Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

45355

Supelco

Bromoxynil

PESTANAL®, analytical standard

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
Br2C6H2(OH)CN
CAS Number:
1689-84-5
Molecular Weight:
276.91
Beilstein/REAXYS Number:
2364039
EC Number:
216-882-7
MDL number:
MFCD00002153
UNSPSC Code:
41116107
PubChem Substance ID:
329756669
NACRES:
NA.24

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

mp

189-191 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Oc1c(Br)cc(cc1Br)C#N

InChI

1S/C7H3Br2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H

InChI key

UPMXNNIRAGDFEH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Bromoxynil is a foliar-applied contact herbicide, for post-emergence control of annual broad-leaved weeds in agriculture. Its mode of action involves the uncoupling of oxidative phosphorylation in plants and animals. It also inhibits photoreduction and photophosphorylation in chloroplasts.
Bromoxynil is a foliar-applied contact herbicide, for post-emergence control of annual broad-leaved weeds in agriculture. Its mode of action involves the uncoupling of oxidative phosphorylation in plants and animals. It also inhibits photoreduction and photophosphorylation in chloroplasts.

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

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL2676
BCCD9901
BCBW8110
BCBW3125
SZBD051XV

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1988)
Robert M Zablotowicz et al.
Pest management science, 65(6), 658-664 (2009-03-17)
The objectives of these laboratory experiments were: (1) to assess bromoxynil sorption, mineralization, bound residue formation and extractable residue persistence in a Dundee silt loam collected from 0-2 cm and 2-10 cm depths under continuous conventional tillage and no-tillage; (2)
Panpan Wang et al.
Bioelectrochemistry (Amsterdam, Netherlands), 136, 107597-107597 (2020-07-17)
Interfacing photosynthetic protein complexes with electrodes is frequently used for the identification of electron transfer mechanisms and the fabrication of biosensors. Binding of herbicide compounds to the terminal plastoquinone QB at photosystem II (PSII) causes disruption of electron flow that
Jiang Zhu et al.
Environmental pollution (Barking, Essex : 1987), 156(1), 136-142 (2008-02-08)
A rapid immunochromatographic one-step strip test was developed to specifically determine bromoxynil in surface and drinking water by competitive inhibition with the nano colloidal gold-conjugated monoclonal antibody (mAb). Bromoxynil standard samples of 0.01-10 mg L(-1) in water were tested by
Hiroshi Ishikita et al.
Biochemistry, 50(24), 5436-5442 (2011-05-19)
The redox potential of the primary quinone Q(A) [E(m)(Q(A))] in photosystem II (PSII) is lowered by replacement of the native plastoquinone (PQ) with bromoxynil (BR) at the secondary quinone Q(B) binding site. Using the BR-bound PSII structure presented in the
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service