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Merck
CN

46426

S-Hydroprene

PESTANAL®, analytical standard

Synonym(s):

Ethyl 3,7,11-trimethyl-2,4-dodecadienoate

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About This Item

Empirical Formula (Hill Notation):
C17H30O2
CAS Number:
Molecular Weight:
266.42
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5255711
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Product Name

S-Hydroprene, PESTANAL®, analytical standard

InChI

1S/C17H30O2/c1-6-19-17(18)13-16(5)12-8-11-15(4)10-7-9-14(2)3/h8,12-15H,6-7,9-11H2,1-5H3/b12-8+,16-13+/t15-/m0/s1

SMILES string

CCOC(=O)\C=C(C)\C=C\C[C@@H](C)CCCC(C)C

InChI key

FYQGBXGJFWXIPP-OJROSNHMSA-N

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

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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.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Skull and crossbonesEnvironment

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 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

WGK 2

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves

Regulatory Information

农药列管产品
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Chloe Hawkings et al.
PloS one, 14(5), e0216800-e0216800 (2019-05-21)
The reproductive ground plan hypothesis proposes that gene networks regulating foraging behavior and reproductive female physiology in social insects emerged from ancestral gene and endocrine factor networks. Expression of storage proteins such as vitellogenins and hexamerins is an example of
A S Downing et al.
Journal of medical entomology, 30(3), 531-536 (1993-05-01)
Insect growth regulators are synthetic chemicals that mimic the function of hormones that occur naturally in arthropods. Two such insect growth regulators, methoprene and hydroprene, were tested to determine effects on growth of laboratory populations of the American house dust
S Mohandass et al.
Journal of economic entomology, 99(4), 1509-1519 (2006-08-30)
Wandering phase Indianmeal moth, Plodia interpunctella (Hübner), larvae were exposed to the label rate of hydroprene (1.9 x 10(-3) mg [AI] /cm2) sprayed on concreted petri dishes. Larvae were exposed for 1, 3, 6, 12, 18, 24, and 30 h
S M Mohandass et al.
Journal of economic entomology, 99(3), 1007-1016 (2006-07-04)
Eggs of the Indianmeal moth, Plodia interpunctella (Hübner), were exposed to the labeled rate of hydroprene (1.9 x 10(-3) mg [AI]/cm2) sprayed on concreted petri dishes. These eggs were exposed for 1, 3, 6, 12, and 18 h and until
Lars Skattebøl et al.
Pest management science, 62(7), 610-616 (2006-05-18)
Analogues of insect juvenile hormones (juvenoids) have been tested for settling inhibition of cyprids from three species of barnacle, Balanus balanoides (L.), Balanus improvisus Darwin and Balanus amphitrite Darwin. Some 3-alkoxypyridine derivatives exhibited strong activity at mg litre(-1) concentrations; 3,7-dimethyloctyl

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