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Crotylbarbital

In this article we are going to address the topic of Crotylbarbital from different perspectives, with the aim of offering a complete and enriching vision of it. Throughout the text we will explore the multiple facets that Crotylbarbital presents, analyzing its impact in different areas and its relevance today. With a critical and reflective approach, we will delve into the different aspects surrounding Crotylbarbital, providing the reader with a deep and detailed understanding of the topic. Through research, analysis and testimonials, we will seek to shed light on Crotylbarbital and offer an informed perspective that encourages debate and reflection.
Crotylbarbital
Clinical data
ATC code
  • none
Identifiers
  • 5-but-2-enyl-5-ethyl-1,3-diazinane-2,4,6-trione
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.016.162 Edit this at Wikidata
Chemical and physical data
FormulaC10H14N2O3
Molar mass210.233 g·mol−1
3D model (JSmol)
  • O=C1NC(=O)NC(=O)C1(CC)C/C=C/C
  • InChI=1S/C10H14N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3,5H,4,6H2,1-2H3,(H2,11,12,13,14,15)/b5-3+ checkY
  • Key:KNMOHCLEINXVBG-HWKANZROSA-N checkY
  (verify)

Crotylbarbital (Mepertan, Kalipnon, Barotal), also known as crotarbital, is a barbiturate derivative developed by Eli Lilly in the 1930s. It has sedative and hypnotic effects, and was used for the treatment of insomnia until it was replaced by newer alternative drugs with fewer side effects and lower risk of overdose.

See also

References

  1. ^ US 2250422, Shonle HA, Doran WJ, "Alkyl-crotyl barbituric acids and their salts", issued 22 July 1941, assigned to Eli Lilly 
  2. ^ Walther T, Meyer FP, Puchta K, Walther H (June 1983). "Effect of an acute dose of crotylbarbital on reaction time and attention testing in healthy human subjects". International Journal of Clinical Pharmacology, Therapy, and Toxicology. 21 (6): 306–10. PMID 6136469.


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