Physicochemical Properties
| Molecular Formula | C11H16O |
| Molecular Weight | 164.24 |
| Exact Mass | 164.12 |
| CAS # | 583-03-9 |
| PubChem CID | 3338 |
| Appearance | Colorless to light yellow liquid |
| Density | 0,96 g/cm3 |
| Boiling Point | 137°C 2mm |
| Flash Point | 137°C/2mm |
| Index of Refraction | 1.5080 |
| LogP | 2.91 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Heavy Atom Count | 12 |
| Complexity | 106 |
| Defined Atom Stereocenter Count | 0 |
| SMILES | CCCCC(C1=CC=CC=C1)O |
| InChi Key | OVGORFFCBUIFIA-UHFFFAOYSA-N |
| InChi Code | InChI=1S/C11H16O/c1-2-3-9-11(12)10-7-5-4-6-8-10/h4-8,11-12H,2-3,9H2,1H3 |
| Chemical Name | 1-phenylpentan-1-ol |
| HS Tariff Code | 2934.99.9001 |
| Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Note: Please store this product in a sealed and protected environment (e.g. under nitrogen), avoid exposure to moisture and light. |
| Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
| ln Vivo | The secretory volume of pancreatic juice and protein output in rats are increased by fenipentol (PHP) administered orally or intraduodenally at doses ranging from 50-200 mg/kg[2]. In rats, fenipentol (50–200 mg/kg for intraperitoneal and 5–10 mg/kg for intravenous) significantly enhances biliary secretion[2]. In dogs, fenipentol (25–200 mg/kg administered intraduodenally) promotes pancreatic secretion[2]. |
| References |
[1]. Therapeutic properties of dihydroxy-dibutylether on sub-acute liver damage induced by several hepatotoxic agents in rats. Int J Tissue React. 1982; 4(4): 309-18. [2]. [Effect of 1-phenyl-1-hydroxy-n-pentane on pancreatic secretion in the rat and the dog]. Nihon Yakurigaku Zasshi. 1971 Nov; 67(6): 637-47. [3]. Biocatalytic and electrochemical reduction of selected phenyl alkanones with antibacterial activity of the corresponding phenyl alkanols. Ijabpt Com, 2011. |
| Additional Infomation |
Fenipentol is a member of benzenes. Fenipentol has been reported in Ligusticum striatum, Vincetoxicum glaucescens, and Ligusticum chuanxiong with data available. |
Solubility Data
| Solubility (In Vitro) | DMSO: 100 mg/mL (608.87 mM) |
| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (15.22 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (15.22 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. Solubility in Formulation 3: ≥ 2.5 mg/mL (15.22 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.  (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 6.0887 mL | 30.4433 mL | 60.8865 mL | |
| 5 mM | 1.2177 mL | 6.0887 mL | 12.1773 mL | |
| 10 mM | 0.6089 mL | 3.0443 mL | 6.0887 mL |