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Fluazifop-P-butyl

PESTANAL®, analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C19H20F3NO4
Numéro CAS:
79241-46-6
Poids moléculaire :
383.36
Numéro MDL:
MFCD06199153
Code UNSPSC :
41116107
ID de substance PubChem :
329753893
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

Chaîne 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

Clé InChI

VAIZTNZGPYBOGF-CYBMUJFWSA-N

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Description générale

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.

Application

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.

Produits recommandés

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.

Informations légales

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

Pictogrammes

FlameHealth hazardEnvironment
GHS02,GHS08,GHS09

Mention d'avertissement

Warning

Mentions de danger

H226,H361d,H410

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

122.0 °F - closed cup - (External MSDS)

Point d'éclair (°C)

50 °C - closed cup - (External MSDS)

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCJ5805
BCBX4137
SZBE190XV
SZB9112XV
SZE9112X

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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)
Fluazifop-P-butyl (herbicide) affects richness and structure of soil bacterial communities.
Darine T, et al.
Soil Biology and Biochemistry, 81, 89-97 (2015)
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)
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)
Evangelia Chronopoulou et al.
Planta, 235(6), 1253-1269 (2011-12-29)
Plant glutathione transferases (GSTs) comprise a large family of inducible enzymes that play important roles in stress tolerance and herbicide detoxification. Treatment of Phaseolus vulgaris leaves with the aryloxyphenoxypropionic herbicide fluazifop-p-butyl resulted in induction of GST activities. Three inducible GST
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