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Merck
CN

W268518

α-甲基苄醇

≥99%, FCC, FG

别名:

(±)-1-苯乙醇, (±)-α-甲基苄醇, 甲基苯基甲醇, 苏合香醇, 苯乙烯醇

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关于此项目

线性分子式:
C6H5CH(OH)CH3
化学文摘社编号:
分子量:
122.16
FEMA Number:
2685
Council of Europe no.:
2030
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
2.064
EC Number:
202-707-1
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
1905149
Organoleptic:
medicinal; chemical; sweet
Grade:
FG, Halal, Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
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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

biological source

synthetic

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%

Quality Level

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

Application


  • RIFM香精成分安全性评估更新,α-甲基苄醇,CAS登记号98-85-1。: 该研究更新了α-甲基苄醇的安全性评估,重点关注其作为香精成分的使用。该研究涉及毒理学数据和合规性,确保化合物在消费品中的安全应用(Api et al., 2024)。

  • 中国三种代表性红茶关键芳香化合物的表征以及水杨酸甲酯和花香剂的感知相互作用.: 该研究鉴定出了中国红茶中的关键芳香化合物,包括α-甲基苄醇。该研究提供了有关感官特性及其在香精香料行业的潜在应用的见解(Niu et al., 2022)。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

存储类别

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

wgk

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yoshio Kasashima et al.
Journal of oleo science, 59(11), 607-613 (2010-10-26)
The reactions of alcohols with nitriles under solvent-free conditions, using molecular iodine as a catalyst, were investigated. The reaction of 1-phenylethanol with propanenitrile produced the amide N-(1-phenylethyl)propanamide, by dehydration and tautomerization, in 71% yield, under the following conditions: temperature=90°C, alcohol:iodine
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)
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
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
Kei Shin-ya et al.
The journal of physical chemistry. A, 111(35), 8598-8605 (2007-08-10)
The absolute configuration and conformation of 1-phenylethanol (1-PhEtOH) have been determined by matrix-isolation infrared (IR) and vibrational circular dichroism (VCD) spectroscopy combined with quantum chemical calculations. Quantum chemical calculations have identified that there are three conformers, namely, I, II, and

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