| Identification | More | [Name]
ALPHA-METHYLBENZYL ALCOHOL | [CAS]
13323-81-4 | [Synonyms]
(+/-)-1-PHENYLETHANOL
1-PHENYLETHANOL
1-PHENYLETHYL ALCOHOL
ALPHA-METHYLBENZYL ALCOHOL
A-METHYLBENZYL ALCOHOL
AURORA KA-7014
DL-1-Phenethylalcohol
DL-1-PHENYLETHANOL
DL-1-PHENYLETHYL ALCOHOL
DL-2-METHYL PHENYL METHANOL
DL-ALPHA-METHYLBENZYL ALCOHOL
DL-ALPHA-METHYLPHENYLCARBINOL
DL-A-METHYLBENZYL ALCOHOL
DL-METHYLPHENYLCARBINOL
DL-PHENYLMETHYLCARBINOL
DL-SEC-PHENETHYL ALCOHOL
dl-sec-phenylethanol
DL-STYRALYL ALCOHOL
FEMA 2685
MBA | [EINECS(EC#)]
202-707-1 | [Molecular Formula]
C8H10O | [MDL Number]
MFCD00004508 | [Molecular Weight]
122.16 | [MOL File]
13323-81-4.mol |
| Chemical Properties | Back Directory | [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)
| [refractive index ]
n20/D 1.527(lit.)
| [Fp ]
185 °F
| [Dielectric constant]
7.6（90℃） | [CAS DataBase Reference]
13323-81-4(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R38:Irritating to the skin.
R41:Risk of serious damage to eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S39:Wear eye/face protection . | [RIDADR ]
UN 2937 6.1/PG 3
| [WGK Germany ]
1
| [RTECS ]
DO9275000
| [HazardClass ]
6.1 | [PackingGroup ]
III | [Toxicity]
The acute oral LD50 in rats was reported as 400 mg/kg (Smyth & Carpenter, 1944). The acute dermal LD50 value in rabbits exceeded 2.5 g/kg (Moreno, 1973). |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless liquid | [Occurrence]
Has apparently not been reported to occur in nature. | [Definition]
ChEBI: 1-phenylethanol is an aromatic alcohol that is ethanol substituted by a phenyl group at position 1. It has a role as a mouse metabolite. | [Preparation]
By hydrogenation or reduction of acetophenone; or from methyl magnesium chloride plus benzaldehyde by a Grignard-type reaction (Bedoukian, 1967). | [Metabolism]
Styrallyl alcohol is converted in rabbits into hippuric acid and methylphenylcarbinyl glucuronide, both optical forms of the carbinol behaving similarly. A small proportion (1-2%) is excreted as mandelic acid (Wjlliams, 1959). | [Purification Methods]
Purify the alcohol via its hydrogen phthalate. [See Houssa & Kenyon J Chem Soc 2260 1930.] Shake it with a solution of ferrous sulfate, and th |
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Energy Chemical
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http://www.energy-chemical.com |
| Company Name: |
HBCChem, Inc.
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