lower tolerance against benzoic acid and its salts, than rats and mice.
 
Sodium benzoate has low toxicity to humans, and recent studies have shown to have some beneficial effects, in preventing Alzheimer and Parkinson's, though the results aren't conclusive so far. Cats however, have a significantly lower tolerance against benzoic acid and its salts, than rats and mice.
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If consumed with ascorbic acid, it may yield benzene, which is carcinogen, phenomenon observed in drinks containing sodium benzoate as preservative. However the levels of benzene obtained are extremely small, and studies have shown that the concentration of benzene is well below the safety limit.
  
 
===Storage===
 
===Storage===
Should be stored in closed bottles, as it's slightly hygroscopic.
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Sodium benzoate should be stored in closed bottles, as it's slightly hygroscopic, though keeping it in a dry chamber is sufficient.
  
 
===Disposal===
 
===Disposal===
Sodium benzoate has low toxicity and doesn't require special disposal.
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Sodium benzoate has low toxicity and doesn't require special disposal. Discard it as you wish.
  
 
==References==
 
==References==
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*[http://www.sciencemadness.org/talk/viewthread.php?tid=29828 Calcium Benzoate from Sodium Benzoate]
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=29828 Calcium Benzoate from Sodium Benzoate]
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=7957 Sodium benzoate to benzoic acid]
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=7957 Sodium benzoate to benzoic acid]
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[[Category:Chemical compounds]]
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[[Category:Organic compounds]]
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[[Category:Sodium compounds]]
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[[Category:Aromatic compounds]]
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[[Category:Readily available chemicals]]
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[[Category:Materials available as food grade]]
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[[Category:Edible chemicals]]

Latest revision as of 18:43, 17 August 2020

Sodium benzoate
Sodium benzoate.jpg
Sodium benzoate from the store.
Names
IUPAC name
Sodium benzoate
Other names
Antimol
Benzoate of soda
E211
Sobenate
Properties
C7H5O2Na
C6H5COONa
Molar mass 144.10 g/mol
Appearance White solid
Odor Odorless
Density 1.497 g/cm3
Melting point 410 °C (770 °F; 683 K) (decomposes)
Boiling point Decomposes
62.69 g/100 ml (0 °C)
62.78 g/100 ml (15 °C)
62.81 g/100 ml (20 °C)
62.87 g/100 ml (30 °C)
71.11 g/100 ml (100 °C)
Solubility Soluble in liq. ammonia, pyridine
Solubility in 1,4-Dioxane 0.0000818 g/100 g (25 °C)
Solubility in ethanol 2.3 g/100 g (25 °C)
8.3 g/100 g (78 °C)
Solubility in methanol 8.22 g/100 g (15 °C)
7.55 g/100 g (66.2 °C)
Vapor pressure 2.9·10-12 mmHg (25 °C)
Hazards
Safety data sheet Sigma-Aldrich
Flash point 100 °C (212 °F; 373 K)
Lethal dose or concentration (LD, LC):
4,100 mg/kg (rat, oral)
Related compounds
Related compounds
Benzoic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Sodium benzoate is an organic chemical compound, used as a food preservative.

Properties

Chemical

Sodium benzoate will react with sodium hydroxide to produce benzene:

C6H5COONa + NaOH → C6H6 + Na2CO3

Small amounts of biphenyl and benzophenone will also be produced as side products.

Ascorbic acid will also reduce the salt to benzene under certain conditions.

Physical

Sodium benzoate is a white hygroscopic compound, with a characteristic smell. It has a solubility in water of 62.7 g/100 ml at standard conditions. Sodium benzoate is also soluble in liquid ammonia and pyridine. It is poorly soluble in most alcohols, like methanol and ethanol.

Availability

Sodium benzoate is available as a food preservative, sold in sealed bags.

Preparation

Sodium benzoate can be prepared by reacting benzoic acid and sodium hydroxide, bicarbonate or carbonate.

Projects

  • Benzene synthesis
  • Make benzoic acid
  • Make benzoic acid esters
  • Whistle mix
  • Food preservative

Handling

Safety

Sodium benzoate has low toxicity to humans, and recent studies have shown to have some beneficial effects, in preventing Alzheimer and Parkinson's, though the results aren't conclusive so far. Cats however, have a significantly lower tolerance against benzoic acid and its salts, than rats and mice.

If consumed with ascorbic acid, it may yield benzene, which is carcinogen, phenomenon observed in drinks containing sodium benzoate as preservative. However the levels of benzene obtained are extremely small, and studies have shown that the concentration of benzene is well below the safety limit.

Storage

Sodium benzoate should be stored in closed bottles, as it's slightly hygroscopic, though keeping it in a dry chamber is sufficient.

Disposal

Sodium benzoate has low toxicity and doesn't require special disposal. Discard it as you wish.

References

Relevant Sciencemadness threads