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45817

Supelco

Haloxyfop

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C15H11ClF3NO4
Numero CAS:
69806-34-4
Peso molecolare:
361.70
Beilstein:
1507817
Numero MDL:
MFCD00871401
Codice UNSPSC:
41116107
ID PubChem:
329756972
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
GOCUAJYOYBLQRH-UHFFFAOYSA-N

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Applicazioni

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

Prodotti consigliati

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.

Note legali

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

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Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302,H318,H412

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG5705
BCBT9661
BCBS7781V

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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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