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Supelco

Ioxynil

PESTANAL®, analytical standard

Synonym(s):

4-Hydroxy-3,5-diiodobenzonitrile

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About This Item

Empirical Formula (Hill Notation):
C7H3I2NO
CAS Number:
1689-83-4
Molecular Weight:
370.91
Beilstein:
2364041
EC Number:
216-881-1
MDL number:
MFCD00016422
UNSPSC Code:
41116107
PubChem Substance ID:
329755281

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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Oc1c(I)cc(cc1I)C#N

InChI

1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H

InChI key

NRXQIUSYPAHGNM-UHFFFAOYSA-N

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General description

Ioxynil is a post-emergent herbicide, which can be used to selectively control broad-leaved weeds in cereals and grass crops. It can be used in combination with phenoxy herbicides in order to control hormone-resistant weeds.

Application

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

Legal Information

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 2 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW5198
SZBD116XV
SZB8114XV
SZE8114X
8114X

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Carsten T Petersen et al.
Pest management science, 59(1), 85-96 (2003-02-01)
Knowledge of the movement of herbicides and soil particles to sub-surface tile drainage may help to predict chemical leaching to surface waters and deeper groundwater systems. The movement of pendimethalin (2 years), ioxynil (1 year) and soil particles (3 years)
Pesticide Chemistry (1989)
Modern Weed Control (1975)
Edward Leithe et al.
Toxicology and applied pharmacology, 247(1), 10-17 (2010-06-01)
Gap junctions are intercellular plasma membrane domains containing channels that mediate transport of ions, metabolites and small signaling molecules between adjacent cells. Gap junctions play important roles in a variety of cellular processes, including regulation of cell growth and differentiation
Akinori Ishihara et al.
General and comparative endocrinology, 134(1), 36-43 (2003-09-18)
We investigated the effect of endocrine disrupting chemicals (EDCs), including medical, industrial, and agricultural chemicals, on 3,3',5-L-[125I]triiodothyronine ([125I]T3) binding to purified Japanese quail transthyretin (qTTR), a major thyroid hormone-binding protein in plasma, and to the ligand-binding domain of thyroid hormone
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