45355
溴苯腈
PESTANAL®, analytical standard
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线性分子式:
Br2C6H2(OH)CN
化学文摘社编号:
分子量:
276.91
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
216-882-7
Beilstein/REAXYS Number:
2364039
MDL number:
InChI key
UPMXNNIRAGDFEH-UHFFFAOYSA-N
InChI
1S/C7H3Br2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H
SMILES string
Oc1c(Br)cc(cc1Br)C#N
grade
analytical standard
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
Quality Level
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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.
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
存储类别
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
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
危险化学品
农药列管产品
此项目有
Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1988)
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
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
J Baxter et al.
Journal of applied microbiology, 104(6), 1605-1616 (2008-01-26)
To study how repeated applications of an herbicide bromoxynil to a soil, mimicking the regime used in the field, affected the degradation of the compound and whether such affects were reflected by changes in the indigenous bacterial community present. Bromoxynil
Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1988)
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