Sodium benzoate

Sodium benzoate
Names
IUPAC name
sodium benzoate
Other names
E211, benzoate of soda
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.760
E number E211 (preservatives)
RTECS number DH6650000
UNII
Properties
C7H5NaO2
Molar mass 144.10 g·mol−1
Appearance white or colorless crystalline powder
Odor odorless
Density 1.497 g/cm3
Melting point 410 °C (770 °F; 683 K)
62.69 g/100 mL (0 °C)
62.78 g/100 mL (15 °C)
62.87 g/100 mL (30 °C)
71.11 g/100 mL (100 °C)[1]
Solubility soluble in liquid ammonia, pyridine[1]
Solubility in methanol 8.22 g/100 g (15 °C)
7.55 g/100 g (66.2 °C)[1]
Solubility in ethanol 2.3 g/100 g (25 °C)
8.3 g/100 g (78 °C)[1]
Solubility in 1,4-Dioxane 0.818 mg/kg (25 °C)[1]
Pharmacology
A16AX11 (WHO)
Hazards
GHS pictograms [2]
GHS signal word Warning
H319[2]
P305+351+338[2]
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oilHealth code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroformReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
1
2
0
Flash point 100 °C (212 °F; 373 K)
500 °C (932 °F; 773 K)
Lethal dose or concentration (LD, LC):
4100 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Sodium benzoate is a substance which has the chemical formula NaC7H5O2. It is a widely used food preservative, with an E number of E211. It is the sodium salt of benzoic acid and exists in this form when dissolved in water. It can be produced by reacting sodium hydroxide with benzoic acid.

Production

Sodium benzoate is produced by the neutralization of benzoic acid,[3] which is itself produced commercially by partial oxidation of toluene with oxygen.

Natural occurrence

Sodium benzoate occurs naturally, along with benzoic acid and its esters, in many foods.[4] Fruits and vegetables can be rich sources, particularly berries such as cranberry and bilberry, other sources include seafood such as prawns, and dairy products like milk, cheese and yogurt.

Uses

Preservative

Sodium benzoate is a preservative, with the E number E211. It is most widely used in acidic foods such as salad dressings (i.e. acetic acid in vinegar), carbonated drinks (carbonic acid), jams and fruit juices (citric acid), pickles (acetic acid), condiments and frogurt toppings. It is also used as a preservative in medicines and cosmetics.[5][6] Under these conditions it is converted into benzoic acid (E210), which is bacteriostatic and fungistatic. Benzoic acid is generally not used directly due to its poor water solubility. Concentration as a food preservative is limited by the FDA in the U.S. to 0.1% by weight.[7] Sodium benzoate is also allowed as an animal food additive at up to 0.1%, according to AFCO's official publication.[8] Sodium benzoate has been replaced by potassium sorbate in the majority of soft drinks in the United Kingdom.[9]

Pharmaceutical applications

Sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids.[10][11] This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia.[12][13][14] Total Positive and Negative Syndrome Scale scores dropped by 21% compared to placebo.

Sodium benzoate, along with phenylbutyrate, is used to treat hyperammonemia.[15][16]

Other uses

Sodium benzoate is also used in fireworks as a fuel in whistle mix, a powder that emits a whistling noise when compressed into a tube and ignited.

Mechanism of food preservation

The mechanism starts with the absorption of benzoic acid into the cell. If the intracellular pH falls to 5 or lower, the anaerobic fermentation of glucose through phosphofructokinase decreases sharply,[17] which inhibits the growth and survival of microorganisms that cause food spoilage.

Health and safety

In the United States, sodium benzoate is designated as generally recognized as safe (GRAS) by the Food and Drug Administration.[18] The International Programme on Chemical Safety found no adverse effects in humans at doses of 647–825 mg/kg of body weight per day.[19][20]

Cats have a significantly lower tolerance against benzoic acid and its salts than rats and mice.[21]

The human body rapidly clears sodium benzoate by combining it with glycine to form hippuric acid which is then excreted.[20] The metabolic pathway for this begins with the conversion of benzoate by butyrate-CoA ligase into an intermediate product, benzoyl-CoA,[22] which is then metabolized by glycine N-acyltransferase into hippuric acid.[23]

Association with benzene in soft drinks

In combination with ascorbic acid (vitamin C, E300), sodium benzoate and potassium benzoate may form benzene, a known carcinogen. When tested by the FDA, most beverages that contained both ascorbic acid and benzoate had benzene levels that were below those considered dangerous for consumption by the World Health Organization (5 ppb).[24] Most of the beverages that tested higher have been reformulated and subsequently tested below the safety limit.[24] Heat, light and shelf life can increase the rate at which benzene is formed.

Hyperactivity

Research published in 2007 for the UK's Food Standards Agency (FSA) suggests that certain artificial colors, when paired with sodium benzoate, may be linked to hyperactive behavior. The results were inconsistent regarding sodium benzoate, so the FSA recommended further study.[25][26][27] The Food Standards Agency concluded that the observed increases in hyperactive behavior, if real, were more likely to be linked to the artificial colors than to sodium benzoate.[27] The report's author, Jim Stevenson from Southampton University, said: "The results suggest that consumption of certain mixtures of artificial food colours and sodium benzoate preservative are associated with increases in hyperactive behaviour in children. . . . Many other influences are at work but this at least is one a child can avoid."[27]

Compendial status

See also

References

  1. 1 2 3 4 5 "sodium benzoate". chemister.ru.
  2. 1 2 3 Sigma-Aldrich Co., Sodium benzoate. Retrieved on 2014-05-23.
  3. ↑ "International Programme On Chemical Safety". Inchem.org. Retrieved 2013-01-14.
  4. ↑ del Olmo, Ana; Calzada, Javier; Nuñez, Manuel (20 November 2015). "Benzoic acid and its derivatives as naturally occurring compounds in foods and as additives: Uses, exposure, and controversy". Critical Reviews in Food Science and Nutrition. 57 (14): 3084–3103. doi:10.1080/10408398.2015.1087964.
  5. ↑ "Skin Deep® Cosmetics Database | Environmental Working Group". Cosmeticsdatabase.com. Retrieved 2013-01-14.
  6. ↑ "Sodium benzoate in Robitussin cough". Rxmed.com. Retrieved 2013-01-14.
  7. ↑ "CFR - Code of Federal Regulations Title 21". www.accessdata.fda.gov.
  8. ↑ AFCO (2004). "Official Publication": 262.
  9. ↑ Saltmarsh, Mike (2015-03-15). "Recent trends in the use of food additives in the United Kingdom". Journal of the Science of Food and Agriculture. 95 (4): 649–652. doi:10.1002/jsfa.6715. ISSN 1097-0010. PMID 24789520. ... the preservative used in the study, sodium benzoate, has been replaced by potassium sorbate in the majority of soft drinks.
  10. ↑ Häberle, J; Boddaert, N; Burlina, A; Chakrapani, A; Dixon, M; Huemer, M; Karall, D; Martinelli, D; Crespo, PS; Santer, R; Servais, A; Valayannopoulos, V; Lindner, M; Rubio, V; Dionisi-Vici, C (2012). "Suggested guidelines for the diagnosis and management of urea cycle disorders". Orphanet Journal of Rare Diseases. 7: 32. doi:10.1186/1750-1172-7-32. PMC 3488504. PMID 22642880.
  11. ↑ Wilcken, B (2004). "Problems in the management of urea cycle disorders". Molecular Genetics and Metabolism. 81 Suppl 1: S86–91. doi:10.1016/j.ymgme.2003.10.016. PMID 15050980.
  12. ↑ Add-on Treatment of Benzoate for Schizophrenia A Randomized, Double-blind, Placebo-Controlled Trial of d-Amino Acid Oxidase Inhibitor December 2013
  13. ↑ "Digest of Neurology and Psychiatry". Institute of Living. 16 April 2018 – via Google Books.
  14. ↑ Mental Health Research Institute Staff Publications, University of Michigan. Mental Health Research Institute
  15. ↑ "Cinnamon May Help Halt Parkinson's Disease Progression - News Releases - Rush University Medical Center".
  16. ↑ "PHENYLBUTYRATE, SODIUM BENZOATE".
  17. ↑ Krebs H. A., Wiggins D., Stubbs M., Sols A., Bedoya F. (September 1983). "Studies on the mechanism of the antifungal action of benzoate". Biochem. J. 214 (3): 657–663. PMC 1152300. PMID 6226283.
  18. ↑ "CFR - Code of Federal Regulations Title 21". www.accessdata.fda.gov.
  19. ↑ "Concise International Chemical Assessment Document 26: Benzoic acid and sodium benzoate". Inchem.org. Retrieved 2013-01-14.
  20. 1 2 Cosmetic Ingredient Review Expert Panel Bindu Nair (2001). "Final Report on the Safety Assessment of Benzyl Alcohol, Benzoic Acid, and Sodium Benzoate". Int J Tox. 20 (Suppl 3): 23–50. doi:10.1080/10915810152630729. PMID 11766131.
  21. ↑ Bedford PG, Clarke EG (January 1972). "Experimental benzoic acid poisoning in the cat". Vet. Rec. 90 (3): 53–8. doi:10.1136/vr.90.3.53. PMID 4672555.
  22. ↑ "butyrate-CoA ligase". BRENDA. Technische Universität Braunschweig. Retrieved 7 May 2014. |section= ignored (help)
  23. ↑ "glycine N-acyltransferase". BRENDA. Technische Universität Braunschweig. Retrieved 7 May 2014. |section= ignored (help)
  24. 1 2 "Data on Benzene in Soft Drinks and Other Beverages". United States Food and Drug Administration. 16 May 2007. Retrieved 7 November 2013.
  25. ↑ Food Standards Agency issues revised advice on certain artificial colours 6 September 2007
  26. ↑ Food Colorings and Hyperactivity "Myomancy" 7 September 2007
  27. 1 2 3 Agency revises advice on certain artificial colours, Food Standards Agency, 11 September 2007
  28. 1 2 3 Sigma Aldrich. "Sodium benzoate". Retrieved 17 July 2009.
  29. ↑ Therapeutic Goods Administration. "Chemical Substances" (PDF). Archived from the original (PDF) on 15 June 2009. Retrieved 17 July 2009.
  30. ↑ British Pharmacopoeia Commission Secretariat. "Index (BP)" (PDF). Archived from the original (PDF) on 11 April 2009. Retrieved 2 March 2010.
  31. ↑ "Japanese Pharmacopoeia 15th Edition". Retrieved 2 March 2010.
  32. ↑ The United States Pharmacopeial Convention. "Revisions to USP 29–NF 24". Retrieved 17 July 2009.
  • International Programme on Chemical Safety - Benzoic Acid and Sodium Benzoate report
  • Kubota K, Ishizaki T (1991). "Dose-dependent pharmacokinetics of benzoic acid following oral administration of sodium benzoate to humans". Eur. J. Clin. Pharmacol. 41 (4): 363–8. doi:10.1007/BF00314969. PMID 1804654. Although the maximum rate of biotransformation of benzoic acid to hippuric acid varied between 17.2 and 28.8 mg.kg-1.h-1 among the six individuals, the mean value (23.0 mg.kg-1.h-1) was fairly close to that provided by daily maximum dose (0.5 g.kg-1.day-1) recommended in the treatment of hyperammonaemia in patients with inborn errors of ureagenesis
  • Safety data for sodium benzoate
  • The Ketchup Conundrum

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