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Merck

45511

Supelco

Fluridon

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C19H14F3NO
CAS-Nummer:
Molekulargewicht:
329.32
Beilstein:
1547990
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

CN1C=C(c2ccccc2)C(=O)C(=C1)c3cccc(c3)C(F)(F)F

InChI

1S/C19H14F3NO/c1-23-11-16(13-6-3-2-4-7-13)18(24)17(12-23)14-8-5-9-15(10-14)19(20,21)22/h2-12H,1H3

InChIKey

YWBVHLJPRPCRSD-UHFFFAOYSA-N

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Anwendung

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

Rechtliche Hinweise

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

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Acute Tox. 3 Dermal - Aquatic Chronic 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves


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Analysenzertifikate (COA)

Lot/Batch Number

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Woong Han et al.
BMB reports, 43(12), 813-817 (2010-12-30)
Plants undergo cell division throughout their life in order to maintain their growth. It is well known that root and shoot tip of plants possess meristems, which contain quiescent cells. Fluridone (1-methyl-3-phenyl-5-(3-trifluoromethyl (phenyl))-4-(1H)-pyridinone) is an established inhibitor of both ABA
Amanda Rasmussen et al.
Plant signaling & behavior, 7(6), 694-697 (2012-05-15)
Roots that form from non-root tissues (adventitious roots) are crucial for cutting propagation in the forestry and horticulture industries. Strigolactone has been demonstrated to be an important regulator of these roots in both Arabidopsis and pea using strigolactone deficient mutants
Xue-Yi Qiao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 32(18), 1848-1850 (2007-12-07)
To study the effect of fluridone concentration, stimulating period, temperature and salt on the seed germination of three species of Cistanche. The seeds were cultured in Petri dish, and the germination percentage was counted. The highest germination percentage was observed
Hanma Zhang et al.
The Plant journal : for cell and molecular biology, 64(5), 764-774 (2010-11-26)
It is well known that abscisic acid (ABA) can halt meristems for long periods without loss of meristem function, and can also promote root growth at low concentrations, but the mechanisms underlying such regulation are largely unknown. Here we show
Sandra A Yi et al.
Ecotoxicology (London, England), 20(1), 81-87 (2010-10-28)
The acute toxicities for technical grade fluridone (Sonar™) and the commercial formulation of fluridone (Sonar®AS) were assessed for male water mites (Hydrachnidiae: Arrenurus: Megaluracarus). Signs of toxicity were evaluated by detection of locomotor dysfunction or death after exposure to concentrations

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