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Merck
CN

34311

Acifluorfen

PESTANAL®, analytical standard

Synonym(s):

5-(2-Chloro-α,α,α-trifluoro-p-tolyloxy)-2-nitrobenzoic acid, 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid

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About This Item

Empirical Formula (Hill Notation):
C14H7ClF3NO5
CAS Number:
50594-66-6
Molecular Weight:
361.66
MDL number:
MFCD00143541
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329754938
EC Number:
256-634-5
Beilstein/REAXYS Number:
2953865

Key Documents

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InChI key

NUFNQYOELLVIPL-UHFFFAOYSA-N

InChI

1S/C14H7ClF3NO5/c15-10-5-7(14(16,17)18)1-4-12(10)24-8-2-3-11(19(22)23)9(6-8)13(20)21/h1-6H,(H,20,21)

SMILES string

OC(=O)c1cc(Oc2ccc(cc2Cl)C(F)(F)F)ccc1[N+]([O-])=O

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Quality Level

100

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Application

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

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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
BCCH9703
BCBW5538

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Lu Sun et al.
Amino acids, 37(3), 523-530 (2009-03-07)
Protoporphyrinogen IX oxidase (PPO), the last common enzyme of heme and chlorophyll biosynthesis, catalyses the oxidation of protoporphyrinogen IX to protoporphyrin IX, with FAD as cofactor. Among PPO, Bacillus subtilis PPO (bsPPO) is unique because of its broad substrate specificity
Hazel R Corradi et al.
The Journal of biological chemistry, 281(50), 38625-38633 (2006-10-19)
Protoporphyrinogen IX oxidase, a monotopic membrane protein, which catalyzes the oxidation of protoporphyrinogen IX to protoporphyrin IX in the heme/chlorophyll biosynthetic pathway, is distributed widely throughout nature. Here we present the structure of protoporphyrinogen IX oxidase from Myxococcus xanthus, an
T A Ezhova et al.
Izvestiia Akademii nauk. Seriia biologicheskaia, (5)(5), 533-543 (2005-06-02)
Selective systems for screening Arabidopsis thaliana (L.) Heynh. mutants with altered sensitivity to the oxidative stress (OS) inductors norflurazon (NF), acifluorfen (AF), and plumbagin (PB) were developed and a collection of 28 mutants was obtained. Dwarf and necrotic forms predominated
Nina Cedergreen et al.
Environmental toxicology and chemistry, 24(12), 3166-3172 (2006-02-01)
During the past two decades, the phenomenon of hormesis has gained increased recognition. To promote research in hormesis, a sound statistical quantification of important parameters, such as the level and significance of the increase in response and the range of
Andreas Richter et al.
Plant & cell physiology, 51(5), 670-681 (2010-04-09)
In photosynthetic organisms chlorophyll and heme biosynthesis is tightly regulated at various levels in response to environmental adaptation and plant development. The formation of 5-aminolevulinic acid (ALA) is the key regulatory step and provides adequate amounts of the common precursor
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