guanidine

Guanidine can be thought of as a nitrogenous analogue of carbonic acid. That is, the C=O group in carbonic acid is replaced by a C=NH group, and each OH is replaced by a {{chem|NH|2}} group.{{cite journal | vauthors = Göbel M, Klapötke TM | title = First structural characterization of guanidine, HN=C(NH(2))(2) | journal = Chemical Communications | volume = 43 | issue = 30 | pages = 3180–3182 | date = August 2007 | pmid = 17653381 | doi = 10.1039/B705100J }} Isobutene can be seen as the carbon analogue in much the same way. A detailed crystallographic analysis of guanidine was elucidated 148 years after its first synthesis, despite the simplicity of the molecule.{{cite journal | vauthors = Yamada T, Liu X, Englert U, Yamane H, Dronskowski R | title = Solid-state structure of free base guanidine achieved at last | journal = Chemistry: A European Journal | volume = 15 | issue = 23 | pages = 5651–5655 | date = June 2009 | pmid = 19388036 | doi = 10.1002/chem.200900508 }} In 2013, the positions of the hydrogen atoms and their displacement parameters were accurately determined using single-crystal neutron diffraction.{{cite journal | vauthors = Sawinski PK, Meven M, Englert U, Dronskowski R | journal = Crystal Growth & Design | year = 2013 | volume = 13 |issue=4 | pages = 1730–5 | doi = 10.1021/cg400054k | title = Single-Crystal Neutron Diffraction Study on Guanidine, CN₃H₅ |doi-access=free }}

Guanidine can be obtained from natural sources, being first isolated in 1861 by Adolph Strecker via the oxidative degradation of an aromatic natural product, guanine, isolated from Peruvian guano.{{cite journal | vauthors = Strecker A | author-link = Adolph Strecker | journal = Liebigs Ann. Chem. | year = 1861 | volume = 118 | pages = 151–177 | issue = 2 | title = Untersuchungen über die chemischen Beziehungen zwischen Guanin, Xanthin, Theobromin, Caffeïn und Kreatinin | trans-title = Studies on the chemical relationships between guanine, xanthine, theobromine, caffeine and creatinine | doi = 10.1002/jlac.18611180203 | url = https://zenodo.org/record/1427163 | access-date = 2019-07-02 | archive-date = 2021-07-16 | archive-url = https://web.archive.org/web/20210716154230/https://zenodo.org/record/1427163 | url-status = live }}

A laboratory method of producing guanidine is gentle (180-190 °C) thermal decomposition of dry ammonium thiocyanate in anhydrous conditions:

:{{chem2|3 NH4SCN -> 2 CH5N3 + H2S + CS2}}

The commercial route involves a two step process starting with the reaction of dicyandiamide with ammonium salts. Via the intermediacy of biguanidine, this ammonolysis step affords salts of the guanidinium cation (see below). In the second step, the salt is treated with base, such as sodium methoxide.{{Ullmann| vauthors = Güthner T, Mertschenk B, Schulz B |title=Guanidine and Derivatives |doi=10.1002/14356007.a12_545.pub2}}

Isothiouronium salts (S-alkylated thioureas) react with amines to give guanidinium salts:{{cite journal|last1=Palmer|first1=David C.|title=S-Methylisothiourea|journal=E-EROS Encyclopedia of Reagents for Organic Synthesis|year=2001|doi=10.1002/047084289X.rm199s|isbn=0471936235}}

:RNH₂ + [CH₃SC(NH₂)₂]⁺X⁻ → [RN(H)C(NH₂)₂]⁺X⁻ + CH₃SH

The resulting guanidinium ions can often be deprotonated to give the guanidine. This approach is sometimes called the Rathke synthesis, in honor of its discoverer. after Bernhard Rathke{{cite journal|title=Heinrich Bernhard Rathke. (1840-1923)|journal=Berichte der Deutschen Chemischen Gesellschaft (A and B Series)|date=8 October 1924|volume=57|issue=9|pages=A83–A92|doi=10.1002/cber.19240570929|doi-access=free}}{{cite journal|last1=Rathke|first1=B.|title=Ueber Derivate und Constitution des Schwefelharnstoffs|journal=Berichte der Deutschen Chemischen Gesellschaft|date=July 1881|volume=14|issue=2|pages=1774–1780|doi=10.1002/cber.18810140247|url=https://zenodo.org/record/1425246}}

The conjugate acid is called the guanidinium cation, ({{chem|C(NH|2|)|3|+}}). This planar, symmetric ion consists of three amino groups each bonded to the central carbon atom with a covalent bond of order 4/3. It is a highly stable +1 cation in aqueous solution due to the efficient resonance stabilization of the charge and efficient solvation by water molecules. As a result, its pK_aH is 13.6{{cite book| vauthors = Perrin DD |title=Dissociation Constants of Organic Bases in Aqueous Solution |publisher=Butterworths |location=London |date=1972 |edition=Supplement }} (pK_b of 0.4) meaning that guanidine is a very strong base in water; in neutral water, it exists almost exclusively as guanidinium. Due to this, most guanidine derivatives are salts containing the conjugate acid.

Image:Guanidinium-ion-3D-balls.png|{{center|ball-and-stick model}}

Image:Guanidinium-ion-2D-skeletal.png|{{center|resonance hybrid}}

Image:Guanidinium-ion-canonical-forms-2D-skeletal.png|{{center|canonical forms}}

Guanidine can be selectively detected using sodium 1,2-naphthoquinone-4-sulfonic acid (Folin's reagent) and acidified urea.{{Cite journal | vauthors = Sullivan MX |date=1935-10-01 |title=A Colorimetric Test for Guanidine |journal=Proceedings of the Society for Experimental Biology and Medicine |language=en |volume=33 |issue=1 |pages=106–108 |doi=10.3181/00379727-33-8270C |s2cid=88290359 |issn=0037-9727}}

The main salt of commercial interest is the nitrate [C({{chem|NH|2}})₃]{{chem|NO|3}}. It is used as a propellant, for example in air bags.

Since the Middle Ages in Europe, guanidine has been used to treat diabetes as the active antihyperglycemic ingredient in French lilac. Due to its long-term hepatotoxicity, further research for blood sugar control was suspended at first after the discovery of insulin. Later development of nontoxic, safe biguanides led to the long-used first-line diabetes control medicine metformin, introduced to Europe in the 1950s & United States in 1995 and now prescribed to over 17 million patients per year in the US.{{cite journal | vauthors = Blaslov K, Naranđa FS, Kruljac I, Renar IP | title = Treatment approach to type 2 diabetes: Past, present and future | journal = World Journal of Diabetes | volume = 9 | issue = 12 | pages = 209–219 | date = December 2018 | pmid = 30588282 | pmc = 6304295 | doi = 10.4239/wjd.v9.i12.209 | doi-access = free }}{{Cite web|title=The Top 300 of 2019|url=https://clincalc.com/DrugStats/Top300Drugs.aspx|access-date=2022-02-17|website=clincalc.com|archive-date=2021-02-12|archive-url=https://web.archive.org/web/20210212142534/https://clincalc.com/DrugStats/Top300Drugs.aspx|url-status=live}}

Guanidinium chloride is a now-controversial adjuvant in treatment of botulism. Recent studies have shown some significant subsets of patients who see no improvement after the administration of this drug.{{cite book| vauthors = Brook I |title=Pediatric Anaerobic Infections: Diagnosis and Management|publisher=Taylor & Francis|year=2001|isbn=0824741862|edition=3rd|page=529}}

Guanidine exists protonated, as guanidinium, in solution at physiological pH.

Guanidinium chloride (also known as guanidine hydrochloride) has chaotropic properties and is used to denature proteins. Guanidinium chloride is known to denature proteins with a linear relationship between concentration and free energy of unfolding. In aqueous solutions containing 6 M guanidinium chloride, almost all proteins lose their entire secondary structure and become randomly coiled peptide chains. Guanidinium thiocyanate is also used for its denaturing effect on various biological samples.

Recent studies suggest that guanidinium is produced by bacteria as a toxic byproduct. To alleviate the toxicity of guanidinium, bacteria have developed a class of transporters known as guanidinium exporters or Gdx proteins to expel the extra amounts of this ion to the outside of the cell.{{cite journal | vauthors = Kermani AA, Macdonald CB, Gundepudi R, Stockbridge RB | title = Guanidinium export is the primal function of SMR family transporters | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 115 | issue = 12 | pages = 3060–3065 | date = March 2018 | pmid = 29507227 | pmc = 5866581 | doi = 10.1073/pnas.1719187115 | bibcode = 2018PNAS..115.3060K | doi-access = free }} Gdx proteins, are highly selective for guanidinium and mono-substituted guanidinyl compounds and share an overlapping set of non-canonical substrates with drug exporter EmrE.{{cite journal | vauthors = Kermani AA, Macdonald CB, Burata OE, Ben Koff B, Koide A, Denbaum E, Koide S, Stockbridge RB | display-authors = 6 | title = The structural basis of promiscuity in small multidrug resistance transporters | journal = Nature Communications | volume = 11 | issue = 1 | pages = 6064 | date = November 2020 | pmid = 33247110 | doi = 10.1038/s41467-020-19820-8 | pmc = 7695847 | bibcode = 2020NatCo..11.6064K }}

Guanidinium hydroxide is the active ingredient in some non-lye hair relaxers.

Image:Guanidine-group-2D-skeletal.png

Guanidines are a group of organic compounds sharing a common functional group with the general structure {{chem|(R|1|R|2|N)(R|3|R|4|N)C{{=}}N−R|5}}. The central bond within this group is that of an imine, and the group is related structurally to amidines and ureas. Examples of guanidines are arginine, triazabicyclodecene, saxitoxin, and creatine.

Galegine is an isoamylene guanidine.{{cite journal | vauthors = Witters LA | title = The blooming of the French lilac | journal = The Journal of Clinical Investigation | volume = 108 | issue = 8 | pages = 1105–1107 | date = October 2001 | pmid = 11602616 | pmc = 209536 | doi = 10.1172/JCI14178 }}

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• Sakaguchi test
• Y-aromaticity
• Amidine

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Category:Guanidines

Category:Bases (chemistry)

Category:Organic compounds with 1 carbon atom