Product Name

  • Name

    Perindoprilat

  • EINECS
  • CAS No. 95153-31-4
  • Article Data3
  • CAS DataBase
  • Density 1.222 g/cm3
  • Solubility
  • Melting Point 153-155掳C
  • Formula C17H28 N2 O5
  • Boiling Point 568.1 °C at 760 mmHg
  • Molecular Weight 340.42
  • Flash Point 297.4 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 95153-31-4 (Perindoprilat)
  • Hazard Symbols
  • Synonyms 1H-Indole-2-carboxylicacid, 1-[2-[(1-carboxybutyl)amino]-1-oxopropyl]octahydro-, [2S-[1[R*(R*)],2a,3ab,7ab]]-; Perindoprilat; S 9780
  • PSA 106.94000
  • LogP 1.79090

Perindoprilat Chemical Properties

Molecular Structure:

Molecular Formula: C17H28N2O5
Molecular Weight: 340.4146
IUPAC Name: (2S,3aS,7aS)-1-[(2S)-2-[[(2S)-1-Hydroxy-1-oxopentan-2-yl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid
Synonyms of Perindoprilat (CAS NO.95153-31-4): 3(2S,3aS,7aS)-1-((S)-N-((S)-1-Carboxybutyl)alanyl)hexahydro-2-indolinecarboxylic acid ; BRN 4207072 ; Perindoprilate ; Perindoprilate [French] ; Perindoprilato ; Perindoprilato [Spanish] ; Perindoprilatum ; Perindoprilatum [Latin] ; S 9780 ; UNII-2UV6ZNQ92K ; 1H-Indole-2-carboxylic acid, octahydro-1-(2-((1-carboxybutyl)amino)-1-oxopropyl)-, (2S-(1(R*(R*)),2-alpha,3a-beta,7a-beta))-
CAS NO: 95153-31-4
Product Categories: Angiotensin-converting enzyme inhibitors ; Cardiovascular agents ; Drug / Therapeutic Agent ; Enzyme Inhibitors ; Protease Inhibitors
Melting point: 153-155°C 
Index of Refraction: 1.534
Molar Refractivity: 86.69 cm3
Molar Volume: 278.4 cm3
Surface Tension: 51.4 dyne/cm
Density: 1.222 g/cm3
Flash Point: 297.4 °C
Enthalpy of Vaporization: 93.19 kJ/mol
Boiling Point: 568.1 °C at 760 mmHg
Vapour Pressure of Perindoprilat (CAS NO.95153-31-4): 2.17E-14 mmHg at 25°C

Perindoprilat Uses

  Perindoprilat (CAS NO.95153-31-4) is used as an angiotensin-converting enzyme (ACE) inhibitor.

Perindoprilat Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous > 2gm/kg (2000mg/kg)   Cardiovascular Drug Reviews. Vol. 10, Pg. 446, 1992.
rat LD50 intravenous > 2gm/kg (2000mg/kg)   Cardiovascular Drug Reviews. Vol. 10, Pg. 446, 1992.

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