DL-1-Phenylethyl Alcohol , 98% , 98-85-1
Synonym(s):
(±)-α-Methylbenzyl alcohol;(±)-1-Phenylethanol;Methyl phenyl carbinol;Styrallyl alcohol;Styrene alcohol
CAS NO.：98-85-1
Empirical Formula: C8H10O
Molecular Weight: 122.16
MDL number: MFCD00004508
EINECS: 202-707-1
PRODUCT Properties
| Melting point: | 19-20 °C(lit.) |
| Boiling point: | 204 °C745 mm Hg(lit.) |
| Density | 1.012 g/mL at 25 °C(lit.) |
| vapor density | 4.21 (vs air) |
| vapor pressure | 0.1 mm Hg ( 20 °C) |
| FEMA | 2685 | ALPHA-METHYLBENZYL ALCOHOL |
| refractive index | n |
| Flash point: | 185 °F |
| solubility | Chloroform (Sparingly), Ethyl Acetate, Methanol (Sparingly) |
| form | Liquid |
| pka | 14.43±0.20(Predicted) |
| color | Clear colorless |
| Odor | at 100.00 %. fresh sweet acetophenone gardenia hyacinth |
| Odor Type | chemical |
| biological source | synthetic |
| Water Solubility | 29 g/L (20 ºC) |
| JECFA Number | 799 |
| BRN | 1905149 |
| Dielectric constant | 7.6（90℃） |
| Stability: | Stable. Combustible. Incompatible with strong acids, strong oxidizing agents. |
| Major Application | flavors and fragrances |
| Cosmetics Ingredients Functions | PERFUMING |
| InChI | 1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3 |
| InChIKey | WAPNOHKVXSQRPX-UHFFFAOYSA-N |
| SMILES | CC(O)c1ccccc1 |
| LogP | 1.636 at 25℃ |
| CAS DataBase Reference | 98-85-1(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzenemethanol, «alpha»-methyl-(98-85-1) |
| EPA Substance Registry System | .alpha.-Methylbenzenemethanol (98-85-1) |
Description and Uses
DL-1-Phenethylalcohol has been identified as a volatile component of food (e.g., in tea aroma and mushrooms). The alcohol is a colorless liquid with a dry, rose-like odor, slightly reminiscent of hawthorn. It can be prepared by catalytic hydrogenation of acetophenone. 1- Phenylethyl alcohol is used in small quantities in perfumery and in larger amounts for the production of its esters, which are more important as fragrance materials.
The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynamic kinetic resolution of 1-phenylethanol by transesterification.
Safety
| Symbol(GHS) |  GHS07 |
| Signal word | Warning |
| Hazard statements | H302-H319 |
| Precautionary statements | P264-P270-P280-P301+P312-P305+P351+P338-P337+P313 |
| PPE | Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter |
| Hazard Codes | Xn |
| Risk Statements | 22-38-41-36/37/38 |
| Safety Statements | 26-39-37/39 |
| RIDADR | UN 2937 6.1/PG 3 |
| WGK Germany | 1 |
| RTECS | DO9275000 |
| TSCA | TSCA listed |
| HazardClass | 6.1(b) |
| PackingGroup | III |
| HS Code | 29400090 |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
| Hazard Classifications | Acute Tox. 4 Oral Eye Irrit. 2 |
| Hazardous Substances Data | 98-85-1(Hazardous Substances Data) |
| Limited Quantities | 5.0 L (1.3 gallons) (liquid) or 5.0 kg (11 lbs) (solid) |
| Excepted Quantities | Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L) |
