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Safety Information

36131

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

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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

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW5198

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Kimmo A Mäenpää et al.
Ecotoxicology and environmental safety, 56(3), 398-410 (2003-10-25)
The benthic macroinvertebrates Lumbriculus variegatus and Chironomus riparius were used in toxicity and bioaccumulation tests to determine the toxic concentrations and accumulation potential of sediment associated herbicides. The tested chemicals were ioxynil, bentazone, and pendimethalin. The bioaccumulation tests with L.
Isabel Morgado et al.
Chemosphere, 69(1), 155-163 (2007-06-08)
A number of chemicals released into the environment share structural similarity to the thyroid hormones (THs), thyroxine (T(4)) and triiodothyronine (T(3)) and it is thought that they may interfere with the thyroid axis and behave as endocrine disruptors (EDs). One
Alison M Cupples et al.
Applied and environmental microbiology, 71(7), 3741-3746 (2005-07-08)
Desulfitobacterium chlororespirans has been shown to grow by coupling the oxidation of lactate to the metabolic reductive dehalogenation of ortho chlorines on polysubstituted phenols. Here, we examine the ability of D. chlororespirans to debrominate and deiodinate the polysubstituted herbicides bromoxynil
Modern Weed Control (1975)
Pesticide Chemistry (1989)
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