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W268518

Sigma-Aldrich

α-Methylbenzyl alcohol

≥99%, FCC, FG

Synonym(s):

(±)-1-Phenylethanol, (±)-α-Methylbenzyl alcohol, Methyl phenyl carbinol, Styrallyl alcohol, Styrene alcohol

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About This Item

Linear Formula:
C6H5CH(OH)CH3
CAS Number:
98-85-1
Molecular Weight:
122.16
FEMA Number:
2685
Beilstein/REAXYS Number:
1905149
EC Number:
202-707-1
Council of Europe no.:
2030
MDL number:
MFCD00004508
UNSPSC Code:
12164502
PubChem Substance ID:
24901252
Flavis number:
2.064
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Halal
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 172.515

vapor density

4.21 (vs air)

vapor pressure

0.1 mmHg ( 20 °C)

assay

≥99%

refractive index

n20/D 1.527 (lit.)

bp

204 °C/745 mmHg (lit.)

mp

19-20 °C (lit.)

density

1.012 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

medicinal; chemical; sweet

SMILES string

CC(O)c1ccccc1

InChI

1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3

InChI key

WAPNOHKVXSQRPX-UHFFFAOYSA-N

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Application


  • Update to RIFM fragrance ingredient safety assessment,a-methylbenzyl alcohol, CAS registry number 98-85-1.: This study updates the safety assessment of a-methylbenzyl alcohol, focusing on its use as a fragrance ingredient. The research addresses toxicological data and regulatory compliance, ensuring the compound′s safe application in consumer products (Api et al., 2024).

  • Characterization of the Key Aroma Compounds of Three Kinds of Chinese Representative Black Tea and Elucidation of the Perceptual Interactions of Methyl Salicylate and Floral Odorants.: This study identifies the key aroma compounds in Chinese black tea, including a-methylbenzyl alcohol. The research provides insights into the sensory properties and potential applications in flavor and fragrance industries (Niu et al., 2022).

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

187.9 °F - Pensky-Martens closed cup

flash_point_c

86.6 °C - Pensky-Martens closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Henry Gruen et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(11), 1344-1352 (2008-10-30)
The photoreactions of 1-nitro-9,10-anthraquinone (N1) and 2-methyl-1-nitro-9,10-anthraquinone (N2) were studied in benzene and acetonitrile in the presence of 1-phenylethanol. For N2, a short-lived 10 ns transient observed upon flash photolysis is attributed to a triplet state, which can be intercepted
Binbin Zhang et al.
ChemSusChem, 5(12), 2469-2473 (2012-10-24)
Exploration of new and effective routes to conduct organic reactions in water using the special properties of water/organics is of great importance. In this work, we performed the disproportionation of various aromatic alcohols in water and in different organic solvents.
Pedro Lozano et al.
Biotechnology letters, 28(19), 1559-1565 (2006-08-11)
Continuous dynamic kinetic resolution processes in different ionic liquid/supercritical carbon dioxide biphasic systems were carried out by simultaneously using both immobilized Candida antarctica lipase B (Novozym 435) and silica modified with benzenosulfonic acid (SCX) catalysts at 40 degrees C and
Directed evolution of galactose oxidase: generation of enantioselective secondary alcohol oxidases.
Franck Escalettes et al.
Chembiochem : a European journal of chemical biology, 9(6), 857-860 (2008-03-12)
Galia Maayan et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(33), 13679-13684 (2009-08-12)
Many naturally occurring biopolymers (i.e., proteins, RNA, DNA) owe their unique properties to their well-defined three-dimensional structures. These attributes have inspired the design and synthesis of folded architectures with functions ranging from molecular recognition to asymmetric catalysis. Among these are
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