51126

Sigma-Aldrich

海胺® 1622 溶液

4 mM in H2O

别名:
苄索氯铵 溶液
CAS号:
Beilstein/REAXYS Number:
3898548
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

100

浓度

4 mM in H2O

密度

0.998 g/mL at 20 °C

SMILES string

[Cl-].CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1

InChI

1S/C27H42NO2.ClH/c1-26(2,3)22-27(4,5)24-13-15-25(16-14-24)30-20-19-29-18-17-28(6,7)21-23-11-9-8-10-12-23;/h8-16H,17-22H2,1-7H3;1H/q+1;/p-1

InChI key

UREZNYTWGJKWBI-UHFFFAOYSA-M

相关类别

一般描述

Hyamine® 1622是阳离子去污剂苄索氯铵。用于Hyamine 1622阳离子的聚(氯乙烯)膜离子选择性电极已被提出。它在土壤表面的吸附已得到研究。由于它具有抗菌和阳离子表面活性剂特性,已被广泛用于化妆品和洗发剂中。

应用

Hyamine® 1622溶液被用作表面活性剂,以检测其对 日本杜鹃的急性毒性以及对氧化应激和胆碱酯酶(ChE)活性的影响。它可以用作改良型红细胞胆碱酯酶Eliman测定法的终止试剂。

包装

5 L in poly drum
1 L in poly bottle

法律信息

Hyamine is a registered trademark of Lonza Group Ltd.

危险声明

预防措施声明

hazcat

Aquatic Chronic 3

storage_class_code

12 - Non Combustible Liquids

WGK Germany

WGK 1

闪点(F)

Not applicable

闪点(C)

Not applicable

个人防护装备

Eyeshields, Gloves

分析证书

原产地证书 (CofO)

P M George et al.
Clinical chemistry, 29(2), 365-368 (1983-02-01)
The procedure of Dietz et al. (Clin. Chem. 19: 1309-1313, 1973) for plasma cholinesterase (EC 3.1.1.7) gives a background absorbance of 1.4 A when extended to erythrocyte cholinesterase (EC 3.1.1.8) measurement, because the peak absorbance of the reaction product, 5-thionitrobenzoate...
Sorption of anionic surfactants SDS, AOT and cationic surfactant Hyamine 1622 on natural soils.
Atay N, et al.
Water, Air, Soil Pollut., 136(1-4), 55-68 (2002)
Mei-Hui Li
Chemosphere, 70(10), 1796-1803 (2007-10-02)
Eight widely used surfactants (cetyltrimethylammonium bromide; CTAB, benzethonium chloride; Hyamine 1622, 4-nonylphenol; NP, octylphenol ethoxylate; Triton X-100, dodecylbenzene sulfonate; LAS, lauryl sulfate; SDS, pentadecafluorooctanoic acid; PFOA, and perfluorooctane sulfonate; PFOS) were selected to examine their acute toxicities and effects on...
Poly (vinyl chloride) containing dibenzo-18-crown-6 as an ion-selective membrane for hyamine 1622.
Khalil MM, et al.
Analytical Letters, 19(7-8), 807-824 (1986)
Naoto Kojima et al.
Bioorganic & medicinal chemistry, 18(24), 8630-8641 (2010-11-16)
The convergent synthesis of fluorescence-labeled solamin, an antitumor Annonaceous acetogenin, was accomplished by two asymmetric alkynylations of 2,5-diformyl tetrahydrofuran with an alkyne tagged with fluorescent groups and another alkyne with an α,β-unsaturated γ-lactone. Assay for the growth inhibitory activity against...

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