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224715

Sigma-Aldrich

trans-3-Hexen-1-ol

97%

Sinónimos:

trans-3-Hexenol

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About This Item

Fórmula lineal:
C2H5CH=CHCH2CH2OH
Número de CAS:
928-97-2
Peso molecular:
100.16
Beilstein/REAXYS Number:
1719713
EC Number:
213-193-3
MDL number:
MFCD00002960
UNSPSC Code:
12352100
PubChem Substance ID:
24853452
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.439 (lit.)

bp

61-62 °C/12 mmHg (lit.)

density

0.817 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

[H]\C(CC)=C(\[H])CCO

InChI

1S/C6H12O/c1-2-3-4-5-6-7/h3-4,7H,2,5-6H2,1H3/b4-3+

InChI key

UFLHIIWVXFIJGU-ONEGZZNKSA-N

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General description

trans-3-Hexen-1-ol (trans 3-Hexenol) stimulates the antennae of male H. cunea moths.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

hcodes

H226,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
02016BX
00310BQ
00104TQ
12517AQ
10919PQ

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Rui Tang et al.
PloS one, 7(11), e49256-e49256 (2012-11-21)
Volatile organic compounds (VOCs) were collected from damaged and intact mulberry leaves (Morus alba L., Moraceae) and from Hyphantria cunea larvae by headspace absorption with Super Q columns. We identified their constituents using gas chromatography-mass spectrometry, and evaluated the responses
Damon J Crook et al.
Journal of economic entomology, 105(2), 429-437 (2012-05-23)
Field trapping assays were conducted in 2009 and 2010 throughout western Michigan, to evaluate lures for adult emerald ash borer, A. planipennis Fairmaire (Coleoptera: Buprestidae). Several ash tree volatiles were tested on purple prism traps in 2009, and a dark
Shigehiro Namiki et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 194(5), 501-515 (2008-04-05)
Pheromone-source orientation behavior can be modified by coexisting plant volatiles. Some host plant volatiles enhance the pheromonal responses of olfactory receptor neurons and increase the sensitivity of orientation behavior in the Lepidoptera species. Although many electrophysiological studies have focused on
Andre F Cruz et al.
Phytochemistry, 78, 72-80 (2012-04-24)
Fusarium diseases cause major economic losses in wheat-based crop rotations. Volatile organic compounds (VOC) in wheat and rotation crops, such as chickpea, may negatively impact pathogenic Fusarium. Using the headspace GC-MS method, 16 VOC were found in greenhouse-grown wheat leaves:
Peter de Groot et al.
Journal of chemical ecology, 34(9), 1170-1179 (2008-07-05)
Green leaf volatiles (GLVs) function as host attractants, pheromone synergists, or sexual kairomones for a number of coleopteran folivores. Hence, we focused on host GLVs to determine if they were attractive to adults of the emerald ash borer, Agrilus planipennis
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