Merck
CN

W268518

Sigma-Aldrich

α-甲基苄醇

≥99%, FCC, FG

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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
线性分子式:
C6H5CH(OH)CH3
CAS号:
分子量:
122.16
FEMA编号:
2685
Beilstein:
1905149
EC 号:
欧洲委员会编号:
2030
MDL编号:
PubChem化学物质编号:
Flavis编号:
2.064
NACRES:
NA.21

生物来源

synthetic

质量水平

等级

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

蒸汽密度

4.21 (vs air)

蒸汽压

0.1 mmHg ( 20 °C)

检测方案

≥99%

折射率

n20/D 1.527 (lit.)

bp

204 °C/745 mmHg (lit.)

mp

19-20 °C (lit.)

密度

1.012 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

性状检查

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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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2

储存分类代码

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

WGK

WGK 1

闪点(°F)

187.9 °F - Pensky-Martens closed cup

闪点(°C)

86.6 °C - Pensky-Martens closed cup

个人防护装备

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

法规信息

危险化学品

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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
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
Shweta Shah et al.
Bioorganic & medicinal chemistry letters, 17(4), 921-924 (2006-12-13)
Lipases from two different sources Candida rugosa (CRL) and Burkholderia cepacia (BCL) were formulated as enzyme precipitated and rinsed with organic solvents, organic solvent rinsed enzyme preparation, cross-linked enzyme aggregates (CLEAs) and protein coated micro-crystals (PCMCs). These various enzyme formulates
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)
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

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