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W256102

Sigma-Aldrich

cis-3-Hexenal solution

50% in triacetin, stabilized

Synonym(s):

(Z)-3-hexenal solution

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About This Item

Linear Formula:
CH3CH2CH2CH=CHCHO
CAS Number:
6789-80-6
Molecular Weight:
98.14
FEMA Number:
2561
Council of Europe no.:
2008
MDL number:
MFCD00065446
UNSPSC Code:
12164502
PubChem Substance ID:
24901150
Flavis number:
5.075
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
FDA 21 CFR 117

contains

α-tocopherol as stabilizer (synthetic)

concentration

50% in triacetin

refractive index

n20/D 1.44

bp

20 °C/0.2 mmHg

density

0.982 g/mL at 25 °C

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

apple; fatty; green; fruity

storage temp.

2-8°C

SMILES string

CC\C=C/CC=O

InChI

1S/C6H10O/c1-2-3-4-5-6-7/h3-4,6H,2,5H2,1H3/b4-3-

InChI key

GXANMBISFKBPEX-ARJAWSKDSA-N

Related Categories

Application

cis-3-Hexenal solution may be used as a standard to identify and quantify the volatile organic compounds emitted by wounded plants using chemical-ionization mass spectrometry.

Disclaimer

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

96.0 °F

Flash Point(C)

35.55 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tristan M Cofer et al.
Plant, cell & environment, 41(7), 1673-1682 (2018-03-31)
Although considerable evidence has accumulated on the defensive activity of plant volatile organic compounds against pathogens and insect herbivores, less is known about the significance of volatile organic compounds emitted by plants under abiotic stress. Here, we report that green
Georg E von Mérey et al.
Frontiers in plant science, 4, 209-209 (2013-07-05)
Plants under herbivore attack emit volatile organic compounds (VOCs) that can serve as foraging cues for natural enemies. Adult females of Lepidoptera, when foraging for host plants to deposit eggs, are commonly repelled by herbivore-induced VOCs, probably to avoid competition
Marie Engelberth et al.
Plants (Basel, Switzerland), 8(6) (2019-06-20)
Green leaf volatiles (GLVs), which have mostly been described as providers of protection against insect herbivory and necrotrophic pathogen infections, were recently shown to provide significant fortification against cold stress damage. It was further demonstrated that cold-damaged maize seedlings released
Negative-ion CIMS: analysis of volatile leaf wound compounds including HCN.
Custer TG, et al.
International Journal of Mass Spectrometry, 223, 427-446 (2003)
Tatyana Savchenko et al.
Planta, 245(6), 1179-1192 (2017-03-18)
This study describes a new role for hydroperoxide lyase branch of oxylipin biosynthesis pathway in protecting photosynthetic apparatus under high light conditions. Lipid-derived signaling molecules, oxylipins, produced by a multi-branch pathway are central in regulation of a wide range of
View All Related Papers

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