DEBRISOQUIN SULFATE
DEBRISOQUIN SULFATE Basic information
- Product Name:
- DEBRISOQUIN SULFATE
- Synonyms:
-
- 3,4-dihydro-2(1h)-isoquinolinecarboximidamidsulfate(2:1)
- 3,4-dihydro-2(1h)-isoquinolinecarboxamidinsulfate(2:1)
- 3,4-Dihydro-2(1H)-isoquinolinecarboximidamide, Debrisoquin sulfate, Ro5-33071
- Tendor
- 3,4-Dihydro-2(1H)-isoquinolinecarboxamide hemisulfate
- 3,4-DIHYDRO-2(1H)-ISOQUINOLINECARBOXAMIDINE 0.5 H2SO4
- 3,4-DIHYDRO-2-[1H]-ISOQUINOLINECARBOXAMIDINE SULFATE SALT
- DEBRISOQUINE SULFATE
- CAS:
- 581-88-4
- MF:
- C20H28N6O4S
- MW:
- 448.54
- EINECS:
- 209-472-4
- Product Categories:
-
- Bases & Related Reagents
- Intermediates & Fine Chemicals
- Nucleotides and Nucleosides
- Nucleotides
- Pharmaceuticals
- Mol File:
- 581-88-4.mol
DEBRISOQUIN SULFATE Chemical Properties
- Melting point:
- 278-280°, 284-285° or 266-268° (H2O)
- storage temp.
- room temp
- solubility
- H2O: 20 mg/mL with heat
- form
- Solid
- color
- Pale Yellow
MSDS
- Language:English Provider:SigmaAldrich
DEBRISOQUIN SULFATE Usage And Synthesis
Chemical Properties
Crystalline Solid
Originator
Declinax,Roche,UK,1967
Uses
Antihypertensive.
Manufacturing Process
27 g of 1,2,3,4-tetrahydroisoquinoline was added at room temperature to a
solution of 28 g of 2-methyl-2-isothiourea sulfate in 80 ml of water. The
resulting mixture was kept at room temperature with occasional shaking. After
a short period of time, methylmercaptan began to escape, and the mixture
warmed up slightly. After then standing for 24 hours, crystals formed. They
were filtered off and rinsed with ice cold water. Recrystallization from
approximately 100 ml of water yielded 1,2,3,4-tetrahydroisoquinoline-2-
carboxamidine sulfate melting at 278°C to 280°C (uncorr.).
Another batch prepared in the same manner melted at 284°C to 285°C due to
a minute difference in moisture content.
Both batches prepared above analyzed correctly for (C10H13N3)2·H2SO4.
brand name
Declinax (HoffmannLaRoche).
Therapeutic Function
Antihypertensive
Biochem/physiol Actions
Debrisoquine is an anti-hypertensive agent. It is metabolized by cytochrome P4502D6.
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