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45817

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Haloxyfop

PESTANAL®, analytical standard

Synonyme(s) :

2-[4-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid, Haloxyfop acid

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About This Item

Formule empirique (notation de Hill):
C15H11ClF3NO4
Numéro CAS:
69806-34-4
Poids moléculaire :
361.70
Numéro Beilstein :
1507817
Numéro MDL:
MFCD00871401
Code UNSPSC :
41116107
ID de substance PubChem :
329756972
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
environmental

Format

neat

Chaîne SMILES 

CC(Oc1ccc(Oc2ncc(cc2Cl)C(F)(F)F)cc1)C(O)=O

InChI

1S/C15H11ClF3NO4/c1-8(14(21)22)23-10-2-4-11(5-3-10)24-13-12(16)6-9(7-20-13)15(17,18)19/h2-8H,1H3,(H,21,22)

Clé InChI

GOCUAJYOYBLQRH-UHFFFAOYSA-N

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Application

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

Produits recommandés

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Informations légales

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

Pictogrammes

CorrosionExclamation mark
GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H318,H412

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG5705
BCBT9661
BCBS7781V
SZBE072XV
SZBC340XV

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Sigma-Aldrich

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A Banaś et al.
Biochemical Society transactions, 28(6), 777-779 (2001-02-15)
Seedlings of wheat were grown for 24 h in control nutrient solution and in solutions containing haloxyfop, alloxydim, diquat or paraquat, and thereafter the roots were used for microsomal preparations. Phosphatidylcholine or diacylglycerol with various 1-(14)C-labelled fatty acids (oleic, linoleic
P Gornicki et al.
Plant molecular biology, 22(3), 547-552 (1993-06-01)
The acetyl-CoA carboxylase present in both wheat germ and total wheat leaf protein contains ca. 220 kDa subunits. It is the major biotin-dependent carboxylase present in wheat chloroplasts. Active acetyl-CoA carboxylase purified from wheat germ is a homodimer with an
A R Rendina et al.
Archives of biochemistry and biophysics, 265(1), 219-225 (1988-08-15)
The selective grass herbicides diclofop, haloxyfop, and trifop were found to be potent reversible inhibitors of acetyl-CoA carboxylase from the susceptible species barley, corn, and wheat. Kis values with variable concentrations of acetyl-CoA ranged from 0.01 to 0.06 microM at
Huajun Bao et al.
Journal of agricultural and food chemistry, 58(14), 8167-8170 (2010-07-03)
An indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) for the herbicide haloxyfop-P-methyl is reported. Two haptens of haloxyfop-P-methyl with different spacer-arm lengths were synthesized, to which polyclonal antibodies were obtained by immunizing New Zealand rabbits. The most sensitive combination of antibody/coating
M J Bartels et al.
Drug metabolism and disposition: the biological fate of chemicals, 17(3), 286-291 (1989-05-01)
The 2-aryloxypropionate haloxyfop is currently being evaluated for use as a herbicide. This compound is structurally similar to a group of 2-arylpropionates that have been shown previously to undergo stereochemical inversion in a variety of mammalian species. To support the
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