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Merck
CN

45511

氟啶草酮

PESTANAL®, analytical standard

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关于此项目

经验公式（希尔记法）:
C19H14F3NO
化学文摘社编号:
59756-60-4
分子量:
329.32
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756798
EC Number:
261-916-6
Beilstein/REAXYS Number:
1547990
MDL number:
MFCD00078682

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产品名称

氟啶草酮, PESTANAL®, analytical standard

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

InChI key

YWBVHLJPRPCRSD-UHFFFAOYSA-N

SMILES string

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

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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相关类别

Application

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Legal Information

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

hcodes

H311,H411

Hazard Classifications

Acute Tox. 3 Dermal - Aquatic Chronic 2

存储类别

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

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves

法规信息

农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCG6207
BCCG4566
BCCC5888
BCBS8623V

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What is the IUPAC name for Product 45511, Fluridon?

    The IUPC name for Product 45511, Fluridon is 4(1H)-Pyridinone, 1-methyl-3-phenyl-5-[3-(trifluoromethyl)phenyl or 1-Methyl-3-phenyl-5-[3-(trifluoromethyl)phenyl]-4(1H)-pyridinone.

  6. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

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
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
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
Kamrun Nahar et al.
The New phytologist, 196(3), 901-913 (2012-09-19)
Studies involving plant-nematode interactions provide an opportunity to unravel plant defense signaling in root tissues. In this study, we have characterized the roles of salicylate (SA), jasmonate (JA), ethylene (ET) and abscisic acid (ABA) in plant defense against the migratory
Lina Sun et al.
Plant cell reports, 31(1), 179-185 (2011-09-29)
Exposure to ozone induced a rapid increase in the levels of the sesquiterpene phytohormone abscisic acid (ABA) and the isoflavone puerarin in suspension cell cultures of Pueraria thomsnii Benth. The observed increases in ABA and puerarin were dependent on the
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