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31635

Supelco

Fenazaquin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C20H22N2O
CAS Number:
Molecular Weight:
306.40
Beilstein:
8331263
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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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
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)
Houneïda Benbouzid et al.
Communications in agricultural and applied biological sciences, 74(1), 129-135 (2009-01-01)
Our biodiversity has long been preserved, but the main constituents of our environment have been particularly affected by the addition of molecules resulting from agricultural and industrial activities. It is well accepted that these changes may stress some species, making
Metabolism of fenazaquin, an acaricide in tea plant.
J Bhattacharyya et al.
Bulletin of environmental contamination and toxicology, 75(3), 569-573 (2006-01-03)

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