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Merck
CN

238465

Sigma-Aldrich

1-氯己烷

99%

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别名:
己基氯
线性分子式:
CH3(CH2)5Cl
CAS号:
分子量:
120.62
Beilstein:
1731289
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

99%

形式

liquid

折射率

n20/D 1.419 (lit.)

bp

133-134 °C (lit.)

mp

−94 °C (lit.)

溶解性

water: insoluble(lit.)

密度

0.879 g/mL at 25 °C (lit.)

SMILES字符串

CCCCCCCl

InChI

1S/C6H13Cl/c1-2-3-4-5-6-7/h2-6H2,1H3

InChI key

MLRVZFYXUZQSRU-UHFFFAOYSA-N

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一般描述

在活性炭或 Al 2 O 3 (催化剂)上,用 Ni、Fe、W、Ni-Mo、Pt 和 Pd 对氯苯和 1-氯己烷蒸气进行加氢脱氯研究 。钛硅分子筛催化用过氧化氢氧化 1-氯己烷

象形图

Flame

警示用语:

Warning

危险声明

危险分类

Flam. Liq. 3

WGK

WGK 1

闪点(°F)

closed cup

闪点(°C)

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

分析证书(COA)

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Oxidation of saturated hydrocarbons with hydrogen peroxide, catalysed by titanium silicalite.
G Clerici M.
Applied Catalysis, 68(1), 249-261 (1999)
Stephen E Repper et al.
Dalton transactions (Cambridge, England : 2003), 46(9), 2821-2828 (2017-02-09)
Absorption of carbon monoxide by copper(i)-containing ionic liquids, [C
Pengfei Li et al.
Journal of chromatography. A, 1623, 461192-461192 (2020-06-09)
An imidazolium ionic-liquid-modified phenolic resin (ILPR) was synthesized using 3-aminophenol as a functional monomer, glyoxylic acid as a green cross-linker, and polyethylene glycol 6000 as a porogen. The obtained ILPR showed better extraction of benzoylurea plant hormones thidiazuron and forchlorfenuron
Horng-Jang Liaw et al.
Journal of hazardous materials, 367, 407-417 (2019-01-06)
Industrial use of ionic liquids may require exposure to high temperatures. We demonstrate that such applications may result in an increase in flammability hazard due to chemical decomposition. The ionic liquid, 1-hexyl-3-methylimidazolium chloride ([C6mim][Cl]), was selected as the study sample.
João P A Reis et al.
Nature communications, 11(1), 1458-1458 (2020-03-21)
Esterification reactions are central to many aspects of industrial and biological chemistry. The formation of carboxyesters typically occurs through nucleophilic attack of an alcohol onto the carboxylate carbon. Under certain conditions employed in organic synthesis, the carboxylate nucleophile can be

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