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45817

Supelco

Haloxyfop

PESTANAL®, analytical standard

Synonym(s):

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

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100 MG
$103.00

$103.00

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100 MG
$103.00

About This Item

Empirical Formula (Hill Notation):
C15H11ClF3NO4
CAS Number:
69806-34-4
Molecular Weight:
361.70
Beilstein/REAXYS Number:
1507817
MDL number:
MFCD00871401
UNSPSC Code:
41116107
PubChem Substance ID:
329756972
NACRES:
NA.24

$103.00

Available to ship onApril 29, 2025Details

Request a Bulk Order

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

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)

InChI key

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.

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Legal Information

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL0225
BCCG5705
BCBT9661
BCBS7781V

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Sigma-Aldrich

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Antonella Messina et al.
Journal of chromatography. A, 1120(1-2), 69-74 (2005-12-21)
The enantioseparation of 2-aryloxypropionic acids by capillary electrochromatography was tested on columns with a monolithic stationary phase prepared from silanized fused-silica capillaries (100 microm I.D.) by in situ copolymerization of glycidyl methacrylate, ethylene glycol dimethacrylate and methyl methacrylate in the
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
W T Stott et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 28(1), 71-79 (1995-11-01)
The potential of haloxyfop [2-(4-((3-chloro-5-(trifluoromethyl)-2- pyridinyl)oxy)phenoxy)propanoic acid; HAL] to induce the proliferation of hepatocellular peroxisomes (PP) was examined in rats, mice, dogs, and monkeys. Chemically induced PP is associated with the development of liver tumors in rodents via an apparent
Hailong Zhang et al.
Science (New York, N.Y.), 299(5615), 2064-2067 (2003-03-29)
Acetyl-coenzyme A carboxylases (ACCs) are required for the biosynthesis and oxidation of long-chain fatty acids. They are targets for therapeutics against obesity and diabetes, and several herbicides function by inhibiting their carboxyltransferase (CT) domain. We determined the crystal structure of
Christophe Délye et al.
Pest management science, 58(5), 474-478 (2002-05-10)
A simple method based upon allele-specific PCR was developed to detect an isoleucine-leucine substitution in the gene encoding chloroplastic acetyl-coenzyme A carboxylase (ACCase) in two gramineous weeds: Lolium rigidum Gaud and Alopecurus myosuroides Huds. Analysis of 1800 A myosuroides and
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