Thiobarbituric acid

Thiobarbituric acid structural formula

CAS Number504-17-6
Molecular FormulaC4H4N2O2S
Molecular Weight144.150
InChI KeyRVBUGGBMJDPOST-UHFFFAOYSA-N
LogP-0.614
Synonyms
  • Thiobarbituric acid
  • 2-Sulfanylidene-1,3-diazinane-4,6-dione
  • 4,6(1H,5H)-Pyrimidinedione, dihydro-2-thioxo-
  • 504-17-6
  • 2-Sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione
  • 4,6(1H,5H)-Pyrimidinedione, dihydro-2-thioxo-
  • Barbituric acid, 2-thio-
  • 4,6-Dihydroxy-2-mercaptopyrimidine
  • 4,6(1H,5H)-pirimidinadiona, dihidro-2-tioxo-
  • 1,2,3,4,5,6-Hexahydro-4,6-dioxopyrimidine-2-thione
  • 2-Mercapto-4,6-dihydroxypyrimidine
  • 2-Mercaptobarbituric acid
  • 2-Mercaptopyrimidine-4,6-diol
  • 2-Thio-4,6-dioxypyrimidine
  • 2-thiobarbituric acid
  • 2-Thiobarbitursaure
  • 2-Thiopyrimidine-4,6-diol
  • 4,6-Dihydroxy-2-mercaptopyrimidine
  • 4,6-Dihydroxy-2-thiopyrimidine
  • Acide 2-thiobarbiturique
  • acido 2-tiobarbiturico
  • Austranal
  • BARBITURIC ACID, 2-THIO-
  • Bathyran
  • Dihydro-2-thioxo-4,6(1H,5H)-pyrimidinedione
  • Hexahydropyrimidine-4,6-dione-2-thione
  • NSC 4733
  • THIOBARBITURIC ACID
  • EINECS 207-985-8
  • 4,6(1H,5H)-Pyrimidinedione, 2-mercapto-
  • USAF EK-660
  • UNII-M1YZW5SS7C
  • 2-thioxodihydropyrimidine-4,6(1H,5H)-dione
  • 1049677-34-0
  • 1076199-44-4
  • 1116339-76-4
  • 118738-55-9
  • 121477-82-5
  • 122508-78-5
  • 1228272-12-5
  • 1236029-05-2
  • 124558-04-9
  • 1256721-97-7
  • 1262632-60-9
  • 126660-87-5
  • 127726-79-8
  • 1287678-13-0
  • 1313510-54-1
  • 1356834-57-5
  • 136771-68-1
  • 1369625-13-7
  • 1393847-12-5
  • 145783-11-5
  • 148021-12-9
  • 157796-99-1
  • 5525-79-1
  • 5658-01-5
  • 709611-98-3
  • 773866-14-1
  • 863970-61-0
  • 878388-18-2
  • 886365-65-7
  • 91759-32-9
  • 924832-30-4
  • 956086-95-6
  • 1423769-56-5
  • 1583284-74-5
  • 1612185-40-6
  • 1622940-33-3
  • 1683524-47-1
  • 1696408-94-2
  • 1773529-72-8
  • 1802859-83-1
  • 1825368-06-6
  • 1850381-77-9

Applications:

Separation of Thiobarbituric acid on Newcrom R1 HPLC column

May 16, 2018
Separation of Thiobarbituric acid on Newcrom R1 HPLC column

Thiobarbituric acid can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
Thiobarbituric acid
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.