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31635

Supelco

Fenazaquin

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C20H22N2O
Número de CAS:
120928-09-8
Peso molecular:
306.40
Beilstein/REAXYS Number:
8331263
EC Number:
410-580-0
MDL number:
MFCD01656049
UNSPSC Code:
41116107
PubChem Substance ID:
329753856
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

CC(C)(C)c1ccc(CCOc2ncnc3ccccc23)cc1

InChI

1S/C20H22N2O/c1-20(2,3)16-10-8-15(9-11-16)12-13-23-19-17-6-4-5-7-18(17)21-14-22-19/h4-11,14H,12-13H2,1-3H3

Inchi Key

DMYHGDXADUDKCQ-UHFFFAOYSA-N

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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.

Legal Information

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

wgk_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ4617
BCCC0050
BCBZ3317
BCBV6671
BCBR9360V

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Regulatory implications of peroxisome proliferation: an industrial perspective.
W T Stott
Annals of the New York Academy of Sciences, 804, 641-648 (1996-12-27)
Jayati Bhattacharyya et al.
Journal of agricultural and food chemistry, 51(14), 4013-4016 (2003-06-26)
Fenazaquin (I) is a new acaricide of the quinazoline class. The photodecomposition of I was studied in aqueous methanolic and 2-propanolic solution under UV light (30 h) and sunlight (70 h) separately. The photolytic half-lives in aqueous methanolic solution were
Anil Duhan et al.
Bulletin of environmental contamination and toxicology, 87(2), 180-183 (2011-06-15)
Degradation of fenazaquin in sandy loam soil was investigated under field and laboratory conditions. Fenazaquin (Magister 10EC) was applied @ 125 and 250 g a.i./ha in field and in pot under field capacity moisture in laboratory. Samples drawn periodically were analyzed
J C Rowlands et al.
Pharmacology & toxicology, 83(5), 214-219 (1998-12-03)
Rotenone is the classical inhibitor of NADH: ubiquinone oxidoreductase and its analogue deguelin is a potent inhibitor of 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced ornithine decarboxylase mRNA steady state level and enzyme activity in mouse 308 cells (Gerhäuser et al. 1995). In MCF-7
S M Boss et al.
Laboratory animal science, 44(1), 31-37 (1994-02-01)
As part of an 18-month carcinogenicity study, 680 Syrian hamsters (Mesocricetus auratus) received daily gavage doses of fenazaquin, an experimental miticide. Mortality associated with severe enteritis was noticed beginning when the hamsters were 4 months old and ranged from one
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