Skip to Content
Merck
CN

224715

trans-3-Hexen-1-ol

97%

Synonym(s):

trans-3-Hexenol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C2H5CH=CHCH2CH2OH
CAS Number:
928-97-2
Molecular Weight:
100.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853452
EC Number:
213-193-3
Beilstein/REAXYS Number:
1719713
MDL number:
MFCD00002960
Assay:
97%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

trans-3-Hexen-1-ol, 97%

InChI key

UFLHIIWVXFIJGU-ONEGZZNKSA-N

InChI

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

SMILES string

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

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

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
02016BX
12517AQ
10919PQ
08404HZ
04803TQ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Krista L Ryall et al.
Environmental entomology, 41(3), 648-656 (2012-06-27)
Attraction of emerald ash borer, Agrilus planipennis Fairmaire, to a volatile pheromone was demonstrated in three field experiments using baited green sticky traps. A dose-response curve was generated for male A. planipennis to increasing release rates of (3Z)-dodecen-12-olide ((3Z)-lactone) in
Tsviya Olender et al.
Chemical senses, 37(7), 581-584 (2012-06-15)
Considerable evidence supports the idea that odorant recognition depends on specific sequence variations in olfactory receptor (OR) proteins. Much of this emerges from in vitro screens in heterogenous expression systems. However, the ultimate proof should arise from measurements of odorant
Gary G Grant et al.
Journal of economic entomology, 104(1), 173-179 (2011-03-17)
We conducted trapping experiments for the emerald ash borer, Agrilus planipennis Fairmaire (Coleoptera: Buprestidae) in Michigan, U.S.A., and Ontario, Canada, to compare unbaited light green sticky prism traps with traps baited with phoebe oil, (Z)-3-hexenol (Z3-6:OH), or blends of other
Y Nikaido et al.
Behavioural brain research, 199(2), 241-246 (2008-12-24)
Although various emotional behaviors and activation of the hypothalamic-pituitary-adrenal (HPA) axis of rats are induced by the exposure of 2,5-dihydro-2,4,5-trimethylthiazoline: TMT, a component of fox odor, these odor-induced responses are influenced by the external environment. Our previous study demonstrated that
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service