AMOBARBITAL SODIUM

Amobarbital Sodium is a research-grade compound used in advanced pharmaceutical and biochemical studies. Chemical & Pharmacological Characteristics Salt formation enhances formulation flexibility compared with the free compound, particularly for aqueous preparations. Pharmacodynamic behavior is consistent with amobarbital, with dose-dependent CNS depression and a barbiturate class safety profile. Regulatory constraints may apply depending on jurisdiction. It is primarily applied to investigate compound-specific mechanisms, physicochemical behavior, and analytical or formulation-relevant characteristics under controlled laboratory conditions.

SKU: b758e5f029b9 Category:

Product Description


Chemical & Pharmacological Characteristics

Salt formation enhances formulation flexibility compared with the free compound, particularly for aqueous preparations. Pharmacodynamic behavior is consistent with amobarbital, with dose-dependent CNS depression and a barbiturate class safety profile. Regulatory constraints may apply depending on jurisdiction.

Mechanism of Action

Amobarbital sodium potentiates GABAA receptor-mediated inhibition by increasing chloride influx and promoting neuronal hyperpolarization. This reduces excitability at the circuit level and can produce sedative-hypnotic or anesthetic-like states depending on exposure.

At elevated exposures, suppression of respiratory drive and cardiovascular reflexes may occur. In vivo protocols should include continuous monitoring, while in vitro studies should account for broad network suppression that can mask more subtle mechanistic signals.

Advanced Research Applications

  • Rapid-onset sedation/anesthesia modeling with controlled aqueous dosing
  • CNS safety pharmacology and comparative GABAergic liability profiling
  • Receptor and network electrophysiology studies requiring soluble barbiturate dosing
  • Benchmark compound for formulation and delivery research in CNS models
  • Translational studies linking exposure to sedation and respiratory endpoints

Toxicodynamics & Cellular Hazard Spectrum

  • High risk of respiratory depression and profound CNS suppression at high dose
  • Dependence/tolerance phenomena with repeated exposure in biological systems
  • Behavioral endpoint confounding due to generalized suppression
  • Controlled substance regulatory requirements for storage and documentation
  • Use strict dosing controls and ethical monitoring in animal models

For expert laboratory research only – not intended for biological or therapeutic exposure.

Datasheet


Molecular Formula

C11H17N2NaO3

Molecular Weight

248.25 g/mol

CAS Number

64-43-7

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Amobarbital sodium (JAN/USP); RefChem:1076932; AMOBARBITAL SODIUM; Amytal sodium; 64-43-7

IUPAC/Chemical Name

sodium 5-ethyl-5-(3-methylbutyl)-4,6-dioxo-1H-pyrimidin-2-olate

InChl Key

BNHGKKNINBGEQL-UHFFFAOYSA-M

InChl Code

InChI=1S/C11H18N2O3.Na/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15;/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16);/q;+1/p-1

References

https://pubchem.ncbi.nlm.nih.gov/compound/23689390; small-molecule

3D Conformer.

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