alpha-Methylbenzolmethanol

Bezeichnung:alpha-Methylbenzolmethanol

CAS-Nr98-85-1

Englisch Name:DL-1-Phenethylalcohol

CBNumberCB4204600

SummenformelC8H10O

Molgewicht122.16

MOL-Datei98-85-1.mol

Synonyma

1-Phenylethanol

alpha-Methylbenzolmethanol

alpha-Methylbenzolmethanol physikalisch-chemischer Eigenschaften

Schmelzpunkt	19-20 °C(lit.)
Siedepunkt	204 °C745 mm Hg(lit.)
Dichte	1.012 g/mL at 25 °C(lit.)
Dampfdichte	4.21 (vs air)
Dampfdruck	0.1 mm Hg ( 20 °C)
FEMA	2685 \| ALPHA-METHYLBENZYL ALCOHOL
Brechungsindex	n20/D 1.527(lit.)
Flammpunkt	185 °F
Löslichkeit	Chloroform (Sparingly), Ethyl Acetate, Methanol (Sparingly)
Aggregatzustand	Liquid
pka	14.43±0.20(Predicted)
Farbe	Clear colorless
Geruch (Odor)	at 100.00 %. fresh sweet acetophenone gardenia hyacinth
Geruchsart	chemical
Wasserlöslichkeit	29 g/L (20 ºC)
JECFA Number	799
BRN	1905149
Dielectric constant	7.6（90℃）
Stabilität	Stable. Combustible. Incompatible with strong acids, strong oxidizing agents.
LogP	1.636 at 25℃
CAS Datenbank	98-85-1(CAS DataBase Reference)
NIST chemische Informationen	Benzenemethanol, «alpha»-methyl-(98-85-1)
EPA chemische Informationen	.alpha.-Methylbenzenemethanol (98-85-1)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-38-41-36/37/38
S-Sätze:	26-39-37/39
RIDADR	UN 2937 6.1/PG 3
WGK Germany	1
RTECS-Nr.	DO9275000
TSCA	Yes
HazardClass	6.1(b)
PackingGroup	III
HS Code	29400090
Giftige Stoffe Daten	98-85-1(Hazardous Substances Data)

Gefahreninformationscode (GHS)

DL-1-Phenethylalcohol Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R38:Reizt die Haut.
R41:Gefahr ernster Augenschäden.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S39:Schutzbrille/Gesichtsschutz tragen.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Beschreibung
α-Methylbenzyl alcohol has a mild hyacinth-gardenia odor.
Chemische Eigenschaften
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.
Chemische Eigenschaften
α-Methylbenzyl alcohol has a mild hyacinth–gardenia odor.
Chemische Eigenschaften
colourless liquid
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.
Verwenden
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.
Vorbereitung Methode
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.
synthetische
By oxidation of ethylbenzene or by reduction of acetophenone.
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
Allgemeine Beschreibung
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 Reaktionen
Insoluble in water.
Reaktivität anzeigen
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.
Brandgefahr
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
Sicherheitsprofil
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.
läuterung methode
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

DL-1-Phenethylalcohol Upstream-Materialien And Downstream Produkte

alpha-Methylbenzolmethanol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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