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B0375

Sigma-Aldrich

Barbital

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C8H12N2O3
Numero CAS:
57-44-3
Peso molecolare:
184.19
Beilstein:
163999
Numero CE:
200-331-2
Numero MDL:
MFCD00036212
Codice UNSPSC:
51361926
ID PubChem:
24891513
NACRES:
NA.21

Stato

powder

Livello qualitativo

200

Controllo stupefacenti

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)

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Stringa SMILE

CCC1(CC)C(=O)NC(=O)NC1=O

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)
FTOAOBMCPZCFFF-UHFFFAOYSA-N

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Applicazioni

<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).</li>
</ul>

Azioni biochim/fisiol

Sedative/hypnotic

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Consigli di prudenza

P301 + P312 + P330

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
SLCL9110
SLCK8770
SLCK5958
SLCH4870
SLBZ7192

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Haixiang Zhao et al.
Analytica chimica acta, 586(1-2), 399-406 (2007-03-28)
A new method was developed for the rapid screening and confirmation analysis of barbital, amobarbital and phenobarbital residues in pork by gas chromatography-tandem mass spectrometry (GC/MS/MS) with ion trap MSD. The residual barbiturates in pork were extracted by ultrasonic extraction
Mamdouh S Masoud et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(1), 230-238 (2007-05-25)
Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II) complexes of barbital, thiouracil, adenine, amino acids (methionine, lysine and alanine) and some mixed ligands were prepared and characterized by elemental analyses, IR, electronic spectra, magnetic susceptibility and ESR spectra. Coordination of
Meiling Wang et al.
Journal of chromatography. A, 1217(17), 2821-2831 (2010-03-17)
This work describes a liquid chromatography-tandem mass spectrometry (LC-MS/MS) procedure for multiplex screening, ultratrace quantification and reliable confirmation of barbital series residues in animal-derived food matrices. The method is developed based on a distinct dependency of the electrospray ionization (ESI)
J M Bossert et al.
Behavioural pharmacology, 14(7), 517-523 (2003-10-15)
We have shown previously that 15 mg/kg pentobarbital induces a conditioned place preference (CPP), but it is unsuitable for intracranial administration. Since the long-acting barbiturate, sodium barbital, is soluble at a neutral pH, we tested whether it would induce a
Marlies Oostendorp et al.
Transfusion, 55(6 Pt 2), 1555-1562 (2015-05-20)
Monoclonal antibodies (MoAbs) are increasingly integrated in the standard of care. The notion that therapeutic MoAbs can interfere with clinical laboratory tests is an emerging concern that requires immediate recognition and the development of appropriate solutions. Here, we describe that
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