Name | Valerophenone |
Synonyms | NSC 58959 Valerophenone Pentanophenone n-Valerophenone 1-Phenyl-1-pentanone 1-PHENYL-1-PENTANONE n-Butyl phenyl ketone Butyl Phenyl KetonePentanophenone |
CAS | 1009-14-9 |
EINECS | 213-767-3 |
InChI | InChI=1/C11H14O/c1-2-3-9-11(12)10-7-5-4-6-8-10/h4-8H,2-3,9H2,1H3 |
InChIKey | XKGLSKVNOSHTAD-UHFFFAOYSA-N |
Molecular Formula | C11H14O |
Molar Mass | 162.23 |
Density | 0.975 g/mL at 20 °C (lit.) |
Melting Point | -9 °C |
Boling Point | 244-245 °C (lit.) |
Flash Point | 217°F |
Water Solubility | Insoluble in water. |
Solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly) |
Appearance | Liquid |
Specific Gravity | 0.98 |
Color | Clear light yellow to yellow-green |
BRN | 1907717 |
Storage Condition | Sealed in dry,Room Temperature |
Stability | Stable. Flammable. Incompatible with strong oxidizing agents, acids, bases, plastics. |
Refractive Index | n20/D 1.5143(lit.) |
Physical and Chemical Properties | Density 0.98 melting point -9°C boiling point 105-107°C (5 mmHg) refractive index 1.5143-1.5163 flash point 102°C |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29143990 |
LogP | 2.79 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Application | 1-phenyl-1-pentanone can be used as intermediates in organic synthesis and pharmaceutical intermediates, can be used in laboratory research and development process and chemical and pharmaceutical synthesis process. |
Use | phenylpentanone is an organic chemical reagent that can be used in organic synthesis. |
preparation | phenylpentanone is an organic intermediate, which can be prepared from benzene and n-valeryl chloride by Friedel-Crafts reaction, alternatively, it can be prepared from methyl benzoate by Grignard reaction. |