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16376-36-6, b-chloralose, CAS:16376-36-6

16376-36-6 , b-chloralose,
CAS:16376-36-6
C8H11Cl3O6 / 309.528
MFCD00064338

b-chloralose , b-氯醛糖

b-Chloralose is a general anesthetic that is used to induce and maintain anesthesia. It has been shown to decrease the heart rate, respiratory rate, and blood pressure in patients. It also causes a reduction of the glomerular filtration rate and delays the recovery of consciousness. Although b-chloralose has been shown to have negative effects on the cardiovascular system, it can be administered safely in combination with other anesthetics because it does not alter their effects. The use of b-chloralose is limited by its short duration of action and by adverse reactions such as nausea, vomiting, and convulsions.

Beta-chloralose is a synthetic derivative of chloralose, a naturally occurring neurotropic compound found in a variety of plants and algae. Beta-chloralose has been widely used as a sedative, an anesthetic, and a neurotoxin in scientific experiments and in veterinary medicine. It acts as a potent agonist of GABA(A) receptors, leading to the inhibition of neurotransmitter release and the induction of a state of sedation or unconsciousness.

Synthesis and Characterization:

Beta-chloralose can be synthesized by the reaction of chloral hydrate with sodium hydroxide in the presence of a catalyst such as potassium iodide. The product is then purified by recrystallization from water or other suitable solvents. The structure and purity of beta-chloralose can be determined by various analytical techniques, including infrared spectroscopy, nuclear magnetic resonance, and mass spectrometry.

Analytical Methods:

Beta-chloralose can be quantified in biological and environmental samples using various analytical methods, such as high-performance liquid chromatography, gas chromatography-mass spectrometry, and enzyme-linked immunosorbent assay. These methods are highly specific and sensitive and can detect beta-chloralose at concentrations as low as 0.1 ng/mL.

Biological Properties:

Beta-chloralose has potent sedative, anesthetic, and neurotoxic properties that make it a useful tool in scientific experiments. It acts primarily as a GABA(A) receptor agonist, leading to the inhibition of neurotransmitter release and the induction of a state of sedation or unconsciousness. It has also been shown to have anticonvulsant, antiepileptic, and analgesic effects.

Toxicity and Safety in Scientific Experiments:

Beta-chloralose is generally considered to be safe for use in scientific experiments at appropriate doses and under appropriate conditions. However, it can be toxic if ingested or inhaled, leading to respiratory depression, coma, and death. Exposure to beta-chloralose should be minimized and appropriate safety measures should be taken to reduce the risk of exposure to laboratory personnel and animals.

Applications in Scientific Experiments:

Beta-chloralose has a wide range of applications in scientific experiments, including as a sedative and anesthetic in animal studies, as a tool for studying the physiology and pharmacology of GABA(A) receptors, and as a method for inducing and studying sleep and anesthesia. It has also been used as a neurotoxin for inducing selective lesions in specific brain regions.

Current State of Research:

Research on beta-chloralose is ongoing and has focused on its pharmacology, toxicology, and applications in various fields of research and industry. There is a growing interest in the development of new drugs and therapies based on the properties of beta-chloralose, as well as the use of beta-chloralose as a tool for studying sleep and anesthesia.

Potential Implications in Various Fields of Research and Industry:

Beta-chloralose has potential implications in various fields of research and industry, including in the development of new drugs and therapies for sleep disorders, anxiety disorders, and epilepsy. It can also be used as a tool for studying the pharmacology and physiology of GABA(A) receptors, and for inducing selective neuronal lesions in animal models of neurological disorders. In the food and beverage industry, beta-chloralose can be used as a preservative and a flavor enhancer.

Limitations and Future Directions:

Despite its potential applications, beta-chloralose has some limitations that need to be addressed in future research. One limitation is the lack of information on the long-term effects of beta-chloralose exposure on human health and the environment. Another limitation is the need for more efficient and selective methods for inducing targeted neuronal lesions. Future research should focus on addressing these limitations and exploring new applications of beta-chloralose in various fields of research and industry.

Future Directions:

1. Development of new drugs and therapies based on the properties of beta-chloralose

2. Investigation of the long-term effects of beta-chloralose exposure on human health and the environment

3. Development of more efficient and selective methods for inducing targeted neuronal lesions

4. Exploration of new applications of beta-chloralose in the food and beverage industry

5. Investigation of the mechanisms of action of beta-chloralose on GABA(A) receptors

6. Examination of the effects of beta-chloralose on the immune system

7. Investigation of the potential use of beta-chloralose as a biomarker for neurological disorders

8. Development of more selective and specific ligands for GABA(A) receptors

9. Exploration of the effects of beta-chloralose on neuronal plasticity

10. Investigation of the effect of beta-chloralose on the gut microbiome

CAS Number16376-36-6
Product Namebeta-Chloralose
IUPAC Name(1R)-1-[(2S,3aR,5R,6S,6aR)-6-hydroxy-2-(trichloromethyl)-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol
Molecular FormulaC8H11Cl3O6
Molecular Weight309.528 g/mol
InChIInChI=1S/C8H11Cl3O6/c9-8(10,11)7-16-5-3(14)4(2(13)1-12)15-6(5)17-7/h2-7,12-14H,1H2/t2-,3+,4-,5-,6-,7+/m1/s1
InChI KeyOJYGBLRPYBAHRT-GVUNPQSCSA-N
SMILESC(C(C1C(C2C(O1)OC(O2)C(Cl)(Cl)Cl)O)O)O
Solubility4.44 mg/mL at 15 °C
Synonymsalpha Chloralose, alpha-Chloralose, Anhydroglucochloral, beta Chloralose, beta-Chloralose, Chloralose, Glucochloral, Glucochloralose
Canonical SMILESC(C(C1C(C2C(O1)OC(O2)C(Cl)(Cl)Cl)O)O)O
Isomeric SMILESC([C@H]([C@@H]1[C@@H]([C@@H]2[C@H](O1)O[C@H](O2)C(Cl)(Cl)Cl)O)O)O


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