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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:
65733-18-8
Molecular Weight:
266.42
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757176
MDL number:
MFCD03095706
Beilstein/REAXYS Number:
5255711

Key Documents

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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

100

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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
GHS06,GHS09

signalword

Danger

hcodes

H331,H410

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCL2331
BCCC8922
BCBW5576

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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
R Rybczynski et al.
Molecular and cellular endocrinology, 141(1-2), 141-151 (1998-09-02)
A rapid increase in ecdysteroid hormone synthesis results when the insect prothoracic gland is stimulated with prothoracicotropic hormone (PTTH), a brain neuropeptide hormone. PTTH also stimulates the specific synthesis of several proteins, one of which is a beta tubulin. To
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
Ivan Hrdý et al.
Pest management science, 62(9), 848-854 (2006-07-13)
The efficacy of juvenile hormone III (JH III) and two JH-mimicking compounds was compared in laboratory experiments with Reticulitermes lucifugus (Rossi), R. santonensis Feytaud and R. virginicus (Banks). Induction of presoldier, soldier and/or soldier-worker intercaste differentiation was taken as positive
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