نتريت

(تم التحويل من Nitrite)
يجب ألا يـُخلـَط بينها وبين nitride, nitrate, or nitrogen dioxide.
نتريت
Nitrit-Ion2.svg
Space-filling model of the nitrite ion
الأسماء
اسم أيوپاك
Nitrite
اسم أيوپاك النظامي
dioxidonitrate(1−)
أسماء أخرى
nitrite
المُعرِّفات
رقم CAS
3D model (JSmol)
ChEBI
ChemSpider
رقم EC
  • 233-272-6
UNII
الخصائص
الصيغة الجزيئية NO2
كتلة مولية 45.99 g mol-1
ما لم يُذكر غير ذلك، البيانات المعطاة للمواد في حالاتهم العيارية (عند 25 °س [77 °ف]، 100 kPa).
مراجع الجدول

The nitrite ion has the chemical formula NO−2. Nitrite (mostly sodium nitrite) is widely used throughout chemical and pharmaceutical industries.[1] The nitrite anion is a pervasive intermediate in the nitrogen cycle in nature. The name nitrite also refers to organic compounds having the –ONO group, which are esters of nitrous acid.

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Production

Sodium nitrite is made industrially by passing a mixture of nitrogen oxides into aqueous sodium hydroxide or sodium carbonate solution:[2][1]

NO + NO
2 + 2 NaOH → 2 NaNO
2 + H
2O
NO + NO
2 + Na
2CO
3 → 2 NaNO
2 + CO
2

The product is purified by recrystallization. Alkali metal nitrites are thermally stable up to and beyond their melting point (441 °C for KNO2). Ammonium nitrite can be made from dinitrogen trioxide, N2O3, which is formally the anhydride of nitrous acid:

2 NH3 + H2O + N2O3 → 2 NH4NO2


Structure

The two canonical structures of NO−2, which contribute to the resonance hybrid for the nitrite ion

The nitrite ion has a symmetrical structure (C2v symmetry), with both N–O bonds having equal length and a bond angle of about 115°. In valence bond theory, it is described as a resonance hybrid with equal contributions from two canonical forms that are mirror images of each other. In molecular orbital theory, there is a sigma bond between each oxygen atom and the nitrogen atom, and a delocalized pi bond made from the p orbitals on nitrogen and oxygen atoms which is perpendicular to the plane of the molecule. The negative charge of the ion is equally distributed on the two oxygen atoms. Both nitrogen and oxygen atoms carry a lone pair of electrons. Therefore, the nitrite ion is a Lewis base.

Reactions

Acid-base properties

Dimensions of trans-HONO (from the microwave spectrum)

Nitrite is the conjugate base of the weak acid nitrous acid:

HNO2 في اتزان مع H+ + NO−2;      pKa ≈ 3.3 at 18 °C[3]

Nitrous acid is also highly volatile – in the gas phase it exists predominantly as a trans-planar molecule. In solution, it is unstable with respect to the disproportionation reaction:

3 HNO2 (aq) في اتزان مع H3O+ + NO−3 + 2 NO

This reaction is slow at 0 °C.[2] Addition of acid to a solution of a nitrite in the presence of a reducing agent, such as iron(II), is a way to make nitric oxide (NO) in the laboratory.

Oxidation and reduction

The formal oxidation state of the nitrogen atom in nitrite is +3. This means that it can be either oxidized to oxidation states +4 and +5, or reduced to oxidation states as low as −3. Standard reduction potentials for reactions directly involving nitrous acid are shown in the table below:[4]

Half-reaction E0 (V)
NO−3 + 3 H+ + 2 e− في اتزان مع HNO2 + H2O +0.94
2 HNO2 + 4 H+ + 4 e− في اتزان مع H2N2O2 + 2 H2O +0.86
N2O4 + 2 H+ + 2 e− في اتزان مع 2 HNO2 +1.065
2 HNO2+ 4 H+ + 4 e− في اتزان مع N2O + 3 H2O +1.29

The data can be extended to include products in lower oxidation states. For example:

H2N2O2 + 2 H+ + 2 e− في اتزان مع N2 + 2 H2O;      E0 = +2.65 V

Oxidation reactions usually result in the formation of the nitrate ion, with nitrogen in oxidation state +5. For example, oxidation with permanganate ion can be used for quantitative analysis of nitrite (by titration):

5 NO−2 + 2 MnO−4 + 6 H+ → 5 NO−3 + 2 Mn2+ + 3 H2O

The product of reduction reactions with nitrite ion are varied, depending on the reducing agent used and its strength. With sulfur dioxide, the products are NO and N2O; with tin(II) (Sn2+) the product is hyponitrous acid (H2N2O2); reduction all the way to ammonia (NH3) occurs with hydrogen sulfide. With the hydrazinium cation (N 2H+5) the product of nitrite reduction is hydrazoic acid (HN3), an instable and explosive compound:

HNO2 + N 2H+5 → HN3 + H2O + H3O+

which can also further react with nitrite:

HNO2 + HN3 → N2O + N2 + H2O

This reaction is unusual in that it involves compounds with nitrogen in four different oxidation states.[2]

Analysis of nitrite

انظر أيضاً: Nitrite test

Nitrite is detected and analyzed by the Griess Reaction, involving the formation of a deep red-colored azo dye upon treatment of a NO−2-containing sample with sulfanilic acid and naphthyl-1-amine in the presence of acid.[5]

Coordination complexes

المقالة الرئيسية: Transition metal nitrite complex

Nitrite is an ambidentate ligand and can form a wide variety of coordination complexes by binding to metal ions in several ways.[2] Two examples are the red nitrito complex [Co(NH3)5(ONO)]2+ is metastable, isomerizing to the yellow nitro complex [Co(NH3)5(NO2)]2+. Nitrite is processed by several enzymes, all of which utilize coordination complexes.


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Biochemistry

A schematic representation of the microbial nitrogen cycle.[6][7] ANAMMOX is anaerobic ammonium oxidation, DNRA is dissimilatory nitrate reduction to ammonium, and COMMAMOX is complete ammonium oxidation.

In nitrification, ammonium is converted to nitrite. Important species include Nitrosomonas. Other bacterial species such as Nitrobacter, are responsible for the oxidation of the nitrite into nitrate.

Nitrite can be reduced to nitric oxide or ammonia by many species of bacteria. Under hypoxic conditions, nitrite may release nitric oxide, which causes potent vasodilation. Several mechanisms for nitrite conversion to NO have been described, including enzymatic reduction by xanthine oxidoreductase, nitrite reductase, and NO synthase (NOS), as well as nonenzymatic acidic disproportionation reactions.

Uses

Chemical precursor

Azo dyes and other colorants are prepared by the process called diazotization, which requires nitrite.[1]

Nitrite in food preservation and biochemistry

انظر أيضاً: Warmed-over flavor

Sodium nitrite is used to speed up the curing of meat and also impart an attractive colour.[8] A 2018 study by the British Meat Producers Association determined that legally permitted levels of nitrite have no effect on the growth of the Clostridium botulinum bacteria which causes botulism, in line with the UK's Advisory Committee on the Microbiological Safety of Food opinion that nitrites are not required to prevent Clostridium botulinum growth and extend shelf life.[9] In the U.S., meat cannot be labeled as "cured" without the addition of nitrite.[10][11][12] In some countries, cured-meat products are manufactured without nitrate or nitrite, and without nitrite from vegetable source. Parma ham, produced without nitrite since 1993, was reported in 2018 to have caused no cases of botulism.[8]

In mice, food rich in nitrites together with unsaturated fats can prevent hypertension, which is one explanation for the apparent health effect of the Mediterranean diet.[13] However, adding nitrites to meat has been shown to generate known carcinogens; the World Health Organization (WHO) advises that eating 50 g (1.8 oz) of nitrite processed meat a day would raise the risk of getting bowel cancer by 18% over a lifetime.[8] The recommended maximum limits by the World Health Organization in drinking water are 3 mg L−1 and 50 mg L−1 for nitrite and nitrate ions, respectively.[14]

Curing of meat

In a reaction with the meat's myoglobin, nitrite gives the product a desirable pink-red "fresh" color, such as with corned beef. In the US, nitrite has been formally used since 1925. According to scientists working for the industry group American Meat Institute, this use of nitrite started in the Middle Ages.[15] Historians[16] and epidemiologists[17] argue that the widespread use of nitrite in meat-curing is closely linked to the development of industrial meat-processing. French investigative journalist Guillaume Coudray asserts that the meat industry chooses to cure its meats with nitrite even though it is established that this chemical gives rise to cancer-causing nitroso-compounds.[18]

Antidote for cyanide poisoning

Nitrites in the form of Sodium Nitrite and Amyl Nitrite are components of many cyanide antidote kits.[19] Both of these compounds bind to hemoglobin and oxidizes the Fe2+ ions to Fe3+ ions forming methaemoglobin. Methaemoglobin in turn binds to cyanide (CN) creating cyanmethaemoglobin, effectively removing cyanide from the Complex IV of the Electron transport chain (ETC) in mitochondria, which is the primary site of disruption caused by cyanide. Another mechanism by which nitrites are useful in treating cyanide toxicity is the generation of Nitric oxide (NO). NO displaces the CN from the Cytochrome c Oxidase (ETC complex IV), making it available for methaemoglobin to bind.[20]

Organic nitrites

A nitrite ester

In organic chemistry, alkyl nitrites are esters of nitrous acid and contain the nitrosoxy functional group. Nitro compounds contain the C–NO2 group. Nitrites have the general formula RONO, where R is an aryl or alkyl group. Amyl nitrite and other alkyl nitrites have a vasodilating action and must be handled in the laboratory with caution. They are sometimes used in medicine for the treatment of heart diseases. A classic named reaction for the synthesis of alkyl nitrites is the Meyer synthesis[21][22] in which alkyl halides react with metallic nitrites to a mixture to nitroalkanes and nitrites.

Safety

انظر أيضاً: Curing (food preservation) § Nitrates and nitrites

Nitrites salts can react with secondary amines to produce N-nitrosamines, which are suspected to cause stomach cancer. The World Health Organization (WHO) advises that each 50 g (1.8 oz) of processed meat eaten a day would raise the risk of getting bowel cancer by 18% over a lifetime; processed meat refers to meat that has been transformed through fermentation, nitrite curing, salting, smoking, or other processes to enhance flavour or improve preservation. The World Health Organization's review of more than 400 studies concluded, in 2015, that there was sufficient evidence that processed meats caused cancer, particularly colon cancer; the WHO's International Agency for Research on Cancer (IARC) classified processed meats as carcinogenic to humans (Group 1).[8][23]

Nitrite (ingested) under conditions that result in endogenous nitrosation, specifically the production of nitrosamine, has been classified as "Probably carcinogenic to humans" (Group 2A) by the IARC.[24][25]

انظر أيضاً

المراجع

  1. ^ أ ب ت Laue W, Thiemann M, Scheibler E, Wiegand KW (2006). "Nitrates and Nitrites". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_265. {{cite encyclopedia}}: Cite has empty unknown parameter: |authors= (help)
  2. ^ أ ب ت ث Greenwood, pp. 461–464.
  3. ^ IUPAC SC-Database Archived 19 يونيو 2017 at the Wayback Machine A comprehensive database of published data on equilibrium constants of metal complexes and ligands
  4. ^ Greenwood, p. 431.
  5. ^ V. M. Ivanov (2004). "The 125th Anniversary of the Griess Reagent". Journal of Analytical Chemistry. 59 (10): 1002–1005. doi:10.1023/B:JANC.0000043920.77446.d7. S2CID 98768756. Translated from V. M. Ivanov (2004). Zhurnal Analiticheskoi Khimii. 59 (10): 1109–1112. {{cite journal}}: Missing or empty |title= (help)
  6. ^ Sparacino-Watkins, Courtney; Stolz, John F.; Basu, Partha (2013-12-16). "Nitrate and periplasmic nitrate reductases". Chem. Soc. Rev. (in الإنجليزية). 43 (2): 676–706. doi:10.1039/c3cs60249d. ISSN 1460-4744. PMC 4080430. PMID 24141308.
  7. ^ Simon, Jörg; Klotz, Martin G. (2013). "Diversity and evolution of bioenergetic systems involved in microbial nitrogen compound transformations". Biochimica et Biophysica Acta (BBA) - Bioenergetics (in الإنجليزية). 1827 (2): 114–135. doi:10.1016/j.bbabio.2012.07.005. PMID 22842521.
  8. ^ أ ب ت ث Wilson, Bee (2018-03-01). "Yes, bacon really is killing us". The Guardian (in الإنجليزية البريطانية). London. ISSN 0261-3077. Archived from the original on 2021-02-10. Retrieved 2021-02-14. In trade journals of the 1960s, the firms who sold nitrite powders to ham-makers spoke quite openly about how the main advantage was to increase profit margins by speeding up production.
  9. ^ Doward, Jamie (2019-03-23). "Revealed: no need to add cancer-risk nitrites to ham". The Observer. London. Archived from the original on 2021-01-26. Retrieved 2021-02-14. The results show that there is no change in levels of inoculated C. botulinum over the curing process, which implies that the action of nitrite during curing is not toxic to C. botulinum spores at levels of 150ppm [parts per million] ingoing nitrite and below.
  10. ^ De Vries, John (1997). Food Safety and Toxicity. CRC Press. p. 70. ISBN 978-0-8493-9488-1.
  11. ^ sodium nitrite and nitrate facts Accessed 12 Dec 2014
  12. ^ Doyle, Michael P.; Sperber, William H. (23 September 2009). Compendium of the Microbiological Spoilage of Foods and Beverages. p. 78. ISBN 9781441908261.
  13. ^ Charles, R. L.; Rudyk, O.; Prysyazhna, O.; Kamynina, A.; Yang, J.; Morisseau, C.; Hammock, B. D.; Freeman, B. A.; Eaton, P. (2014). "Protection from hypertension in mice by the Mediterranean diet is mediated by nitro fatty acid inhibition of soluble epoxide hydrolase". Proceedings of the National Academy of Sciences. 111 (22): 8167–72. Bibcode:2014PNAS..111.8167C. doi:10.1073/pnas.1402965111. PMC 4050620. PMID 24843165.
  14. ^ Bagheri, H.; Hajian, A.; Rezaei, M.; Shirzadmehr, A. (2017). "Composite of Cu metal nanoparticles—multiwall carbon nanotubes—reduced graphene oxide as a novel and high performance platform of the electrochemical sensor for simultaneous determination of nitrite and nitrate". Journal of Hazardous Materials. 324 (Pt B): 762–772. doi:10.1016/j.jhazmat.2016.11.055. PMID 27894754.
  15. ^ Binkerd, E. F.; Kolari, O. E. (1975-01-01). "The history and use of nitrate and nitrite in the curing of meat". Food and Cosmetics Toxicology. 13 (6): 655–661. doi:10.1016/0015-6264(75)90157-1. ISSN 0015-6264. PMID 1107192.
  16. ^ coudray, guillaume, eric (2017). Cochonneries : comment la charcuterie est devenue un poison. paris: Decouverte. pp. part I, chapter 2 (p. 40–55) and chapter 3 (p. 56–70). ISBN 9782707193582. OCLC 1011036745.{{cite book}}: CS1 maint: multiple names: authors list (link)
  17. ^ Lauer, Klaus (1991-01-01). "The history of nitrite in human nutrition: A contribution from German cookery books". Journal of Clinical Epidemiology (in الإنجليزية). 44 (3): 261–264. doi:10.1016/0895-4356(91)90037-A. ISSN 0895-4356. PMID 1999685.
  18. ^ "Guillaume Coudray on the Nitro Meat Cancer Connection". 14 April 2021.
  19. ^ Meillier, Andrew; Heller, Cara (2015). "Acute Cyanide Poisoning: Hydroxocobalamin and Sodium Thiosulfate Treatments with Two Outcomes following One Exposure Event". Case Reports in Medicine. 2015: 217951. doi:10.1155/2015/217951. ISSN 1687-9627. PMC 4620268. PMID 26543483.
  20. ^ Bebarta, Vikhyat S.; Brittain, Matthew; Chan, Adriano; Garrett, Norma; Yoon, David; Burney, Tanya; Mukai, David; Babin, Michael; Pilz, Renate B.; Mahon, Sari B.; Brenner, Matthew (June 2017). "Sodium Nitrite and Sodium Thiosulfate Are Effective Against Acute Cyanide Poisoning when Administered by Intramuscular Injection". Annals of Emergency Medicine. 69 (6): 718–725.e4. doi:10.1016/j.annemergmed.2016.09.034. ISSN 0196-0644. PMC 5446299. PMID 28041825.
  21. ^ Victor Meyer (1872). "Ueber die Nitroverbindungen der Fettreihe". Justus Liebig's Annalen der Chemie. 171 (1): 1–56. doi:10.1002/jlac.18741710102.; Victor Meyer, J. Locher (1876). "Ueber die Pseudonitrole, die Isomeren der Nitrolsäuren". Justus Liebig's Annalen der Chemie. 180 (1–2): 133–55. doi:10.1002/jlac.18761800113.; V. Meyer and Stüber (1872). "Vorläufige Mittheilung". Chemische Berichte. 5: 203–05. doi:10.1002/cber.18720050165.; Victor Meyer, O. Stüber (1872). "Ueber die Nitroverbindungen der Fettreihe". Chemische Berichte. 5: 399–406. doi:10.1002/cber.187200501121. S2CID 95188274.; Victor Meyer, A. Rilliet (1872). "Ueber die Nitroverbindungen der Fettreiche. Dritte Mittheilung". Chemische Berichte. 5 (2): 1029–34. doi:10.1002/cber.187200502133.; Victor Meyer, C. Chojnacki (1872). "Ueber die Nitroverbindungen der Fettreihe. Vierte Mittheilung". Chemische Berichte. 5 (2): 1034–38. doi:10.1002/cber.187200502134.
  22. ^ Robert B. Reynolds, Homer Adkins (1929). "The Relationship of the Constitution of Certain Alky Halides to the Formation of Nitroparaffins and Alkyl Nitrites". Journal of the American Chemical Society. 51 (1): 279–87. doi:10.1021/ja01376a037.
  23. ^ "IARC Monographs evaluate consumption of red meat and processed meat" (PDF). International Agency for Research on Cancer. 2015-10-26. Archived from the original (PDF) on 2021-01-18. Retrieved 2021-02-14. Processed meat was classified as carcinogenic to humans (Group 1), based on sufficient evidence in humans that the consumption of processed meat causes colorectal cancer.
  24. ^ "List of classifications, Volumes 1–116 – IARC Monographs on the Evaluation of Carcinogenic Risks to Humans". International Agency for Research on Cancer (IARC) – World Health Organization (WHO). 2010. Archived from the original on 10 June 2017. Retrieved 25 September 2016.
  25. ^ VOLUME 94 – Ingested Nitrate and Nitrite, and Cyanobacterial Peptide Toxins – IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 2010. ISBN 9789283212942. Retrieved 25 September 2016. {{cite book}}: |work= ignored (help)


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