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Bromoxynil

PESTANAL®, analytical standard

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About This Item

Formule linéaire :
Br2C6H2(OH)CN
Numéro CAS:
1689-84-5
Poids moléculaire :
276.91
Numéro Beilstein :
2364039
Numéro CE :
216-882-7
Numéro MDL:
MFCD00002153
Code UNSPSC :
41116107
ID de substance PubChem :
329756669
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

189-191 °C (lit.)

Application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

Chaîne SMILES 

Oc1c(Br)cc(cc1Br)C#N

InChI

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

Clé InChI

UPMXNNIRAGDFEH-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Informations légales

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

Pictogrammes

Skull and crossbonesHealth hazardEnvironment
GHS06,GHS08,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301,H317,H330,H361d,H410

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCD9901
BCBW8110
BCBW3125
SZBD051XV
SZB8021XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
Purification and Properties of a Nitrilase Specific for the Herbicide Bromoxynil and Corresponding Nucleotide Sequence Analysis of the bxn Gene.
Stalker MD, et al.
The Journal of Biological Chemistry, 263(13), 6310-6314 (1988)
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
Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1988)
Alain Boussac et al.
Biochimica et biophysica acta, 1807(1), 119-129 (2010-10-13)
The main cofactors involved in Photosystem II (PSII) oxygen evolution activity are borne by two proteins, D1 (PsbA) and D2 (PsbD). In Thermosynechococcus elongatus, a thermophilic cyanobacterium, the D1 protein is predominantly encoded by either the psbA(1) or the psbA(3)
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