51126
Hyamine® 1622 solution
4 mM in H2O
Synonym(s):
(Diisobutylphenoxyethoxyethyl)dimethylbenzylammonium chloride solution
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About This Item
CAS Number:
Beilstein:
3898548
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
concentration
4 mM in H2O
density
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
General description
Hyamine® 1622 is a cationic detergent benzethonium chloride. Poly(vinyl chloride) membrane ion-selective electrode for the Hyamine 1622 cation has been proposed. Its sorption on soil surfaces has been investigated. It is widely used in cosmetics and shampoos due to its antimicrobial and cationic surfactant properties.
Application
Hyamine® 1622 solution was used as surfactant to examine its acute toxicity and effect on oxidative stress and cholinesterase (ChE) activity in Dugesia japonica. It may be employed as stopping reagent in the improved Eliman procedure for erythrocyte cholinesterase.
Legal Information
Hyamine is a registered trademark of Lonza Group Ltd.
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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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
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)
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C4-Fluorinated analogues of solamin, an antitumor acetogenin, were synthesized and investigated for their antitumor activities against 39 tumor cell lines. C4-Fluorinated solamins showed more potent growth inhibitory activity against cancer cell lines than solamin.
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