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Merck

34343

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329754956
EC Number:
276-696-7
Beilstein/REAXYS Number:
6932817
MDL number:
MFCD00144303

Key Documents

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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

SMILES string

CCOC(=O)NCCOc1ccc(Oc2ccccc2)cc1

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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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

signalword

Warning

hcodes

H351,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

34343-1EA: + 34343-250MG: + 34343-BULK: + 34343-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK5935
BCCG3127
BCBT7968

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Quang Dang Nong et al.
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
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
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)
Shigeto Oda et al.
Ecotoxicology and environmental safety, 67(3), 399-405 (2007-02-10)
Acute and reproductive toxicity tests were conducted on seven strains of Daphnia magna from six laboratories in five countries. 3,4-Dichloroaniline (DCA) and fenoxycarb were used as test chemicals. Acute toxicity tests revealed that estimated EC(50) (50% effective concentration) values for
H Jin et al.
Science advances, 5(4), eaav7569-eaav7569 (2019-04-17)
Color patterns often function as camouflage to protect insects from predators. In most swallowtail butterflies, younger larvae mimic bird droppings but change their pattern to mimic their host plants during their final molt. This pattern change is determined during the
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