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Merck
CN

186260

Sigma-Aldrich

乙基磺酸

95%

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别名:
1-Ethanesulfonic acid, Ethylsulfonic acid
线性分子式:
CH3CH2SO3H
CAS号:
分子量:
110.13
Beilstein:
1743071
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

95%

折射率

n20/D 1.434 (lit.)

bp

123 °C/0.01 mmHg (lit.)

mp

−17 °C (lit.)

溶解性

water: soluble

密度

1.35 g/mL at 25 °C (lit.)

SMILES字符串

O=S(O)(CC)=O

InChI

1S/C2H6O3S/c1-2-6(3,4)5/h2H2,1H3,(H,3,4,5)

InChI key

CCIVGXIOQKPBKL-UHFFFAOYSA-N

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一般描述

乙基磺酸参与高铼酸盐溶液的电解还原

乙基磺酸是一种磺酸,通常用作烷化和聚合反应的催化剂。

应用

乙基磺酸可用作ACPO(酸性粗棕榈油)预处理的酯化催化剂,用于生产生物柴油。

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

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


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Advanced fuel cell catalysts: sulfonation of carbon-supported catalysts using 2-aminoethanesulfonic acid
Xu Z, et al.
Electrochemical and Solid-State Letters, 6(9), A171-A171 (2003)
The Action of Sulfuric Acid, Ethanesulfonic Acid and Chlorosulfonic Acid on Aliphatic Hydrocarbons
Gordon GS and Burwell RL
Journal of the American Chemical Society, 71(7), 2355-2359 (1949)
Electrolytic Reduction of Perrhenate. I. Studies in Perchloric, Ethanesulfonic, Trifluoroacetic and Hydrochloric Acids.
Hindman JC and Wehner P.
Journal of the American Chemical Society, 75(12), 2869-2872 (1953)
Adeeb Hayyan et al.
Bioresource technology, 102(20), 9564-9570 (2011-08-23)
An industrial grade acidic crude palm oil (ACPO) pre-treatment process was carried out using ethanesulfonic acid (ESA) as a catalyst in the esterification reaction. ESA was used in different dosages to reduce free fatty acid (FFA) to a minimum level
E M Thurman et al.
Journal of chromatography. A, 957(1), 3-9 (2002-07-10)
Degradates of acetochlor and alachlor (ethanesulfonic acids, ESAs) were analyzed in both standards and in a groundwater sample using high-performance liquid chromatography-time-of-flight mass spectrometry with electrospray ionization. The negative pseudomolecular ion of the secondary amide of acetochlor ESA and alachlor

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