Barbital

SIGMA/B0375

Synonym: 5,5-Diethyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 5,5-Diethylbarbituric acid; Barbitone; Veronal

CAS Number: 57-44-3
Empirical Formula (Hill Notation): C₈H₁₂N₂O₃
Molecular Weight: 184.19
EC Number: 200-331-2
MDL Number: MFCD00036212
Linear Formula: C₈H₁₂N₂O₃
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-B0375-25G	25 g	$0.00 1/EA CALL FOR PRICE	Add To Favorites
45-B0375-100G	100 g	$0.00 1/EA CALL FOR PRICE	Add To Favorites
45-B0375-500G	500 g	$1700.00 1/EA	Add To Favorites

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This image depicts SKU: B0375-100G

Properties
Descriptions
Safety Info.
Basic Data

application(s)	forensics and toxicology pharmaceutical (small molecule) veterinary
drug control	USDEA Schedule IV; Home Office Schedule 3; psychotrope (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada; psicótropo (Spain); Decreto Lei 15/93: Tabela IV (Portugal); Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet
form	powder
InChI	1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)
InChI key	FTOAOBMCPZCFFF-UHFFFAOYSA-N
Quality Level	200
SMILES string	CCC1(CC)C(=O)NC(=O)NC1=O
technique(s)	gas chromatography (GC): suitable
	HPLC: suitable

Application:

<ul>
<li><strong>Synthesis and characterization of some pyrimidine, purine, amino acid and mixed ligand complexes: </strong> This study explores the use of Barbital in the synthesis of various ligand complexes, highlighting its application in the development of life science reagents and pharmaceutical intermediates. This could inform R and D strategies for pharmaceutical manufacturing using Barbital as a key intermediate (Masoud et al., 2008). External link

</li>
</ul>

Biochem/physiol Actions:

Sedative/hypnotic

Symbol	GHS07
Signal word	Warning
Hazard statements	H302
Precautionary statements	P301 + P312 + P330
Hazard Codes	Xn
Risk Statements	22
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

UNSPSC

51361926

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