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W435600

Sigma-Aldrich

trans-3-Hexen-1-ol

≥95%, stabilized

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Synonym(s):
trans-3-Hexenol
Linear Formula:
C2H5CH=CHCH2CH2OH
CAS Number:
Molecular Weight:
100.16
FEMA Number:
4356
Beilstein:
1719713
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.21

biological source

synthetic

grade

Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009

Assay

≥95%

contains

alpha-tocopherol, synthetic as stabilizer

refractive index

n20/D 1.439 (lit.)

bp

61-62 °C/12 mmHg (lit.)

density

0.817 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

green

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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1 of 4

This Item
W256218W368903W256102
trans-3-Hexen-1-ol ≥95%, stabilized

Sigma-Aldrich

W435600

trans-3-Hexen-1-ol

trans-2-Hexen-1-ol ≥95%, FCC, FG

Sigma-Aldrich

W256218

trans-2-Hexen-1-ol

grade

Fragrance grade, Halal, Kosher

grade

FG, Halal, Kosher

grade

FG, Fragrance grade, Halal, Kosher

grade

Fragrance grade, Halal, Kosher

agency

follows IFRA guidelines

agency

-

agency

follows IFRA guidelines

agency

follows IFRA guidelines

assay

≥95%

assay

≥95%

assay

≥95%

assay

-

refractive index

n20/D 1.439 (lit.)

refractive index

n20/D 1.438 (lit.)

refractive index

n20/D 1.452 (lit.)

refractive index

n20/D 1.44

bp

61-62 °C/12 mmHg (lit.)

bp

158-160 °C (lit.)

bp

60 °C/0.5 mmHg (lit.)

bp

20 °C/0.2 mmHg

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

138.2 °F - closed cup

Flash Point(C)

59 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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:
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
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
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
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

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