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Merck
CN

421464

Zonyl® FSP fluorosurfactant

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About This Item

CAS Number:
UNSPSC Code:
12162002
MDL number:
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refractive index

n20/D 1.358 (lit.)

bp

84 °C (lit.)

density

1.15 g/mL at 25 °C (lit.)

Legal Information

DuPont Product
Zonyl is a registered trademark of E. I. du Pont de Nemours and Company

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Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

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

Regulatory Information

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V Caslavska et al.
Caries research, 25(1), 27-33 (1991-01-01)
After in vitro treatments of bovine enamel with NaF/Zonyl FSC and NH4F in-depth profiles of the chemical composition of the outermost zone of surface enamel were obtained with electron spectroscopy. The most important finding of the study was that after
Effects of laundering upon the removal of atrazine and metolachlor from cotton, cotton/polyester, and polyester fabrics treated with fluorochemical finishes.
A Shaw et al.
Bulletin of environmental contamination and toxicology, 66(3), 319-325 (2001-02-15)
Chao Lu et al.
Analytical chemistry, 79(2), 666-672 (2007-01-16)
Gold nanoparticles (GNPs) capped with nonionic fluorosurfactant molecules (Zonyl FSN) were synthesized, and with the colloidal solution as a probe reagent, a new postcolumn colorimetric detection method for HPLC assay of homocysteine (Hcy) has been developed. The FSN-capped GNPs exhibited
Ingrid Machado de Andrade et al.
The International journal of prosthodontics, 25(2), 157-159 (2012-03-01)
The aim of this study was to evaluate the efficacy of experimental toothpastes for removing denture biofilm by means of a randomized crossover trial. Thirty volunteers brushed their dentures using a brush and four pastes: (1) Corega refreshing mint (control)
Natalia Quinete et al.
Archives of environmental contamination and toxicology, 59(1), 20-30 (2010-01-08)
Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) are manmade, stable perfluorosurfactants. The properties of perfluoroalkylated compounds that cause them to persist in the environment are also the properties that made them attractive compounds for industrial usage for over 50 years.

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