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Merck
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Documenti fondamentali

46426

Supelco

S-Hydroprene

PESTANAL®, analytical standard

Sinonimo/i:

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

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250 MG
CHF 209.00

CHF 209.00


Spedizione prevista il26 marzo 2025


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Cambia visualizzazione
250 MG
CHF 209.00

About This Item

Formula empirica (notazione di Hill):
C17H30O2
Numero CAS:
Peso molecolare:
266.42
Beilstein:
5255711
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

CHF 209.00


Spedizione prevista il26 marzo 2025


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Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
FYQGBXGJFWXIPP-OJROSNHMSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Prodotti consigliati

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.

Note legali

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

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Pittogrammi

Skull and crossbonesEnvironment

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

No data available

Punto d’infiammabilità (°C)

No data available

Dispositivi di protezione individuale

Eyeshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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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
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
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
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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