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Merck
CN

77848

Supelco

(R)-(+)-1-苯基乙醇

for chiral derivatization, LiChropur, ≥99.0%

别名:

(+)-甲基苯基甲醇, (R)-(+)-α-甲基苯甲醇

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About This Item

经验公式(希尔记法):
C8H10O
CAS号:
分子量:
122.16
Beilstein:
2039798
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.05

等级

for chiral derivatization

质量水平

产品线

ChiraSelect

方案

≥99.0% (sum of enantiomers, GC)
≥99.0%

表单

liquid

旋光性

[α]20/D +45±1°, c = 5% in methanol

光学纯度

enantiomeric ratio: ≥99.5:0.5 (GC)

质量

LiChropur

技术

HPLC: suitable

折射率

n20/D 1.528

沸点

88-89 °C/10 mmHg (lit.)

mp

9-11 °C (lit.)

密度

1.012 g/mL at 20 °C (lit.)

SMILES字符串

C[C@@H](O)c1ccccc1

InChI

1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1

InChI key

WAPNOHKVXSQRPX-SSDOTTSWSA-N

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一般描述

(R)-(+)-1-Phenylethanol is a chiral derivatizating agent, which is employed for derivatizing acids for their subsequent analysis using gas chromatography as the analytical technique.

其他说明

于检测对映体纯度和分离酸的手性试剂;环酐和环氧化物的不对称开环

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Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律信息

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a 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 Oral - Eye Irrit. 2 - Skin 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 3

闪点(°F)

185.0 °F - closed cup

闪点(°C)

85 °C - closed cup

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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S.V. Ley et al.
Tetrahedron, 46, 4995-4995 (1990)
Y. Takeuchi et al.
Journal of the Chemical Society. Perkin Transactions 1, 2203-2203 (1987)
T. Rosen et al.
Journal of the American Chemical Society, 107, 3731-3731 (1985)
H. Niwa et al.
Tetrahedron Letters, 29, 5139-5139 (1988)
Sachiko Sugimoto et al.
Phytochemistry, 108, 189-195 (2014-12-03)
Three aromatic glycosides (1-3), two sulfur and nitrogen-containing compound glucosides (4, 5), and one flavonoid glycoside (6) were isolated from the leaves of Ixora undulata. Their structures were established by extensive 1D, 2D NMR, and HRESIMS experiments, and structure 4

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