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Merck

31712

Supelco

Fluazifop-P-butyl

PESTANAL®, analytical standard

Sinónimos:

Butyl (R)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionate

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About This Item

Fórmula empírica (notación de Hill):
C19H20F3NO4
Número de CAS:
Peso molecular:
383.36
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

formato

neat

cadena SMILES

CCCCOC(=O)[C@@H](C)Oc1ccc(Oc2ccc(cn2)C(F)(F)F)cc1

InChI

1S/C19H20F3NO4/c1-3-4-11-25-18(24)13(2)26-15-6-8-16(9-7-15)27-17-10-5-14(12-23-17)19(20,21)22/h5-10,12-13H,3-4,11H2,1-2H3/t13-/m1/s1

Clave InChI

VAIZTNZGPYBOGF-CYBMUJFWSA-N

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Descripción general

Fluazifop-P-butyl belongs to the arylophenoxypropionate group of graminicides. It is a post-emergence herbicide that acts by inhibiting acetyl-CoA carboxylase enzyme activity, involved in the catalysis of the formation of malonyl-CoA during metabolism of lipids.

Aplicación

Fluazifop-P-butyl may be used as a reference standard for the determination of the analyte:
  • In different varieties of lettuce (Lactuca sativum) by capillary gas chromatography with nitrogen–phosphorus detection (NPD).
  • In tea samples by modified QuEChERS (quick, easy, cheap, effective, rugged, and safe) sample preparation procedure combined with ultra-performance liquid chromatography-electrospray tandem mass spectrometry (UPLC/MS/MS).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Productos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Información legal

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

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 3 - Repr. 2

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

122.0 °F - closed cup - (External MSDS)

Punto de inflamabilidad (°C)

50 °C - closed cup - (External MSDS)

Equipo de protección personal

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number

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Los clientes también vieron

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A multi-residue method for fast determination of pesticides in tea by ultra performance liquid chromatography- electrospray tandem mass spectrometry combined with modified QuEChERS sample preparation procedure.
Chen G, et al.
Food Chemistry, 125(4), 1406- 1411 (2011)
Effect of fluazifop-p-butyl treatment on pigments and polyamines level within tissues of non-target maize plants.
Horbowicz M, et al.
Pesticide Biochemistry and Physiology, 107(1), 78- 85 (2013)
Fluazifop-P-butyl (herbicide) affects richness and structure of soil bacterial communities.
Darine T, et al.
Soil Biology and Biochemistry, 81, 89- 97 (2015)
Simplified multiresidue method for determination of pesticide residues in lettuce by gas chromatography with nitrogen- phosphorus detection.
Fenoll J, et al.
Analytical and Bioanalytical Chemistry, 389(2), 643- 651 (2007)
N W Clark et al.
Archives of toxicology, 67(1), 44-48 (1993-01-01)
Enzyme mediated hydrolysis of fluazifop butyl has been measured with rat and human skin post-mitochondrial fractions. Rat skin had a ten times greater capacity to metabolise fluazifop butyl than human skin, but the enzyme affinities were similar. The post-mitochondrial fraction

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