48750
Genapol® X-080
Synonym(s):
Polyethylene glycol monoalkyl ether, Iso-tridecyl alchohol polyglycol ether (8EO), Oligoethylene glycol monoalkyl ether
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About This Item
Linear Formula:
HO(CH2CH2O)n(CH2)mH
CAS Number:
MDL number:
UNSPSC Code:
12161902
NACRES:
NA.25
description
non-ionic
Quality Level
form
liquid
mol wt
552.78 g/mol
refractive index
n20/D 1.461±0.001
CMC
0.06-0.15
transition temp
cloud point >45 °C
density
1.000 g/mL±0.003 g/mL at 20 °C
HLB
13
SMILES string
O(CCOCCOCCOCCOCCO)CCOCCOCCOCCOCCCCCCCCCCCC
InChI
1S/C30H62O10/c1-2-3-4-5-6-7-8-9-10-11-13-32-15-17-34-19-21-36-23-25-38-27-29-40-30-28-39-26-24-37-22-20-35-18-16-33-14-12-31/h31H,2-30H2,1H3
InChI key
ONJQDTZCDSESIW-UHFFFAOYSA-N
Related Categories
General description
Contains 8 ethylene oxides.
Application
<ul>
<li><strong>Micelle-mediated extraction and cloud point preconcentration for the analysis of aesculin and aesculetin in Cortex fraxini by HPLC.</strong> Genapol® X-080 was employed in the cloud point extraction process to improve the efficiency of isolating bioactive compounds, demonstrating its utility in biocompatible surfactant applications within pharmaceutical testing (Shi et al., 2007).</li>
<li><strong>Determination of benzimidazole fungicides in soil samples using microwave-assisted micellar extraction and liquid chromatography with fluorescence detection.</strong> This study highlights the efficiency of Genapol® X-080 in enhancing micellar mediated extractions, applicable in environmental and agrochemical analyses (Halko et al., 2006).</li>
<li><strong>Development and performance evaluation of a positive reference material for hemolysis testing.</strong> Utilizes Genapol® X-080 for its non-ionic, biocompatible properties in the development of IVD reagents, ensuring safety and compatibility in medical diagnostics (Haishima et al., 2014).</li>
<li><strong>Micelle-mediated extraction of dibenzocyclooctadiene lignans from Schisandra chinensis with analysis by high-performance liquid chromatography.</strong> The paper documents the application of Genapol® X-080 in traditional medicine compound extraction, supporting its use in complex biological matrices (Lee et al., 2014).</li>
<li><strong>Green techniques in comparison to conventional ones in the extraction of Amaryllidaceae alkaloids: Best solvents selection and parameters optimization.</strong> Genapol® X-080 is highlighted for its role in green chemistry applications, emphasizing its effectiveness and environmental safety in the extraction processes (Takla et al., 2018).</li>
</ul>
<li><strong>Micelle-mediated extraction and cloud point preconcentration for the analysis of aesculin and aesculetin in Cortex fraxini by HPLC.</strong> Genapol® X-080 was employed in the cloud point extraction process to improve the efficiency of isolating bioactive compounds, demonstrating its utility in biocompatible surfactant applications within pharmaceutical testing (Shi et al., 2007).</li>
<li><strong>Determination of benzimidazole fungicides in soil samples using microwave-assisted micellar extraction and liquid chromatography with fluorescence detection.</strong> This study highlights the efficiency of Genapol® X-080 in enhancing micellar mediated extractions, applicable in environmental and agrochemical analyses (Halko et al., 2006).</li>
<li><strong>Development and performance evaluation of a positive reference material for hemolysis testing.</strong> Utilizes Genapol® X-080 for its non-ionic, biocompatible properties in the development of IVD reagents, ensuring safety and compatibility in medical diagnostics (Haishima et al., 2014).</li>
<li><strong>Micelle-mediated extraction of dibenzocyclooctadiene lignans from Schisandra chinensis with analysis by high-performance liquid chromatography.</strong> The paper documents the application of Genapol® X-080 in traditional medicine compound extraction, supporting its use in complex biological matrices (Lee et al., 2014).</li>
<li><strong>Green techniques in comparison to conventional ones in the extraction of Amaryllidaceae alkaloids: Best solvents selection and parameters optimization.</strong> Genapol® X-080 is highlighted for its role in green chemistry applications, emphasizing its effectiveness and environmental safety in the extraction processes (Takla et al., 2018).</li>
</ul>
Other Notes
Sales restrictions may apply
Used for the isolation of hydrogenase-cytochrome b complex from cytoplasmic membranes of Xanthobacter autotrophicus; Activator in the stabilization of aqueous solutions of cholesterol oxidase from Pseudomonads
Legal Information
Genapol is a registered trademark of Clariant GmbH
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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H. Buschek et al.
Ger. offen. DE 3200274 null
Júlio C Fonseca et al.
Environmental monitoring and assessment, 75(1), 1-10 (2005-05-20)
This work reports studies of the degradation rates of a fatty alcohol polyglycol ether non-ionic surfactant, Genapol OXD-080, putatively useful for the control of red swamp crayfish (Procambarus clarkii Girard) in rice fields under laboratory and field conditions. The influence
Radoslav Halko et al.
Journal of AOAC International, 89(5), 1403-1409 (2006-10-18)
A simple and fast analytical method was developed for the determination of benzimidazole fungicides (benomyl, carbendazim, thiabendazole, and fuberidazole) in soil samples. The analytes were extracted from the soil samples by means of conventional microwave-assisted extraction, using the non-ionic surfactants
E Chantelau
Diabetes & metabolism, 26(4), 304-306 (2000-09-30)
A case of a type 1 diabetic woman with auto-immune thyroiditis is reported, in whom repeated exposure to insulin containing Genapol(R) (polyethylen-polypropylenglycol) over 3 years reproducibly parallels with an increase of serum TSH (thyroid-stimulating hormone) above the normal limit. Previously
B. Schink
FEMS Microbiology Letters, 13, 289-289 (1982)
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