Chloral hydrate

Chloral hydrate

Chloral hydrate
Names
IUPAC name
2,2,2-trichloroethane-1,1-diol
Other names
Trichloroacetaldehyde monohydrate
Tradenames: Aquachloral, Novo-Chlorhydrate, Somnos, Noctec, Somnote
Identifiers
 Y
ATC code N05
ChEBI  Y
ChEMBL  Y
ChemSpider  Y
DrugBank  Y
EC number 206-117-5
Jmol-3D images Image
KEGG  Y
PubChem
RTECS number FM875000
UNII  Y
Properties
C2H3Cl3O2
Molar mass 165.39 g·mol−1
Appearance Colorless solid
Odor aromatic, slightly acrid
Density 1.9081 g/cm3
Melting point 57 °C (135 °F; 330 K)
Boiling point 98 °C (208 °F; 371 K)
very soluble
Solubility very soluble in benzene, ethyl ether, ethanol
log P 0.99
Acidity (pKa) 9.66, 11.0[1]
Structure
monoclinic
Pharmacology
Legal status
  • US: C (Risk not ruled out)
Oral codeine/syrup, rectal suppository
Pharmacokinetics:
well absorbed
converted to trichloroethanol, hepatic and renal
8–10 hours in plasma
bile, feces, urine (various metabolites not unchanged)
Hazards
Safety data sheet External MSDS
Harmful (Xn)
R-phrases R22 R36 R37 R38
Lethal dose or concentration (LD, LC):
LD50 (Median dose)
1100 mg/kg (mouse, oral)
Related compounds
Related compounds
Chloral, chlorobutanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 Y  (: Y/N?)

Chloral hydrate is an formula C2H3Cl3O2. It is a colorless solid. It has limited use as a sedative and hypnotic pharmaceutical drug. It is also a useful laboratory chemical reagent and precursor. It is derived from chloral (trichloroacetaldehyde) by the addition of one equivalent of water.

It was discovered through the chlorination (

Media related to at Wikimedia Commons

External links

  1. ^ Gawron, O., Draus, F. (1958). J. Am. Chem. Soc. 80 (20): 5392.  
  2. ^ Justus Liebig (1832). "Ueber die Zersetzung des Alkohols durch Chlor". Annalen der Pharmacie 1 (1): 31–32.  
  3. ^ Justus Liebig (1832). "Ueber die Verbindungen, welche durch die Einwirkung des Chlors auf Alkohol, Aether, ölbildendes Gas und Essiggeist entstehen". Annalen der Pharmacie 1 (2): 182–230.  
  4. ^ Liebreich, Oskar (1869). Das Chloralhydrat : ein neues Hypnoticum und Anaestheticum und dessen Anwendung in der Medicin ; eine Arzneimittel-Untersuchung. Berlin: Müller. 
  5. ^ http://www.justice.gov/dea/concern/chloral_hydrate.html Archived 11 May 2012 at the Wayback Machine
  6. ^ "An Improved Clearing and Mounting Solution to Replace Chloral Hydrate in Microscopic Applications". Applications in Plant Sciences, 1(5).  
  7. ^ "Pyrrole Alkaloids with Potential Cancer Chemopreventive Activity Isolated from a Goji Berry-Contaminated Commercial Sample of African Mango". Journal of Agricultural and Food Chemistry, 62 (22).  
  8. ^ "Summary statement - 12.20 Chloral hydrate (trichloroacetaldehyde)" (PDF). World Health Organization. Retrieved March 14, 2013. 
  9. ^ Michelle Meadows (January–February 2007). "The FDA Takes Action Against Unapproved Drugs" (PDF). FDA Consumer magazine. 
  10. ^ Takahashi, Yasuo; Onodera, Sukeo; Morita, Masatoshi; and Terao, Yoshiyasu (2003). "A Problem in the Determination of Trihalomethane by Headspace-Gas Chromatography/Mass Spectrometry" (PDF). Journal of Health Science 49 (1): 3.  
  11. ^ C. S. Marvel and G. S. Hiers (1941). "Isatin".  
  12. ^ Tariq, Syed H.; Pulisetty, Shailaja (2008). "Pharmacotherapy for Insomnia". Clinics in Geriatric Medicine 24 (1): 93–105.  
  13. ^ http://jcc.kau.edu.sa/Files/140/Researches/11822_Chloral.pdf
  14. ^ Gauillard J, Cheref S, Vacherontrystram MN, Martin JC. (May–Jun 2002). "Chloral hydrate: a hypnotic best forgotten?". Encephale 28 (3 Pt 1): 200–204.  
  15. ^ Beland, Frederick A. "NTP Technical Report on the Toxicity and Metabolism Studies of Chloral Hydrate" (PDF). Toxicity Report Series Number 59. National Toxicology Program. p. 10. Retrieved March 14, 2013. 
  16. ^ Gelder, M., Mayou, R. and Geddes, J. (2005). Psychiatry (3rd ed.). New York: Oxford. p. 238. 
  17. ^ R. Baselt (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City, CA: Biomedical Publications. pp. 259–261. 
  18. ^ Trichloroethanol
  19. ^ Reinhard Jira, Erwin Kopp, Blaine C. McKusick, Gerhard Röderer, Axel Bosch and Gerald Fleischmann "Chloroacetaldehydes" in Ullmann's Encyclopedia of Industrial Chemistry, 2007, Wiley-VCH, Weinheim. doi:10.1002/14356007.a06_527.pub2
  20. ^ Lu, J; Greco, MA (2006). "Sleep circuitry and the hypnotic mechanism of GABAA drugs". Journal of Clinical Sleep Medicine 2 (2): S19–26.  
  21. ^ New York Daily News, 10/25/2008
  22. ^ Rathmell, George W. (2002). A Passport to Hell: The Mystery of Richard Realf. Lincoln, Nebraska: Authors Choice Press. pp. ix, 134.  
  23. ^ Anna Nicole Smith Autopsy Report. XI. Manner of death. A. The Exclusion of Homicide The Smoking Gun
  24. ^ Anna Nicole Smith Autopsy Released. Coroner: Ex-Playmate died from accidental sedative overdose The Smoking Gun
  25. ^ Hank Williams summary Book Rags
  26. ^ Gide, André and Dorothy Bussey (trans). If It Die...An Autobiography. New York: Vintage International, 2001. p105
  27. ^ Sacks, Oliver. "Altered States". The New Yorker, 27 Aug 2012. The New Yorker. Retrieved 2 September 2015. 

References

See also

  • The Jonestown mass suicides, which involved the communal drinking of Flavor Aid poisoned with Valium, chloral hydrate, cyanide, and Phenergan
  • Richard Realf (1832–1878) killed himself with a combination of chloral hydrate and laudanum.[22]
  • Jennie Bosschieter (1882–1900) who was murdered with chloral hydrate in Paterson, New Jersey on 12 October 1900.
  • John Tyndall (1820–1893) who died of an accidental overdose.
  • Anna Nicole Smith (1967–2007) who died of an accidental[23] combination of chloral hydrate with four benzodiazepines and several other drugs, as announced by forensic pathologist Dr. Joshua Perper on 26 March 2007. Chloral hydrate was the major factor, but it was unclear if any of these drugs would have been sufficient by itself to cause her death.[24]
  • Marilyn Monroe had chloral hydrate in her system at her death.
  • [25]
  • William S. Burroughs was expelled from school for experimenting with chloral hydrate along with another pupil. The incident is detailed in the writer's foreword to Junkie.
  • Mary Todd Lincoln was given chloral hydrate for sleep problems. See Mary Todd Lincoln by Jean Baker and Mary: Mrs. A. Lincoln, by Janis Cooke Newman.
  • André Gide (1869–1951) was given chloral hydrate as a boy for sleep problems by a physician named Lizart. Gide states in his autobiography, If It Die... that "all my later weaknesses of will or memory I attribute to him."[26]
  • Dante Gabriel Rossetti (1828–1882), the English painter, was a regular user of chloral hydrate, originally against insomnia. He is quoted as saying to his friend Hall Caine: "Everyone has skeletons in their cupboards, and this is mine."
  • Friedrich Nietzsche regularly used chloral hydrate in the years leading up to his nervous breakdown, according to Lou Salome and other associates. Whether the drug contributed to his insanity is a point of controversy.
  • Antonin Artaud allegedly died of an overdose of chloral hydrate.
  • Oliver Sacks abused chloral hydrate in 1965 as a depressed insomniac. He found himself taking fifteen times the usual dose of chloral hydrate every night before he eventually ran out, causing violent withdrawal symptoms.[27]
  • William James experimented with chloral hydrate in order to investigate the nature of mystical experiences.

Notable uses

Chloral hydrate is also an ingredient used for Hoyer's solution, a bryophytes, ferns, seeds, and small arthropods (especially mites). One recipe for making Hoyer's is dissolving gum arabic (30.0 g) in water (50.0 mL), then adding chloral hydrate (200.0 g), and then finally adding glycerol (16.0 mL). An advantage of this medium include a high refraction index and clearing (macerating) properties of the small specimens (especially advantageous if specimens require observation with differential interference contrast microscopy). The major disadvantage of Hoyer's is its susceptibility to the effects of rehydration, which causes the mountant to crystallize and threatening the slide to become unusable. It is therefore absolutely necessary, after drying a mounted specimen, to thoroughly ring (2 layers are best) cover slips with a protective coating (e.g., insulating glyptol), which prevents rehydration and mountant deterioration. Chloral hydrate reportedly does not effectively clear larger specimens, or arthropods that are more heavily sclerotized (e.g., larger insects). These should first be cleared with another product (e.g., 10% KOH or NaOH), and then mounted in Hoyer's. Other disadvantages of Hoyer's (principally due to chloral hydrate) include toxicity (see above), and procurement problems due to chloral hydrate being a controlled substance.

Hoyer's mounting medium

Chloral hydrate is a prescription-only-medicine (POM) in the Netherlands, but possession without a valid prescription will result only in seizure of the drug, not prosecution. Production, sale and distribution are however punishable by law. It is not listed under the Dutch Opium Law, but when the intent is human consumption, it is covered by the Geneesmiddelenwet (Medicine Act).

The United Kingdom does not consider chloral hydrate to be a controlled substance.

It is not controlled in Canada except that a prescription is required to purchase the pharmaceutical forms. Possession without a prescription is not illegal and industrial trade is not regulated.

Chloral hydrate is illegal without a prescription and is a schedule IV controlled substance in the United States. Its properties have sometimes led to its use as a date rape drug.[21] Chloral hydrate is still available in the United States, albeit it is relatively uncommon and not often kept in the inventory of major pharmacies. It has largely been abandoned for the treatment of insomnia in favor of newer drugs such as the "Z-drugs" family, which includes zolpidem (Ambien), zaleplon (Sonata), and eszopiclone (Lunesta). A small number of medical practitioners continue to prescribe it to treat insomnia when all other more modern medications have failed. In the United States, it is commonly supplied in syrup form in a 500 mg/5mL concentration. It is also supplied in suppository form, though use of this method of administration is extremely rare.

Legal status

The metabolite of chloral hydrate exerts its pharmacological properties via enhancing the GABA receptor complex[20] and therefore is similar in action to benzodiazepines, nonbenzodiazepines and barbiturates. It can be moderately addictive, as chronic use is known to cause dependency and withdrawal symptoms. The chemical can potentiate various anticoagulants and is weakly mutagenic in vitro and in vivo.

Chloral hydrate is metabolized in vivo[18] to trichloroethanol, which is responsible for its physiological and psychological effects.[19]

Pharmacodynamics

Acute overdosage is often characterized by nausea, vomiting, confusion, convulsions, slow and irregular breathing, cardiac arrhythmia, and coma. The plasma, serum or blood concentrations of chloral hydrate and/or trichloroethanol, its major active metabolite, may be measured to confirm a diagnosis of poisoning in hospitalized patients or to aid in the medicolegal investigation of fatalities. Accidental overdosage of young children undergoing simple dental or surgical procedures has occurred. Hemodialysis has been used successfully to accelerate clearance of the drug in poisoning victims.[17]

Chloral hydrate was routinely administered to patients on the gram scale. Prolonged exposure to the vapors is unhealthy however, with a LC50 for 4-h exposure of 440 mg/m3. Long-term use of chloral hydrate is associated with a rapid development of tolerance to its effects and possible addiction as well as adverse effects including rashes, gastric discomfort and severe kidney, heart, and liver failure.[16]

Safety

In therapeutic doses for insomnia, chloral hydrate is effective within 20 to 60 minutes.[14] In humans it is metabolized within 7 hours into trichloroethanol and trichloroethanol glucuronide by erythrocytes and plasma esterases and into trichloroacetic acid in 4 to 5 days.[15] It has a very narrow therapeutic window making this drug difficult to use. Higher doses can depress respiration and blood pressure.

Chloral hydrate is used for the short-term treatment of insomnia and as a sedative before minor medical or dental treatment. It was largely displaced in the mid-20th century by barbiturates[12] and subsequently by benzodiazepines. It was also formerly used in veterinary medicine as a general anesthetic. It is also still used as a sedative prior to EEG procedures, as it is one of the few available sedatives that does not suppress epileptiform discharges.[13]

Hypnotic

Notably, it is used to synthesize isatin. In this synthesis, chloral hydrate reacts with aniline and hydroxylamine to give a condensation product which cyclicizes in sulfuric acid to give the target compound:[11]

Chloral hydrate is a starting point for the synthesis of other organic compounds. It is the starting material for the production of chloral, which is produced by the distillation of a mixture of chloral hydrate and sulfuric acid, which serves as the desiccant.

Building block in organic synthesis

Uses

4 Cl2 + C2H5OH + H2O → Cl3CCH(OH)2 + 5 HCl

Chloral hydrate is produced from chlorine and ethanol in acidic solution. In basic conditions the haloform reaction takes place and chloral hydrate is decomposed by hydrolysis to form chloroform.[10]

Production

Contents

  • Production 1
  • Uses 2
    • Building block in organic synthesis 2.1
    • Hypnotic 2.2
  • Safety 3
  • Pharmacodynamics 4
  • Legal status 5
  • Hoyer's mounting medium 6
  • Notable uses 7
  • See also 8
  • References 9
  • External links 10

Chloral hydrate has not been approved by the FDA in the United States or the EMA in the European Union for any medical indication and is on the list of unapproved drugs that are still prescribed by clinicians.[9] Usage of the drug as a sedative or hypnotic may carry some risk given the lack of clinical trials.

It is, together with humic acids are present. It has been detected in drinking water at concentrations of up to 100 micrograms per litre (µg/L) but concentrations are normally found to be below 10 µg/L. Levels are generally found to be higher in surface water than in ground water.[8]

in microscopy procedures. [7][6]