1-Phenylethanol

HCID 7409CAS 13323-81-4

Basic information

Standard SMILES
CC(O)c1ccccc1
InChIKey
WAPNOHKVXSQRPX-UHFFFAOYSA-N
Molecular formula
C8H10O
Average molar mass
122.16 g/mol
Monoisotopic mass
122.07316494

Overview

Alpha-methylbenzyl alcohol appears as 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.

Names & identifiers

Preferred name
1-Phenylethanol
IUPAC
1-phenylethanol
English name
alpha-Methylbenzyl alcohol
Molecular formula
C8H10O
Molecular weight
122.16

Names & synonyms

1-Phenylethanol98-85-1ALPHA-METHYLBENZYL ALCOHOLStyrallyl alcoholMethylphenyl carbinolStyralyl alcoholMethylphenylcarbinol1-Phenethyl alcohol(1-Hydroxyethyl)benzene1-Phenylethyl alcoholPhenylmethylcarbinolalpha-Methylbenzenemethanol
Show more names
FEMA 2685α-METHYLBENZYLALCOHOLAURORA KA-7014STYRENE ALCOHOLPHENYLETHANOL,1-DL-1-PHENYLETHANOLDL-STYRALYL ALCOHOL
alpha-Phenylethanolalpha-Phenylethyl alcohol1-Phenyl-1-hydroxyethaneEthanol, 1-phenyl-NCI-C55685alpha-HydroxyethylbenzeneFEMA No. 2685FEMA Number 2685

Database identifiers

CAS
13323-81-4、98-85-1
PubChem CID
7409
DTXSID
DTXSID1020859
ChEMBL
CHEMBL508917
ChEBI
CHEBI:669
UNII
E6O895DQ52
EC Number
202-707-1、236-361-8
Nikkaji
J2.520.944C、J3.224G

Properties

Computed structural properties

XLogP
1.4
Topological polar surface area
20.2 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
1
Heavy atoms
9

Experimental & physicochemical properties

Chemical ClassesFlammable agents - 2nd degree
PolymersOther Classes -> Alcohols and Polyols, Other
pHNeutral
FragrancesFragrance Ingredient (alpha-Methylbenzyl alcohol) -> IFRA transparency List
Odor · 3 items

MILD FLORAL ODOR

MILD HYACINTH-GARDENIA ODOR

Weak, bitter, almond-like odor

Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food

Physicochemical properties

Melting point
19 · 19-20 °C(lit.)
Boiling point
204 °C745 · 204 °C745 mm Hg(lit.)
Density
1.012 g/mL · 1.012 g/mL at 25 °C(lit.)
vapor density
4.21 · 4.21 (vs air)
vapor pressure
0.1 mm · 0.1 mm Hg ( 20 °C)
refractive index
20 · n20/D 1.527(lit.)

Safety & regulation

GHS classification

GHS Classification · 6 items

This chemical does not meet GHS hazard criteria for 1.9% (37 of 1934) of reports.

Warning

H302 (98.1%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 1934 reports by companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

Hazard information

Regulatory Information · 6 items

Chemical: Benzenemethanol, .alpha.-methyl-

Regulation (EC) No 1831/2003 (amended)

Benzenemethanol, .alpha.-methyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenemethanol, .alpha.-methyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 07-09-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/5405

1-Phenylethanol: Does not have an individual approval but may be used under an appropriate group standard

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelPoison
Fire Hazards · 5 items

Excerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:

· Combustible material: may burn but does not ignite readily.

· Combustible material: may burn but does not ignite readily.

· Combustible material: may burn but does not ignite readily.

· Combustible material: may burn but does not ignite readily.

Health Hazards · 5 items

Irritating to the skin, eyes, nose, throat, and upper respiratory tract. (USCG, 1999)

· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.

· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.

· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.

· TOXIC and/or CORROSIVE; inhalation, ingestion or skin contact with material may cause severe injury or death.

Hazards Summary · 1 item

A skin, eye, nose, throat, and upper respiratory tract irritant; [CAMEO] Increased liver weights and centrilobular necrosis observed in high-dose animal studies; Kidney injury and increased benign tumors of kidneys observed in male rats (not relevant to humans); Safe when used as a flavoring agent; [JECFA] Ataxia, labored breathing, and lethargy for up to 30 minutes after receiving high dose in rodent studies; [NTP] A moderate skin irritant; A severe eye irritant; Based on animal studies; [CHEMINFO] An irritant; May cause serious eye injury; Targets kidneys; [MSDSonline]

DOT ID and Guide · 4 items

3438 153

3438 153

2937 153

2937 153

Safety & protection

Fire FightingExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Accidental Release Measures · 6 items

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 5 items

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

General First Aid:

General First Aid:

General First Aid:

General First Aid:

Exposure Control and Personal Protection · 4 items

· Wear positive pressure self-contained breathing apparatus (SCBA).

· Wear positive pressure self-contained breathing apparatus (SCBA).

· Wear positive pressure self-contained breathing apparatus (SCBA).

· Wear positive pressure self-contained breathing apparatus (SCBA).

Fire Fighting Procedures"ALCOHOL" FOAM
Nonfire Spill ResponseExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:

Toxicology

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a recommended classification scheme(1), measured Koc values of <5-52, with higher values corresponding to soils with a greater organic content(2), indicate that alpha-methylbenzyl alcohol will have very high mobility in soil(SRC). Biodegradation is expected to be a major fate process for this compound(SRC). Alpha-methylbenzyl alcohol was completely biodegraded within 2-3 weeks under aerobic conditions using an activated sludge inoculum(3). Under anaerobic conditions, this compound had a half-life of 7 days(3). Acetophenone was reported as a major metabolite for both oxygen conditions(3). Volatilization of alpha-methylbenzyl alcohol from either moist surfaces will not be a major fate process(SRC) based on estimated values for Henry's Law constant (2.9X10-7 atm-cu m/mole)(4,SRC). Volatilization from dry soil surfaces should not be significant based on an estimated vapor pressure (0.058 mm Hg)(5,SRC).

AQUATIC FATE: Based on a recommended classification scheme(1), experimental Koc values of <5 to 52(2) indicate that alpha-methylbenzyl alcohol will not adsorb to suspended solids and sediment(SRC) in the water column. Biodegradation is expected to be a major fate process for this compound(SRC). Alpha-methylbenzyl alcohol was completely biodegraded within 2-3 weeks under aerobic conditions using an activated sludge inoculum(3). Under anaerobic conditions, this compound had a half-life of 7 days(3). Acetophenone was reported as the major metabolite for both oxygen conditions(3). Retention pond and aerated lagoon systems reported 12 and 17% biodegradation after 260 hours(3) indicating that under some conditions, biodegradation may not occur rapidly(SRC). Alpha-methylbenzyl alcohol should not volatilize from water surfaces based on an estimated Henry's Law constant of 2.9X10-7 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). An estimated BCF value of 9(3,SRC), from a measured water solubility(2), suggests that alpha-methylbenzyl alcohol will not bioconcentrate in aquatic organisms(SRC), according to a recommended classification scheme(5).

ATMOSPHERIC FATE: According to a suggested classification scheme(1), an estimated vapor pressure of 0.058 mm Hg at 25 °C(2,SRC) indicates that alpha-methylbenzyl alcohol will mainly exist in the vapor phase in the ambient atmosphere. Vapor-phase alpha-methylbenzyl alcohol is degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be about 1.1 days(3,SRC).

Food Survey ValuesAlpha-methylbenzyl alcohol was identified in Beaufort cheese in France at unreported concentrations(1).
Adverse EffectsNeurotoxin - Acute solvent syndrome
Ongoing Test Status · 1 item

The following link will take the user to the National Toxicology Program (NTP) Test Agent Search Results page, which tabulates all of the "Standard Toxicology & Carcinogenesis Studies", "Developmental Studies", and "Genetic Toxicity Studies" performed with this chemical. Clicking on the "Testing Status" link will take the user to the status (i.e., in review, in progress, in preparation, on test, completed, etc.) and results of all the studies that the NTP has done on this chemical. [http://ntp-apps.niehs.nih.gov/ntp_tox/index.cfm?fuseaction=ntpsearch.searchresults&searchterm=98-85-1]

Effluent Concentrations · 1 item

Alpha-methylbenzyl alcohol was detected once in the wastewater from a mechanical products industry(1). Wastewater from a petrochemical company contained alpha-methylbenzyl alcohol at unreported concentrations(2). Alpha-methylbenzyl alcohol was detected in finished water from the Blue Plains Advanced Waste Treatment Plant in Washington, DC in September, 1974(3).

Soil Adsorption/Mobility · 1 item

Koc values for alpha-methylbenzyl alcohol were determined for three subsoils: Apison (organic content = 0.11%) had a Koc of 37, Fullerton (organic content = 0.06%) had a Koc of <5, and Dormont (organic content = 1.2%) had a Koc of 52(1). According to a recommended classification scheme(2), these Koc values suggest that alpha-methylbenzyl alcohol has very high mobility in soil, although increasing organic content will act to reduce mobility slightly(SRC).

Regulatory information

FDA Requirements · 1 item

alpha-Methylbenzyl alcohol is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: 1) the quantity added to food does not exceed the amount reasonably required to accomplish its intended physical, nutritive, or other technical effect in food, and 2) when intended for use in or on food it is of appropriate food grade and is prepared and handled as a food ingredient.

Safety data

wgk
1
rtecs
DO9275000
ridadr
UN 3438
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).
risk_code
22-38-41
Signal word
Danger

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 5 items

DEHYDROGENASE PRESENT IN RAT CYTOSOL & MICROSOMES CONVERTS 1-PHENYLETHANOL INTO ACETOPHENONES.

...METHYL PHENYLCARBINOL GIVEN TO RATS SHOWS SUBSTRATE STEREOSELECTIVITY IN ITS OWN METABOLISM; WHILE R-(+)-ISOMER IS EXCRETED LARGELY AS GLUCURONIDE, S-(-)-ISOMER UNDERGOES FURTHER OXIDATIVE METABOLISM.

YIELDS ACETOPHENONE IN RAT. 1-PHENYLETHYL-BETA-D-GLUCURONIDE IN RABBIT. /FROM TABLE/

Site directed mutants were constructed in cytochrome p450cam to re-engineer the stereochemistry and coupling of ethylbenzene hydroxylation. The reaction with the wild type enzyme produces one regioisomer 1-phenylethanol with 5% reduced nicotinamide adenine deoxyribonucleic acid product conversion of and a ration of 73:27 for the R and S enantiomers respectively. Ethylbenzene was modeled into the active site of wild type p450cam in a rigid mode and oriented to optimize either pro-R or pro-S hydrogen abstraction. Residues T101, T185 and V247 make extensive contacts with the substrate in the static complexes and were therefore chosen for site directed mutagenesis. Single mutants T101M, V247A and V247M are more stereospecific producing 89, 87 and 82% (R)-1-phenylethanol respectively. The coupling of the reaction is doubled for the single mutants T185L, T185F and V247M. In an effort to engineer incr stereospecificity and coupling into a single catalyst the T101M, T185F and V247M mutants were combined in a multiple mutant of p450cam. This protein hydroxylates ethylbenzene resulting in an R:S ratio of 87:13 for the 1-phenylethanols and 13% coupling of reducing equivalents to product. The catalytic stereospecificity and stoichiometry with T101-T185F-V247M does not represent a summation of changes observed for the single mutants. A portion of the individual effects on substrate recognition produced by the single substitutions is either eliminated or degenerate within the triple mutant.

Alpha-methyl benzyl alcohol has known human metabolites that include (2S,3S,4S,5R)-3,4,5-trihydroxy-6-(1-phenylethoxy)oxane-2-carboxylic acid.

Cellular LocationsCytoplasm

Uses & manufacturing

Uses · 4 items

Used in perfumery; as a flavoring agent; in dyes; as a laboratory reagent; in stoving enamels; in cellulose nitrate and acetyl cellulose lacquers; as an additive in paint-removal agents; [HSDB] Used as an un-isolated intermediate in styrene production; as an antimicrobial agent; [CHEMINFO]

Painting (Solvents) [Category: Paint]

PERFUMERY; FLAVORING; DYES; LABORATORY REAGENT

Methylbenzyl alcohol can be used like benzyl alcohol, and can be employed in stoving enamels. In cellulose nitrate and acetyl cellulose lacquers, methylbenzyl alcohol helps to improve flow and film formation and prevents blushing at relatively high atmospheric humidity levels. It has also proved to be a useful additive in paint-removal agents on account of its dissolution properties and long evaporation time.

U.S. Imports · 2 items

(1977) 1.05X10+8 GRAMS (PRINCPL CUSTMS DISTS)

(1979) 6.81X10+7 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 3 items

2023: 1,000,000 - <5,000,000 lb

(1974) 4.54X10+6 G (CONSUMPTION AS FRAGRANCE)

(1977) LESS THAN 2.7X10+11 G-UNISOLATED INT

Industry UsesIntermediate
Methods of Manufacturing · 2 items

REDUCTION OF ACETOPHENONE; REACTION OF METHYL MAGNESIUM CHLORIDE AND BENZALDEHYDE; OXIDATION OF ETHYLBENZENE

In the hydroperoxide process, an organic hydroperoxide is used to epoxidize propylene; an organic alcohol is a coproduct.

Formulations/PreparationsGRADE: FCC

Applications

OccurrenceHas apparently not been reported to occur in nature.

Preparation methods

PreparationBy hydrogenation or reduction of acetophenone; or from methyl magnesium chloride plus benzaldehyde by a Grignard-type reaction (Bedoukian, 1967).

Suppliers49 total

湖北万得化工有限公司15377098680 15377098680 · [email protected]
Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
怀化元研达生物技术有限责任公司18711085600 · [email protected]
广州隽沐生物科技股份有限公司020-36607679; 13502246435 · [email protected]
陕西缔都新材料有限公司029-63373950 17392216152 · [email protected]

Additional notes

DefinitionChEBI: 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.

Related reactions

147 records

Linked notes

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