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46426

Supelco

S-Hydroprene

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C17H30O2
Número de CAS:
65733-18-8
Peso molecular:
266.42
Beilstein/REAXYS Number:
5255711
MDL number:
MFCD03095706
UNSPSC Code:
41116107
PubChem Substance ID:
329757176
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)\C=C(C)\C=C\C[C@@H](C)CCCC(C)C

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

InChI key

FYQGBXGJFWXIPP-OJROSNHMSA-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.

Recommended products

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_germany

WGK 2

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCL2331
BCCC8922
BCBW5576
SZB9168XV
SZE9168X

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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
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
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
Said A M Mazyad et al.
Journal of the Egyptian Society of Parasitology, 36(3), 1101-1114 (2006-12-13)
Two insect growth regulators, Methorprene and Hydroprene were evaluated as growth hormones on the common house dust mite; Dermatophagoides farinae. The adults and immature stages were treated with 4 concentrations of each regulator as contact and as diet. The data
Yuichiro Suzuki et al.
Development (Cambridge, England), 135(3), 569-577 (2008-01-04)
The evolution of complete metamorphosis in insects is a key innovation that has led to the successful diversification of holometabolous insects, yet the origin of the pupa remains an enigma. Here, we analyzed the expression of the pupal specifier gene
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