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Merck

91242

Supelco

Sulfluramid

PESTANAL®, analytical standard

Sinónimos:

N-Ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-1-octanesulfonamide, N-Ethylperfluorooctane-1-sulfonamide

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About This Item

Fórmula empírica (notación de Hill):
C10H6F17NO2S
Número de CAS:
Peso molecular:
527.20
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

Análisis

≥98.0% (GC)

caducidad

limited shelf life, expiry date on the label

composición

carbon content, 22.3-23.3 wt. %

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

formato

neat

cadena SMILES

CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C10H6F17NO2S/c1-2-28-31(29,30)10(26,27)8(21,22)6(17,18)4(13,14)3(11,12)5(15,16)7(19,20)9(23,24)25/h28H,2H2,1H3

Clave InChI

CCEKAJIANROZEO-UHFFFAOYSA-N

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Categorías relacionadas

Descripción general

Sulfluramid is a slow-acting insecticide for controlling ants.

Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfluramid may be used as a reference standard for the determination of sulfluramid and its isomers in ant bait by capillary column gas chromatography.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Información legal

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Lact. - Repr. 1B - STOT RE 1

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Certificados de análisis (COA)

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R O Manning et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(1), 205-211 (1991-01-01)
The objectives of this study were to characterize the absorption, distribution, and elimination of sulfluramid (N-ethyl perfluorooctane sulfonamide) and its major metabolite, perfluorooctane sulfonamide (DESFA), in order to assess the effect of dosage vehicle on their pharmacokinetics. In Trial 1
R G Schnellmann et al.
Biochimica et biophysica acta, 1016(3), 344-348 (1990-04-26)
The effects of sulfluramide (N-ethylperfluorooctane sulfonamide) and perfluorooctane sulfonamide (DESFA) on isolated rabbit renal cortical mitochondria (RCM) were examined. Sulfluramid (1-100 microM) and DESFA (0.5-50 microM) increased state 4 respiration of RCM respiring on pyruvate/malate or succinate in a concentration
Margie M Peden-Adams et al.
Journal of toxicology and environmental health. Part A, 70(13), 1130-1141 (2007-06-15)
Perfluorinated hydrocarbons have been manufactured for over 40 yr and have numerous applications in industry. This group of compounds has recently generated much interest, as some of these compounds such as perfluorooctane sulfonate (PFOS) and perfluoroctanic acid (PFOA) are persistent
Timothy M O'Brien et al.
Toxicology and applied pharmacology, 227(2), 184-195 (2007-12-01)
N-alkyl perfluorooctane sulfonamides have been widely used as surfactants on fabrics and papers, fire retardants, and anti-corrosion agents, among many other commercial applications. The global distribution and environmental persistence of these compounds has generated considerable interest regarding potential toxic effects.
Jonathan P Benskin et al.
Environmental science & technology, 47(3), 1381-1389 (2013-01-12)
Investigations into the biodegradation potential of perfluorooctane sulfonate (PFOS)-precursor candidates have focused on low molecular weight substances (e.g., N-ethyl perfluorooctane sulfonamido ethanol (EtFOSE)) in wastewater treatment plant sludge. Few data are available on PFOS-precursor biodegradation in other environmental compartments, and

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