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Merck

46426

Supelco

S-Hydroprene

PESTANAL®, analytical standard

Sinónimos:

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

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250 MG
MXP 4,011.00

MXP 4,011.00


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250 MG
MXP 4,011.00

About This Item

Fórmula empírica (notación de Hill):
C17H30O2
Número de CAS:
Peso molecular:
266.42
Beilstein:
5255711
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

MXP 4,011.00


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grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

Formato

neat

cadena SMILES

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

Clave InChI

FYQGBXGJFWXIPP-OJROSNHMSA-N

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Aplicación

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

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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.

Información legal

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

Pictogramas

Skull and crossbonesEnvironment

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

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

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

No data available

Punto de inflamabilidad (°C)

No data available

Equipo de protección personal

Eyeshields, Gloves


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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
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
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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