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Merck

O5284

Sigma-Aldrich

1-Octen-3-ol

98%

Synonym(e):

Pentyl-vinylcarbinol

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About This Item

Lineare Formel:
CH3(CH2)4CH(OH)CH=CH2
CAS-Nummer:
Molekulargewicht:
128.21
Beilstein:
1744110
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

98%

Brechungsindex

n20/D 1.437 (lit.)

bp

84-85 °C/25 mmHg (lit.)

Dichte

0.837 g/mL at 20 °C
0.83 g/mL at 25 °C (lit.)

SMILES String

CCCCCC(O)C=C

InChI

1S/C8H16O/c1-3-5-6-7-8(9)4-2/h4,8-9H,2-3,5-7H2,1H3

InChIKey

VSMOENVRRABVKN-UHFFFAOYSA-N

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Piktogramme

Skull and crossbones

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Skin Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

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

WGK

WGK 2

Flammpunkt (°F)

154.4 °F - closed cup

Flammpunkt (°C)

68 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Associative learning has been shown in a variety of insects, including the mosquitoes Culex quinquefasciatus and Anopheles gambiae. This study demonstrates associative learning for the first time in Aedes aegypti, an important vector of dengue, yellow fever and chikungunya viruses.
J I Cook et al.
Bulletin of entomological research, 101(5), 541-550 (2011-07-07)
1-Octen-3-ol is a kairomone for many haematophagous insects including mosquitoes. Numerous studies have examined the effects of racemic 1-octen-3-ol; however, few studies have investigated the role of individual enantiomers in relation to mosquito attraction. In the present study, we investigated
L E Harrup et al.
Journal of medical entomology, 49(1), 112-121 (2012-02-09)
The host kairomones carbon dioxide (CO2) and 1-octen-3-ol elicit a host seeking response in a wide range of haematophagous Diptera. This study investigates the response of Culicoides biting midges (Diptera: Ceratopogonidae) to these cues using field-based experiments at two sites

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