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Hydantoin
Hydantoin.svg
IUPAC name
Identifiers
CAS number 461-72-3
PubChem 10006
SMILES
Properties
Molecular formula C3H4N2O2
Molar mass 100.076
Melting point

220°C

Solubility in water 39.7 g/L (100°C)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Hydantoin, which is also known as glycolylurea, is a heterocyclic organic compound that can be thought of as a cyclic "double-condensation reaction" product of glycolic acid and urea. Its chemical structure, shown in the Table of Properties at right, is similar to that of imidazolidine except that the molecule of hydantoin has carbonyl groups in the number 2 and 4 positions in the ring. Imidazolidine is the hydrogen-saturated analogue of imidazole. Imidazole is a heterocyclic aromatic organic compound.

In a more general sense, hydantoins can refer to chemical compounds that have substituent groups bonded to a hydantoin ring skeletal structure. For example, phenytoin (mentioned below) has two phenyl groups substituted onto the number 5 carbon in a hydantoin molecule.[1]

Contents

Synthesis

Hydantoin was first isolated in 1861 by Adolf von Baeyer in the course of his study of uric acid. He obtained it by hydrogenation of Allantoin, hence the name. Urech in 1873 [2] synthesized the derivative 5-methylhydantoin from alanine sulfate and potassium cyanate in what is now known as the Urech hydantoin synthesis:

Urech Hydantoin synthesis

The 5,5-dimethyl compound can also be obtained from acetone cyanohydrin (also discovered by Urech: see cyanohydrin reaction) and ammonium carbonate.[3]. This reaction type is called the Bucherer-Bergs reaction.[4][5]

According to the 1911 Encyclopedia Britannica, hydantoin can also be synthesized either by heating allantoin with hydroiodic acid or by "heating bromacetyl urea with alcoholic ammonia".

Uses

Chemical

When hydantoin reacts with hot, dilute hydrochloric acid, glycine is one of the products.

Medicine

Derivatives

Dantrolene is used in malignant hyperthermia, neuroleptic malignant syndrome, spasticity, and Ecstasy intoxication.

Halogenated analogues of hydantoin are used as chlorinating or brominating agents in disinfectant/sanitizer or biocide products. The three major halogenated derivatives are dichlorodimethylhydantoin (DCDMH), bromochlorodimethylhydantoin (BCDMH), and dibromodimethylhydantoin (DBDMH).

Pharmaceutical Industry

Hydantoin is used to synthesize the following anticonvulsants:

DNA Damage

A high proportion of cytosine and thymine bases in DNA are oxidized to hydantoins over time after the death of an organism. Such modifications block DNA polymerases and thus prevents PCR from working. Such damage is a problem with dealing with ancient DNA samples [6].

External links

ChemExper.com.

References

  1. ^ The Chemistry of the Hydantoins.Elinor Ware Chem. Rev.; 1950; 46(3) pp 403 - 470; doi:10.1021/cr60145a001
  2. ^ Urech, Ann., 165, 99 (1873).
  3. ^ Organic Syntheses, Coll. Vol. 3, p.323 (1955); Vol. 20, p.42 (1940) Link.
  4. ^ Bucherer and Steiner, J. prakt. Chem., 140, 291 (1934).
  5. ^ Bergs, Ger. pat. 566,094 (1929) [C. A., 27, 1001 (1933)].
  6. ^ Hofreiter M., Serre D., Poinar H.N., Kuch M., and Paabo S. Nature Reviews Genetics (2001) 2:353.

This article incorporates text from the Encyclopædia Britannica, Eleventh Edition, a publication now in the public domain.


1911 encyclopedia

Up to date as of January 14, 2010

From LoveToKnow 1911

HYDANTOIN (glycolyl urea), C3H4N202 (glycoluric) acid,H 2 N CO-NH. CH 2 CO 2 H, which is readily soluble in hot water, and on heating with hydriodic acid decomposes into ammonia, carbon dioxide and glycocoll, CH2 NH2 C02 H. Many substituted hydantoins are known; the a-alkyl hydantoins are formed on fusion of aldehydeor ketone-cyanhydrins with urea, the 13-alkyl hydantoins from the fusion of mono-alkyl glycocolls with urea, and the 'y-alkyl hydantoins from the action of alkalis and alkyl iodides on the a-compounds. y-Methyl hydantoin has been obtained as a splitting product of caffeine (E. Fischer, Ann., 1882, 215, p. 253).


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