DL-1-Phenethylalcohol Chemical 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)

refractive index 

n20/D 1.527(lit.)

FEMA 

2685 | ALPHA-METHYLBENZYL ALCOHOL

Flash point:

185 °F

solubility 

Chloroform (Sparingly), Ethyl Acetate, Methanol (Sparingly)

pka

14.43±0.20(Predicted)

form 

Liquid

color 

Clear colorless

Odor

at 100.00 %. fresh sweet acetophenone gardenia hyacinth

Odor Type

chemical

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.

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)

Safety Information

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 

Yes

HazardClass 

6.1(b)

PackingGroup 

III

HS Code 

29400090

Hazardous Substances Data

98-85-1(Hazardous Substances Data)

MSDS

• Language:English Provider:DL-1-Phenethylalcohol
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

DL-1-Phenethylalcohol Usage And Synthesis

Description

α-Methylbenzyl alcohol has a mild hyacinth-gardenia odor.

Chemical Properties

α-Methylbenzyl alcohol has a mild hyacinth–gardenia odor.

Chemical Properties

colourless liquid

Chemical Properties

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.

Occurrence

Two optically active isomers exist; the commercial product is the racemic form. Reported found in cranberry, grapes, chive, Scotch spearmint oil, cheeses, cognac, rum, white wine, cocoa, black tea, filbert, cloudberry, beans, mushroom and endive.

Uses

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.

Preparation

By oxidation of ethylbenzene or by reduction of acetophenone.

Production Methods

1-Phenylethanol is coproduced with propylene oxide by reaction of a-peroxyethylbenzene (formed by the oxidation of ethylbenzene) with propylene. It is used as a fragrance additive in cosmetics such as perfumes, creams, and soaps and is an intermediate in styrene production. 1-Phenylethanol is also added to foods as a flavoring agent. Industrial exposure may occur from dermal contact and ingestion.

Definition

ChEBI: An aromatic alcohol that is ethanol substituted by a phenyl group at position 1.

Taste threshold values

Taste characteristics at 50 ppm: chemical, medicinal, with a balsamic vanilla woody nuance.

Synthesis Reference(s)

Tetrahedron Letters, 36, p. 3861, 1995 DOI: 10.1016/0040-4039(95)00679-7

General Description

A colorless liquid. Insoluble in water and less dense than water. Contact may slightly irritate skin, eyes and mucous membranes. May be slightly toxic by ingestion, inhalation and skin absorption. Used to make other chemicals.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Attacks plastics. [Handling Chemicals Safely, 1980. p. 236]. Acetyl bromide reacts violently with alcohols or water [Merck 11th ed. 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid [Chem. Eng. News 45(43):73. 1967; J, Org. Chem. 28:1893. 1963]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites [NFPA 491 M. 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence [Wischmeyer 1969].

Health Hazard

Irritating to the skin, eyes, nose, throat, and upper respiratory tract.

Fire Hazard

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Flammability and Explosibility

Not classified

Safety Profile

Poison by ingestion and subcutaneous routes. Moderately toxic by skin contact. A skin and severe eye irritant. Questionable carcinogen. Combustible when exposed to heat or flame; can react with oxidming materials. To fight fire, use alcohol foam, foam, CO2, dry chemical

Carcinogenicity

In an NTP study, both sexes of F344 rats were dosed by gavage with 0, 375, and 750 mg/kg 1-phenylethanol 5 days/week for 2 years. There was an increased incidence of neoplastic kidney tumors in the high-dose male rats but no evidence of carcinogenicity in the female rats . In the same NTP study, both sexes of B6C3F1 mice were dosed by oral gavage with 0, 375, and 750 mg/kg 1-phenylethanol 5 days/week for 2 years. There was no evidence that 1-phenylethanol was carcinogenic to mice in this study.

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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