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Merck
CN

108006

Sigma-Aldrich

苯甲醇

ReagentPlus®, ≥99%

别名:

苯甲醇

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About This Item

线性分子式:
C6H5CH2OH
CAS号:
分子量:
108.14
Beilstein:
878307
EC 号:
MDL编号:
UNSPSC代码:
12352104
eCl@ss:
39023110
PubChem化学物质编号:
NACRES:
NA.21
方案:
≥99%
沸点:
203-205 °C (lit.)
蒸汽压:
13.3 mmHg ( 100 °C)
3.75 mmHg ( 77 °C)

蒸汽密度

3.7 (vs air)

质量水平

蒸汽压

13.3 mmHg ( 100 °C)
3.75 mmHg ( 77 °C)

产品线

ReagentPlus®

方案

≥99%

表单

liquid

自燃温度

817 °F

expl. lim.

0.34-6.3 %

折射率

n20/D 1.539 (lit.)

沸点

203-205 °C (lit.)

mp

−16-−13 °C (lit.)

溶解性

water: soluble 33 g/L at 20 °C

密度

1.045 g/mL at 25 °C (lit.)

SMILES字符串

OCc1ccccc1

InChI

1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2

InChI key

WVDDGKGOMKODPV-UHFFFAOYSA-N

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一般描述

苯甲醇是一种芳香醇,广泛用于化妆品和染发剂中。它在没有溶剂的情况下发生氧化,由负载在用不同数量的3-氨基丙基三乙氧基硅烷(APTES)官能化的TiO2上的Pd催化剂催化。

应用

苄醇可以用于通过氧化法制备苯甲酸。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

213.8 °F - DIN 51758

闪点(°C)

101 °C - DIN 51758


历史批次信息供参考:

分析证书(COA)

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Surface functionalized TiO2 supported Pd catalysts for solvent-free selective oxidation of benzyl alcohol.
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Catalysis Today, 250, 218-225 (2015)
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Concise Encyclopedia Chemistry, 122-122 (1994)
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The Journal of pharmacology and experimental therapeutics, 314(1), 232-243 (2005-03-29)
Our aim was to determine whether the newly described P2X1 antagonist NF449 [4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt] could selectively antagonize the platelet P2X1 receptor and how it affected platelet function. NF449 inhibited alpha,beta-methyleneadenosine 5'-triphosphate-induced shape change (IC50 = 83 +/- 13
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Inorganic chemistry, 51(18), 10025-10036 (2012-09-08)
The rate of oxidation of 2,5-dimethoxybenzyl alcohol (2,5-(MeO)(2)C(6)H(3)CH(2)OH) by [Fe(IV)(O)(N4Py)](2+) (N4Py = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) was enhanced significantly in the presence of Sc(OTf)(3) (OTf(-) = trifluoromethanesulfonate) in acetonitrile (e.g., 120-fold acceleration in the presence of Sc(3+)). Such a remarkable enhancement of the
Luis E Santos-Figueroa et al.
Chemical Society reviews, 42(8), 3489-3613 (2013-02-13)
This review focuses on examples reported in the years 2010-2011 dealing with the design of chromogenic and fluorogenic chemosensors or reagents for anions.

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