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Supelco

Fenoxycarb

PESTANAL®, analytical standard

Synonym(s):

Ethyl 2-(4-phenoxyphenoxy)ethylcarbamate

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About This Item

Empirical Formula (Hill Notation):
C17H19NO4
CAS Number:
72490-01-8
Molecular Weight:
301.34
Beilstein:
6932817
EC Number:
276-696-7
MDL number:
MFCD00144303
UNSPSC Code:
41116107
PubChem Substance ID:
329754956
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

CCOC(=O)NCCOc1ccc(Oc2ccccc2)cc1

InChI

1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)

InChI key

HJUFTIJOISQSKQ-UHFFFAOYSA-N

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General description

Fenoxycarb is a neurotoxic carbamate, insect growth regulator or public health insecticide, which can exhibit potent insect juvenile hormone-mimic activity, which causes disturbance in the development, reproduction and behaviour of insects. It can be used to control a wide variety of insect pests, basically in agriculture, forestry, and stored products.

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

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H351,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class Code

11 - Combustible Solids

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)

Lot/Batch Number
BCCK5935
BCCG3127
BCBT7968
SZBC157XV
SZBC048XV

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Scientific reports, 7(1), 13521-13521 (2017-11-04)
Sexually dimorphic traits are common and widespread among animals. The expression of the Doublesex-/Mab-3-domain (DM-domain) gene family has been widely studied in model organisms and has been proven to be essential for the development and maintenance of sex-specific traits. However
Synthesis of haptens and protein conjugates for the development of immunoassays for the insect growth regulator fenoxycarb
Szurdoki F, et al.
Journal of Agricultural and Food Chemistry, 50, 29-40 (2002)
R Bober et al.
Insect molecular biology, 19(1), 77-86 (2009-12-17)
Sex pheromone production in Helicoverpa armigera is regulated by pheromone-biosynthesis-activating neuropeptide (PBAN), which binds to a G-protein coupled receptor at the pheromone gland. We demonstrate the temporal differential expression levels of the PBAN receptor (PBAN-R) gene, reaching peak levels at
David Jarriault et al.
Hormones and behavior, 56(1), 185-191 (2009-05-05)
Male moths use sex pheromones to find their mating partners. In the moth, Agrotis ipsilon, the behavioral response and the neuron sensitivity within the primary olfactory centre, the antennal lobe (AL), to sex pheromone increase with age and juvenile hormone
Takeru Matsumoto et al.
Chemosphere, 72(3), 451-456 (2008-04-02)
It was reported that males daphnid Daphnia magna that have been induced by methyl farnesoate exposure exhibit higher tolerance to chemical compounds such as potassium dichromate and pentachlorophenol than females. Male neonates are also known to be induced by exposure
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