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161950

Sigma-Aldrich

1,3-Diethyl-2-thiobarbituric acid

99%

Synonyme(s) :

1,3-Diethyl-2-sulfanylidene-1,3-diazinane-4,6-dione, 1,3-Diethyldihydro-2-thioxo-4,6(1H,5H)-pyrimidinedione, 1,3-Diethylthiobarbituric acid, N,N′-Diethyl-2-thiobarbituric acid

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About This Item

Formule empirique (notation de Hill):
C8H12N2O2S
Numéro CAS:
5217-47-0
Poids moléculaire :
200.26
Numéro CE :
226-010-7
Numéro MDL:
MFCD00006676
Code UNSPSC :
12352100
ID de substance PubChem :
24849962
Nomenclature NACRES :
NA.22

Niveau de qualité

100

Pureté

99%

Contrôle du médicament

regulated under CDSA - not available from Sigma-Aldrich Canada

Pf

109-112 °C (lit.)

Solubilité

1 M NaOH: soluble 50 mg/mL, clear, colorless to light yellow

Chaîne SMILES 

CCN1C(=O)CC(=O)N(CC)C1=S

InChI

1S/C8H12N2O2S/c1-3-9-6(11)5-7(12)10(4-2)8(9)13/h3-5H2,1-2H3

Clé InChI

SHBTUGJAKBRBBJ-UHFFFAOYSA-N

Application

1,3-Diethyl-2-thiobarbituric acid (DETBA) was used as coinitiator during the photopolymerization of dental materials. It was used as reagent in electrochemical oxidation of 3,4-dihydroxybenzoic acid to yield benzofuro[2,3-d]pyrimidine derivatives. It was used in DETBA assay for determination of nicotine metabolites in human urine by HPLC.

Pictogrammes

Skull and crossbones
GHS06

Mention d'avertissement

Danger

Mentions de danger

H301,H317

Classification des risques

Acute Tox. 3 Oral - Skin Sens. 1

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
MKCH2520
MKCJ4376
MKCH2519
MKBV9273V
MKCB7193

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Jadwiga Turło et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(4), 1085-1091 (2010-02-09)
Preparations derived from Lentinula edodes (Berk.) Pegl. mycelium are worldwide used as dietary supplements containing compounds active as immune system enhancers, demonstrating chemopreventive and anticancer activity. L. edodes mycelium enriched with organic forms of selenium like selenized yeast possess putative
K Nakashima et al.
Biomedical chromatography : BMC, 6(2), 55-58 (1992-03-01)
The peroxyoxalate chemiluminescence(CL) detection method for the evaluation of the CL intensity of malondialdehyde(MDA) condensates with seven 2-thiobarbituric acid derivatives is described. The method consists of a flow injection technique together with a CL detection system using bis(2,4,6-trichlorophenyl) oxalate(TCPO) and
H Peach et al.
IARC scientific publications, (74)(74), 183-193 (1986-01-01)
Three novel colorimetric methods of detecting urinary nicotine metabolites called the barbituric acid, diethylthiobarbituric acid (DETB) and DETB-extraction methods were evaluated for use as a simple cheap objective test of smoking. Urine samples were collected from 103 male smokers and
T Sakai et al.
Journal of chromatography. B, Biomedical sciences and applications, 726(1-2), 313-316 (1999-05-29)
The reaction conditions of 1,3-diethyl-2-thiobarbituric acid (DETBA)-malonaldehyde (MA) adduct formation were examined in order to analyze MA in fish tissue by high-performance liquid chromatography. A reaction mixture containing 4 mM butyl hydroxytoluene was heated at 100 degrees C for 150
R F Smith et al.
Clinical chemistry, 44(2), 275-280 (1998-02-25)
The performance of a simple colorimetric assay for urinary nicotine metabolites to assess smoking status in diabetic subjects (n = 251) was investigated. Several variations of the colorimetric assay and a qualitative extraction procedure were evaluated in comparison with a
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